| Year |
Citation |
Score |
| Low-probability matches (unlikely to be authored by this person) |
| 2024 |
Orrú CD, Groveman BR, Hughson AG, Barrio T, Isiofia K, Race B, Ferreira NC, Gambetti P, Schneider DA, Masujin K, Miyazawa K, Ghetti B, Zanusso G, Caughey B. Sensitive detection of pathological seeds of α-synuclein, tau and prion protein on solid surfaces. Plos Pathogens. 20: e1012175. PMID 38640117 DOI: 10.1371/journal.ppat.1012175 |
0.01 |
|
| 2024 |
Horne RI, Andrzejewska EA, Alam P, Brotzakis ZF, Srivastava A, Aubert A, Nowinska M, Gregory RC, Staats R, Possenti A, Chia S, Sormanni P, Ghetti B, Caughey B, Knowles TPJ, et al. Discovery of potent inhibitors of α-synuclein aggregation using structure-based iterative learning. Nature Chemical Biology. PMID 38632492 DOI: 10.1038/s41589-024-01580-x |
0.01 |
|
| 2024 |
Valentino RR, Scotton WJ, Roemer SF, Lashley T, Heckman MG, Shoai M, Martinez-Carrasco A, Tamvaka N, Walton RL, Baker MC, Macpherson HL, Real R, Soto-Beasley AI, Mok K, Revesz T, ... ... Ghetti B, et al. MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association study. The Lancet. Neurology. 23: 487-499. PMID 38631765 DOI: 10.1016/S1474-4422(24)00083-8 |
0.01 |
|
| 2024 |
Fernandez A, Hoq MR, Hallinan GI, Li D, Bharath SR, Vago FS, Zhang X, Ozcan KA, Newell KL, Garringer HJ, Jiang W, Ghetti B, Vidal R. Cryo-EM structures of amyloid-β and tau filaments in Down syndrome. Nature Structural & Molecular Biology. PMID 38553642 DOI: 10.1038/s41594-024-01252-3 |
0.01 |
|
| 2024 |
Klingstedt T, Lantz L, Shirani H, Ge J, Hanrieder J, Vidal R, Ghetti B, Nilsson KPR. Thiophene-Based Ligands for Specific Assignment of Distinct Aβ Pathologies in Alzheimer's Disease. Acs Chemical Neuroscience. 15: 1581-1595. PMID 38523263 DOI: 10.1021/acschemneuro.4c00021 |
0.01 |
|
| 2024 |
Wang H, Chang TS, Dombroski BA, Cheng PL, Si YQ, Tucci A, Patil V, Valiente-Banuet L, Farrell K, Mclean C, Molina-Porcel L, Alex R, Paul De Deyn P, Le Bastard N, Gearing M, ... ... Ghetti BF, et al. Association of Structural Forms of 17q21.31 with the Risk of Progressive Supranuclear Palsy and Sub-haplotypes. Medrxiv : the Preprint Server For Health Sciences. PMID 38464214 DOI: 10.1101/2024.02.26.24303379 |
0.01 |
|
| 2024 |
Joseph-Mathurin N, Feldman RL, Lu R, Shirzadi Z, Toomer C, Saint Clair JR, Ma Y, McKay NS, Strain JF, Kilgore C, Friedrichsen KA, Chen CD, Gordon BA, Chen G, Hornbeck RC, ... ... Ghetti B, et al. Presenilin-1 mutation position influences amyloidosis, small vessel disease, and dementia with disease stage. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 38380882 DOI: 10.1002/alz.13729 |
0.01 |
|
| 2023 |
Björk L, Shirani H, Todarwal Y, Linares M, Vidal R, Ghetti B, Norman P, Klingstedt T, Nilsson KPR. Distinct Heterocyclic Moieties Govern the Selectivity of Thiophene-Vinylene-Based Ligands Towards Aβ or Tau Pathology in Alzheime's Disease. European Journal of Organic Chemistry. 26. PMID 38585413 DOI: 10.1002/ejoc.202300583 |
0.01 |
|
| 2023 |
Wang H, Chang TS, Dombroski BA, Cheng PL, Patil V, Valiente-Banuet L, Farrell K, Mclean C, Molina-Porcel L, Rajput A, Paul De Deyn P, Le Bastard N, Gearing M, Donker Kaat L, Van Swieten JC, ... ... Ghetti BF, et al. Whole-Genome Sequencing Analysis Reveals New Susceptibility Loci and Structural Variants Associated with Progressive Supranuclear Palsy. Medrxiv : the Preprint Server For Health Sciences. PMID 38234807 DOI: 10.1101/2023.12.28.23300612 |
0.01 |
|
| 2023 |
Tetter S, Arseni D, Murzin AG, Buhidma Y, Peak-Chew SY, Garringer HJ, Newell KL, Vidal R, Apostolova LG, Lashley T, Ghetti B, Ryskeldi-Falcon B. TAF15 amyloid filaments in frontotemporal lobar degeneration. Nature. PMID 38057661 DOI: 10.1038/s41586-023-06801-2 |
0.01 |
|
| 2023 |
Yang Y, Murzin AG, Peak-Chew S, Franco C, Garringer HJ, Newell KL, Ghetti B, Goedert M, Scheres SHW. Cryo-EM structures of Aβ40 filaments from the leptomeninges of individuals with Alzheimer's disease and cerebral amyloid angiopathy. Acta Neuropathologica Communications. 11: 191. PMID 38049918 DOI: 10.1186/s40478-023-01694-8 |
0.01 |
|
| 2023 |
Cracco L, Cali I, Cohen ML, Aslam R, Notari S, Kong Q, Newell KL, Ghetti B, Appleby BS, Gambetti P. Efficient transmission of human prion diseases to a glycan-free prion protein-expressing host. Brain : a Journal of Neurology. PMID 38000783 DOI: 10.1093/brain/awad399 |
0.01 |
|
| 2023 |
Fontana E, Bongianni M, Benussi A, Bronzato E, Scialo C, Sacchetto L, Cagnin A, Castriciano S, Buratti E, Gardoni F, Italia M, Schreiber A, Ferracin C, Fiorini M, Newell KL, ... ... Ghetti B, et al. Detection of TDP-43 seeding activity in the olfactory mucosa from patients with frontotemporal dementia. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 37908186 DOI: 10.1002/alz.13541 |
0.01 |
|
| 2023 |
Touroutoglou A, Katsumi Y, Brickhouse M, Zaitsev A, Eckbo R, Aisen P, Beckett L, Dage JL, Eloyan A, Foroud T, Ghetti B, Griffin P, Hammers D, Jack CR, Kramer JH, et al. The Sporadic Early-onset Alzheimer's Disease Signature Of Atrophy: Preliminary Findings From The Longitudinal Early-onset Alzheimer's Disease Study (LEADS) Cohort. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 37850549 DOI: 10.1002/alz.13466 |
0.01 |
|
| 2023 |
Rajewski BH, Makwana KM, Angera IJ, Geremia DK, Zepeda AR, Hallinan GI, Vidal R, Ghetti B, Serrano AL, Del Valle JR. β-Bracelets: Macrocyclic Cross-β Epitope Mimics Based on a Tau Conformational Strain. Journal of the American Chemical Society. 145: 23131-23142. PMID 37844142 DOI: 10.1021/jacs.3c06830 |
0.01 |
|
| 2023 |
Sepulveda-Falla D, Villegas Lanau CA, White C, Serrano GE, Acosta-Uribe J, Mejía-Cupajita B, Villalba-Moreno ND, Lu P, Glatzel M, Kofler JK, Ghetti B, Frosch MP, Lopera Restrepo F, Kosik KS, Beach TG. Comorbidities in Early-Onset Sporadic versus Presenilin-1 Mutation-Associated Alzheimer's Disease Dementia: Evidence for Dependency on Alzheimer's Disease Neuropathological Changes. Medrxiv : the Preprint Server For Health Sciences. PMID 37646002 DOI: 10.1101/2023.08.14.23294081 |
0.01 |
|
| 2023 |
Arseni D, Chen R, Murzin AG, Peak-Chew SY, Garringer HJ, Newell KL, Kametani F, Robinson AC, Vidal R, Ghetti B, Hasegawa M, Ryskeldi-Falcon B. TDP-43 forms amyloid filaments with a distinct fold in type A FTLD-TDP. Nature. PMID 37532939 DOI: 10.1038/s41586-023-06405-w |
0.01 |
|
| 2023 |
Eloyan A, Thangarajah M, An N, Borowski BJ, Reddy AL, Aisen P, Dage JL, Foroud T, Ghetti B, Griffin P, Hammers D, Iaccarino L, Jack CR, Kirby K, Kramer J, et al. White matter hyperintensities are higher among early-onset Alzheimer's disease participants than their cognitively normal and early-onset nonAD peers: Longitudinal Early-onset Alzheimer's Disease Study (LEADS). Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 37491599 DOI: 10.1002/alz.13402 |
0.01 |
|
| 2023 |
Rajabli F, Benchek P, Tosto G, Kushch N, Sha J, Bazemore K, Zhu C, Lee WP, Haut J, Hamilton-Nelson KL, Wheeler NR, Zhao Y, Farrell JJ, Grunin MA, Leung YY, ... ... Ghetti B, et al. Multi-ancestry genome-wide meta-analysis of 56,241 individuals identifies and nominates ancestry-specific loci , , and as novel risk loci for Alzheimer's disease: the Alzheimer's Disease Genetics Consortium. Medrxiv : the Preprint Server For Health Sciences. PMID 37461624 DOI: 10.1101/2023.07.06.23292311 |
0.01 |
|
| 2023 |
McKay NS, Gordon BA, Hornbeck RC, Dincer A, Flores S, Keefe SJ, Joseph-Mathurin N, Jack CR, Koeppe R, Millar PR, Ances BM, Chen CD, Daniels A, Hobbs DA, Jackson K, ... ... Ghetti B, et al. Positron emission tomography and magnetic resonance imaging methods and datasets within the Dominantly Inherited Alzheimer Network (DIAN). Nature Neuroscience. PMID 37429916 DOI: 10.1038/s41593-023-01359-8 |
0.01 |
|
| 2023 |
Kaivola K, Chia R, Ding J, Rasheed M, Fujita M, Menon V, Walton RL, Collins RL, Billingsley K, Brand H, Talkowski M, Zhao X, Dewan R, Stark A, Ray A, ... ... Ghetti B, et al. Genome-wide structural variant analysis identifies risk loci for non-Alzheimer's dementias. Cell Genomics. 3: 100316. PMID 37388914 DOI: 10.1016/j.xgen.2023.100316 |
0.01 |
|
| 2023 |
Schweighauser M, Garringer HJ, Klingstedt T, Nilsson KPR, Masuda-Suzukake M, Murrell JR, Risacher SL, Vidal R, Scheres SHW, Goedert M, Ghetti B, Newell KL. Mutation ∆K281 in MAPT causes Pick's disease. Acta Neuropathologica. 146: 211-226. PMID 37351604 DOI: 10.1007/s00401-023-02598-6 |
0.01 |
|
| 2023 |
Shi Y, Ghetti B, Goedert M, Scheres SHW. Cryo-EM Structures of Chronic Traumatic Encephalopathy Tau Filaments with PET Ligand Flortaucipir. Journal of Molecular Biology. 168025. PMID 37330290 DOI: 10.1016/j.jmb.2023.168025 |
0.01 |
|
| 2023 |
Valentino RR, Scotton WJ, Roemer SF, Lashley T, Heckman MG, Shoai M, Martinez-Carrasco A, Tamvaka N, Walton RL, Baker MC, Macpherson HL, Real R, Soto-Beasley AI, Mok K, Revesz T, ... ... Ghetti B, et al. Creating the Pick's disease International Consortium: Association study of H2 haplotype with risk of Pick's disease. Medrxiv : the Preprint Server For Health Sciences. PMID 37163045 DOI: 10.1101/2023.04.17.23288471 |
0.01 |
|
| 2023 |
Merrihew GE, Park J, Plubell D, Searle BC, Keene CD, Larson EB, Bateman R, Perrin RJ, Chhatwal JP, Farlow MR, McLean CA, Ghetti B, Newell KL, Frosch MP, Montine TJ, et al. A peptide-centric quantitative proteomics dataset for the phenotypic assessment of Alzheimer's disease. Scientific Data. 10: 206. PMID 37059743 DOI: 10.1038/s41597-023-02057-7 |
0.01 |
|
| 2023 |
Hoq MR, Bharath SR, Hallinan GI, Fernandez A, Vago FS, Ozcan KA, Li D, Garringer HJ, Vidal R, Ghetti B, Jiang W. Cross-β helical filaments of Tau and TMEM106B in gray and white matter of multiple system tauopathy with presenile dementia. Acta Neuropathologica. PMID 36952000 DOI: 10.1007/s00401-023-02563-3 |
0.01 |
|
| 2023 |
Yang Y, Garringer HJ, Shi Y, Lövestam S, Peak-Chew S, Zhang X, Kotecha A, Bacioglu M, Koto A, Takao M, Spillantini MG, Ghetti B, Vidal R, Murzin AG, Scheres SHW, et al. New SNCA mutation and structures of α-synuclein filaments from juvenile-onset synucleinopathy. Acta Neuropathologica. PMID 36847833 DOI: 10.1007/s00401-023-02550-8 |
0.01 |
|
| 2023 |
Hoq MR, Bharath SR, Hallinan GI, Fernandez A, Vago FS, Ozcan KA, Li D, Garringer HJ, Vidal R, Ghetti B, Jiang W. Cross-β helical filaments of Tau and TMEM106B in Gray and White Matter of Multiple System Tauopathy with presenile Dementia. Biorxiv : the Preprint Server For Biology. PMID 36711790 DOI: 10.1101/2023.01.09.523314 |
0.01 |
|
| 2023 |
Lantz L, Shirani H, Ghetti B, Vidal R, Klingstedt T, Nilsson P. Thiophene-Based Ligands for Histological Multiplex Spectral Detection of Distinct Protein Aggregates in Alzheimer´s Disease. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 36645413 DOI: 10.1002/chem.202203568 |
0.01 |
|
| 2023 |
Yang Y, Zhang W, Murzin AG, Schweighauser M, Huang M, Lövestam S, Peak-Chew SY, Saito T, Saido TC, Macdonald J, Lavenir I, Ghetti B, Graff C, Kumar A, Nordberg A, et al. Cryo-EM structures of amyloid-β filaments with the Arctic mutation (E22G) from human and mouse brains. Acta Neuropathologica. PMID 36611124 DOI: 10.1007/s00401-022-02533-1 |
0.01 |
|
| 2022 |
Nelson PT, Lee EB, Cykowski MD, Alafuzoff I, Arfanakis K, Attems J, Brayne C, Corrada MM, Dugger BN, Flanagan ME, Ghetti B, Grinberg LT, Grossman M, Grothe MJ, Halliday GM, et al. LATE-NC staging in routine neuropathologic diagnosis: an update. Acta Neuropathologica. PMID 36512061 DOI: 10.1007/s00401-022-02524-2 |
0.01 |
|
| 2022 |
Yang Y, Shi Y, Schweighauser M, Zhang X, Kotecha A, Murzin AG, Garringer HJ, Cullinane PW, Saito Y, Foroud T, Warner TT, Hasegawa K, Vidal R, Murayama S, Revesz T, ... Ghetti B, et al. Structures of α-synuclein filaments from human brains with Lewy pathology. Nature. PMID 36108674 DOI: 10.1038/s41586-022-05319-3 |
0.01 |
|
| 2022 |
Hopfner F, Tietz AK, Ruf VC, Ross OA, Koga S, Dickson D, Aguzzi A, Attems J, Beach T, Beller A, Cheshire WP, van Deerlin V, Desplats P, Deuschl G, Duyckaerts C, ... ... Ghetti B, et al. Common Variants Near ZIC1 and ZIC4 in Autopsy-Confirmed Multiple System Atrophy. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 35997131 DOI: 10.1002/mds.29164 |
0.01 |
|
| 2022 |
Björk L, Bäck M, Lantz L, Ghetti B, Vidal R, Klingstedt T, Nilsson P. Proteophenes - amino acid functionalized thiophene-based fluorescent ligands for visualization of protein deposits in tissue sections with Alzheimer´s disease pathology. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 35950816 DOI: 10.1002/chem.202201557 |
0.01 |
|
| 2022 |
Cracco L, Doud EH, Hallinan GI, Garringer HJ, Jacobsen MH, Richardson RM, Buratti E, Vidal R, Ghetti B, Newell KL. Distinguishing post-translational modifications in dominantly inherited frontotemporal dementias: FTLD-TDP Type A (GRN) vs Type B (C9orf72). Neuropathology and Applied Neurobiology. e12836. PMID 35836354 DOI: 10.1111/nan.12836 |
0.01 |
|
| 2022 |
Hallinan GI, Ozcan KA, Hoq MR, Cracco L, Vago FS, Bharath SR, Li D, Jacobsen M, Doud EH, Mosley AL, Fernandez A, Garringer HJ, Jiang W, Ghetti B, Vidal R. Cryo-EM structures of prion protein filaments from Gerstmann-Sträussler-Scheinker disease. Acta Neuropathologica. PMID 35819518 DOI: 10.1007/s00401-022-02461-0 |
0.01 |
|
| 2022 |
Vöglein J, Franzmeier N, Morris JC, Dieterich M, McDade E, Simons M, Preische O, Hofmann A, Hassenstab J, Benzinger TL, Fagan A, Noble JM, Berman SB, Graff-Radford NR, Ghetti B, et al. Patterns and implications of neurological examination findings in autosomal dominant Alzheimer disease. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 35609137 DOI: 10.1002/alz.12684 |
0.01 |
|
| 2022 |
Morris JC, Weiner M, Xiong C, Beckett L, Coble D, Saito N, Aisen PS, Allegri R, Benzinger TLS, Berman SB, Cairns NJ, Carrillo MC, Chui HC, Chhatwal JP, Cruchaga C, ... ... Ghetti B, et al. Autosomal dominant and sporadic late onset Alzheimer disease share a common in vivo pathophysiology. Brain : a Journal of Neurology. PMID 35580594 DOI: 10.1093/brain/awac181 |
0.01 |
|
| 2022 |
Luckett PH, Chen C, Gordon BA, Wisch J, Berman SB, Chhatwal JP, Cruchaga C, Fagan AM, Farlow MR, Fox NC, Jucker M, Levin J, Masters CL, Mori H, Noble JM, ... ... Ghetti B, et al. Biomarker clustering in autosomal dominant Alzheimer's disease. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 35362200 DOI: 10.1002/alz.12661 |
0.01 |
|
| 2022 |
Schweighauser M, Arseni D, Bacioglu M, Huang M, Lövestam S, Shi Y, Yang Y, Zhang W, Kotecha A, Garringer HJ, Vidal R, Hallinan GI, Newell KL, Tarutani A, Murayama S, ... ... Ghetti B, et al. Age-dependent formation of TMEM106B amyloid filaments in human brains. Nature. PMID 35344985 DOI: 10.1038/s41586-022-04650-z |
0.01 |
|
| 2022 |
Kovacs GG, Ghetti B, Goedert M. Classification of diseases with accumulation of Tau protein. Neuropathology and Applied Neurobiology. e12792. PMID 35064600 DOI: 10.1111/nan.12792 |
0.01 |
|
| 2022 |
Yang Y, Arseni D, Zhang W, Huang M, Lövestam S, Schweighauser M, Kotecha A, Murzin AG, Peak-Chew SY, Macdonald J, Lavenir I, Garringer HJ, Gelpi E, Newell KL, Kovacs GG, ... ... Ghetti B, et al. Cryo-EM structures of amyloid-β 42 filaments from human brains. Science (New York, N.Y.). 375: 167-172. PMID 35025654 DOI: 10.1126/science.abm7285 |
0.01 |
|
| 2021 |
Abrahamson EE, Kofler JK, Becker CR, Price JC, Newell KL, Ghetti B, Murrell JR, McLean CA, Lopez OL, Mathis CA, Klunk WE, Villemagne VL, Ikonomovic MD. 11C-PiB PET can underestimate brain amyloid-β burden when cotton wool plaques are numerous. Brain : a Journal of Neurology. PMID 34918018 DOI: 10.1093/brain/awab434 |
0.01 |
|
| 2021 |
Buckles VD, Xiong C, Bateman RJ, Hassenstab J, Allegri R, Berman SB, Chhatwal JP, Danek A, Fagan AM, Ghetti B, Goate A, Graff-Radford N, Jucker M, Levin J, Marcus DS, et al. Different rates of cognitive decline in autosomal dominant and late-onset Alzheimer disease. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 34854530 DOI: 10.1002/alz.12505 |
0.01 |
|
| 2021 |
Hubbard EE, Heil LR, Merrihew GE, Chhatwal JP, Farlow MR, McLean CA, Ghetti B, Newell KL, Frosch MP, Bateman RJ, Larson EB, Keene CD, Perrin RJ, Montine TJ, MacCoss MJ, et al. Does Data-Independent Acquisition Data Contain Hidden Gems? A Case Study Related to Alzheimer's Disease. Journal of Proteome Research. PMID 34818016 DOI: 10.1021/acs.jproteome.1c00558 |
0.01 |
|
| 2021 |
Brelstaff JH, Mason M, Katsinelos T, McEwan WA, Ghetti B, Tolkovsky AM, Spillantini MG. Microglia become hypofunctional and release metalloproteases and tau seeds when phagocytosing live neurons with P301S tau aggregates. Science Advances. 7: eabg4980. PMID 34669475 DOI: 10.1126/sciadv.abg4980 |
0.01 |
|
| 2021 |
Todarwal Y, Gustafsson C, Thi Minh NN, Ertzgaard I, Klingstedt T, Ghetti B, Vidal R, König C, Lindgren M, Nilsson KPR, Linares M, Norman P. Tau Protein Binding Modes in Alzheimer's Disease for Cationic Luminescent Ligands. The Journal of Physical Chemistry. B. 125: 11628-11636. PMID 34643404 DOI: 10.1021/acs.jpcb.1c06019 |
0.01 |
|
| 2021 |
Shi Y, Zhang W, Yang Y, Murzin AG, Falcon B, Kotecha A, van Beers M, Tarutani A, Kametani F, Garringer HJ, Vidal R, Hallinan GI, Lashley T, Saito Y, Murayama S, ... ... Ghetti B, et al. Structure-based classification of tauopathies. Nature. PMID 34588692 DOI: 10.1038/s41586-021-03911-7 |
0.01 |
|
| 2021 |
Baiardi S, Rossi M, Mammana A, Appleby BS, Barria MA, Calì I, Gambetti P, Gelpi E, Giese A, Ghetti B, Herms J, Ladogana A, Mikol J, Pal S, Ritchie DL, et al. Phenotypic diversity of genetic Creutzfeldt-Jakob disease: a histo-molecular-based classification. Acta Neuropathologica. PMID 34324063 DOI: 10.1007/s00401-021-02350-y |
0.01 |
|
| 2021 |
Chen CD, Joseph-Mathurin N, Sinha N, Zhou A, Li Y, Friedrichsen K, McCullough A, Franklin EE, Hornbeck R, Gordon B, Sharma V, Cruchaga C, Goate A, Karch C, McDade E, ... ... Ghetti B, et al. Comparing amyloid-β plaque burden with antemortem PiB PET in autosomal dominant and late-onset Alzheimer disease. Acta Neuropathologica. PMID 34319442 DOI: 10.1007/s00401-021-02342-y |
0.01 |
|
| 2021 |
Keret O, Staffaroni AM, Ringman JM, Cobigo Y, Goh SM, Wolf A, Allen IE, Salloway S, Chhatwal J, Brickman AM, Reyes-Dumeyer D, Bateman RJ, Benzinger TLS, Morris JC, Ances BM, ... ... Ghetti B, et al. Pattern and degree of individual brain atrophy predicts dementia onset in dominantly inherited Alzheimer's disease. Alzheimer's & Dementia (Amsterdam, Netherlands). 13: e12197. PMID 34258377 DOI: 10.1002/dad2.12197 |
0.01 |
|
| 2021 |
Hallinan GI, Hoq MR, Ghosh M, Vago FS, Fernandez A, Garringer HJ, Vidal R, Jiang W, Ghetti B. Structure of Tau filaments in Prion protein amyloidoses. Acta Neuropathologica. PMID 34128081 DOI: 10.1007/s00401-021-02336-w |
0.01 |
|
| 2021 |
Klingstedt T, Shirani H, Ghetti B, Vidal R, Nilsson P. Thiophene-Based Optical Ligands That Selectively Detect Aβ Pathology in Alzheimer's Disease. Chembiochem : a European Journal of Chemical Biology. PMID 34101954 DOI: 10.1002/cbic.202100199 |
0.01 |
|
| 2021 |
Kumar A, Koistinen NA, Malarte ML, Nennesmo I, Ingelsson M, Ghetti B, Lemoine L, Nordberg A. Astroglial tracer BU99008 detects multiple binding sites in Alzheimer's disease brain. Molecular Psychiatry. PMID 33888872 DOI: 10.1038/s41380-021-01101-5 |
0.01 |
|
| 2021 |
Shi Y, Murzin AG, Falcon B, Epstein A, Machin J, Tempest P, Newell KL, Vidal R, Garringer HJ, Sahara N, Higuchi M, Ghetti B, Jang MK, Scheres SHW, Goedert M. Correction to: Cryo-EM structures of tau filaments from Alzheimer's disease with PET ligand APN-1607. Acta Neuropathologica. PMID 33830331 DOI: 10.1007/s00401-021-02303-5 |
0.01 |
|
| 2021 |
Sorrentino S, Ascari R, Maderna E, Catania M, Ghetti B, Tagliavini F, Giaccone G, Di Fede G. Microglial Heterogeneity and Its Potential Role in Driving Phenotypic Diversity of Alzheimer's Disease. International Journal of Molecular Sciences. 22. PMID 33803478 DOI: 10.3390/ijms22052780 |
0.01 |
|
| 2021 |
Shi Y, Murzin AG, Falcon B, Epstein A, Machin J, Tempest P, Newell KL, Vidal R, Garringer HJ, Sahara N, Higuchi M, Ghetti B, Jang MK, Scheres SHW, Goedert M. Cryo-EM structures of tau filaments from Alzheimer's disease with PET ligand APN-1607. Acta Neuropathologica. PMID 33723967 DOI: 10.1007/s00401-021-02294-3 |
0.01 |
|
| 2021 |
Chia R, Sabir MS, Bandres-Ciga S, Saez-Atienzar S, Reynolds RH, Gustavsson E, Walton RL, Ahmed S, Viollet C, Ding J, Makarious MB, Diez-Fairen M, Portley MK, Shah Z, Abramzon Y, ... ... Ghetti B, et al. Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture. Nature Genetics. PMID 33589841 DOI: 10.1038/s41588-021-00785-3 |
0.01 |
|
| 2021 |
Joseph-Mathurin N, Wang G, Kantarci K, Jack CR, McDade E, Hassenstab J, Blazey TM, Gordon BA, Su Y, Chen G, Massoumzadeh P, Hornbeck RC, Allegri RF, Ances BM, Berman SB, ... ... Ghetti B, et al. Longitudinal Accumulation of Cerebral Microhemorrhages in Dominantly Inherited Alzheimer Disease. Neurology. PMID 33495373 DOI: 10.1212/WNL.0000000000011542 |
0.01 |
|
| 2021 |
Luckett PH, McCullough A, Gordon BA, Strain J, Flores S, Dincer A, McCarthy J, Kuffner T, Stern A, Meeker KL, Berman SB, Chhatwal JP, Cruchaga C, Fagan AM, Farlow MR, ... ... Ghetti B, et al. Modeling autosomal dominant Alzheimer's disease with machine learning. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 33480178 DOI: 10.1002/alz.12259 |
0.01 |
|
| 2021 |
Goedert M, Spillantini MG, Falcon B, Zhang W, Newell KL, Hasegawa M, Scheres SHW, Ghetti B. Tau Protein and Frontotemporal Dementias. Advances in Experimental Medicine and Biology. 1281: 177-199. PMID 33433876 DOI: 10.1007/978-3-030-51140-1_12 |
0.01 |
|
| 2020 |
Buciuc M, Whitwell JL, Kasanuki K, Graff-Radford J, Machulda MM, Duffy JR, Strand EA, Lowe VJ, Graff-Radford NR, Rush BK, Franczak MB, Flanagan ME, Baker MC, Rademakers R, Ross OA, ... Ghetti BF, et al. Lewy body disease is a contributor to logopenic progressive aphasia phenotype. Annals of Neurology. PMID 33274526 DOI: 10.1002/ana.25979 |
0.01 |
|
| 2020 |
Irimia-Dominguez J, Sun C, Li K, Muhoberac BB, Hallinan GI, Garringer HJ, Ghetti B, Jiang W, Vidal R. Cryo-EM structures and functional characterization of homo- and heteropolymers of human ferritin variants. Scientific Reports. 10: 20666. PMID 33244127 DOI: 10.1038/s41598-020-77717-4 |
0.01 |
|
| 2020 |
Groveman BR, Orrù CD, Hughson AG, Raymond LD, Zanusso G, Ghetti B, Campbell KJ, Safar J, Galasko D, Caughey B. Correction to: Rapid and ultra-sensitive quantitation of disease-associated α-synuclein seeds in brain and cerebrospinal fluid by αSyn RT-QuIC. Acta Neuropathologica Communications. 8: 180. PMID 33153488 DOI: 10.1186/s40478-020-01052-y |
0.01 |
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| 2020 |
Vermunt L, Dicks E, Wang G, Dincer A, Flores S, Keefe SJ, Berman SB, Cash DM, Chhatwal JP, Cruchaga C, Fox NC, Ghetti B, Graff-Radford NR, Hassenstab J, Karch CM, et al. Single-subject grey matter network trajectories over the disease course of autosomal dominant Alzheimer's disease. Brain Communications. 2: fcaa102. PMID 32954344 DOI: 10.1093/braincomms/fcaa102 |
0.01 |
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| 2020 |
Luo J, Agboola F, Grant E, Masters CL, Albert MS, Johnson SC, McDade EM, Vöglein J, Fagan AM, Benzinger T, Massoumzadeh P, Hassenstab J, Bateman RJ, Morris JC, Perrin RJ, ... ... Ghetti B, et al. Sequence of Alzheimer disease biomarker changes in cognitively normal adults: A cross-sectional study. Neurology. PMID 32873693 DOI: 10.1212/Wnl.0000000000010747 |
0.01 |
|
| 2020 |
Aschenbrenner AJ, Petros J, McDade E, Wang G, Balota DA, Benzinger TL, Cruchaga C, Goate A, Xiong C, Perrin R, Fagan AM, Graff-Radford N, Ghetti B, Levin J, Weidinger E, et al. Relationships between big-five personality factors and Alzheimer's disease pathology in autosomal dominant Alzheimer's disease. Alzheimer's & Dementia (Amsterdam, Netherlands). 12: e12038. PMID 32587883 DOI: 10.1002/Dad2.12038 |
0.01 |
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| 2020 |
Schultz SA, Strain JF, Adedokun A, Wang Q, Preische O, Kuhle J, Flores S, Keefe S, Dincer A, Ances BM, Berman SB, Brickman AM, Cash DM, Chhatwal J, Cruchaga C, ... ... Ghetti B, et al. Serum neurofilament light chain levels are associated with white matter integrity in autosomal dominant Alzheimer's disease. Neurobiology of Disease. 104960. PMID 32522711 DOI: 10.1016/J.Nbd.2020.104960 |
0.01 |
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| 2020 |
Abskharon R, Seidler PM, Sawaya MR, Cascio D, Yang TP, Philipp S, Williams CK, Newell KL, Ghetti B, DeTure MA, Dickson DW, Vinters HV, Felgner PL, Nakajima R, Glabe CG, et al. Crystal structure of a conformational antibody that binds tau oligomers and inhibits pathological seeding by extracts from donors with Alzheimer's disease. The Journal of Biological Chemistry. PMID 32493775 DOI: 10.1074/Jbc.Ra120.013638 |
0.01 |
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| 2020 |
Schweighauser M, Shi Y, Tarutani A, Kametani F, Murzin AG, Ghetti B, Matsubara T, Tomita T, Ando T, Hasegawa K, Murayama S, Yoshida M, Hasegawa M, Scheres SHW, Goedert M. Structures of α-synuclein filaments from multiple system atrophy. Nature. PMID 32461689 DOI: 10.1038/S41586-020-2317-6 |
0.01 |
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| 2020 |
Morgan SA, Lavenir I, Fan J, Masuda-Suzukake M, Passarella D, DeTure MA, Dickson DW, Ghetti B, Goedert M. α-Synuclein filaments from transgenic mouse and human synucleinopathy-containing brains are major seed-competent species. The Journal of Biological Chemistry. PMID 32209651 DOI: 10.1074/Jbc.Ra119.012179 |
0.01 |
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| 2020 |
Brozzetti L, Sacchetto L, Cecchini MP, Avesani A, Perra D, Bongianni M, Portioli C, Scupoli M, Ghetti B, Monaco S, Buffelli M, Zanusso G. Neurodegeneration-Associated Proteins in Human Olfactory Neurons Collected by Nasal Brushing. Frontiers in Neuroscience. 14: 145. PMID 32194369 DOI: 10.3389/Fnins.2020.00145 |
0.01 |
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| 2020 |
Metrick MA, Ferreira NDC, Saijo E, Kraus A, Newell K, Zanusso G, Vendruscolo M, Ghetti B, Caughey B. A single ultrasensitive assay for detection and discrimination of tau aggregates of Alzheimer and Pick diseases. Acta Neuropathologica Communications. 8: 22. PMID 32087764 DOI: 10.1186/S40478-020-0887-Z |
0.01 |
|
| 2020 |
Zhang W, Tarutani A, Newell KL, Murzin AG, Matsubara T, Falcon B, Vidal R, Garringer HJ, Shi Y, Ikeuchi T, Murayama S, Ghetti B, Hasegawa M, Goedert M, Scheres SHW. Novel tau filament fold in corticobasal degeneration. Nature. PMID 32050258 DOI: 10.1038/S41586-020-2043-0 |
0.01 |
|
| 2020 |
Reiman EM, Arboleda-Velasquez JF, Quiroz YT, Huentelman MJ, Beach TG, Caselli RJ, Chen Y, Su Y, Myers AJ, Hardy J, Paul Vonsattel J, Younkin SG, Bennett DA, De Jager PL, Larson EB, ... ... Ghetti BF, et al. Exceptionally low likelihood of Alzheimer's dementia in APOE2 homozygotes from a 5,000-person neuropathological study. Nature Communications. 11: 667. PMID 32015339 DOI: 10.1038/S41467-019-14279-8 |
0.01 |
|
| 2020 |
Aschenbrenner AJ, James BD, McDade E, Wang G, Lim YY, Benzinger TLS, Cruchaga C, Goate A, Xiong C, Perrin R, Buckles V, Allegri R, Berman SB, Chhatwal JP, Fagan A, ... ... Ghetti B, et al. Awareness of genetic risk in the Dominantly Inherited Alzheimer Network (DIAN). Alzheimer's & Dementia : the Journal of the Alzheimer's Association. 16: 219-228. PMID 31914221 DOI: 10.1002/Alz.12010 |
0.01 |
|
| 2019 |
Klingstedt T, Ghetti B, Holton JL, Ling H, Nilsson KPR, Goedert M. Luminescent conjugated oligothiophenes distinguish between α-synuclein assemblies of Parkinson's disease and multiple system atrophy. Acta Neuropathologica Communications. 7: 193. PMID 31796099 DOI: 10.1186/S40478-019-0840-1 |
0.01 |
|
| 2019 |
Saijo E, Metrick MA, Koga S, Parchi P, Litvan I, Spina S, Boxer A, Rojas JC, Galasko D, Kraus A, Rossi M, Newell K, Zanusso G, Grinberg LT, Seeley WW, ... Ghetti B, et al. Correction to: 4-Repeat tau seeds and templating subtypes as brain and CSF biomarkers of frontotemporal lobar degeneration. Acta Neuropathologica. PMID 31748840 DOI: 10.1007/S00401-019-02092-Y |
0.01 |
|
| 2019 |
Metrick MA, do Carmo Ferreira N, Saijo E, Hughson AG, Kraus A, Orrú C, Miller MW, Zanusso G, Ghetti B, Vendruscolo M, Caughey B. Million-fold sensitivity enhancement in proteopathic seed amplification assays for biospecimens by Hofmeister ion comparisons. Proceedings of the National Academy of Sciences of the United States of America. PMID 31641070 DOI: 10.1073/Pnas.1909322116 |
0.01 |
|
| 2019 |
Saijo E, Metrick MA, Koga S, Parchi P, Litvan I, Spina S, Boxer A, Rojas JC, Galasko D, Kraus A, Rossi M, Newell K, Zanusso G, Grinberg LT, Seeley WW, ... Ghetti B, et al. 4-Repeat tau seeds and templating subtypes as brain and CSF biomarkers of frontotemporal lobar degeneration. Acta Neuropathologica. PMID 31616982 DOI: 10.1007/S00401-019-02080-2 |
0.01 |
|
| 2019 |
Bongianni M, Ladogana A, Capaldi S, Klotz S, Baiardi S, Cagnin A, Perra D, Fiorini M, Poleggi A, Legname G, Cattaruzza T, Janes F, Tabaton M, Ghetti B, Monaco S, et al. α-Synuclein RT-QuIC assay in cerebrospinal fluid of patients with dementia with Lewy bodies. Annals of Clinical and Translational Neurology. PMID 31599499 DOI: 10.1002/Acn3.50897 |
0.01 |
|
| 2019 |
Seidler PM, Boyer DR, Murray KA, Yang TP, Bentzel M, Sawaya MR, Rosenberg G, Cascio D, Williams CK, Newell KL, Ghetti B, DeTure MA, Dickson DW, Vinters HV, Eisenberg DS. Structure-based inhibitors halt prion-like seeding by Alzheimer's disease- and tauopathy-derived brain tissue samples. The Journal of Biological Chemistry. PMID 31537646 DOI: 10.1074/Jbc.Ra119.009688 |
0.01 |
|
| 2019 |
Lavenir I, Passarella D, Masuda-Suzukake M, Curry A, Holton JL, Ghetti B, Goedert M. Silver staining (Campbell-Switzer) of neuronal α-synuclein assemblies induced by multiple system atrophy and Parkinson's disease brain extracts in transgenic mice. Acta Neuropathologica Communications. 7: 148. PMID 31522685 DOI: 10.1186/S40478-019-0804-5 |
0.01 |
|
| 2019 |
Kunkle BW, Grenier-Boley B, Sims R, Bis JC, Damotte V, Naj AC, Boland A, Vronskaya M, van der Lee SJ, Amlie-Wolf A, Bellenguez C, Frizatti A, Chouraki V, Martin ER, Sleegers K, ... ... Ghetti B, et al. Author Correction: Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing. Nature Genetics. PMID 31417202 DOI: 10.1038/s41588-019-0495-7 |
0.01 |
|
| 2019 |
Josephs KA, Mackenzie I, Frosch MP, Bigio EH, Neumann M, Arai T, Dugger BN, Ghetti B, Grossman M, Hasegawa M, Herrup K, Holton J, Jellinger K, Lashley T, McAleese KE, et al. LATE to the PART-y. Brain : a Journal of Neurology. PMID 31359030 DOI: 10.1093/Brain/Awz224 |
0.01 |
|
| 2019 |
Cali CP, Patino M, Tai YK, Ho WY, McLean CA, Morris CM, Seeley WW, Miller BL, Gaig C, Vonsattel JPG, White CL, Roeber S, Kretzschmar H, Troncoso JC, Troakes C, ... ... Ghetti B, et al. C9orf72 intermediate repeats are associated with corticobasal degeneration, increased C9orf72 expression and disruption of autophagy. Acta Neuropathologica. PMID 31327044 DOI: 10.1007/S00401-019-02045-5 |
0.01 |
|
| 2019 |
Gondim DD, Oblak A, Murrell JR, Richardson R, Epperson F, Ross OA, Ghetti B. Diffuse Lewy Body Disease and Alzheimer Disease: Neuropathologic Phenotype Associated With the PSEN1 p.A396T Mutation. Journal of Neuropathology and Experimental Neurology. PMID 31165862 DOI: 10.1093/Jnen/Nlz039 |
0.01 |
|
| 2019 |
Cracco L, Xiao X, Nemani SK, Lavrich J, Cali I, Ghetti B, Notari S, Surewicz WK, Gambetti P. Gerstmann-Sträussler-Scheinker disease revisited: accumulation of covalently-linked multimers of internal prion protein fragments. Acta Neuropathologica Communications. 7: 1. PMID 31142381 DOI: 10.1186/S40478-019-0734-2 |
0.01 |
|
| 2019 |
Vöglein J, Paumier K, Jucker M, Preische O, McDade E, Hassenstab J, Benzinger TL, Noble JM, Berman SB, Graff-Radford NR, Ghetti B, Farlow MR, Chhatwal J, Salloway S, Xiong C, et al. Clinical, pathophysiological and genetic features of motor symptoms in autosomal dominant Alzheimer's disease. Brain : a Journal of Neurology. PMID 30897203 DOI: 10.1093/Brain/Awz050 |
0.01 |
|
| 2019 |
Falcon B, Zivanov J, Zhang W, Murzin AG, Garringer HJ, Vidal R, Crowther RA, Newell KL, Ghetti B, Goedert M, Scheres SHW. Novel tau filament fold in chronic traumatic encephalopathy encloses hydrophobic molecules. Nature. PMID 30894745 DOI: 10.1038/S41586-019-1026-5 |
0.01 |
|
| 2019 |
Goedert M, Falcon B, Zhang W, Ghetti B, Scheres SHW. Distinct Conformers of Assembled Tau in Alzheimer's and Pick's Diseases. Cold Spring Harbor Symposia On Quantitative Biology. PMID 30886056 DOI: 10.1101/Sqb.2018.83.037580 |
0.01 |
|
| 2019 |
Kunkle BW, Grenier-Boley B, Sims R, Bis JC, Damotte V, Naj AC, Boland A, Vronskaya M, van der Lee SJ, Amlie-Wolf A, Bellenguez C, Frizatti A, Chouraki V, Martin ER, Sleegers K, ... ... Ghetti B, et al. Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing. Nature Genetics. 51: 414-430. PMID 30820047 DOI: 10.1038/s41588-019-0358-2 |
0.01 |
|
| 2019 |
Pottier C, Ren Y, Perkerson RB, Baker M, Jenkins GD, van Blitterswijk M, DeJesus-Hernandez M, van Rooij JGJ, Murray ME, Christopher E, McDonnell SK, Fogarty Z, Batzler A, Tian S, Vicente CT, ... ... Ghetti B, et al. Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD. Acta Neuropathologica. PMID 30739198 DOI: 10.1007/S00401-019-01962-9 |
0.01 |
|
| 2019 |
Pardini M, Huey ED, Spina S, Kreisl WC, Morbelli S, Wassermann EM, Nobili F, Ghetti B, Grafman J. FDG-PET patterns associated with underlying pathology in corticobasal syndrome. Neurology. PMID 30700592 DOI: 10.1212/Wnl.0000000000007038 |
0.01 |
|
| 2019 |
Preische O, Schultz SA, Apel A, Kuhle J, Kaeser SA, Barro C, Gräber S, Kuder-Buletta E, LaFougere C, Laske C, Vöglein J, Levin J, Masters CL, Martins R, Schofield PR, ... ... Ghetti B, et al. Serum neurofilament dynamics predicts neurodegeneration and clinical progression in presymptomatic Alzheimer's disease. Nature Medicine. PMID 30664784 DOI: 10.1038/S41591-018-0304-3 |
0.01 |
|
| 2018 |
Vöglein J, Noachtar S, McDade E, Quaid KA, Salloway S, Ghetti B, Noble J, Berman S, Chhatwal J, Mori H, Fox N, Allegri R, Masters CL, Buckles V, Ringman JM, et al. Seizures as an early symptom of autosomal dominant Alzheimer's disease. Neurobiology of Aging. 76: 18-23. PMID 30616208 DOI: 10.1016/J.Neurobiolaging.2018.11.022 |
0.01 |
|
| 2018 |
Kraus A, Saijo E, Metrick MA, Newell K, Sigurdson CJ, Zanusso G, Ghetti B, Caughey B. Seeding selectivity and ultrasensitive detection of tau aggregate conformers of Alzheimer disease. Acta Neuropathologica. PMID 30570675 DOI: 10.1007/S00401-018-1947-3 |
0.01 |
|
| 2018 |
Newell K, Paron F, Mompean M, Murrell J, Salis E, Stuani C, Pattee G, Romano M, Laurents D, Ghetti B, Buratti E. Dysregulation of TDP-43 Intracellular Localization and Early-Onset ALS are Associated with a TARDBP S375G Variant. Brain Pathology (Zurich, Switzerland). PMID 30461104 DOI: 10.1111/bpa.12680 |
0.01 |
|
| 2018 |
Risacher SL, Farlow MR, Bateman DR, Epperson F, Tallman EF, Richardson R, Murrell JR, Unverzagt FW, Apostolova LG, Bonnin JM, Ghetti B, Saykin AJ. Detection of tau in Gerstmann-Sträussler-Scheinker disease (PRNP F198S) by [F]Flortaucipir PET. Acta Neuropathologica Communications. 6: 114. PMID 30373672 DOI: 10.1186/S40478-018-0608-Z |
0.01 |
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| 2018 |
Falcon B, Zhang W, Schweighauser M, Murzin AG, Vidal R, Garringer HJ, Ghetti B, Scheres SHW, Goedert M. Tau filaments from multiple cases of sporadic and inherited Alzheimer's disease adopt a common fold. Acta Neuropathologica. PMID 30276465 DOI: 10.1007/S00401-018-1914-Z |
0.01 |
|
| 2018 |
Müller S, Preische O, Sohrabi HR, Gräber S, Jucker M, Ringman JM, Martins RN, McDade E, Schofield PR, Ghetti B, Rossor M, Fox NN, Graff-Radford NR, Levin J, Danek A, et al. Relationship between physical activity, cognition, and Alzheimer pathology in autosomal dominant Alzheimer's disease. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 30266303 DOI: 10.1016/J.Jalz.2018.06.3059 |
0.01 |
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| 2018 |
McDade E, Wang G, Gordon BA, Hassenstab J, Benzinger TLS, Buckles V, Fagan AM, Holtzman DM, Cairns NJ, Goate AM, Marcus DS, Morris JC, Paumier K, Xiong C, Allegri R, ... ... Ghetti B, et al. Longitudinal cognitive and biomarker changes in dominantly inherited Alzheimer disease. Neurology. PMID 30217935 DOI: 10.1212/Wnl.0000000000006277 |
0.01 |
|
| 2018 |
Falcon B, Zhang W, Murzin AG, Murshudov G, Garringer HJ, Vidal R, Crowther RA, Ghetti B, Scheres SHW, Goedert M. Structures of filaments from Pick's disease reveal a novel tau protein fold. Nature. PMID 30158706 DOI: 10.1038/S41586-018-0454-Y |
0.01 |
|
| 2018 |
Brelstaff J, Tolkovsky AM, Ghetti B, Goedert M, Spillantini MG. Living Neurons with Tau Filaments Aberrantly Expose Phosphatidylserine and Are Phagocytosed by Microglia. Cell Reports. 24: 1939-1948.e4. PMID 30134156 DOI: 10.1016/J.Celrep.2018.07.072 |
0.01 |
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| 2018 |
Karch CM, Hernández D, Wang JC, Marsh J, Hewitt AW, Hsu S, Norton J, Levitch D, Donahue T, Sigurdson W, Ghetti B, Farlow M, Chhatwal J, Berman S, Cruchaga C, et al. Human fibroblast and stem cell resource from the Dominantly Inherited Alzheimer Network. Alzheimer's Research & Therapy. 10: 69. PMID 30045758 DOI: 10.1186/S13195-018-0400-0 |
0.01 |
|
| 2018 |
Ghetti B, Piccardo P, Zanusso G. Dominantly inherited prion protein cerebral amyloidoses - a modern view of Gerstmann-Sträussler-Scheinker. Handbook of Clinical Neurology. 153: 243-269. PMID 29887140 DOI: 10.1016/B978-0-444-63945-5.00014-3 |
0.01 |
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| 2018 |
Lee S, Zimmerman ME, Narkhede A, Nasrabady SE, Tosto G, Meier IB, Benzinger TLS, Marcus DS, Fagan AM, Fox NC, Cairns NJ, Holtzman DM, Buckles V, Ghetti B, McDade E, et al. White matter hyperintensities and the mediating role of cerebral amyloid angiopathy in dominantly-inherited Alzheimer's disease. Plos One. 13: e0195838. PMID 29742105 DOI: 10.1371/Journal.Pone.0195838 |
0.01 |
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| 2018 |
Pottier C, Zhou X, Perkerson RB, Baker M, Jenkins GD, Serie DJ, Ghidoni R, Benussi L, Binetti G, López de Munain A, Zulaica M, Moreno F, Le Ber I, Pasquier F, Hannequin D, ... ... Ghetti B, et al. Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study. The Lancet. Neurology. PMID 29724592 DOI: 10.1016/S1474-4422(18)30126-1 |
0.01 |
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| 2018 |
Chhatwal JP, Schultz AP, Johnson KA, Hedden T, Jaimes S, Benzinger TLS, Jack C, Ances BM, Ringman JM, Marcus DS, Ghetti B, Farlow MR, Danek A, Levin J, Yakushev I, et al. Preferential degradation of cognitive networks differentiates Alzheimer's disease from ageing. Brain : a Journal of Neurology. PMID 29522171 DOI: 10.1093/Brain/Awy053 |
0.01 |
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| 2018 |
Di Fede G, Catania M, Maderna E, Ghidoni R, Benussi L, Tonoli E, Giaccone G, Moda F, Paterlini A, Campagnani I, Sorrentino S, Colombo L, Kubis A, Bistaffa E, Ghetti B, et al. Molecular subtypes of Alzheimer's disease. Scientific Reports. 8: 3269. PMID 29459625 DOI: 10.1038/s41598-018-21641-1 |
0.01 |
|
| 2018 |
Groveman BR, Orrù CD, Hughson AG, Raymond LD, Zanusso G, Ghetti B, Campbell KJ, Safar J, Galasko D, Caughey B. Rapid and ultra-sensitive quantitation of disease-associated α-synuclein seeds in brain and cerebrospinal fluid by αSyn RT-QuIC. Acta Neuropathologica Communications. 6: 7. PMID 29422107 DOI: 10.1186/s40478-018-0508-2 |
0.01 |
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| 2018 |
Taylor LM, McMillan PJ, Liachko NF, Strovas TJ, Ghetti B, Bird TD, Dirk Keene C, Kraemer BC. Pathological phosphorylation of tau and TDP-43 by TTBK1 and TTBK2 drives neurodegeneration. Molecular Neurodegeneration. 13: 7. PMID 29409526 DOI: 10.1186/S13024-018-0237-9 |
0.01 |
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| 2017 |
Lemoine L, Gillberg PG, Svedberg M, Stepanov V, Jia Z, Huang J, Nag S, Tian H, Ghetti B, Okamura N, Higuchi M, Halldin C, Nordberg A. Comparative binding properties of the tau PET tracers THK5117, THK5351, PBB3, and T807 in postmortem Alzheimer brains. Alzheimer's Research & Therapy. 9: 96. PMID 29229003 DOI: 10.1186/S13195-017-0325-Z |
0.01 |
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| 2017 |
Rasmussen J, Mahler J, Beschorner N, Kaeser SA, Häsler LM, Baumann F, Nyström S, Portelius E, Blennow K, Lashley T, Fox NC, Sepulveda-Falla D, Glatzel M, Oblak AL, Ghetti B, et al. Amyloid polymorphisms constitute distinct clouds of conformational variants in different etiological subtypes of Alzheimer's disease. Proceedings of the National Academy of Sciences of the United States of America. PMID 29158413 DOI: 10.1073/Pnas.1713215114 |
0.01 |
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| 2017 |
Eskandari-Sedighi G, Daude N, Gapeshina H, Sanders DW, Kamali-Jamil R, Yang J, Shi B, Wille H, Ghetti B, Diamond MI, Janus C, Westaway D. The CNS in inbred transgenic models of 4-repeat Tauopathy develops consistent tau seeding capacity yet focal and diverse patterns of protein deposition. Molecular Neurodegeneration. 12: 72. PMID 28978354 DOI: 10.1186/S13024-017-0215-7 |
0.01 |
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| 2017 |
Kinnunen KM, Cash DM, Poole T, Frost C, Benzinger TLS, Ahsan RL, Leung KK, Cardoso MJ, Modat M, Malone IB, Morris JC, Bateman RJ, Marcus DS, Goate A, Salloway S, ... ... Ghetti B, et al. Presymptomatic atrophy in autosomal dominant Alzheimer's disease: A serial MRI study. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 28738187 DOI: 10.1016/J.Jalz.2017.06.2268 |
0.01 |
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| 2017 |
Sims R, van der Lee SJ, Naj AC, Bellenguez C, Badarinarayan N, Jakobsdottir J, Kunkle BW, Boland A, Raybould R, Bis JC, Martin ER, Grenier-Boley B, Heilmann-Heimbach S, Chouraki V, Kuzma AB, ... ... Ghetti B, et al. Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease. Nature Genetics. PMID 28714976 DOI: 10.1038/Ng.3916 |
0.01 |
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| 2017 |
Fitzpatrick AWP, Falcon B, He S, Murzin AG, Murshudov G, Garringer HJ, Crowther RA, Ghetti B, Goedert M, Scheres SHW. Cryo-EM structures of tau filaments from Alzheimer's disease. Nature. PMID 28678775 DOI: 10.1038/Nature23002 |
0.01 |
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| 2017 |
Müller S, Preische O, Sohrabi HR, Gräber S, Jucker M, Dietzsch J, Ringman JM, Martins RN, McDade E, Schofield PR, Ghetti B, Rossor M, Graff-Radford NR, Levin J, Galasko D, et al. Decreased body mass index in the preclinical stage of autosomal dominant Alzheimer's disease. Scientific Reports. 7: 1225. PMID 28450713 DOI: 10.1038/S41598-017-01327-W |
0.01 |
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| 2017 |
Saijo E, Ghetti B, Zanusso G, Oblak A, Furman JL, Diamond MI, Kraus A, Caughey B. Ultrasensitive and selective detection of 3-repeat tau seeding activity in Pick disease brain and cerebrospinal fluid. Acta Neuropathologica. PMID 28293793 DOI: 10.1007/S00401-017-1692-Z |
0.01 |
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| 2017 |
Cracco L, Notari S, Cali I, Sy MS, Chen SG, Cohen ML, Ghetti B, Appleby BS, Zou WQ, Caughey B, Safar JG, Gambetti P. Novel strain properties distinguishing sporadic prion diseases sharing prion protein genotype and prion type. Scientific Reports. 7: 38280. PMID 28091514 DOI: 10.1038/Srep38280 |
0.01 |
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| 2017 |
McEwan WA, Falcon B, Vaysburd M, Clift D, Oblak AL, Ghetti B, Goedert M, James LC. Cytosolic Fc receptor TRIM21 inhibits seeded tau aggregation. Proceedings of the National Academy of Sciences of the United States of America. PMID 28049840 DOI: 10.1073/Pnas.1607215114 |
0.01 |
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| 2017 |
Annette Contreras J, Risacher SL, Dzemidzic M, West JD, McDonald BC, Farlow MR, Matthews BR, Apostolova LG, Brosch J, Ghetti B, GoÑi J. 2307 Journal of Clinical and Translational Science. 1: 6-6. DOI: 10.1017/cts.2017.38 |
0.01 |
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| 2017 |
Fitzpatrick A, Falcon B, He S, Murzin A, Murshudov G, Garringer H, Crowther A, Ghetti BF, Goedert M, Scheres S. CRYO-EM STRUCTURES OF TAU FILAMENTS FROM ALZHEIMER'S DISEASE BRAIN Alzheimer's & Dementia. 13: P892. DOI: 10.1016/J.Jalz.2017.07.298 |
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| 2017 |
Ghetti BF. [EC‐03–01]: FRONTOTEMPORAL LOBAR DEGENERATION: CLINICAL PICTURES, NEUROPATHOLOGIES AND GENETICS Alzheimer's & Dementia. 13. DOI: 10.1016/j.jalz.2017.07.297 |
0.01 |
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| 2017 |
McDade E, Wang G, Benzinger TL, Buckles VD, Fagan AM, Gordon BA, Hassenstab J, Holtzman DM, Cairns NJ, Goate AM, Marcus DS, Morris JC, Paumier KL, Xiong C, Ricardo A, ... ... Ghetti BF, et al. LONGITUDINAL BIOMARKER CHANGES IN AUTOSOMAL DOMINANT ALZHEIMER'S DISEASE FROM THE DIAN STUDY Alzheimer's & Dementia. 13: P879-P880. DOI: 10.1016/J.Jalz.2017.07.265 |
0.01 |
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| 2017 |
Saijo E, Ghetti BF, Zanusso G, Oblak AL, Furman JL, Diamond M, Caughey B. [P1-128]: ULTRASENSITIVE AND SELECTIVE DETECTION OF 3-REPEAT TAU SEEDING ACTIVITY IN PICK DISEASE BRAIN AND CEREBROSPINAL FLUID USING TAU RT-QUIC Alzheimer's & Dementia. 13: P290-P291. DOI: 10.1016/J.Jalz.2017.06.195 |
0.01 |
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| 2017 |
Zanusso G, Sacchetto L, Brozzetti L, Olivieri D, Ferrari S, Faccioli L, Bongianni M, Pedrazzoli M, Buffelli M, Monaco S, Pocchiari M, Caughey B, Ghetti BF. [P2-442]: NEURODEGENERATION-ASSOCIATED PROTEINS IN HUMAN OLFACTORY NEURONS Alzheimer's & Dementia. 13: P805-P806. DOI: 10.1016/J.Jalz.2017.06.1098 |
0.01 |
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| 2016 |
Garringer HJ, Sammeta N, Oblak A, Ghetti B, Vidal R. Amyloid and intracellular accumulation of BRI2. Neurobiology of Aging. 52: 90-97. PMID 28131015 DOI: 10.1016/J.Neurobiolaging.2016.12.018 |
0.01 |
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| 2016 |
Galimberti D, Cioffi SM, Fenoglio C, Serpente M, Oblak AL, Rodriguez-Porcel F, Oldoni E, Hagen MC, Arcaro M, Scarpini E, Ghetti B, Espay AJ. Rapidly progressive primary progressive aphasia and parkinsonism with novel GRN mutation. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 27859661 DOI: 10.1002/Mds.26872 |
0.01 |
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| 2016 |
Tang M, Ryman DC, McDade E, Jasielec MS, Buckles VD, Cairns NJ, Fagan AM, Goate A, Marcus DS, Xiong C, Allegri RF, Chhatwal JP, Danek A, Farlow MR, Fox NC, ... Ghetti B, et al. Neurological manifestations of autosomal dominant familial Alzheimer's disease: a comparison of the published literature with the Dominantly Inherited Alzheimer Network observational study (DIAN-OBS). The Lancet. Neurology. PMID 27777020 DOI: 10.1016/S1474-4422(16)30229-0 |
0.01 |
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| 2016 |
Su Y, Blazey TM, Owen CJ, Christensen JJ, Friedrichsen K, Joseph-Mathurin N, Wang Q, Hornbeck RC, Ances BM, Snyder AZ, Cash LA, Koeppe RA, Klunk WE, Galasko D, Brickman AM, ... ... Ghetti B, et al. Correction: Quantitative Amyloid Imaging in Autosomal Dominant Alzheimer's Disease: Results from the DIAN Study Group. Plos One. 11: e0163669. PMID 27649320 DOI: 10.1371/journal.pone.0163669 |
0.01 |
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| 2016 |
Umeh CC, Kalakoti P, Greenberg MK, Notari S, Cohen Y, Gambetti P, Oblak AL, Ghetti B, Mari Z. Clinicopathological Correlates in a PRNP P102L Mutation Carrier with Rapidly Progressing Parkinsonism-dystonia. Movement Disorders Clinical Practice. 3: 355-358. PMID 27617269 DOI: 10.1002/Mdc3.12307 |
0.01 |
|
| 2016 |
Garringer HJ, Irimia JM, Li W, Goodwin CB, Richine B, Acton A, Chan RJ, Peacock M, Muhoberac BB, Ghetti B, Vidal R. Effect of Systemic Iron Overload and a Chelation Therapy in a Mouse Model of the Neurodegenerative Disease Hereditary Ferritinopathy. Plos One. 11: e0161341. PMID 27574973 DOI: 10.1371/Journal.Pone.0161341 |
0.01 |
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| 2016 |
Liachko NF, Saxton AD, McMillan PJ, Strovas TJ, Currey HN, Taylor LM, Wheeler JM, Oblak AL, Ghetti B, Montine TJ, Keene CD, Raskind MA, Bird TD, Kraemer BC. The phosphatase calcineurin regulates pathological TDP-43 phosphorylation. Acta Neuropathologica. PMID 27473149 DOI: 10.1007/S00401-016-1600-Y |
0.01 |
|
| 2016 |
Catafau AM, Bullich S, Seibyl JP, Barthel H, Ghetti B, Leverenz J, Ironside JW, Schulz-Schaefer WJ, Hoffmann A, Sabri O. Cerebellar amyloid-beta plaques: How frequent are they, and do they influence 18F-Florbetaben SUVR? Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine. PMID 27363836 DOI: 10.2967/jnumed.115.171652 |
0.01 |
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| 2016 |
Deng HX, Shi Y, Yang Y, Ahmeti KB, Miller N, Huang C, Cheng L, Zhai H, Deng S, Nuytemans K, Corbett NJ, Kim MJ, Deng H, Tang B, Yang Z, ... ... Ghetti B, et al. Identification of TMEM230 mutations in familial Parkinson's disease. Nature Genetics. PMID 27270108 DOI: 10.1038/Ng.3589 |
0.01 |
|
| 2016 |
Dardis A, Zampieri S, Canterini S, Newell KL, Stuani C, Murrell JR, Ghetti B, Fiorenza MT, Bembi B, Buratti E. Altered localization and functionality of TAR DNA Binding Protein 43 (TDP-43) in niemann- pick disease type C. Acta Neuropathologica Communications. 4: 52. PMID 27193329 DOI: 10.1186/s40478-016-0325-4 |
0.01 |
|
| 2016 |
Deters KD, Risacher SL, Yoder KK, Oblak AL, Unverzagt FW, Murrell JR, Epperson F, Tallman EF, Quaid KA, Farlow MR, Saykin AJ, Ghetti B. [(11)C]PiB PET in Gerstmann-Sträussler-Scheinker disease. American Journal of Nuclear Medicine and Molecular Imaging. 6: 84-93. PMID 27069768 |
0.01 |
|
| 2016 |
Lee S, Viqar F, Zimmerman ME, Narkhede A, Tosto G, Benzinger TL, Marcus DS, Fagan AM, Goate A, Fox NC, Cairns NJ, Holtzman DM, Buckles V, Ghetti B, McDade E, et al. White matter hyperintensities are a core feature of Alzheimer's disease: Evidence from the Dominantly Inherited Alzheimer Network. Annals of Neurology. PMID 27016429 DOI: 10.1002/ana.24647 |
0.01 |
|
| 2016 |
Su Y, Blazey TM, Owen CJ, Christensen JJ, Friedrichsen K, Joseph-Mathurin N, Wang Q, Hornbeck RC, Ances BM, Snyder AZ, Cash LA, Koeppe RA, Klunk WE, Galasko D, Brickman AM, ... ... Ghetti B, et al. Quantitative Amyloid Imaging in Autosomal Dominant Alzheimer's Disease: Results from the DIAN Study Group. Plos One. 11: e0152082. PMID 27010959 DOI: 10.1371/Journal.Pone.0152082 |
0.01 |
|
| 2016 |
Rodriguez-Porcel F, Lowder L, Rademakers R, Ravenscroft T, Ghetti B, Hagen MC, Espay AJ. Fulminant corticobasal degeneration: Agrypnia excitata in corticobasal syndrome. Neurology. PMID 26873956 DOI: 10.1212/Wnl.0000000000002491 |
0.01 |
|
| 2016 |
Pirisinu L, Di Bari MA, D'Agostino C, Marcon S, Riccardi G, Poleggi A, Cohen ML, Appleby BS, Gambetti P, Ghetti B, Agrimi U, Nonno R. Gerstmann-Sträussler-Scheinker disease subtypes efficiently transmit in bank voles as genuine prion diseases. Scientific Reports. 6: 20443. PMID 26841849 DOI: 10.1038/Srep20443 |
0.01 |
|
| 2016 |
Seibyl J, Catafau AM, Barthel H, Ishii K, Rowe CC, Leverenz JB, Ghetti B, Ironside JW, Takao M, Akatsu H, Murayama S, Bullich S, Mueller A, Koglin N, Schulz-Schaeffer WJ, et al. Impact of training method on the robustness of the visual assessment of 18F-florbetaben PET scans: results from a Phase 3 trial. Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine. PMID 26823561 DOI: 10.2967/jnumed.115.161927 |
0.01 |
|
| 2016 |
McDade E, Weng H, Wang G, Xiong C, Fagan AM, Hassenstab J, Marcus DS, Morris JC, Benzinger TL, Cairns NJ, Goate AM, Buckles V, Holtzman DM, Berman S, Ghetti B, et al. O5-02-01: Longitudinal Clinical and Biomarker Changes in Dominantly Inherited Alzheimer's Disease: The Dominantly Inherited Alzheimer Network Alzheimer's & Dementia. 12: P378-P379. DOI: 10.1016/J.Jalz.2016.06.710 |
0.01 |
|
| 2016 |
Buckles V, Xiong C, Weng H, Bateman R, Chhatwal JP, Ghetti B, Goate A, Graff-Radford NR, Hassenstab J, Mayeux R, Masters CL, McDade E, Moulder KL, Paumier KL, Ringman JM, et al. The Dian-Nacc Uds Comparison Study: Rates Of Cognitive Decline Alzheimers & Dementia. 12: 309. DOI: 10.1016/J.Jalz.2016.06.559 |
0.01 |
|
| 2016 |
Lee S, Zimmerman ME, Viqar F, Narkhede A, Tosto G, Lee Smith Benzinger T, Marcus DS, Goate AM, Fox NC, Cairns NJ, Holtzman DM, Buckles V, Ghetti B, McDade E, Martins RN, et al. O2-03-02: are White Matter Hyperintensities a Core Feature of Alzheimer’s Disease or Just a Reflection of Amyloid Angiopathy? Evidence From the Dominantly Inherited Alzheimer Network (DIAN) Alzheimer's & Dementia. 12: P226-P226. DOI: 10.1016/J.Jalz.2016.06.406 |
0.01 |
|
| 2016 |
Ghetti B, Murrell JR, Richardson RM, Epperson F, Gambetti P, Oblak AL. P4-228: Neuronal Intracytoplasmic PrP Deposits in Dominantly Inherited Creutzfeldt-Jakob Disease Associated With the PRNP
E200K-129V Haplotype Alzheimer's & Dementia. 12: P1116-P1117. DOI: 10.1016/J.Jalz.2016.06.2320 |
0.01 |
|
| 2016 |
Ghetti B, Dlouhy SR, Dupree B, Epperson F, Murrell JR, Oblak AL, Piccardo P, Richardson RM, Spina S, Takao M, Vidal R, Yamaguchi K, Young K. Contribution Of The Neuropathology Laboratory At Indiana University To The Deciphering Of Dominantly Inherited Dementias: 1976-2016 Alzheimers & Dementia. 12. DOI: 10.1016/J.Jalz.2016.06.1553 |
0.01 |
|
| 2016 |
Ghetti B, Murrell JR, Oblak AL, Epperson F, Foroud TM. P1-348: Neuropathology of Familial Alzheimer's Disease Associated with a Presenilin 1 A396T Mutation Reveals The Coexistence of Aβ, TAU, and A-Synuclein Proteinopathies Alzheimer's & Dementia. 12: P562-P563. DOI: 10.1016/J.Jalz.2016.06.1099 |
0.01 |
|
| 2015 |
Kovacs GG, Ferrer I, Grinberg LT, Alafuzoff I, Attems J, Budka H, Cairns NJ, Crary JF, Duyckaerts C, Ghetti B, Halliday GM, Ironside JW, Love S, Mackenzie IR, Munoz DG, et al. Aging-related tau astrogliopathy (ARTAG): harmonized evaluation strategy. Acta Neuropathologica. PMID 26659578 DOI: 10.1007/S00401-015-1509-X |
0.01 |
|
| 2015 |
Ringman JM, Liang LJ, Zhou Y, Vangala S, Teng E, Kremen S, Wharton D, Goate A, Marcus DS, Farlow M, Ghetti B, McDade E, Masters CL, Mayeux RP, Rossor M, et al. Erratum: Early behavioural changes in familial Alzheimers disease in the Dominantly Inherited Alzheimer Network (Brain (2015) 138 (103645) (10.1093/brain/awv004)) Brain. 138. PMID 26598496 DOI: 10.1093/Brain/Awv210 |
0.01 |
|
| 2015 |
Orrú CD, Groveman BR, Raymond LD, Hughson AG, Nonno R, Zou W, Ghetti B, Gambetti P, Caughey B. Correction: Bank Vole Prion Protein As an Apparently Universal Substrate for RT-QuIC-Based Detection and Discrimination of Prion Strains. Plos Pathogens. 11: e1005117. PMID 26284358 DOI: 10.1371/Journal.Ppat.1005117 |
0.01 |
|
| 2015 |
Wang F, Gordon BA, Ryman DC, Ma S, Xiong C, Hassenstab J, Goate A, Fagan AM, Cairns NJ, Marcus DS, McDade E, Ringman JM, Graff-Radford NR, Ghetti B, Farlow MR, et al. Cerebral amyloidosis associated with cognitive decline in autosomal dominant Alzheimer disease. Neurology. PMID 26245925 DOI: 10.1212/Wnl.0000000000001903 |
0.01 |
|
| 2015 |
Ehrlich M, Hallmann AL, Reinhardt P, Araúzo-Bravo MJ, Korr S, Röpke A, Psathaki OE, Ehling P, Meuth SG, Oblak AL, Murrell JR, Ghetti B, Zaehres H, Schöler HR, Sterneckert J, et al. Distinct Neurodegenerative Changes in an Induced Pluripotent Stem Cell Model of Frontotemporal Dementia Linked to Mutant TAU Protein. Stem Cell Reports. 5: 83-96. PMID 26143746 DOI: 10.1016/J.Stemcr.2015.06.001 |
0.01 |
|
| 2015 |
Lemoine L, Saint-Aubert L, Marutle A, Antoni G, Eriksson JP, Ghetti B, Okamura N, Nennesmo I, Gillberg PG, Nordberg A. Visualization of regional tau deposits using (3)H-THK5117 in Alzheimer brain tissue. Acta Neuropathologica Communications. 3: 40. PMID 26134112 DOI: 10.1186/S40478-015-0220-4 |
0.01 |
|
| 2015 |
Orrú CD, Groveman BR, Raymond LD, Hughson AG, Nonno R, Zou W, Ghetti B, Gambetti P, Caughey B. Bank Vole Prion Protein As an Apparently Universal Substrate for RT-QuIC-Based Detection and Discrimination of Prion Strains. Plos Pathogens. 11: e1004983. PMID 26086786 DOI: 10.1371/Journal.Ppat.1004983 |
0.01 |
|
| 2015 |
Kouri N, Ross OA, Dombroski B, Younkin CS, Serie DJ, Soto-Ortolaza A, Baker M, Finch NC, Yoon H, Kim J, Fujioka S, McLean CA, Ghetti B, Spina S, Cantwell LB, et al. Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy. Nature Communications. 6: 7247. PMID 26077951 DOI: 10.1038/Ncomms8247 |
0.01 |
|
| 2015 |
Cairns NJ, Perrin RJ, Franklin EE, Carter D, Vincent B, Xie M, Bateman RJ, Benzinger T, Friedrichsen K, Brooks WS, Halliday GM, McLean C, Ghetti B, Morris JC, et al. Neuropathologic assessment of participants in two multi-center longitudinal observational studies: The Alzheimer Disease Neuroimaging Initiative (ADNI) and the Dominantly Inherited Alzheimer Network (DIAN). Neuropathology : Official Journal of the Japanese Society of Neuropathology. PMID 25964057 DOI: 10.1111/Neup.12205 |
0.01 |
|
| 2015 |
Sabri O, Sabbagh MN, Seibyl J, Barthel H, Akatsu H, Ouchi Y, Senda K, Murayama S, Ishii K, Takao M, Beach TG, Rowe CC, Leverenz JB, Ghetti B, Ironside JW, et al. Florbetaben PET imaging to detect amyloid beta plaques in Alzheimer disease: Phase 3 study. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 25824567 DOI: 10.1016/j.jalz.2015.02.004 |
0.01 |
|
| 2015 |
Kaushal V, Dye R, Pakavathkumar P, Foveau B, Flores J, Hyman B, Ghetti B, Koller BH, LeBlanc AC. Neuronal NLRP1 inflammasome activation of Caspase-1 coordinately regulates inflammatory interleukin-1-beta production and axonal degeneration-associated Caspase-6 activation. Cell Death and Differentiation. PMID 25744023 DOI: 10.1038/Cdd.2015.16 |
0.01 |
|
| 2015 |
Ringman JM, Liang LJ, Zhou Y, Vangala S, Teng E, Kremen S, Wharton D, Goate A, Marcus DS, Farlow M, Ghetti B, McDade E, Masters CL, Mayeux RP, Rossor M, et al. Early behavioural changes in familial Alzheimer's disease in the Dominantly Inherited Alzheimer Network. Brain : a Journal of Neurology. 138: 1036-45. PMID 25688083 DOI: 10.1093/Brain/Awv004 |
0.01 |
|
| 2015 |
Beecham GW, Dickson DW, Scott WK, Martin ER, Schellenberg G, Nuytemans K, Larson EB, Buxbaum JD, Trojanowski JQ, Van Deerlin VM, Hurtig HI, Mash DC, Beach TG, Troncoso JC, Pletnikova O, ... ... Ghetti B, et al. PARK10 is a major locus for sporadic neuropathologically confirmed Parkinson disease. Neurology. 84: 972-80. PMID 25663231 DOI: 10.1212/Wnl.0000000000001332 |
0.01 |
|
| 2015 |
Li W, Garringer HJ, Goodwin CB, Richine B, Acton A, VanDuyn N, Muhoberac BB, Irimia-Dominguez J, Chan RJ, Peacock M, Nass R, Ghetti B, Vidal R. Systemic and cerebral iron homeostasis in ferritin knock-out mice. Plos One. 10: e0117435. PMID 25629408 DOI: 10.1371/Journal.Pone.0117435 |
0.01 |
|
| 2015 |
Nho K, Kim S, Risacher SL, Shen L, Corneveaux JJ, Swaminathan S, Lin H, Ramanan VK, Liu Y, Foroud TM, Inlow MH, Siniard AL, Reiman RA, Aisen PS, Petersen RC, ... ... Ghetti B, et al. Protective variant for hippocampal atrophy identified by whole exome sequencing. Annals of Neurology. 77: 547-52. PMID 25559091 DOI: 10.1002/Ana.24349 |
0.01 |
|
| 2015 |
Ghetti B, Oblak AL, Boeve BF, Johnson KA, Dickerson BC, Goedert M. Invited review: Frontotemporal dementia caused by microtubule-associated protein tau gene (MAPT) mutations: a chameleon for neuropathology and neuroimaging. Neuropathology and Applied Neurobiology. 41: 24-46. PMID 25556536 DOI: 10.1111/Nan.12213 |
0.01 |
|
| 2015 |
Wang LS, Naj AC, Graham RR, Crane PK, Kunkle BW, Cruchaga C, Murcia JD, Cannon-Albright L, Baldwin CT, Zetterberg H, Blennow K, Kukull WA, Faber KM, Schupf N, Norton MC, ... ... Ghetti B, et al. Rarity of the Alzheimer disease-protective APP A673T variant in the United States. Jama Neurology. 72: 209-16. PMID 25531812 DOI: 10.1001/Jamaneurol.2014.2157 |
0.01 |
|
| 2015 |
Su Y, Blazey TM, Snyder AZ, Raichle ME, Marcus DS, Ances BM, Bateman RJ, Cairns NJ, Aldea P, Cash L, Christensen JJ, Friedrichsen K, Hornbeck RC, Farrar AM, Owen CJ, ... ... Ghetti B, et al. Partial volume correction in quantitative amyloid imaging. Neuroimage. 107: 55-64. PMID 25485714 DOI: 10.1016/J.Neuroimage.2014.11.058 |
0.01 |
|
| 2015 |
Catafau AM, Bullich S, Seibyl J, Barthel H, Ghetti B, Leverenz JB, Ironside JW, Schulz-Schaeffer WJ, Hoffman A, Sabri O. O4‐08‐03: Do cerebellar plaques influence
18
F‐florbetaben amyloid PET scan quantification? Alzheimer's & Dementia. 11. DOI: 10.1016/j.jalz.2015.07.389 |
0.01 |
|
| 2015 |
Leverenz JB, Sabri O, Catafau AM, Barthel H, Seibyl J, Ghetti B, Ironside JW, Bullich S, Schulz-Schaeffer WJ, Hoffman A. O4‐08‐02: Impact of morphologically distinct amyloid ß (Aß) deposits on 18F‐florbetaben (FBB) PET scans Alzheimer's & Dementia. 11. DOI: 10.1016/j.jalz.2015.07.388 |
0.01 |
|
| 2015 |
Deters K, Risacher SL, Farlow MR, Unverzagt FW, Hutchins GD, Yoder KK, Murrell JR, Epperson F, Saykin AJ, Ghetti B. P2-124: Glucose hypometabolism in gerstmann-sträussler-scheinker patients with the F198S mutation Alzheimer's & Dementia. 11: P530-P531. DOI: 10.1016/j.jalz.2015.06.662 |
0.01 |
|
| 2015 |
Newell K, Murrell JR, Sundararajan J, Hylton P, Ghetti B. P1-212: Neuropathologic characterization of cerebral β-amyloid angiopathy in familial cerebral hemorrhage Alzheimer's & Dementia. 11: P431-P432. DOI: 10.1016/j.jalz.2015.06.412 |
0.01 |
|
| 2015 |
Ghetti B, Oblak AL, Abdulkader MM, Murrell JR, Richardson RM, Epperson F, Farlow MR, Matthews BR, Unverzagt FW. P1-086: Multiple proteinopathies underlying atypical dementia Alzheimer's & Dementia. 11: P372-P372. DOI: 10.1016/J.Jalz.2015.06.283 |
0.01 |
|
| 2015 |
Abdulkader MM, Hagen MC, Murrell JR, Oblak AL, Rodriguez-Porcel F, Cioffi SM, Fenoglio C, Scarpini E, Espay A, Ghetti B, Galimberti D. P4-009: Frontotemporal dementia and parkinsonism linked to chromosome 17 granulin: Clinical and pathologic study of a patient from a new pedigree Alzheimer's & Dementia. 11: P768-P769. DOI: 10.1016/J.Jalz.2015.06.1713 |
0.01 |
|
| 2015 |
Deters K, Risacher SL, Farlow MR, Unverzagt FW, Hutchins GD, Yoder KK, Murrell JR, Epperson F, Saykin AJ, Ghetti B. IC-P-055: Glucose hypometabolism in gerstmann-sträussler-scheinker patients with the F198S mutation Alzheimer's & Dementia. 11: P43-P43. DOI: 10.1016/J.Jalz.2015.06.076 |
0.01 |
|
| 2015 |
Leverenz JB, Sabri O, Catafau AM, Barthel H, Seibyl J, Ghetti B, Ironside JW, Bullich S, Schulz-Schaeffer WJ, Hoffman A. IC‐P‐002: Impact of morphologically distinct amyloid ß (Aß) deposits on 18F‐florbetaben (FBB) PET scans Alzheimer's & Dementia. 11. DOI: 10.1016/j.jalz.2015.06.022 |
0.01 |
|
| 2015 |
Catafau AM, Bullich S, Seibyl J, Barthel H, Ghetti B, Leverenz JB, Ironside JW, Schulz-Schaeffer WJ, Hoffman A, Sabri O. IC‐P‐001: Do cerebellar plaques influence
18
F‐florbetaben amyloid PET scan quantification? Alzheimer's & Dementia. 11. DOI: 10.1016/j.jalz.2015.06.021 |
0.01 |
|
| 2014 |
Deters KD, Risacher SL, Farlow MR, Unverzagt FW, Kareken DA, Hutchins GD, Yoder KK, Murrell JR, Spina S, Epperson F, Gao S, Saykin AJ, Ghetti B. Cerebral hypometabolism and grey matter density in MAPT intron 10 +3 mutation carriers. American Journal of Neurodegenerative Disease. 3: 103-14. PMID 25628962 |
0.01 |
|
| 2014 |
Liachko NF, McMillan PJ, Strovas TJ, Loomis E, Greenup L, Murrell JR, Ghetti B, Raskind MA, Montine TJ, Bird TD, Leverenz JB, Kraemer BC. The tau tubulin kinases TTBK1/2 promote accumulation of pathological TDP-43. Plos Genetics. 10: e1004803. PMID 25473830 DOI: 10.1371/Journal.Pgen.1004803 |
0.01 |
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| 2014 |
Ringman JM, Goate A, Masters CL, Cairns NJ, Danek A, Graff-Radford N, Ghetti B, Morris JC. Genetic heterogeneity in Alzheimer disease and implications for treatment strategies. Current Neurology and Neuroscience Reports. 14: 499. PMID 25217249 DOI: 10.1007/S11910-014-0499-8 |
0.01 |
|
| 2014 |
Naj AC, Jun G, Reitz C, Kunkle BW, Perry W, Park YS, Beecham GW, Rajbhandary RA, Hamilton-Nelson KL, Wang LS, Kauwe JS, Huentelman MJ, Myers AJ, Bird TD, Boeve BF, ... ... Ghetti B, et al. Effects of multiple genetic loci on age at onset in late-onset Alzheimer disease: a genome-wide association study. Jama Neurology. 71: 1394-404. PMID 25199842 DOI: 10.1001/Jamaneurol.2014.1491 |
0.01 |
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| 2014 |
Beecham GW, Hamilton K, Naj AC, Martin ER, Huentelman M, Myers AJ, Corneveaux JJ, Hardy J, Vonsattel JP, Younkin SG, Bennett DA, De Jager PL, Larson EB, Crane PK, Kamboh MI, ... ... Ghetti B, et al. Genome-wide association meta-analysis of neuropathologic features of Alzheimer's disease and related dementias. Plos Genetics. 10: e1004606. PMID 25188341 DOI: 10.1371/Journal.Pgen.1004606 |
0.01 |
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| 2014 |
Thomas JB, Brier MR, Bateman RJ, Snyder AZ, Benzinger TL, Xiong C, Raichle M, Holtzman DM, Sperling RA, Mayeux R, Ghetti B, Ringman JM, Salloway S, McDade E, Rossor MN, et al. Functional connectivity in autosomal dominant and late-onset Alzheimer disease. Jama Neurology. 71: 1111-22. PMID 25069482 DOI: 10.1001/Jamaneurol.2014.1654 |
0.01 |
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| 2014 |
Boyd CD, Tierney M, Wassermann EM, Spina S, Oblak AL, Ghetti B, Grafman J, Huey E. Visuoperception test predicts pathologic diagnosis of Alzheimer disease in corticobasal syndrome. Neurology. 83: 510-9. PMID 24991033 DOI: 10.1212/Wnl.0000000000000667 |
0.01 |
|
| 2014 |
Ryman DC, Acosta-Baena N, Aisen PS, Bird T, Danek A, Fox NC, Goate A, Frommelt P, Ghetti B, Langbaum JB, Lopera F, Martins R, Masters CL, Mayeux RP, McDade E, et al. Symptom onset in autosomal dominant Alzheimer disease: a systematic review and meta-analysis. Neurology. 83: 253-60. PMID 24928124 DOI: 10.1212/Wnl.0000000000000596 |
0.01 |
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| 2014 |
Oblak AL, Hagen MC, Sweadner KJ, Haq I, Whitlow CT, Maldjian JA, Epperson F, Cook JF, Stacy M, Murrell JR, Ozelius LJ, Brashear A, Ghetti B. Rapid-onset dystonia-parkinsonism associated with the I758S mutation of the ATP1A3 gene: a neuropathologic and neuroanatomical study of four siblings. Acta Neuropathologica. 128: 81-98. PMID 24803225 DOI: 10.1007/S00401-014-1279-X |
0.01 |
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| 2014 |
Fagan AM, Xiong C, Jasielec MS, Bateman RJ, Goate AM, Benzinger TL, Ghetti B, Martins RN, Masters CL, Mayeux R, Ringman JM, Rossor MN, Salloway S, Schofield PR, Sperling RA, et al. Longitudinal change in CSF biomarkers in autosomal-dominant Alzheimer's disease. Science Translational Medicine. 6: 226ra30. PMID 24598588 DOI: 10.1126/Scitranslmed.3007901 |
0.01 |
|
| 2014 |
Gallagher MD, Suh E, Grossman M, Elman L, McCluskey L, Van Swieten JC, Al-Sarraj S, Neumann M, Gelpi E, Ghetti B, Rohrer JD, Halliday G, Van Broeckhoven C, Seilhean D, Shaw PJ, et al. TMEM106B is a genetic modifier of frontotemporal lobar degeneration with C9orf72 hexanucleotide repeat expansions. Acta Neuropathologica. 127: 407-18. PMID 24442578 DOI: 10.1007/S00401-013-1239-X |
0.01 |
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| 2014 |
Hoffmann S, Murrell J, Harms L, Miller K, Meisel A, Brosch T, Scheel M, Ghetti B, Goebel HH, Stenzel W. Enlarging the nosological spectrum of hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS). Brain Pathology (Zurich, Switzerland). 24: 452-8. PMID 24428556 DOI: 10.1111/Bpa.12120 |
0.01 |
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| 2014 |
Zanusso G, Fiorini M, Ferrari S, Meade-White K, Barbieri I, Brocchi E, Ghetti B, Monaco S. Gerstmann-Sträussler-Scheinker disease and "anchorless prion protein" mice share prion conformational properties diverging from sporadic Creutzfeldt-Jakob disease. The Journal of Biological Chemistry. 289: 4870-81. PMID 24398683 DOI: 10.1074/Jbc.M113.531335 |
0.01 |
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| 2014 |
Ehrlich M, Hallmann AL, Reinhardt P, Araúzo-Bravo MJ, Korr S, Röpke A, Psathaki OE, Ehling P, Meuth SG, Oblak AL, Murrell JR, Ghetti B, Zaehres H, Schöler HR, Sterneckert J, et al. Distinct Neurodegenerative Changes in an Induced Pluripotent Stem Cell Model of Frontotemporal Dementia Linked to Mutant TAU Protein Stem Cell Reports. DOI: 10.1016/j.stemcr.2015.06.001 |
0.01 |
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| 2014 |
Goni F, Prelli F, Drummond E, Herline K, Marta M, Sun Y, Ghetti BF, Wisniewski T. Anti-Conformational Monoclonal Antibody With Selective Preference For Prp Res Strains From Different Animal Species And Humans Alzheimers & Dementia. 10: 924. DOI: 10.1016/J.Jalz.2014.07.141 |
0.01 |
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| 2014 |
Sabri O, Catafau A, Barthel H, Ishii K, Rowe CC, Leverenz J, Ghetti BF, Ironside J, Takao M, Akatsu H, Murayama S, Koglin N, Schulz‐Schaeffer W, Sabbagh M, Stephens A, et al. P2‐225: POSTMORTEM HISTOPATHOLOGY‐PROOFED EFFICACY AND RELIABILITY OF THE VISUAL ASSESSMENT OF 18F‐FLORBETABEN PET SCANS IN THE DETECTION OF CEREBRAL BETA‐AMYLOID NEURITIC PLAQUES Alzheimer's & Dementia. 10. DOI: 10.1016/j.jalz.2014.05.902 |
0.01 |
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| 2014 |
Newell K, Vonsattel JP, Murrell J, Ghetti BF, Gambetti P, Dubinsky R, Swerdlow RH. P4-147: PHENOTYPIC CHARACTERIZATION OF EARLY ONSET FAMILIAL AD ASSOCIATED WITH A PSEN1 L418F MUTATION Alzheimer's & Dementia. 10: P842-P843. DOI: 10.1016/J.Jalz.2014.05.1663 |
0.01 |
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| 2014 |
Newell KL, Murrell JR, Oblak AL, Epperson F, Ottley B, Unverzagt FW, Farlow MR, Risacher SL, Saykin AJ, Morris JC, Cairns NJ, Ghetti BF. P4-146: POSTERIOR CEREBRAL ATROPHY ASSOCIATED WITH THE PSEN1 I229F MUTATION Alzheimer's & Dementia. 10: P842-P842. DOI: 10.1016/j.jalz.2014.05.1662 |
0.01 |
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| 2014 |
West JD, Risacher SL, Tallman EM, McDonald BC, Wang Y, Epperson F, Murrell J, Benzinger TL, Bateman R, Morris JC, Farlow MR, Ghetti BF, Saykin AJ. P4-105: ALTERED FMRI ACTIVATION PATTERN DURING VISUAL SCENE ENCODING IN AFFECTED AND NON-AFFECTED CARRIERS OF PSEN1 AND APP MUTATIONS Alzheimer's & Dementia. 10: P822-P823. DOI: 10.1016/j.jalz.2014.05.1621 |
0.01 |
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| 2014 |
Newell KL, Murrell J, Oblak AL, Epperson F, Ottley B, Unverzagt F, Farlow MR, Risacher SL, Saykin AJ, Morris JC, Cairns NJ, Ghetti BF. IC-P-138: POSTERIOR CEREBRAL ATROPHY ASSOCIATED WITH THE PSEN1 I229F MUTATION Alzheimer's & Dementia. 10: P78-P79. DOI: 10.1016/J.Jalz.2014.05.144 |
0.01 |
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| 2014 |
Ghetti BF, Dickson DW, Ilangovan S, Reyes MG, Oblak AL, Epperson F, Murrell JR. Psen1 M233V Mutation Causes Very Early Onset Alzheimer Disease: The Importance Of Neuropathologic Archival Tissue Alzheimers & Dementia. 10. DOI: 10.1016/J.Jalz.2014.05.1096 |
0.01 |
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| 2014 |
Ghetti BF, Miller DC, Zou W, Cohen Y, Richardson R, Oblak AL, Gambetti P, Murrell JR. Early Onset And Rapid Course Of Alzheimer Disease Associated With The I143T Psen1 Mutation Alzheimers & Dementia. 10: 629. DOI: 10.1016/J.Jalz.2014.05.1095 |
0.01 |
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| 2014 |
Risacher SL, West JD, Tallman EM, McDonald BC, Wang Y, Epperson F, Murrell J, Benzinger TL, Bateman R, Morris JC, Farlow MR, Ghetti BF, Saykin AJ. IC-P-094: ALTERED FMRI ACTIVATION PATTERN DURING VISUAL SCENE ENCODING IN AFFECTED AND NON-AFFECTED CARRIERS OF PSEN1 AND APP MUTATIONS Alzheimer's & Dementia. 10: P53-P53. DOI: 10.1016/J.Jalz.2014.05.099 |
0.01 |
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| 2014 |
Ghetti BF, Newell KL, Abrahamson EE, Cairns NJ, Murrell JR, Oblak AL, Unverzagt FW, Farlow MR, Epperson F, Richardson R, Dupree B, Morris JC, Klunk WE, Saykin AJ, Risacher SL, et al. IC-P-032: COMPARATIVE ANALYSIS OF PIB IN VIVO
WITH 6-CN-PIB AND Aβ-IMMUNOHISTOCHEMISTRY POSTMORTEM IN FAMILIAL ALZHEIMER DISEASE ASSOCIATED WITH THE PSEN1 I229F MUTATION Alzheimer's & Dementia. 10: P20-P21. DOI: 10.1016/J.Jalz.2014.05.036 |
0.01 |
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| 2014 |
Clavaguera F, Ghetti B, Schweighauser G, Akatsu H, Hench J, Tolnay M, Goedert M. F2‐04‐03: TRANSMISSION AND SPREADING OF TAUOPATHIES IN TRANSGENIC MOUSE BRAIN Alzheimer's & Dementia. 10. DOI: 10.1016/j.jalz.2014.04.152 |
0.01 |
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| 2014 |
Ghetti BF, Newell KL, Abrahamson EE, Cairns NJ, Murrell JR, Oblak AL, Unverzagt FW, Farlow MR, Epperson F, Richardson R, Dupree B, Morris JC, Klunk WE, Saykin AJ, Risacher SL, et al. O1-01-03: COMPARATIVE ANALYSIS OF PIB IN VIVO
WITH 6-CN-PIB AND AB-IMMUNOHISTOCHEMISTRY POSTMORTEM IN FAMILIAL ALZHEIMER'S DISEASE ASSOCIATED WITH THE PSEN1 I229F MUTATION Alzheimer's & Dementia. 10: P129-P129. DOI: 10.1016/j.jalz.2014.04.058 |
0.01 |
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| 2013 |
Kim S, Nho K, Risacher SL, Inlow M, Swaminathan S, Yoder KK, Shen L, West JD, McDonald BC, Tallman EF, Hutchins GD, Fletcher JW, Farlow MR, Ghetti B, Saykin AJ. PARP1 gene variation and microglial activity on [(11)C]PBR28 PET in older adults at risk for Alzheimer's disease. Multimodal Brain Image Analysis : Third International Workshop, Mbia 2013, Held in Conjunction With Miccai 2013, Nagoya, Japan, September 22, 2013 : Proceedings / Li Shen, Tianming Liu, Pew-Thian Yap, Heng Huang, Dinggang Shen, Carl-Fre.... 8159: 150-158. PMID 25383391 DOI: 10.1007/978-3-319-02126-3_15 |
0.01 |
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| 2013 |
Alonso Adel C, ElAkkad E, Gong C, Liu F, Tanaka T, Kudo T, Tatebayashi Y, Pei J, Wang J, Khatoon S, Flory M, Ghetti B, Gozes I, Novak M, Novak M, et al. Inge Grundke-Iqbal, Ph.D. (1937–2012): the discoverer of the abnormal hyperphosphorylation of tau in Alzheimer’s disease. Journal of Molecular Neuroscience : Mn. 49: 430-5. PMID 24883456 DOI: 10.1007/S12031-012-9925-Z |
0.01 |
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| 2013 |
Benzinger TL, Blazey T, Jack CR, Koeppe RA, Su Y, Xiong C, Raichle ME, Snyder AZ, Ances BM, Bateman RJ, Cairns NJ, Fagan AM, Goate A, Marcus DS, Aisen PS, ... ... Ghetti B, et al. Regional variability of imaging biomarkers in autosomal dominant Alzheimer's disease. Proceedings of the National Academy of Sciences of the United States of America. 110: E4502-9. PMID 24194552 DOI: 10.1073/Pnas.1317918110 |
0.01 |
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| 2013 |
Roher AE, Maarouf CL, Malek-Ahmadi M, Wilson J, Kokjohn TA, Daugs ID, Whiteside CM, Kalback WM, Macias MP, Jacobson SA, Sabbagh MN, Ghetti B, Beach TG. Subjects harboring presenilin familial Alzheimer's disease mutations exhibit diverse white matter biochemistry alterations. American Journal of Neurodegenerative Disease. 2: 187-207. PMID 24093083 |
0.01 |
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| 2013 |
Cash DM, Ridgway GR, Liang Y, Ryan NS, Kinnunen KM, Yeatman T, Malone IB, Benzinger TL, Jack CR, Thompson PM, Ghetti BF, Saykin AJ, Masters CL, Ringman JM, Salloway SP, et al. The pattern of atrophy in familial Alzheimer disease: volumetric MRI results from the DIAN study. Neurology. 81: 1425-33. PMID 24049139 DOI: 10.1212/Wnl.0B013E3182A841C6 |
0.01 |
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| 2013 |
Mills SM, Mallmann J, Santacruz AM, Fuqua A, Carril M, Aisen PS, Althage MC, Belyew S, Benzinger TL, Brooks WS, Buckles VD, Cairns NJ, Clifford D, Danek A, Fagan AM, ... ... Ghetti B, et al. Preclinical trials in autosomal dominant AD: implementation of the DIAN-TU trial. Revue Neurologique. 169: 737-43. PMID 24016464 DOI: 10.1016/J.Neurol.2013.07.017 |
0.01 |
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| 2013 |
Ahmed Z, Bigio EH, Budka H, Dickson DW, Ferrer I, Ghetti B, Giaccone G, Hatanpaa KJ, Holton JL, Josephs KA, Powers J, Spina S, Takahashi H, White CL, Revesz T, et al. Globular glial tauopathies (GGT): consensus recommendations. Acta Neuropathologica. 126: 537-44. PMID 23995422 DOI: 10.1007/S00401-013-1171-0 |
0.01 |
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| 2013 |
Kim S, Swaminathan S, Inlow M, Risacher SL, Nho K, Shen L, Foroud TM, Petersen RC, Aisen PS, Soares H, Toledo JB, Shaw LM, Trojanowski JQ, Weiner MW, McDonald BC, ... ... Ghetti B, et al. Influence of genetic variation on plasma protein levels in older adults using a multi-analyte panel. Plos One. 8: e70269. PMID 23894628 DOI: 10.1371/Journal.Pone.0070269 |
0.01 |
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| 2013 |
Nho K, Corneveaux JJ, Kim S, Lin H, Risacher SL, Shen L, Swaminathan S, Ramanan VK, Liu Y, Foroud T, Inlow MH, Siniard AL, Reiman RA, Aisen PS, Petersen RC, ... ... Ghetti B, et al. Identification of functional variants from whole-exome sequencing, combined with neuroimaging genetics. Molecular Psychiatry. 18: 739. PMID 23787478 DOI: 10.1038/Mp.2013.81 |
0.01 |
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| 2013 |
Sundal C, Fujioka S, Van Gerpen JA, Wider C, Nicholson AM, Baker M, Shuster EA, Aasly J, Spina S, Ghetti B, Roeber S, Garbern J, Tselis A, Swerdlow RH, Miller BB, et al. Parkinsonian features in hereditary diffuse leukoencephalopathy with spheroids (HDLS) and CSF1R mutations. Parkinsonism & Related Disorders. 19: 869-77. PMID 23787135 DOI: 10.1016/J.Parkreldis.2013.05.013 |
0.01 |
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| 2013 |
Clavaguera F, Akatsu H, Fraser G, Crowther RA, Frank S, Hench J, Probst A, Winkler DT, Reichwald J, Staufenbiel M, Ghetti B, Goedert M, Tolnay M. Brain homogenates from human tauopathies induce tau inclusions in mouse brain. Proceedings of the National Academy of Sciences of the United States of America. 110: 9535-40. PMID 23690619 DOI: 10.1073/Pnas.1301175110 |
0.01 |
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| 2013 |
Nho K, Corneveaux JJ, Kim S, Lin H, Risacher SL, Shen L, Swaminathan S, Ramanan VK, Liu Y, Foroud T, Inlow MH, Siniard AL, Reiman RA, Aisen PS, Petersen RC, ... ... Ghetti B, et al. Whole-exome sequencing and imaging genetics identify functional variants for rate of change in hippocampal volume in mild cognitive impairment. Molecular Psychiatry. 18: 781-7. PMID 23608917 DOI: 10.1038/Mp.2013.24 |
0.01 |
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| 2013 |
Nalls MA, Duran R, Lopez G, Kurzawa-Akanbi M, McKeith IG, Chinnery PF, Morris CM, Theuns J, Crosiers D, Cras P, Engelborghs S, De Deyn PP, Van Broeckhoven C, Mann DM, Snowden J, ... ... Ghetti B, et al. A multicenter study of glucocerebrosidase mutations in dementia with Lewy bodies. Jama Neurology. 70: 727-35. PMID 23588557 DOI: 10.1001/Jamaneurol.2013.1925 |
0.01 |
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| 2013 |
Garringer HJ, Murrell J, Sammeta N, Gnezda A, Ghetti B, Vidal R. Increased tau phosphorylation and tau truncation, and decreased synaptophysin levels in mutant BRI2/tau transgenic mice. Plos One. 8: e56426. PMID 23418567 DOI: 10.1371/Journal.Pone.0056426 |
0.01 |
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| 2013 |
Spina S, Van Laar AD, Murrell JR, Hamilton RL, Kofler JK, Epperson F, Farlow MR, Lopez OL, Quinlan J, DeKosky ST, Ghetti B. Phenotypic variability in three families with valosin-containing protein mutation. European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies. 20: 251-8. PMID 22900631 DOI: 10.1111/J.1468-1331.2012.03831.X |
0.01 |
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| 2013 |
Mills S, Mallmann J, Santacruz A, Fuqua A, Carril M, Aisen P, Althage M, Belyew S, Benzinger T, Brooks W, Buckles V, Cairns N, Clifford D, Danek A, Fagan A, ... ... Ghetti B, et al. Erratum to “Preclinical trials in autosomal dominant AD: Implementation of the DIAN-TU trial” [Rev. Neurol. 169 (10) (2013) 737–743] Revue Neurologique. 169: 1018. DOI: 10.1016/J.Neurol.2013.10.005 |
0.01 |
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| 2013 |
Newell K, Murrell J, Glazier B, Epperson F, Ghetti B. P2-228: Familial neurodegenerative disease with dementia, pyramidal tract signs, hydrocephalus and leukoencephalopathy: Just atypical Alzheimer's disease? Alzheimer's & Dementia. 9: P440-P440. DOI: 10.1016/j.jalz.2013.05.874 |
0.01 |
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| 2013 |
Oblak A, Murrell I, Huey E, Wassermann E, Grafman J, Pietrini P, Kapogiannis D, Glazier B, Ghetti B. P2-226: Frontotemporal dementia associated with the MAPT IVS10+16C>T mutation: A multidisciplinary study Alzheimer's & Dementia. 9: P439-P440. DOI: 10.1016/J.Jalz.2013.05.872 |
0.01 |
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| 2013 |
Wang Y, West J, Shen L, Risacher S, Sporns O, McDonald B, Tallman E, Ghetti B, Gao S, Farlow M, O'Neill D, Xiao H, Saykin A. P1-324: Altered connectome mapping in people with mild cognitive impairment and older adults with cognitive complaints Alzheimer's & Dementia. 9: P276-P276. DOI: 10.1016/J.Jalz.2013.05.550 |
0.01 |
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| 2013 |
Wang Y, West J, Risacher S, McDonald B, Tallman E, Ghetti B, Farlow M, Gao S, O'Neill D, Saykin A. P1-323: Characterization of regional cerebral blood flow in people with mild cognitive impairment and older adults with cognitive complaints Alzheimer's & Dementia. 9: P276-P276. DOI: 10.1016/j.jalz.2013.05.549 |
0.01 |
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| 2013 |
Risacher S, Kim S, Yoder K, Shen L, West J, McDonald B, Wang Y, Nho K, Tallman E, Hutchins G, Fletcher J, Ghetti B, Gao S, Farlow M, Saykin A. P1-315: Relationship of microglial activation measured by [11C]PBR28 PET, atrophy on MRI and plasma biomarkers in individuals with and at-risk for Alzheimer's disease Alzheimer's & Dementia. 9: P272-P273. DOI: 10.1016/j.jalz.2013.05.541 |
0.01 |
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| 2013 |
Swaminathan S, Nho K, Risacher S, Yoder K, Kim S, Shen L, Tallman E, McDonald B, Hutchins G, Fletcher J, Farlow M, Ghetti B, Foroud T, Saykin A. P1-276: Gene-based analyses of microglial activation on [11C]PBR28 PET in older adults at risk for Alzheimer's disease Alzheimer's & Dementia. 9: P255-P255. DOI: 10.1016/j.jalz.2013.05.501 |
0.01 |
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| 2013 |
Thomas J, Brier M, Bateman R, Snyder A, Benzinger T, Xiong C, Raichle M, Sperling R, Mayeux R, Ghetti B, Ringman J, Salloway S, McDade E, Rossor M, Schofield P, et al. P1-271: Resting state functional connectivity in autosomal dominant and sporadic Alzheimer's disease Alzheimer's & Dementia. 9: P252-P253. DOI: 10.1016/j.jalz.2013.05.496 |
0.01 |
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| 2013 |
Kinnunen K, Ryan N, Cash D, Leite AB, Finnegan S, Cardoso M, Leung K, Modat M, Benzinger T, Jack C, Marcus D, Raichle M, Thompson P, Ringman J, Ghetti B, et al. P1-269: Are early atrophy patterns in autosomal dominant familial Alzheimer's disease gene-dependent? Alzheimer's & Dementia. 9: P251-P252. DOI: 10.1016/j.jalz.2013.05.494 |
0.01 |
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| 2013 |
Risacher S, Kim S, Klaunig J, Shen L, McDonald B, Farlow M, Ghetti B, Gao S, Wang Z, Zhou S, Saykin A. P1-051: DNA damage in peripheral blood cells is associated with Alzheimer's-related plasma proteins in individuals at risk for progression to Alzheimer's disease Alzheimer's & Dementia. 9: P171-P171. DOI: 10.1016/J.Jalz.2013.05.272 |
0.01 |
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| 2013 |
Thomas J, Brier M, Bateman R, Snyder A, Benzinger T, Xiong C, Raichle M, Sperling R, Mayeux R, Ghetti B, Ringman J, Salloway S, McDade E, Rossor M, Schofield P, et al. IC-P-184: Resting state functional connectivity in autosomal dominant and sporadic Alzheimer's disease Alzheimer's & Dementia. 9: P105-P105. DOI: 10.1016/J.Jalz.2013.05.181 |
0.01 |
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| 2013 |
Kim S, Nho K, Risacher S, Swaminathan S, Yoder K, Shen L, West J, McDonald B, Tallman E, Hutchins G, Fletcher J, Farlow M, Ghetti B, Saykin A. IC-P-143: Influence of PARP1 haplotype on [11C]PBR28 PET brain uptake Alzheimer's & Dementia. 9: P84-P85. DOI: 10.1016/j.jalz.2013.05.140 |
0.01 |
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| 2013 |
Kim S, Nho K, Risacher S, Swaminathan S, Yoder K, Shen L, West J, McDonald B, Tallman E, Hutchins G, Fletcher J, Farlow M, Ghetti B, Saykin A. P4-006: Influence of PARP1 haplotype on [11C]PBR28 PET brain uptake Alzheimer's & Dementia. 9: P706-P707. DOI: 10.1016/J.Jalz.2013.05.1394 |
0.01 |
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| 2013 |
Swaminathan S, Nho K, Risacher S, Yoder K, Kim S, Shen L, Tallman E, McDonald B, Hutchins G, Fletcher J, Farlow M, Ghetti B, Foroud T, Saykin A. IC-P-137: Gene-based analyses of microglial activation on [11C] PBR28 PET in older adults at risk for Alzheimer's disease Alzheimer's & Dementia. 9: P81-P81. DOI: 10.1016/J.Jalz.2013.05.134 |
0.01 |
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| 2013 |
Cash D, Ridgway G, Modat M, Ryan N, Kinnunen K, Cardoso J, Benzinger T, Jack CR, Raichle M, Marcus D, Ringman J, Thompson P, Ghetti B, Salloway S, Sperling R, et al. P3-134: Dissociating volume and intensity differences in familial Alzheimer's disease Alzheimer's & Dementia. 9: P603-P603. DOI: 10.1016/j.jalz.2013.05.1205 |
0.01 |
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| 2013 |
Wang Y, West J, Shen L, Risacher S, Sporns O, McDonald B, Tallman E, Ghetti B, Gao S, Farlow M, O'Neill D, Xiao H, Saykin A. IC-P-118: Altered connectome mapping in mild cognitive impairment and older adults with cognitive complaints Alzheimer's & Dementia. 9: P71-P71. DOI: 10.1016/J.Jalz.2013.05.115 |
0.01 |
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| 2013 |
Wang Y, West J, Risacher S, McDonald B, Tallman E, Ghetti B, Farlow M, Gao S, O'Neill D, Saykin A. IC-P-117: Characterization of regional cerebral blood flow in mild cognitive impairment and older adults with cognitive complaints Alzheimer's & Dementia. 9: P71-P71. DOI: 10.1016/J.Jalz.2013.05.114 |
0.01 |
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| 2013 |
Nho K, Swaminathan S, Kim S, Risacher S, Ramanan V, Shen L, Mackin S, Aisen P, Petersen R, Weiner M, McDonald B, Farlow M, Ghetti B, Gao S, Saykin A, et al. Genome-wide analysis of genetic variants associated with depressive symptoms in older adults Alzheimers & Dementia. 9. DOI: 10.1016/J.Jalz.2013.05.1077 |
0.01 |
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| 2013 |
Risacher S, Kim S, Yoder K, Shen L, West J, McDonald B, Wang Y, Nho K, Tallman E, Hutchins G, Fletcher J, Ghetti B, Gao S, Farlow M, Saykin A. IC-P-107: Relationship of microglial activation measured by [11C]PBR28 PET, atrophy on MRI and plasma biomarkers in individuals with and at risk for Alzheimer's disease Alzheimer's & Dementia. 9: P63-P63. DOI: 10.1016/J.Jalz.2013.05.104 |
0.01 |
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| 2013 |
Blazey T, Jack C, Kantarci K, Preboske G, Ringman J, Brickman A, Raichle M, Hornbeck R, Saykin A, Salloway S, McDade E, Rossor M, Fox N, Thompson P, Correia S, ... ... Ghetti B, et al. Prevalence and growth of cerebral microhemorrhages in autosomal dominant Alzheimer's disease Alzheimers & Dementia. 9. DOI: 10.1016/J.Jalz.2013.05.100 |
0.01 |
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| 2013 |
Cash D, Ridgway G, Modat M, Ryan N, Kinnunen K, Cardoso J, Benzinger T, Jack CR, Raichle M, Marcus D, Ringman J, Thompson P, Ghetti B, Salloway S, Sperling R, et al. Dissociating volume and intensity differences in familial Alzheimer's disease Alzheimers & Dementia. 9: 603. DOI: 10.1016/J.Jalz.2013.05.075 |
0.01 |
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| 2013 |
Blazey T, Jack C, Kantarci K, Preboske G, Ringman J, Brickman A, Raichle M, Hornbeck R, Saykin A, Salloway S, McDade E, Rossor M, Fox N, Thompson P, Correia S, ... ... Ghetti B, et al. O1-03-05: Prevalence and growth of cerebral microhemorrhages in autosomal dominant Alzheimer's disease Alzheimer's & Dementia. 9: P130-P131. DOI: 10.1016/j.jalz.2013.04.065 |
0.01 |
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| 2013 |
Kinnunen K, Ryan N, Cash D, Leite AB, Finnegan S, Cardoso M, Leung K, Modat M, Benzinger T, Jack C, Marcus D, Raichle M, Thompson P, Ringman J, Ghetti B, et al. Are early atrophy patterns in autosomal dominant familial Alzheimer's disease gene-dependent? Alzheimers & Dementia. 9. DOI: 10.1016/J.Jalz.2013.04.017 |
0.01 |
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| 2013 |
del Carmen Alonso A, ElAkkad E, Gong C, Liu F, Tanaka T, Kudo T, Tatebayashi Y, Pei J, Wang J, Khatoon S, Flory M, Ghetti B, Gozes I, Novak M, Novak M, et al. Erratum to: Inge Grundke-Iqbal, Ph.D. (1937–2012): the Discoverer of the Abnormal Hyperphosphorylation of Tau in Alzheimer’s Disease Journal of Molecular Neuroscience. 49: 639-640. DOI: 10.1007/s12031-013-9963-1 |
0.01 |
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| 2013 |
Moro ML, Giaccone G, Lombardi R, Indaco A, Uggetti A, Morbin M, Saccucci S, Di Fede G, Catania M, Walsh DM, Demarchi A, Rozemuller A, Bogdanovic N, Bugiani O, Ghetti B, et al. Erratum to: APP mutations in the Aβ coding region are associated with abundant cerebral deposition of Aβ38 Acta Neuropathologica. 125: 467-467. DOI: 10.1007/S00401-013-1094-9 |
0.01 |
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| 2012 |
Dickson DW, Miller BL, Ghetti B. American Journal of Neurodegenerative Disease: Editorial Board (2012) e-Century Publishing Corporation. American Journal of Neurodegenerative Disease. 1: 119-21. PMID 23383384 |
0.01 |
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| 2012 |
Moro ML, Giaccone G, Lombardi R, Indaco A, Uggetti A, Morbin M, Saccucci S, Di Fede G, Catania M, Walsh DM, Demarchi A, Rozemuller A, Bogdanovic N, Bugiani O, Ghetti B, et al. APP mutations in the Aβ coding region are associated with abundant cerebral deposition of Aβ38. Acta Neuropathologica. 124: 809-21. PMID 23143229 DOI: 10.1007/S00401-012-1061-X |
0.01 |
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| 2012 |
Morris JC, Aisen PS, Bateman RJ, Benzinger TL, Cairns NJ, Fagan AM, Ghetti B, Goate AM, Holtzman DM, Klunk WE, McDade E, Marcus DS, Martins RN, Masters CL, Mayeux R, et al. Developing an international network for Alzheimer research: The Dominantly Inherited Alzheimer Network. Clinical Investigation. 2: 975-984. PMID 23139856 DOI: 10.4155/Cli.12.93 |
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| 2012 |
Vidal R, Ghetti B. Generation of a novel murine model of Aβ deposition based on the expression of human wild-type amyloid precursor protein gene. Prion. 6: 346-9. PMID 22874668 DOI: 10.4161/Pri.21023 |
0.01 |
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| 2012 |
Sundal C, Van Gerpen JA, Nicholson AM, Wider C, Shuster EA, Aasly J, Spina S, Ghetti B, Roeber S, Garbern J, Borjesson-Hanson A, Tselis A, Swerdlow RH, Miller BB, Fujioka S, et al. MRI characteristics and scoring in HDLS due to CSF1R gene mutations. Neurology. 79: 566-74. PMID 22843259 DOI: 10.1212/Wnl.0B013E318263575A |
0.01 |
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| 2012 |
Bateman RJ, Xiong C, Benzinger TL, Fagan AM, Goate A, Fox NC, Marcus DS, Cairns NJ, Xie X, Blazey TM, Holtzman DM, Santacruz A, Buckles V, Oliver A, Moulder K, ... ... Ghetti B, et al. Clinical and biomarker changes in dominantly inherited Alzheimer's disease. The New England Journal of Medicine. 367: 795-804. PMID 22784036 DOI: 10.1056/Nejmoa1202753 |
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| 2012 |
Allen M, Zou F, Chai HS, Younkin CS, Crook J, Pankratz VS, Carrasquillo MM, Rowley CN, Nair AA, Middha S, Maharjan S, Nguyen T, Ma L, Malphrus KG, Palusak R, ... ... Ghetti B, et al. Novel late-onset Alzheimer disease loci variants associate with brain gene expression. Neurology. 79: 221-8. PMID 22722634 DOI: 10.1212/Wnl.0B013E3182605801 |
0.01 |
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| 2012 |
Coppola G, Chinnathambi S, Lee JJ, Dombroski BA, Baker MC, Soto-Ortolaza AI, Lee SE, Klein E, Huang AY, Sears R, Lane JR, Karydas AM, Kenet RO, Biernat J, Wang LS, ... ... Ghetti B, et al. Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases. Human Molecular Genetics. 21: 3500-12. PMID 22556362 DOI: 10.1093/Hmg/Dds161 |
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| 2012 |
Ferrari R, Mok K, Moreno JH, Cosentino S, Goldman J, Pietrini P, Mayeux R, Tierney MC, Kapogiannis D, Jicha GA, Murrell JR, Ghetti B, Wassermann EM, Grafman J, Hardy J, et al. Screening for C9ORF72 repeat expansion in FTLD. Neurobiology of Aging. 33: 1850.e1-11. PMID 22459598 DOI: 10.1016/J.Neurobiolaging.2012.02.017 |
0.01 |
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| 2012 |
Vidal R, Sammeta N, Garringer HJ, Sambamurti K, Miravalle L, Lamb BT, Ghetti B. The Psen1-L166P-knock-in mutation leads to amyloid deposition in human wild-type amyloid precursor protein YAC transgenic mice. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 26: 2899-910. PMID 22459153 DOI: 10.1096/Fj.12-205542 |
0.01 |
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| 2012 |
Monaco S, Fiorini M, Farinazzo A, Ferrari S, Gelati M, Piccardo P, Zanusso G, Ghetti B. Allelic origin of protease-sensitive and protease-resistant prion protein isoforms in Gerstmann-Sträussler-Scheinker disease with the P102L mutation. Plos One. 7: e32382. PMID 22384235 DOI: 10.1371/Journal.Pone.0032382 |
0.01 |
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| 2012 |
Goedert M, Ghetti B, Spillantini MG. Frontotemporal dementia: implications for understanding Alzheimer disease. Cold Spring Harbor Perspectives in Medicine. 2: a006254. PMID 22355793 DOI: 10.1101/Cshperspect.A006254 |
0.01 |
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| 2012 |
Rademakers R, Baker M, Nicholson AM, Rutherford NJ, Finch N, Soto-Ortolaza A, Lash J, Wider C, Wojtas A, DeJesus-Hernandez M, Adamson J, Kouri N, Sundal C, Shuster EA, Aasly J, ... ... Ghetti B, et al. Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids. Nature Genetics. 44: 200-5. PMID 22197934 DOI: 10.1038/Ng.1027 |
0.01 |
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| 2012 |
Jeffrey M, McGovern G, Chambers EV, King D, González L, Manson JC, Ghetti B, Piccardo P, Barron RM. Mechanism of PrP-amyloid formation in mice without transmissible spongiform encephalopathy. Brain Pathology (Zurich, Switzerland). 22: 58-66. PMID 21645162 DOI: 10.1111/j.1750-3639.2011.00508.x |
0.01 |
|
| 2012 |
Ghetti B, Perry KW, Fuller RW. Norepinephrine metabolism in the cerebellum of the purkinje cell degeneration (pcd) mutant mouse. Neurochemistry International. 10: 39-47. PMID 20501080 DOI: 10.1016/0197-0186(87)90170-7 |
0.01 |
|
| 2012 |
Sundal C, Fujioka S, Van Gerpen J, Wider C, Aasly J, Roeber S, Shuster E, Ghetti B, Garbern J, Tselis A, Swerdlow R, Miller B, Rademakers R, Dickson D, Broderick D, et al. Observational Study for MRI Characteristics in HDLS with a Known Gene Mutation on Chromosome 5 (P06.180) Neurology. 78: P06.180-P06.180. DOI: 10.1212/Wnl.78.1_Meetingabstracts.P06.180 |
0.01 |
|
| 2012 |
Sundal C, Van Gerpen J, Fujioka S, Aasly J, Wider C, Roeber S, Shuster E, Ghetti B, Garbern J, Tselis A, Swerdlow R, Rademakers R, Dickson D, Broderick D, Wszolek Z. HDLS: Due to CSF1R Gene Mutation; Clinical Characteristics (P05.119) Neurology. 78: P05.119-P05.119. DOI: 10.1212/Wnl.78.1_Meetingabstracts.P05.119 |
0.01 |
|
| 2012 |
Kinnunen K, Cash D, Liang Y, Leung K, Cardoso J, Modat M, Malone I, Yeatman T, Nicholas J, Benzinger T, Koeppe R, Jack C, Raichle M, Marcus D, Ringman J, ... ... Ghetti B, et al. P2-226: Cross-sectional cerebral volumetric differences and associations with estimated time to age-at-onset in familial Alzheimer's disease: Findings from the DIAN study Alzheimer's & Dementia. 8: P338-P339. DOI: 10.1016/j.jalz.2012.05.933 |
0.01 |
|
| 2012 |
Becker J, Koeppe R, Benzinger T, Jack C, Marcus D, Raichle M, Thompson P, Saykin A, Correia S, Schofield P, Rowe C, Fox N, Brickman A, Ghetti B, Masters C, et al. FDG metabolism in the DIAN study of autosomal dominant Alzheimer's disease Alzheimers & Dementia. 8. DOI: 10.1016/J.Jalz.2012.05.655 |
0.01 |
|
| 2012 |
Chhatwal J, Schultz A, Johnson K, Benzinger T, Jack C, Salloway S, Ringman J, Koeppe R, Marcus D, Thompson P, Saykin A, Correia S, Schofield P, Rowe C, Fox N, ... ... Ghetti B, et al. O2-06-01: Disrupted functional connectivity in autosomal dominant Alzheimer's disease: Preliminary findings from the DIAN study Alzheimer's & Dementia. 8: P244-P245. DOI: 10.1016/J.Jalz.2012.05.654 |
0.01 |
|
| 2012 |
Murrell J, Farlow M, Ghetti B, Unverzagt F, Spina S. P1-172: Phenotypic heterogenity in different individuals of a family with expanded hexanucleotide repeat at C9ORF72 Alzheimer's & Dementia. 8: P168-P168. DOI: 10.1016/J.Jalz.2012.05.450 |
0.01 |
|
| 2012 |
Kinnunen K, Cash D, Leung K, Liang Y, Cardoso M, Modat M, Malone I, Benzinger T, Koeppe R, Jack C, Raichle M, Marcus D, Ringman J, Thompson P, Saykin A, ... Ghetti B, et al. P1-015: Brain and hippocampal rates of atrophy in familial Alzheimer's disease mutation carriers: Preliminary findings from the DIAN study Alzheimer's & Dementia. 8: P112-P113. DOI: 10.1016/j.jalz.2012.05.290 |
0.01 |
|
| 2012 |
Sabbagh M, Seibyl J, Akatsu H, Ouchi Y, Beach T, Charny A, Barthel H, Senda K, Muryama S, Iishi K, Leverenz J, Ghetti B, Ironside J, Roth K, Hoffmann A, et al. O1‐04‐01: Multicentre phase 3 trial on florbetaben for beta‐amyloid brain PET in Alzheimer's disease Alzheimer's & Dementia. 8. DOI: 10.1016/j.jalz.2012.05.220 |
0.01 |
|
| 2012 |
Ghetti B, Vidal R, Sammeta N, Garringer H, Sambamurti K, Miravalle L, Lamb B. The Psen1-L166P knock-in mutation leads to amyloid deposition in human wild-type amyloid precursor protein YAC transgenic mice Alzheimers & Dementia. 8: 86. DOI: 10.1016/J.Jalz.2012.05.209 |
0.01 |
|
| 2012 |
Seibyl J, Sabri O, Sabbagh M, Akatsu H, Ouchi Y, Beach T, Charny A, Barthel H, Senda K, Murayama S, Ishii K, Leverenz J, Ghetti B, Ironside J, Roth K, et al. P4‐167: Techniques for histopathological verification of florbetaben PET in a global phase III clinical trial Alzheimer's & Dementia. 8. DOI: 10.1016/j.jalz.2012.05.1871 |
0.01 |
|
| 2012 |
Benzinger T, Blazey T, Ances B, Raichle M, Ances B, Snyder A, Su Y, Marcus D, Ringman J, Thompson P, Ghetti B, Saykin A, Salloway S, Correia S, Johnson K, et al. IC-P-128: Progressive white matter abnormalities in autosomal dominant Alzheimer's disease: Results of the DIAN study Alzheimer's & Dementia. 8: P68-P69. DOI: 10.1016/j.jalz.2012.05.1858 |
0.01 |
|
| 2012 |
Benzinger T, Blazey T, Koeppe R, Jack C, Raichle M, Su Y, Snyder A, Marcus D, Johnson K, Sperling R, Ringman J, Thompson P, Ghetti B, Saykin A, Schofield P, et al. P4-153: Elevated PiB precedes dementia in autosomal-dominant Alzheimer's disease: PiB, FDG and atrophy in the DIAN cohort Alzheimer's & Dementia. 8: P687-P688. DOI: 10.1016/j.jalz.2012.05.1857 |
0.01 |
|
| 2012 |
Ghetti B, Murrell J, Koeppe R, Gilman S, Fink J, Miravalle L, Albin R, Vidal R, Foster N. Follow-up of the first American report of familial Alzheimer's disease Alzheimers & Dementia. 8: 665. DOI: 10.1016/J.Jalz.2012.05.1793 |
0.01 |
|
| 2012 |
Ghetti B, Murrell J, Boyer P, Piccardo P, Vidal R, Hargrave K, Scott K, Silber M, Filley C, DeMasters B, Iyriboz T, Towfighi J. P4-090: Early-onset Alzheimer's disease associated with PSEN1 L166P mutation: An atypical clinical phenotype Alzheimer's & Dementia. 8: P664-P665. DOI: 10.1016/J.Jalz.2012.05.1792 |
0.01 |
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| 2012 |
Di Fede G, Ghidoni R, Catania M, Giaccone G, Benussi L, Moda F, Gobbi M, Moro M, Kubis A, Ruggerone M, Ghetti B, Binetti G, Salmona M, Tagliavini F. P4‐052: Phenotypic heterogeneity of Alzheimer's disease: Toward the identification of molecular determinants underlying distinct clinicopathological subgroups Alzheimer's & Dementia. 8. DOI: 10.1016/j.jalz.2012.05.1754 |
0.01 |
|
| 2012 |
Kinnunen K, Cash D, Leung K, Liang Y, Cardoso M, Modat M, Malone I, Benzinger T, Koeppe R, Jack C, Raichle M, Marcus D, Ringman J, Thompson P, Saykin A, ... Ghetti B, et al. Brain and hippocampal rates of atrophy in familial Alzheimer's disease mutation carriers: Preliminary findings from the DIAN study Alzheimers & Dementia. 8. DOI: 10.1016/J.Jalz.2012.05.172 |
0.01 |
|
| 2012 |
Benzinger T, Blazey T, Ances B, Raichle M, Ances B, Snyder A, Su Y, Marcus D, Ringman J, Thompson P, Ghetti B, Saykin A, Salloway S, Correia S, Johnson K, et al. IC-P-128: Progressive white matter abnormalities in autosomal dominant Alzheimer's disease: Results of the DIAN study Alzheimer's & Dementia. 8: P68-P69. DOI: 10.1016/j.jalz.2012.05.162 |
0.01 |
|
| 2012 |
Wang Y, West J, Magee T, McDonald B, Risacher S, Shen L, Ramanan V, Kim S, O'Neill D, Farlow M, Ghetti B, Saykin A. P3-215: Hippocampal subfield atrophy on 3T MRI in prodromal Alzheimer's disease and older adults with cognitive complaints Alzheimer's & Dementia. 8: P535-P535. DOI: 10.1016/j.jalz.2012.05.1437 |
0.01 |
|
| 2012 |
Benzinger T, Blazey T, Koeppe R, Jack C, Raichle M, Su Y, Snyder A, Marcus D, Ringman J, Thompson P, Ghetti B, Saykin A, Salloway S, Correia S, Johnson K, et al. Elevated PiB precedes dementia in autosomal dominant Alzheimer's disease: PiB, FDG and atrophy in the DIAN cohort Alzheimers & Dementia. 8. DOI: 10.1016/J.Jalz.2012.05.132 |
0.01 |
|
| 2012 |
West J, Wang Y, Magee T, McDonald B, Risacher S, Shen L, Ramanan V, Kim S, O'Neill D, Farlow M, Ghetti B, Saykin A. IC-P-060: Hippocampal subfield atrophy on 3T MRI in prodromal Alzheimer's disease and older adults with cognitive complaints Alzheimer's & Dementia. 8: P36-P36. DOI: 10.1016/J.Jalz.2012.05.093 |
0.01 |
|
| 2012 |
Kinnunen K, Cash D, Liang Y, Leung K, Cardoso M, Modat M, Malone I, Yeatman T, Nicholas J, Benzinger T, Koeppe R, Jack C, Raichle M, Marcus D, Ringman J, ... ... Ghetti B, et al. Cross-sectional cerebral volumetric differences and associations with estimated time to age-at-onset in familial Alzheimer's disease: Findings from the DIAN study Alzheimers & Dementia. 8: 23. DOI: 10.1016/J.Jalz.2012.05.064 |
0.01 |
|
| 2012 |
Bateman R, Benzinger T, Cairns N, Fagan A, Goate A, Marcus D, Storandt M, Xiong C, Buckles V, Holtzman D, Moulder K, Oliver A, Santacruz A, Fox N, Ghetti B, et al. Presymptomatic Alzheimer's disease in the Dominantly Inherited Alzheimer's Network (DIAN) Alzheimers & Dementia. 8: 4. DOI: 10.1016/J.Jalz.2012.05.015 |
0.01 |
|
| 2011 |
Vidal R, Ghetti B. Characterization of amyloid deposits in neurodegenerative diseases. Methods in Molecular Biology (Clifton, N.J.). 793: 241-58. PMID 21913105 DOI: 10.1007/978-1-61779-328-8_16 |
0.01 |
|
| 2011 |
Chen-Plotkin AS, Martinez-Lage M, Sleiman PM, Hu W, Greene R, Wood EM, Bing S, Grossman M, Schellenberg GD, Hatanpaa KJ, Weiner MF, White CL, Brooks WS, Halliday GM, Kril JJ, ... ... Ghetti B, et al. Genetic and clinical features of progranulin-associated frontotemporal lobar degeneration. Archives of Neurology. 68: 488-97. PMID 21482928 DOI: 10.1001/Archneurol.2011.53 |
0.01 |
|
| 2011 |
Naj AC, Jun G, Beecham GW, Wang LS, Vardarajan BN, Buros J, Gallins PJ, Buxbaum JD, Jarvik GP, Crane PK, Larson EB, Bird TD, Boeve BF, Graff-Radford NR, De Jager PL, ... ... Ghetti B, et al. Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease. Nature Genetics. 43: 436-41. PMID 21460841 DOI: 10.1038/Ng.801 |
0.01 |
|
| 2011 |
Hagen MC, Murrell JR, Delisle MB, Andermann E, Andermann F, Guiot MC, Ghetti B. Encephalopathy with neuroserpin inclusion bodies presenting as progressive myoclonus epilepsy and associated with a novel mutation in the Proteinase Inhibitor 12 gene. Brain Pathology (Zurich, Switzerland). 21: 575-82. PMID 21435071 DOI: 10.1111/J.1750-3639.2011.00481.X |
0.01 |
|
| 2011 |
Jayadev S, Nochlin D, Poorkaj P, Steinbart EJ, Mastrianni JA, Montine TJ, Ghetti B, Schellenberg GD, Bird TD, Leverenz JB. Familial prion disease with Alzheimer disease-like tau pathology and clinical phenotype. Annals of Neurology. 69: 712-20. PMID 21416485 DOI: 10.1002/Ana.22264 |
0.01 |
|
| 2011 |
Wijsman EM, Pankratz ND, Choi Y, Rothstein JH, Faber KM, Cheng R, Lee JH, Bird TD, Bennett DA, Diaz-Arrastia R, Goate AM, Farlow M, Ghetti B, Sweet RA, Foroud TM, et al. Genome-wide association of familial late-onset Alzheimer's disease replicates BIN1 and CLU and nominates CUGBP2 in interaction with APOE. Plos Genetics. 7: e1001308. PMID 21379329 DOI: 10.1371/Journal.Pgen.1001308 |
0.01 |
|
| 2011 |
Bellucci A, Bugiani O, Ghetti B, Spillantini MG. Presence of reactive microglia and neuroinflammatory mediators in a case of frontotemporal dementia with P301S mutation. Neuro-Degenerative Diseases. 8: 221-9. PMID 21212632 DOI: 10.1159/000322228 |
0.01 |
|
| 2011 |
Espay AJ, Spina S, Houghton DJ, Murrell JR, de Courten-Myers GM, Ghetti B, Litvan I. Rapidly progressive atypical parkinsonism associated with frontotemporal lobar degeneration and motor neuron disease. Journal of Neurology, Neurosurgery, and Psychiatry. 82: 751-3. PMID 20587488 DOI: 10.1136/Jnnp.2009.201608 |
0.01 |
|
| 2011 |
Fagan A, Xiong C, Bateman R, Goate A, Holtzman D, Ghetti B, Martins R, Masters C, Mayeux R, Ringman J, Rossor M, Salloway S, Schofield P, Sperling R, Morris J. O2-01-01: Plasma and Cerebrospinal Fluid Markers in the DIAN Study of Autosomal-Dominant Alzheimer's Disease Alzheimer's & Dementia. 7: S287-S287. DOI: 10.1016/j.jalz.2011.05.833 |
0.01 |
|
| 2010 |
Barbeito AG, Levade T, Delisle MB, Ghetti B, Vidal R. Abnormal iron metabolism in fibroblasts from a patient with the neurodegenerative disease hereditary ferritinopathy. Molecular Neurodegeneration. 5: 50. PMID 21067605 DOI: 10.1186/1750-1326-5-50 |
0.01 |
|
| 2010 |
Parchi P, Cescatti M, Notari S, Schulz-Schaeffer WJ, Capellari S, Giese A, Zou WQ, Kretzschmar H, Ghetti B, Brown P. Agent strain variation in human prion disease: insights from a molecular and pathological review of the National Institutes of Health series of experimentally transmitted disease. Brain : a Journal of Neurology. 133: 3030-42. PMID 20823086 DOI: 10.1093/Brain/Awq234 |
0.01 |
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| 2010 |
Garcia-Reitböck P, Anichtchik O, Bellucci A, Iovino M, Ballini C, Fineberg E, Ghetti B, Della Corte L, Spano P, Tofaris GK, Goedert M, Spillantini MG. SNARE protein redistribution and synaptic failure in a transgenic mouse model of Parkinson's disease. Brain : a Journal of Neurology. 133: 2032-44. PMID 20534649 DOI: 10.1093/Brain/Awq132 |
0.01 |
|
| 2010 |
Van Deerlin VM, Sleiman PM, Martinez-Lage M, Chen-Plotkin A, Wang LS, Graff-Radford NR, Dickson DW, Rademakers R, Boeve BF, Grossman M, Arnold SE, Mann DM, Pickering-Brown SM, Seelaar H, Heutink P, ... ... Ghetti B, et al. Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions. Nature Genetics. 42: 234-9. PMID 20154673 DOI: 10.1038/Ng.536 |
0.01 |
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| 2010 |
Cupidi C, Capobianco R, Goffredo D, Marcon G, Ghetti B, Bugiani O, Tagliavini F, Giaccone G. Neocortical variation of Abeta load in fully expressed, pure Alzheimer's disease. Journal of Alzheimer's Disease : Jad. 19: 57-68. PMID 20061626 DOI: 10.3233/Jad-2010-1205 |
0.01 |
|
| 2010 |
Mackenzie IR, Neumann M, Bigio EH, Cairns NJ, Alafuzoff I, Kril J, Kovacs GG, Ghetti B, Halliday G, Holm IE, Ince PG, Kamphorst W, Revesz T, Rozemuller AJ, Kumar-Singh S, et al. Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update. Acta Neuropathologica. 119: 1-4. PMID 19924424 DOI: 10.1007/S00401-009-0612-2 |
0.01 |
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| 2010 |
Garringer HJ, Murrell J, D'Adamio L, Ghetti B, Vidal R. Modeling familial British and Danish dementia. Brain Structure & Function. 214: 235-44. PMID 19779737 DOI: 10.1007/S00429-009-0221-9 |
0.01 |
|
| 2010 |
Kepe V, Ghetti B, Farlow MR, Bresjanac M, Miller K, Huang SC, Wong KP, Murrell JR, Piccardo P, Epperson F, Repovs G, Smid LM, Petric A, Siddarth P, Liu J, et al. PET of brain prion protein amyloid in Gerstmann-Sträussler-Scheinker disease. Brain Pathology (Zurich, Switzerland). 20: 419-30. PMID 19725833 DOI: 10.1111/J.1750-3639.2009.00306.X |
0.01 |
|
| 2010 |
Ghetti B, Glazier BS. Title Page / Table of Contents Dementia and Geriatric Cognitive Disorders. 30: I-III. DOI: 10.1159/000320291 |
0.01 |
|
| 2010 |
Albrecht S, Bogdanovic N, Ghetti B, Winblad B, Leblanc A. Erratum: Caspase-6 activation in familial alzheimer disease brains carrying amyloid precursor protein or pesenilin I or presenilin II mutations (Journal of Neuropathology and Experimental Neurology (2009) 68 (1282-1293) Journal of Neuropathology and Experimental Neurology. 69. DOI: 10.1097/Nen.0B013E3181Cf7162 |
0.01 |
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| 2010 |
Ghetti B, Hagen MC, Murrell JR, Takao M, Piccardo P, Glazier BS, Epperson F, Spina S, Rentz C. P4-140: Alzheimer's Disease Associated with the F105L Mutation in the Presenilin 1 (PSEN1) Gene Alzheimer's & Dementia. 6: e64-e65. DOI: 10.1016/J.Jalz.2010.08.199 |
0.01 |
|
| 2010 |
Ghetti B. S4‐02‐03: Molecular neuropathology of tauopathies Alzheimer's & Dementia. 6. DOI: 10.1016/j.jalz.2010.05.460 |
0.01 |
|
| 2010 |
Unverzagt FW, Farlow MR, Gao S, Saykin AJ, Murrell JR, Risacher SL, Lane KA, West JD, Matthews BR, Piccardo P, Miravalle L, Vidal RG, Ghetti B. P3-156: Cognition and brain structure in Gerstmann-Straussler-Scheinker disease (PRNP F198S) Alzheimer's & Dementia. 6: S495-S495. DOI: 10.1016/J.Jalz.2010.05.1654 |
0.01 |
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| 2009 |
Albrecht S, Bogdanovic N, Ghetti B, Winblad B, LeBlanc AC. Caspase-6 activation in familial alzheimer disease brains carrying amyloid precursor protein or presenilin i or presenilin II mutations. Journal of Neuropathology and Experimental Neurology. 68: 1282-93. PMID 19915487 DOI: 10.1097/NEN.0b013e3181c1da10 |
0.01 |
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| 2009 |
Huey ED, Pardini M, Cavanagh A, Wassermann EM, Kapogiannis D, Spina S, Ghetti B, Grafman J. Association of ideomotor apraxia with frontal gray matter volume loss in corticobasal syndrome. Archives of Neurology. 66: 1274-80. PMID 19822784 DOI: 10.1001/Archneurol.2009.218 |
0.01 |
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| 2009 |
Parchi P, Strammiello R, Notari S, Giese A, Langeveld JP, Ladogana A, Zerr I, Roncaroli F, Cras P, Ghetti B, Pocchiari M, Kretzschmar H, Capellari S. Incidence and spectrum of sporadic Creutzfeldt-Jakob disease variants with mixed phenotype and co-occurrence of PrPSc types: an updated classification. Acta Neuropathologica. 118: 659-71. PMID 19718500 DOI: 10.1007/S00401-009-0585-1 |
0.01 |
|
| 2009 |
Ghetti B. Old age before cognitive impairment. Current Alzheimer Research. 6: 323. PMID 19689229 |
0.01 |
|
| 2009 |
Kovacs GG, Murrell JR, Horvath S, Haraszti L, Majtenyi K, Molnar MJ, Budka H, Ghetti B, Spina S. TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and chorea. Movement Disorders : Official Journal of the Movement Disorder Society. 24: 1843-7. PMID 19609911 DOI: 10.1002/Mds.22697 |
0.01 |
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| 2009 |
Marti J, Santa-Cruz MC, Molina V, Serra R, Bayer SA, Ghetti B, Hervás JP. Regional differences in the vulnerability of substantia nigra dopaminergic neurons in weaver mice. Acta Neurobiologiae Experimentalis. 69: 198-206. PMID 19593334 |
0.01 |
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| 2009 |
Barbeito AG, Garringer HJ, Baraibar MA, Gao X, Arredondo M, Núñez MT, Smith MA, Ghetti B, Vidal R. Abnormal iron metabolism and oxidative stress in mice expressing a mutant form of the ferritin light polypeptide gene. Journal of Neurochemistry. 109: 1067-78. PMID 19519778 DOI: 10.1111/J.1471-4159.2009.06028.X |
0.01 |
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| 2009 |
Ory-Magne F, Brefel-Courbon C, Payoux P, Debruxelles S, Sibon I, Goizet C, Labauge P, Menegon P, Uro-Coste E, Ghetti B, Delisle MB, Vidal R, Rascol O. Clinical phenotype and neuroimaging findings in a French family with hereditary ferritinopathy (FTL498-499InsTC). Movement Disorders : Official Journal of the Movement Disorder Society. 24: 1676-83. PMID 19514068 DOI: 10.1002/Mds.22669 |
0.01 |
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| 2009 |
Xiao X, Miravalle L, Yuan J, McGeehan J, Dong Z, Wyza R, MacLennan GT, Golichowski AM, Kneale G, King N, Kong Q, Spina S, Vidal R, Ghetti B, Roos K, et al. Failure to detect the presence of prions in the uterine and gestational tissues from a Gravida with Creutzfeldt-Jakob disease. The American Journal of Pathology. 174: 1602-8. PMID 19349373 DOI: 10.2353/Ajpath.2009.081045 |
0.01 |
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| 2009 |
Giliberto L, Borghi R, Piccini A, Mangerini R, Sorbi S, Cirmena G, Garuti A, Ghetti B, Tagliavini F, Mughal MR, Mattson MP, Zhu X, Wang X, Guglielmotto M, Tamagno E, et al. Mutant presenilin 1 increases the expression and activity of BACE1. The Journal of Biological Chemistry. 284: 9027-38. PMID 19196715 DOI: 10.1074/Jbc.M805685200 |
0.01 |
|
| 2009 |
Mackenzie IR, Neumann M, Bigio EH, Cairns NJ, Alafuzoff I, Kril J, Kovacs GG, Ghetti B, Halliday G, Holm IE, Ince PG, Kamphorst W, Revesz T, Rozemuller AJ, Kumar-Singh S, et al. Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendations. Acta Neuropathologica. 117: 15-8. PMID 19015862 DOI: 10.1007/S00401-008-0460-5 |
0.01 |
|
| 2009 |
Vidal R, Barbeito AG, Miravalle L, Ghetti B. Cerebral amyloid angiopathy and parenchymal amyloid deposition in transgenic mice expressing the Danish mutant form of human BRI2. Brain Pathology (Zurich, Switzerland). 19: 58-68. PMID 18410407 DOI: 10.1111/J.1750-3639.2008.00164.X |
0.01 |
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| 2009 |
Kovacs GG, Murrell JR, Horvath S, Haraszti L, Majtenyi K, Budka H, Ghetti B, Spina S. Novel TARDBP mutation associated with frontotemporal dementia and movement disorder but not motor neuron disease Alzheimers & Dementia. 5: 501. DOI: 10.1016/J.Jalz.2009.04.707 |
0.01 |
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| 2008 |
Chiesa R, Piccardo P, Biasini E, Ghetti B, Harris DA. Aggregated, wild-type prion protein causes neurological dysfunction and synaptic abnormalities. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 28: 13258-67. PMID 19052217 DOI: 10.1523/JNEUROSCI.3109-08.2008 |
0.01 |
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| 2008 |
Maarouf CL, Daugs ID, Spina S, Vidal R, Kokjohn TA, Patton RL, Kalback WM, Luehrs DC, Walker DG, Castaño EM, Beach TG, Ghetti B, Roher AE. Histopathological and molecular heterogeneity among individuals with dementia associated with Presenilin mutations. Molecular Neurodegeneration. 3: 20. PMID 19021905 DOI: 10.1186/1750-1326-3-20 |
0.01 |
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| 2008 |
Kovacs GG, Majtenyi K, Spina S, Murrell JR, Gelpi E, Hoftberger R, Fraser G, Crowther RA, Goedert M, Budka H, Ghetti B. White matter tauopathy with globular glial inclusions: a distinct sporadic frontotemporal lobar degeneration. Journal of Neuropathology and Experimental Neurology. 67: 963-75. PMID 18800011 DOI: 10.1097/Nen.0B013E318187A80F |
0.01 |
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| 2008 |
Notari S, Strammiello R, Capellari S, Giese A, Cescatti M, Grassi J, Ghetti B, Langeveld JP, Zou WQ, Gambetti P, Kretzschmar HA, Parchi P. Characterization of truncated forms of abnormal prion protein in Creutzfeldt-Jakob disease. The Journal of Biological Chemistry. 283: 30557-65. PMID 18753138 DOI: 10.1074/Jbc.M801877200 |
0.01 |
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| 2008 |
Ghetti B, Spina S, Murrell JR, Huey ED, Pietrini P, Sweeney B, Wassermann EM, Keohane C, Farlow MR, Grafman J. In vivo and postmortem clinicoanatomical correlations in frontotemporal dementia and parkinsonism linked to chromosome 17. Neuro-Degenerative Diseases. 5: 215-7. PMID 18322394 DOI: 10.1159/000113706 |
0.01 |
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| 2008 |
Van Vickle GD, Esh CL, Kokjohn TA, Patton RL, Kalback WM, Luehrs DC, Beach TG, Newel AJ, Lopera F, Ghetti B, Vidal R, Castaño EM, Roher AE. Presenilin-1 280Glu-->Ala mutation alters C-terminal APP processing yielding longer abeta peptides: implications for Alzheimer's disease. Molecular Medicine (Cambridge, Mass.). 14: 184-94. PMID 18317569 DOI: 10.2119/2007-00094.Vanvickle |
0.01 |
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| 2008 |
Velasco A, Fraser G, Delobel P, Ghetti B, Lavenir I, Goedert M. Detection of filamentous tau inclusions by the fluorescent Congo red derivative FSB [(trans,trans)-1-fluoro-2,5-bis(3-hydroxycarbonyl-4-hydroxy)styrylbenzene]. Febs Letters. 582: 901-6. PMID 18291106 DOI: 10.1016/J.Febslet.2008.02.025 |
0.01 |
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| 2008 |
Vidal R, Miravalle L, Gao X, Barbeito AG, Baraibar MA, Hekmatyar SK, Widel M, Bansal N, Delisle MB, Ghetti B. Expression of a mutant form of the ferritin light chain gene induces neurodegeneration and iron overload in transgenic mice. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 28: 60-7. PMID 18171923 DOI: 10.1523/Jneurosci.3962-07.2008 |
0.01 |
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| 2008 |
Delobel P, Lavenir I, Fraser G, Ingram E, Holzer M, Ghetti B, Spillantini MG, Crowther RA, Goedert M. Analysis of tau phosphorylation and truncation in a mouse model of human tauopathy. The American Journal of Pathology. 172: 123-31. PMID 18079436 DOI: 10.2353/Ajpath.2008.070627 |
0.01 |
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| 2008 |
Spina S, Farlow MR, Unverzagt FW, Kareken DA, Murrell JR, Fraser G, Epperson F, Crowther RA, Spillantini MG, Goedert M, Ghetti B. The tauopathy associated with mutation +3 in intron 10 of Tau: characterization of the MSTD family. Brain : a Journal of Neurology. 131: 72-89. PMID 18065436 DOI: 10.1093/Brain/Awm280 |
0.01 |
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| 2008 |
Vidal R, Miravalle L, Barbeito AG, Baraibar MA, Bansal N, Smith MA, Delisle MB, Ghetti B. P1-105: Neurodegeneration and iron overload in transgenic mice expressing a mutant form of the ferritin light polypeptide gene Alzheimers & Dementia. 4. DOI: 10.1016/J.Jalz.2008.05.692 |
0.01 |
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| 2008 |
Vidal R, Barbeito AG, Miravalle L, Ghetti B. O3-01-04: Vascular amyloid deposition and related pathology in a transgenic mouse model of familial Danish dementia Alzheimers & Dementia. 4. DOI: 10.1016/J.Jalz.2008.05.408 |
0.01 |
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| 2008 |
Spina S, Laar ADV, Murrell JR, Courten-Myers Gd, Hamilton RL, Vidal R, Farlow MR, Quinlan J, DeKosky ST, Ghetti B. O2-05-03: Inclusion body myopathy with paget disease of the bone and frontotemporal dementia: New families, a novel mutation, and a new clinical presentation Alzheimers & Dementia. 4. DOI: 10.1016/J.Jalz.2008.05.342 |
0.01 |
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| 2008 |
Ghetti B, Hake AM, Murrell JR, Epperson F, Farlow MR, Vidal R, Spina S. P3-221: Familial Alzheimer's disease associated with the V717L amyloid precursor protein gene mutation: Neuropathological characterization Alzheimers & Dementia. 4. DOI: 10.1016/J.Jalz.2008.05.1788 |
0.01 |
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| 2008 |
Spina S, Murrell JR, Vidal R, Ghetti B. P2-205: Neuropathologic and genetic characterization of frontotemporal lobar degeneration with ubiquitin- and/or TDP-43-positive inclusions: A large series Alzheimers & Dementia. 4. DOI: 10.1016/J.Jalz.2008.05.1280 |
0.01 |
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| 2007 |
Spina S, Murrell JR, Huey ED, Wassermann EM, Pietrini P, Grafman J, Ghetti B. Corticobasal syndrome associated with the A9D Progranulin mutation. Journal of Neuropathology and Experimental Neurology. 66: 892-900. PMID 17917583 DOI: 10.1097/Nen.0B013E3181567873 |
0.01 |
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| 2007 |
Martà J, Santa-Cruz MC, Bayer SA, Ghetti B, Hervás JP. Purkinje cell age-distribution in fissures and in foliar crowns: a comparative study in the weaver cerebellum. Brain Structure & Function. 212: 347-57. PMID 17899183 DOI: 10.1007/S00429-007-0159-8 |
0.01 |
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| 2007 |
Filley CM, Rollins YD, Anderson CA, Arciniegas DB, Howard KL, Murrell JR, Boyer PJ, Kleinschmidt-DeMasters BK, Ghetti B. The genetics of very early onset Alzheimer disease. Cognitive and Behavioral Neurology : Official Journal of the Society For Behavioral and Cognitive Neurology. 20: 149-56. PMID 17846513 DOI: 10.1097/Wnn.0B013E318145A8C8 |
0.01 |
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| 2007 |
Rademakers R, Baker M, Gass J, Adamson J, Huey ED, Momeni P, Spina S, Coppola G, Karydas AM, Stewart H, Johnson N, Hsiung GY, Kelley B, Kuntz K, Steinbart E, ... ... Ghetti B, et al. Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiative. The Lancet. Neurology. 6: 857-68. PMID 17826340 DOI: 10.1016/S1474-4422(07)70221-1 |
0.01 |
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| 2007 |
Ingelsson M, Ramasamy K, Russ C, Freeman SH, Orne J, Raju S, Matsui T, Growdon JH, Frosch MP, Ghetti B, Brown RH, Irizarry MC, Hyman BT. Increase in the relative expression of tau with four microtubule binding repeat regions in frontotemporal lobar degeneration and progressive supranuclear palsy brains. Acta Neuropathologica. 114: 471-9. PMID 17721707 DOI: 10.1007/S00401-007-0280-Z |
0.01 |
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| 2007 |
Martà J, Santa-Cruz MC, Bayer SA, Ghetti B, Hervás JP. Generation and survival of midbrain dopaminergic neurons in weaver mice. International Journal of Developmental Neuroscience : the Official Journal of the International Society For Developmental Neuroscience. 25: 299-307. PMID 17582722 DOI: 10.1016/J.Ijdevneu.2007.05.002 |
0.01 |
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| 2007 |
Li A, Piccardo P, Barmada SJ, Ghetti B, Harris DA. Prion protein with an octapeptide insertion has impaired neuroprotective activity in transgenic mice. The Embo Journal. 26: 2777-85. PMID 17510630 DOI: 10.1038/Sj.Emboj.7601726 |
0.01 |
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| 2007 |
Piccini A, Zanusso G, Borghi R, Noviello C, Monaco S, Russo R, Damonte G, Armirotti A, Gelati M, Giordano R, Zambenedetti P, Russo C, Ghetti B, Tabaton M. Association of a presenilin 1 S170F mutation with a novel Alzheimer disease molecular phenotype. Archives of Neurology. 64: 738-45. PMID 17502474 DOI: 10.1001/Archneur.64.5.738 |
0.01 |
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| 2007 |
Goedert M, Ghetti B. Alois Alzheimer: his life and times. Brain Pathology (Zurich, Switzerland). 17: 57-62. PMID 17493039 DOI: 10.1111/J.1750-3639.2007.00056.X |
0.01 |
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| 2007 |
Piccardo P, Manson JC, King D, Ghetti B, Barron RM. Accumulation of prion protein in the brain that is not associated with transmissible disease. Proceedings of the National Academy of Sciences of the United States of America. 104: 4712-7. PMID 17360589 DOI: 10.1073/pnas.0609241104 |
0.01 |
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| 2007 |
Baba Y, Baker MC, Le Ber I, Brice A, Maeck L, Kohlhase J, Yasuda M, Stoppe G, Bugiani O, Sperfeld AD, Tsuboi Y, Uitti RJ, Farrer MJ, Ghetti B, Hutton ML, et al. Clinical and genetic features of families with frontotemporal dementia and parkinsonism linked to chromosome 17 with a P301S tau mutation. Journal of Neural Transmission (Vienna, Austria : 1996). 114: 947-50. PMID 17318302 DOI: 10.1007/S00702-007-0632-9 |
0.01 |
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| 2007 |
Di Fede G, Giaccone G, Limido L, Mangieri M, Suardi S, Puoti G, Morbin M, Mazzoleni G, Ghetti B, Tagliavini F. The epsilon isoform of 14-3-3 protein is a component of the prion protein amyloid deposits of Gerstmann-Sträussler-Scheinker disease. Journal of Neuropathology and Experimental Neurology. 66: 124-30. PMID 17278997 DOI: 10.1097/Nen.0B013E3180302060 |
0.01 |
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| 2007 |
Spina S, Murrell JR, Huey ED, Wassermann EM, Pietrini P, Baraibar MA, Barbeito AG, Troncoso JC, Vidal R, Ghetti B, Grafman J. Clinicopathologic features of frontotemporal dementia with progranulin sequence variation. Neurology. 68: 820-7. PMID 17202431 DOI: 10.1212/01.Wnl.0000254460.31273.2D |
0.01 |
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| 2007 |
Spina S, Murrell JR, Yoshida H, Ghetti B, Bermingham N, Sweeney B, Dlouhy SR, Crowther RA, Goedert M, Keohane C. The novel Tau mutation G335S: clinical, neuropathological and molecular characterization. Acta Neuropathologica. 113: 461-70. PMID 17186252 DOI: 10.1007/S00401-006-0182-5 |
0.01 |
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| 2007 |
Ringman JM, Rodriguez Y, Diaz-Olavarrieta C, Chavez M, Thompson M, Fairbanks L, Paz F, Varpetian A, Chaparro H, Macias-Islas MA, Murrell J, Ghetti B, Kawas C. Performance on MMSE sub-items and education level in presenilin-1 mutation carriers without dementia. International Psychogeriatrics / Ipa. 19: 323-32. PMID 16805926 DOI: 10.1017/S1041610206003772 |
0.01 |
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| 2007 |
Ghetti B, Goedert M. Symposium: Tau protein and neurodegeneration Brain Pathology. 17: 56. DOI: 10.1111/j.1750-3639.2007.00057.x |
0.01 |
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| 2006 |
Ghetti B. Neurodegeneration and hereditary dementias: 40 years of learning. Journal of Alzheimer's Disease : Jad. 9: 45-52. PMID 17004363 |
0.01 |
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| 2006 |
Huey ED, Grafman J, Wassermann EM, Pietrini P, Tierney MC, Ghetti B, Spina S, Baker M, Hutton M, Elder JW, Berger SL, Heflin KA, Hardy J, Momeni P. Characteristics of frontotemporal dementia patients with a Progranulin mutation. Annals of Neurology. 60: 374-80. PMID 16983677 DOI: 10.1002/Ana.20969 |
0.01 |
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| 2006 |
Ghetti B, Goebel HH. Frontotemporal dementia: the post-tau era. Neurology. 67: 560-1. PMID 16924003 DOI: 10.1212/01.wnl.0000237005.54105.d7 |
0.01 |
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| 2006 |
Spillantini MG, Murrell JR, Goedert M, Farlow M, Klug A, Ghetti B. Mutations in the tau gene (MAPT) in FTDP-17: the family with Multiple System Tauopathy with Presenile Dementia (MSTD). Journal of Alzheimer's Disease : Jad. 9: 373-80. PMID 16914875 DOI: 10.3233/Jad-2006-9S342 |
0.01 |
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| 2006 |
Radde R, Bolmont T, Kaeser SA, Coomaraswamy J, Lindau D, Stoltze L, Calhoun ME, Jäggi F, Wolburg H, Gengler S, Haass C, Ghetti B, Czech C, Hölscher C, Mathews PM, et al. Abeta42-driven cerebral amyloidosis in transgenic mice reveals early and robust pathology. Embo Reports. 7: 940-6. PMID 16906128 DOI: 10.1038/Sj.Embor.7400784 |
0.01 |
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| 2006 |
Wszolek ZK, Tsuboi Y, Ghetti B, Pickering-Brown S, Baba Y, Cheshire WP. Frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17). Orphanet Journal of Rare Diseases. 1: 30. PMID 16899117 DOI: 10.1186/1750-1172-1-30 |
0.01 |
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| 2006 |
Murrell J, Ghetti B, Cochran E, Macias-Islas MA, Medina L, Varpetian A, Cummings JL, Mendez MF, Kawas C, Chui H, Ringman JM. The A431E mutation in PSEN1 causing familial Alzheimer's disease originating in Jalisco State, Mexico: an additional fifteen families. Neurogenetics. 7: 277-9. PMID 16897084 DOI: 10.1007/S10048-006-0053-1 |
0.01 |
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| 2006 |
Schweitzer K, Decker E, Zhu L, Miller RE, Mirra SS, Spina S, Ghetti B, Wang M, Murrell J. Aberrantly regulated proteins in frontotemporal dementia. Biochemical and Biophysical Research Communications. 348: 465-72. PMID 16890190 DOI: 10.1016/J.Bbrc.2006.07.113 |
0.01 |
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| 2006 |
Moroncini G, Mangieri M, Morbin M, Mazzoleni G, Ghetti B, Gabrielli A, Williamson RA, Giaccone G, Tagliavini F. Pathologic prion protein is specifically recognized in situ by a novel PrP conformational antibody. Neurobiology of Disease. 23: 717-24. PMID 16876426 DOI: 10.1016/j.nbd.2006.06.008 |
0.01 |
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| 2006 |
Shiarli AM, Jennings R, Shi J, Bailey K, Davidson Y, Tian J, Bigio EH, Ghetti B, Murrell JR, Delisle MB, Mirra S, Crain B, Zolo P, Arima K, Iseki E, et al. Comparison of extent of tau pathology in patients with frontotemporal dementia with Parkinsonism linked to chromosome 17 (FTDP-17), frontotemporal lobar degeneration with Pick bodies and early onset Alzheimer's disease. Neuropathology and Applied Neurobiology. 32: 374-87. PMID 16866983 DOI: 10.1111/J.1365-2990.2006.00736.X |
0.01 |
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| 2006 |
Colucci M, Moleres FJ, Xie ZL, Ray-Chaudhury A, Gutti S, Butefisch CM, Cervenakova L, Wang W, Goldfarb LG, Kong Q, Ghetti B, Chen SG, Gambetti P. Gerstmann-Sträussler-Scheinker: a new phenotype with 'curly' PrP deposits. Journal of Neuropathology and Experimental Neurology. 65: 642-51. PMID 16825951 DOI: 10.1097/01.Jnen.0000228198.81797.4D |
0.01 |
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| 2006 |
Tofaris GK, Garcia Reitböck P, Humby T, Lambourne SL, O'Connell M, Ghetti B, Gossage H, Emson PC, Wilkinson LS, Goedert M, Spillantini MG. Pathological changes in dopaminergic nerve cells of the substantia nigra and olfactory bulb in mice transgenic for truncated human alpha-synuclein(1-120): implications for Lewy body disorders. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 26: 3942-50. PMID 16611810 DOI: 10.1523/Jneurosci.4965-05.2006 |
0.01 |
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| 2006 |
Baba Y, Ghetti B, Baker MC, Uitti RJ, Hutton ML, Yamaguchi K, Bird T, Lin W, DeLucia MW, Dickson DW, Wszolek ZK. Hereditary diffuse leukoencephalopathy with spheroids: clinical, pathologic and genetic studies of a new kindred. Acta Neuropathologica. 111: 300-11. PMID 16523341 DOI: 10.1007/S00401-006-0046-Z |
0.01 |
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| 2006 |
Delobel P, Lavenir I, Ghetti B, Holzer M, Goedert M. Cell-cycle markers in a transgenic mouse model of human tauopathy: increased levels of cyclin-dependent kinase inhibitors p21Cip1 and p27Kip1. The American Journal of Pathology. 168: 878-87. PMID 16507903 DOI: 10.2353/Ajpath.2006.050540 |
0.01 |
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| 2006 |
Brelstaff JH, Tolkovsky A, Ghetti BF, Goedert M, Spillantini MG. P4-257: NEURONS WITH TAU AGGREGATES EXPOSE PHOSPHATIDYLSERINE AND ARE PHAGOCYTOSED LIVE BY MICROGLIA Alzheimer's & Dementia. 14: P1545-P1545. DOI: 10.1016/J.Jalz.2018.07.079 |
0.01 |
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| 2006 |
Galasko DR, Groveman BR, Orru CD, Hughson AG, Raymond LD, Zanusso G, Ghetti BF, Campbell KJ, Safar J, Caughey B. P1-250: RAPID AND ULTRA-SENSITIVE DETECTION OF α-SYNUCLEIN SEEDS IN BRAIN AND CEREBROSPINAL FLUID BY α-SYN RT-QUIC: AN AID TO DIAGNOSIS FOR PD AND DLB Alzheimer's & Dementia. 14: P375-P375. DOI: 10.1016/j.jalz.2018.06.255 |
0.01 |
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| 2006 |
Joe EB, Joseph-Mathurin N, Benzinger TL, Bateman RJ, McDade E, Ghetti BF, Levin J, Vöglein J, Fox NC, Sperling RA, Chhatwal JP, Noble J, Salloway S, Chui HC, Ringman JM. P4-094: OCCIPITAL TO GLOBAL PIB UPTAKE IS ASSOCIATED WITH THE PRESENCE OF MICROHEMORRHAGES AND MUTATIONS ASSOCIATED WITH CEREBRAL AMYLOID ANGIOPATHY IN THE DOMINANTLY INHERITED ALZHEIMER'S NETWORK Alzheimer's & Dementia. 14: P1472-P1473. DOI: 10.1016/J.Jalz.2018.06.2497 |
0.01 |
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| 2006 |
Spina S, Murrell JR, Farlow MR, Ghetti B. P4-109: Clinical symptoms and brainstem pathology in FTDP-17 associated with the EXON 10 +3 intronic Tau mutation Alzheimers & Dementia. 2. DOI: 10.1016/J.Jalz.2006.05.1848 |
0.01 |
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| 2006 |
Piccini A, Zanusso G, Borghi R, Noviello C, Monaco S, Russo R, Damonte G, Armirotti A, Gelati M, Giordano R, Zambenedetti P, Russo C, Zaccheo D, Ghetti B, Tabaton M. P3-418: A cerebellar variant of Alzheimer's disease caused by presenilin 1 S170F mutation Alzheimer's & Dementia. 2: S499-S499. DOI: 10.1016/J.Jalz.2006.05.1689 |
0.01 |
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| 2006 |
Cupidi C, Giaccone G, Capobianco R, Ghetti B, Bugiani O, Tagliavini F. P3-200: Relationship between neurofibrillary pathology and Aβ deposition in Alzheimer disease Alzheimers & Dementia. 2. DOI: 10.1016/J.Jalz.2006.05.1468 |
0.01 |
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| 2006 |
Spina S, Murrell JR, Sweeney B, Bermingham N, Ghetti B, Keohane C. P3-156: Early onset frontotemporal dementia and parkinsonism associated with the G335S Tau mutation Alzheimers & Dementia. 2. DOI: 10.1016/J.Jalz.2006.05.1424 |
0.01 |
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| 2005 |
Ghetti B. Recognition: Robert Terry. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. 1: 78. PMID 19595824 DOI: 10.1016/j.jalz.2005.06.006 |
0.01 |
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| 2005 |
Castellani RJ, Siedlak SL, Fortino AE, Perry G, Ghetti B, Smith MA. Chitin-like polysaccharides in Alzheimer's disease brains. Current Alzheimer Research. 2: 419-23. PMID 16248847 DOI: 10.2174/156720505774330555 |
0.01 |
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| 2005 |
Esh C, Patton L, Kalback W, Kokjohn TA, Lopez J, Brune D, Newell AJ, Beach T, Schenk D, Games D, Paul S, Bales K, Ghetti B, Castaño EM, Roher AE. Altered APP processing in PDAPP (Val717 --> Phe) transgenic mice yields extended-length Abeta peptides. Biochemistry. 44: 13807-19. PMID 16229470 DOI: 10.1021/Bi051213+ |
0.01 |
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| 2005 |
Ringman JM, Diaz-Olavarrieta C, Rodriguez Y, Chavez M, Fairbanks L, Paz F, Varpetian A, Maldonado HC, Macias-Islas MA, Murrell J, Ghetti B, Kawas C. Neuropsychological function in nondemented carriers of presenilin-1 mutations. Neurology. 65: 552-8. PMID 16116115 DOI: 10.1212/01.Wnl.0000172919.50001.D6 |
0.01 |
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| 2005 |
Petersen RB, Siedlak SL, Lee HG, Kim YS, Nunomura A, Tagliavini F, Ghetti B, Cras P, Moreira PI, Castellani RJ, Guentchev M, Budka H, Ironside JW, Gambetti P, Smith MA, et al. Redox metals and oxidative abnormalities in human prion diseases. Acta Neuropathologica. 110: 232-8. PMID 16096758 DOI: 10.1007/S00401-005-1034-4 |
0.01 |
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| 2005 |
Miravalle L, Calero M, Takao M, Roher AE, Ghetti B, Vidal R. Amino-terminally truncated Abeta peptide species are the main component of cotton wool plaques. Biochemistry. 44: 10810-21. PMID 16086583 DOI: 10.1021/Bi0508237 |
0.01 |
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| 2005 |
Yamaguchi K, Cochran EJ, Murrell JR, Polymeropoulos MH, Shannon KM, Crowther RA, Goedert M, Ghetti B. Abundant neuritic inclusions and microvacuolar changes in a case of diffuse Lewy body disease with the A53T mutation in the alpha-synuclein gene. Acta Neuropathologica. 110: 298-305. PMID 15981014 DOI: 10.1007/S00401-005-1042-4 |
0.01 |
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| 2005 |
Baba Y, Tsuboi Y, Baker MC, Uitti RJ, Hutton ML, Dickson DW, Farrer M, Putzke JD, Woodruff BK, Ghetti B, Murrell JR, Boeve BF, Petersen RC, Verpillat P, Brice A, et al. The effect of tau genotype on clinical features in FTDP-17. Parkinsonism & Related Disorders. 11: 205-8. PMID 15878580 DOI: 10.1016/J.Parkreldis.2005.01.003 |
0.01 |
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| 2005 |
Zaidi SI, Richardson SL, Capellari S, Song L, Smith MA, Ghetti B, Sy MS, Gambetti P, Petersen RB. Characterization of the F198S prion protein mutation: enhanced glycosylation and defective refolding. Journal of Alzheimer's Disease : Jad. 7: 159-71; discussion 1. PMID 15851854 DOI: 10.3233/Jad-2005-7209 |
0.01 |
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| 2005 |
Gemignani A, Pietrini P, Murrell JR, Glazier BS, Zolo P, Guazzelli M, Ghetti B. Slow wave and rem sleep mechanisms are differently altered in hereditary pick disease associated with the TAU G389R mutation. Archives Italiennes De Biologie. 143: 65-79. PMID 15844669 DOI: 10.4449/Aib.V143I1.340 |
0.01 |
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| 2005 |
Stewart RS, Piccardo P, Ghetti B, Harris DA. Neurodegenerative illness in transgenic mice expressing a transmembrane form of the prion protein. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 25: 3469-77. PMID 15800202 DOI: 10.1523/JNEUROSCI.0105-05.2005 |
0.01 |
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| 2005 |
Chiesa R, Piccardo P, Dossena S, Nowoslawski L, Roth KA, Ghetti B, Harris DA. Bax deletion prevents neuronal loss but not neurological symptoms in a transgenic model of inherited prion disease. Proceedings of the National Academy of Sciences of the United States of America. 102: 238-43. PMID 15618403 DOI: 10.1073/pnas.0406173102 |
0.01 |
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| 2005 |
Boeve BF, Tremont-Lukats IW, Waclawik AJ, Murrell JR, Hermann B, Jack CR, Shiung MM, Smith GE, Nair AR, Lindor N, Koppikar V, Ghetti B. Longitudinal characterization of two siblings with frontotemporal dementia and parkinsonism linked to chromosome 17 associated with the S305N tau mutation. Brain : a Journal of Neurology. 128: 752-72. PMID 15615814 DOI: 10.1093/Brain/Awh356 |
0.01 |
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| 2005 |
Bugiani O, Giaccone G, Capobianco R, Tagliavini F, Ghetti B. Alzheimer's disease (AD) : AT8 recognizes degenerating ectopic neurons and astrocytes in the subcortical white matter. Revue Neurologique. 161: 338-339. DOI: 10.1016/S0035-3787(05)85050-7 |
0.01 |
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| 2004 |
Vidal R, Delisle MB, Ghetti B. Neurodegeneration caused by proteins with an aberrant carboxyl-terminus. Journal of Neuropathology and Experimental Neurology. 63: 787-800. PMID 15330334 DOI: 10.1093/Jnen/63.8.787 |
0.01 |
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| 2004 |
Woodruff BK, Baba Y, Hutton ML, Wszolek ZK, Tsuboi Y, Kobayashi T, Ghetti B, Arima K, Yasuda M, Rascol O. Haplotype-phenotype correlations in kindreds with the N279K mutation in the tau gene. Archives of Neurology. 61: 1327; author reply 1. PMID 15313857 DOI: 10.1001/archneur.61.8.1327-a |
0.01 |
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| 2004 |
Barmada S, Piccardo P, Yamaguchi K, Ghetti B, Harris DA. GFP-tagged prion protein is correctly localized and functionally active in the brains of transgenic mice. Neurobiology of Disease. 16: 527-37. PMID 15262264 DOI: 10.1016/J.Nbd.2004.05.005 |
0.01 |
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| 2004 |
Takao M, Ghetti B, Yoshida H, Piccardo P, Narain Y, Murrell JR, Vidal R, Glazier BS, Jakes R, Tsutsui M, Spillantini MG, Crowther RA, Goedert M, Koto A. Early-onset dementia with Lewy bodies. Brain Pathology (Zurich, Switzerland). 14: 137-47. PMID 15193026 DOI: 10.1111/J.1750-3639.2004.Tb00046.X |
0.01 |
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| 2004 |
Vidal R, Ghetti B, Takao M, Brefel-Courbon C, Uro-Coste E, Glazier BS, Siani V, Benson MD, Calvas P, Miravalle L, Rascol O, Delisle MB. Intracellular ferritin accumulation in neural and extraneural tissue characterizes a neurodegenerative disease associated with a mutation in the ferritin light polypeptide gene. Journal of Neuropathology and Experimental Neurology. 63: 363-80. PMID 15099026 DOI: 10.1093/Jnen/63.4.363 |
0.01 |
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| 2004 |
Vitali A, Piccini A, Borghi R, Fornaro P, Siedlak SL, Smith MA, Gambetti P, Ghetti B, Tabaton M. Soluble amyloid beta-protein is increased in frontotemporal dementia with tau gene mutations. Journal of Alzheimer's Disease : Jad. 6: 45-51. PMID 15004327 DOI: 10.3233/Jad-2004-6106 |
0.01 |
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| 2004 |
Notari S, Capellari S, Giese A, Westner I, Baruzzi A, Ghetti B, Gambetti P, Kretzschmar HA, Parchi P. Effects of different experimental conditions on the PrPSc core generated by protease digestion: implications for strain typing and molecular classification of CJD. The Journal of Biological Chemistry. 279: 16797-804. PMID 14754888 DOI: 10.1074/Jbc.M313220200 |
0.01 |
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| 2004 |
Roher AE, Kokjohn TA, Esh C, Weiss N, Childress J, Kalback W, Luehrs DC, Lopez J, Brune D, Kuo YM, Farlow M, Murrell J, Vidal R, Ghetti B. The human amyloid-beta precursor protein770 mutation V717F generates peptides longer than amyloid-beta-(40-42) and flocculent amyloid aggregates. The Journal of Biological Chemistry. 279: 5829-36. PMID 14645225 DOI: 10.1074/Jbc.M311380200 |
0.01 |
|
| 2004 |
Kong Q, Surewicz WK, Petersen RB, Zou W, Chen SG, Gambetti P, Parchi P, Capellari S, Goldfarb L, Montagna P, Lugaresi E, Piccardo P, Ghetti B. 14 Inherited Prion Diseases Cold Spring Harbor Monograph Archive. 41: 673-775. DOI: 10.1101/087969693.41.673 |
0.01 |
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| 2004 |
Vidal R, Ghetti B, Delisle MB, Rascol O, Perry G, Smith MA. P4-242 Oxidative damage in ferritin-induced neurodegeneration Neurobiology of Aging. 25. DOI: 10.1016/S0197-4580(04)81800-1 |
0.01 |
|
| 2004 |
Murrell J, Tremont-Lukats IW, Waclawik AJ, Lindor N, Ghetti B, Boeve BF. P4-148 Genetic analyses of a family with frontotemporal dementia Neurobiology of Aging. 25: S517. DOI: 10.1016/S0197-4580(04)81706-8 |
0.01 |
|
| 2004 |
Boeve BF, Tremont IW, Waclawik AJ, Murrell J, Hermann B, Jack CR, Smith GE, Knopman DS, Nair AR, Lindor N, Koppikar V, Ghetti B. P3-339 Longitudinal characterization of two siblings with frontotemporal dementia associated with the S305N tau mutation Neurobiology of Aging. 25. DOI: 10.1016/S0197-4580(04)81488-X |
0.01 |
|
| 2004 |
Miravalle L, Ghetti B, Calero M, Rentz CA, Richardson RM, Takao M, Vidal R. P1-216 Cotton wool plaques associated with a novel mutation in the presenilin 1 gene (V261I): immunohistological, genetic and biochemicals studies Neurobiology of Aging. 25. DOI: 10.1016/S0197-4580(04)80529-3 |
0.01 |
|
| 2003 |
De Michele G, Pocchiari M, Petraroli R, Manfredi M, Caneve G, Coppola G, Casali C, Saccà F, Piccardo P, Salvatore E, Berardelli A, Orio M, Barbieri F, Ghetti B, Filla A. Variable phenotype in a P102L Gerstmann-Sträussler-Scheinker Italian family. The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques. 30: 233-6. PMID 12945948 DOI: 10.1017/S0317167100002651 |
0.01 |
|
| 2003 |
Tofaris GK, Razzaq A, Ghetti B, Lilley KS, Spillantini MG. Ubiquitination of alpha-synuclein in Lewy bodies is a pathological event not associated with impairment of proteasome function. The Journal of Biological Chemistry. 278: 44405-11. PMID 12923179 DOI: 10.1074/Jbc.M308041200 |
0.01 |
|
| 2003 |
Chiesa R, Piccardo P, Quaglio E, Drisaldi B, Si-Hoe SL, Takao M, Ghetti B, Harris DA. Molecular distinction between pathogenic and infectious properties of the prion protein. Journal of Virology. 77: 7611-22. PMID 12805461 DOI: 10.1128/JVI.77.13.7611-7622.2003 |
0.01 |
|
| 2003 |
Powers JM, Byrne NP, Ito M, Takao M, Yankopoulou D, Spillantini MG, Ghetti B. A novel leukoencephalopathy associated with tau deposits primarily in white matter glia. Acta Neuropathologica. 106: 181-7. PMID 12783250 DOI: 10.1007/S00401-003-0719-9 |
0.01 |
|
| 2003 |
Harris DA, Chiesa R, Drisaldi B, Quaglio E, Migheli A, Piccardo P, Ghetti B. A murine model of a familial prion disease. Clinics in Laboratory Medicine. 23: 175-86. PMID 12733431 DOI: 10.1016/S0272-2712(02)00069-0 |
0.01 |
|
| 2003 |
Ghetti B, Tagliavini F, Takao M, Bugiani O, Piccardo P. Hereditary prion protein amyloidoses. Clinics in Laboratory Medicine. 23: 65-85, viii. PMID 12733425 DOI: 10.1016/S0272-2712(02)00064-1 |
0.01 |
|
| 2003 |
Vidal R, Delisle MB, Rascol O, Ghetti B. Hereditary ferritinopathy. Journal of the Neurological Sciences. 207: 110-1. PMID 12614943 |
0.01 |
|
| 2002 |
Tsuboi Y, Baker M, Hutton ML, Uitti RJ, Rascol O, Delisle MB, Soulages X, Murrell JR, Ghetti B, Yasuda M, Komure O, Kuno S, Arima K, Sunohara N, Kobayashi T, et al. Clinical and genetic studies of families with the tau N279K mutation (FTDP-17). Neurology. 59: 1791-3. PMID 12473774 DOI: 10.1212/01.Wnl.0000038909.49164.4B |
0.01 |
|
| 2002 |
Allen B, Ingram E, Takao M, Smith MJ, Jakes R, Virdee K, Yoshida H, Holzer M, Craxton M, Emson PC, Atzori C, Migheli A, Crowther RA, Ghetti B, Spillantini MG, et al. Abundant tau filaments and nonapoptotic neurodegeneration in transgenic mice expressing human P301S tau protein. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 22: 9340-51. PMID 12417659 DOI: 10.1523/Jneurosci.22-21-09340.2002 |
0.01 |
|
| 2002 |
Ogunnyi A, Akang EE, Gureje O, Takao M, Piccardo P, Baiyewu O, Hall KS, Ghetti B, Hendrie HC. Dementia with Lewy bodies in a Nigerian: a case report. International Psychogeriatrics / Ipa. 14: 211-8. PMID 12243211 DOI: 10.1017/S1041610202008402 |
0.01 |
|
| 2002 |
Zhong J, Deng J, Ghetti B, Lee WH. Inhibition of insulin-like growth factor I activity contributes to the premature apoptosis of cerebellar granule neuron in weaver mutant mice: in vitro analysis. Journal of Neuroscience Research. 70: 36-45. PMID 12237862 DOI: 10.1002/jnr.10360 |
0.01 |
|
| 2002 |
Adamec E, Murrell JR, Takao M, Hobbs W, Nixon RA, Ghetti B, Vonsattel JP. P301L tauopathy: confocal immunofluorescence study of perinuclear aggregation of the mutated protein. Journal of the Neurological Sciences. 200: 85-93. PMID 12127682 DOI: 10.1016/S0022-510X(02)00150-8 |
0.01 |
|
| 2002 |
Martà J, Wills KV, Ghetti B, Bayer SA. A combined immunohistochemical and autoradiographic method to detect midbrain dopaminergic neurons and determine their time of origin. Brain Research. Brain Research Protocols. 9: 197-205. PMID 12113779 |
0.01 |
|
| 2002 |
Takao M, Ghetti B, Hayakawa I, Ikeda E, Fukuuchi Y, Miravalle L, Piccardo P, Murrell JR, Glazier BS, Koto A. A novel mutation (G217D) in the Presenilin 1 gene ( PSEN1) in a Japanese family: presenile dementia and parkinsonism are associated with cotton wool plaques in the cortex and striatum. Acta Neuropathologica. 104: 155-70. PMID 12111359 DOI: 10.1007/s00401-002-0536-6 |
0.01 |
|
| 2002 |
Davis RL, Shrimpton AE, Carrell RW, Lomas DA, Gerhard L, Baumann B, Lawrence DA, Yepes M, Kim TS, Ghetti B, Piccardo P, Takao M, Lacbawan F, Muenke M, Sifers RN, et al. Association between conformational mutations in neuroserpin and onset and severity of dementia. Lancet. 359: 2242-7. PMID 12103288 DOI: 10.1016/S0140-6736(02)09293-0 |
0.01 |
|
| 2002 |
Tsuboi Y, Uitti RJ, Delisle MB, Ferreira JJ, Brefel-Courbon C, Rascol O, Ghetti B, Murrell JR, Hutton M, Baker M, Wszolek ZK. Clinical features and disease haplotypes of individuals with the N279K tau gene mutation: a comparison of the pallidopontonigral degeneration kindred and a French family. Archives of Neurology. 59: 943-50. PMID 12056930 DOI: 10.1001/Archneur.59.6.943 |
0.01 |
|
| 2002 |
Moehlmann T, Winkler E, Xia X, Edbauer D, Murrell J, Capell A, Kaether C, Zheng H, Ghetti B, Haass C, Steiner H. Presenilin-1 mutations of leucine 166 equally affect the generation of the Notch and APP intracellular domains independent of their effect on Abeta 42 production. Proceedings of the National Academy of Sciences of the United States of America. 99: 8025-30. PMID 12048239 DOI: 10.1073/Pnas.112686799 |
0.01 |
|
| 2002 |
Marti J, Wills KV, Ghetti B, Bayer SA. Regional differences in the Purkinje cells settled pattern: a comparative autoradiographic study in control and homozygous weaver mice. Experimental Neurology. 175: 168-81. PMID 12009769 DOI: 10.1006/exnr.2002.7873 |
0.01 |
|
| 2002 |
Taratuto AL, Piccardo P, Reich EG, Chen SG, Sevlever G, Schultz M, Luzzi AA, Rugiero M, Abecasis G, Endelman M, Garcia AM, Capellari S, Xie Z, Lugaresi E, Gambetti P, ... ... Ghetti B, et al. Insomnia associated with thalamic involvement in E200K Creutzfeldt-Jakob disease. Neurology. 58: 362-7. PMID 11839833 DOI: 10.1212/Wnl.58.3.362 |
0.01 |
|
| 2001 |
Harris DA, Chiesa R, Migheli A, Piccardo P, Ghetti B. Cellular and transgenic models of familial prion diseases. Methods in Molecular Medicine. 59: 149-61. PMID 21374503 DOI: 10.1385/1-59259-134-5:149 |
0.01 |
|
| 2001 |
Atzori C, Ghetti B, Piva R, Srinivasan AN, Zolo P, Delisle MB, Mirra SS, Migheli A. Activation of the JNK/p38 pathway occurs in diseases characterized by tau protein pathology and is related to tau phosphorylation but not to apoptosis. Journal of Neuropathology and Experimental Neurology. 60: 1190-7. PMID 11764091 DOI: 10.1093/Jnen/60.12.1190 |
0.01 |
|
| 2001 |
Takao M, Ghetti B, Murrell JR, Unverzagt FW, Giaccone G, Tagliavini F, Bugiani O, Piccardo P, Hulette CM, Crain BJ, Farlow MR, Heyman A. Ectopic white matter neurons, a developmental abnormality that may be caused by the PSEN1 S169L mutation in a case of familial AD with myoclonus and seizures. Journal of Neuropathology and Experimental Neurology. 60: 1137-52. PMID 11764087 DOI: 10.1093/Jnen/60.12.1137 |
0.01 |
|
| 2001 |
Panegyres PK, Toufexis K, Kakulas BA, Cernevakova L, Brown P, Ghetti B, Piccardo P, Dlouhy SR. A new PRNP mutation (G131V) associated with Gerstmann-Sträussler-Scheinker disease. Archives of Neurology. 58: 1899-902. PMID 11709001 |
0.01 |
|
| 2001 |
Martà J, Wills KV, Ghetti B, Bayer SA. Evidence that the loss of Purkinje cells and deep cerebellar nuclei neurons in homozygous weaver is not related to neurogenetic patterns. International Journal of Developmental Neuroscience : the Official Journal of the International Society For Developmental Neuroscience. 19: 599-610. PMID 11600321 |
0.01 |
|
| 2001 |
Piccardo P, Liepnieks JJ, William A, Dlouhy SR, Farlow MR, Young K, Nochlin D, Bird TD, Nixon RR, Ball MJ, DeCarli C, Bugiani O, Tagliavini F, Benson MD, Ghetti B. Prion proteins with different conformations accumulate in Gerstmann-Sträussler-Scheinker disease caused by A117V and F198S mutations. The American Journal of Pathology. 158: 2201-7. PMID 11395398 DOI: 10.1016/S0002-9440(10)64692-5 |
0.01 |
|
| 2001 |
Chiesa R, Pestronk A, Schmidt RE, Tourtellotte WG, Ghetti B, Piccardo P, Harris DA. Primary myopathy and accumulation of PrPSc-like molecules in peripheral tissues of transgenic mice expressing a prion protein insertional mutation. Neurobiology of Disease. 8: 279-88. PMID 11300723 DOI: 10.1006/Nbdi.2001.0400 |
0.01 |
|
| 2001 |
Levy E, Sastre M, Kumar A, Gallo G, Piccardo P, Ghetti B, Tagliavini F. Codeposition of cystatin C with amyloid-beta protein in the brain of Alzheimer disease patients. Journal of Neuropathology and Experimental Neurology. 60: 94-104. PMID 11202179 |
0.01 |
|
| 2001 |
Yazaki M, Liepnieks JJ, Murrell JR, Takao M, Guenther B, Piccardo P, Farlow MR, Ghetti B, Benson MD. Biochemical characterization of a neuroserpin variant associated with hereditary dementia. The American Journal of Pathology. 158: 227-33. PMID 11141496 DOI: 10.1016/S0002-9440(10)63961-2 |
0.01 |
|
| 2001 |
Tagliavini F, Lievens PM, Tranchant C, Warter JM, Mohr M, Giaccone G, Perini F, Rossi G, Salmona M, Piccardo P, Ghetti B, Beavis RC, Bugiani O, Frangione B, Prelli F. A 7-kDa prion protein (PrP) fragment, an integral component of the PrP region required for infectivity, is the major amyloid protein in Gerstmann-Sträussler-Scheinker disease A117V. The Journal of Biological Chemistry. 276: 6009-15. PMID 11087738 DOI: 10.1074/Jbc.M007062200 |
0.01 |
|
| 2001 |
Russo C, Schettini G, Saido TC, Hulette C, Lippa C, Lannfelt L, Ghetti B, Gambetti P, Tabaton M, Teller JK. Molecular consequences of presenilin-1 mutation Nature. 411: 655-655. DOI: 10.1038/35079684 |
0.01 |
|
| 2001 |
Harris DA, Chiesa R, Drisaldi B, Quaglio E, Migheli A, Piccardo P, Ghetti B. A transgenic model of a familial prion disease Archives of Virology, Supplement. 103-112. |
0.01 |
|
| 2000 |
Harris DA, Chiesa R, Drisaldi B, Quaglio E, Migheli A, Piccardo P, Ghetti B. A transgenic model of a familial prion disease. Archives of Virology. Supplementum. 103-12. PMID 11214912 DOI: 10.1007/978-3-7091-6308-5_9 |
0.01 |
|
| 2000 |
Sorbi S, Alberoni M, Alfieri P, Amici S, Antana D, Appollonio I, Avanzi S, Bartoli A, Bergamasco B, Bracco L, Bruni A, Bugiani O, Caffarra P, Caltagirone C, Carolei A, ... ... Ghetti B, et al. Guidelines for the diagnosis of dementia and Alzheimer's disease Neurological Sciences. 21: 187-194. PMID 11214656 DOI: 10.1007/S100720070075 |
0.01 |
|
| 2000 |
Goedert M, Ghetti B, Spillantini MG. Tau gene mutations in frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17). Their relevance for understanding the neurogenerative process. Annals of the New York Academy of Sciences. 920: 74-83. PMID 11193179 DOI: 10.1111/J.1749-6632.2000.Tb06907.X |
0.01 |
|
| 2000 |
Ghetti B, Murrell JR, Zolo P, Spillantini MG, Goedert M. Progress in hereditary tauopathies: a mutation in the Tau gene (G389R) causes a Pick disease-like syndrome. Annals of the New York Academy of Sciences. 920: 52-62. PMID 11193177 DOI: 10.1111/J.1749-6632.2000.Tb06905.X |
0.01 |
|
| 2000 |
Takao M, Benson MD, Murrell JR, Yazaki M, Piccardo P, Unverzagt FW, Davis RL, Holohan PD, Lawrence DA, Richardson R, Farlow MR, Ghetti B. Neuroserpin mutation S52R causes neuroserpin accumulation in neurons and is associated with progressive myoclonus epilepsy. Journal of Neuropathology and Experimental Neurology. 59: 1070-86. PMID 11138927 DOI: 10.1093/Jnen/59.12.1070 |
0.01 |
|
| 2000 |
Delisle MB, Uro-Coste E, Murrell JR, Rascol O, Ghetti B. [Neurodegenerative disease associated with a mutation of codon 279 (N279K) in exon 10 of Tau protein]. Bulletin De L'Acadã©Mie Nationale De Mã©Decine. 184: 799-809; discussion . PMID 10989564 |
0.01 |
|
| 2000 |
Lippa CF, Swearer JM, Kane KJ, Nochlin D, Bird TD, Ghetti B, Nee LE, St George-Hyslop P, Pollen DA, Drachman DA. Familial Alzheimer's disease: site of mutation influences clinical phenotype. Annals of Neurology. 48: 376-9. PMID 10976645 DOI: 10.1002/1531-8249(200009)48:3<376::Aid-Ana13>3.0.Co;2-U |
0.01 |
|
| 2000 |
Parchi P, Zou W, Wang W, Brown P, Capellari S, Ghetti B, Kopp N, Schulz-Schaeffer WJ, Kretzschmar HA, Head MW, Ironside JW, Gambetti P, Chen SG. Genetic influence on the structural variations of the abnormal prion protein. Proceedings of the National Academy of Sciences of the United States of America. 97: 10168-72. PMID 10963679 DOI: 10.1073/Pnas.97.18.10168 |
0.01 |
|
| 2000 |
Martà J, Wills KV, Ghetti B, Bayer SA. The weaver gene continues to target late-generated dopaminergic neurons in midbrain areas at P90. Brain Research. Developmental Brain Research. 122: 173-81. PMID 10960686 |
0.01 |
|
| 2000 |
Martà J, Wills KV, Ghetti B, Bayer SA. The weaver gene has no effect on the generation patterns of mesencephalic dopaminergic neurons. Brain Research. Developmental Brain Research. 122: 165-72. PMID 10960685 |
0.01 |
|
| 2000 |
Vidal R, Calero M, Piccardo P, Farlow MR, Unverzagt FW, Méndez E, Jiménez-Huete A, Beavis R, Gallo G, Gomez-Tortosa E, Ghiso J, Hyman BT, Frangione B, Ghetti B. Senile dementia associated with amyloid beta protein angiopathy and tau perivascular pathology but not neuritic plaques in patients homozygous for the APOE-epsilon4 allele. Acta Neuropathologica. 100: 1-12. PMID 10912914 DOI: 10.1007/S004010051186 |
0.01 |
|
| 2000 |
Bugiani O, Giaccone G, Piccardo P, Morbin M, Tagliavini F, Ghetti B. Neuropathology of Gerstmann-Sträussler-Scheinker disease. Microscopy Research and Technique. 50: 10-5. PMID 10871543 DOI: 10.1002/1097-0029(20000701)50:1<10::Aid-Jemt3>3.0.Co;2-6 |
0.01 |
|
| 2000 |
Murrell JR, Hake AM, Quaid KA, Farlow MR, Ghetti B. Early-onset Alzheimer disease caused by a new mutation (V717L) in the amyloid precursor protein gene. Archives of Neurology. 57: 885-7. PMID 10867787 DOI: 10.1001/Archneur.57.6.885 |
0.01 |
|
| 2000 |
Russo C, Schettini G, Saido TC, Hulette C, Lippa C, Lannfelt L, Ghetti B, Gambetti P, Tabaton M, Teller JK. Presenilin-1 mutations in Alzheimer's disease. Nature. 405: 531-2. PMID 10850703 DOI: 10.1038/35014735 |
0.01 |
|
| 2000 |
Chiesa R, Drisaldi B, Quaglio E, Migheli A, Piccardo P, Ghetti B, Harris DA. Accumulation of protease-resistant prion protein (PrP) and apoptosis of cerebellar granule cells in transgenic mice expressing a PrP insertional mutation. Proceedings of the National Academy of Sciences of the United States of America. 97: 5574-9. PMID 10805813 DOI: 10.1073/pnas.97.10.5574 |
0.01 |
|
| 2000 |
Harkins AB, Dlouhy S, Ghetti B, Cahill AL, Won L, Heller B, Heller A, Fox AP. Evidence of elevated intracellular calcium levels in weaver homozygote mice. The Journal of Physiology. 524: 447-55. PMID 10766925 DOI: 10.1111/J.1469-7793.2000.T01-2-00447.X |
0.01 |
|
| 2000 |
Quaid KA, Murrell JR, Hake AM, Farlow MR, Ghetti B. Presymptomatic genetic testing with an APP mutation in Early-onset Alzheimer disease: A descriptive study of sibship dynamics Journal of Genetic Counseling. 9: 327-341. DOI: 10.1023/A:1009406229745 |
0.01 |
|
| 2000 |
Piccardo P, Liepnieks JJ, William A, Dlouhy SR, Bugiani O, Tagliavini F, Benson MD, Ghetti B. Determination of the amino-terminal cleavage site of PRPRES in GSS F198S Neurobiology of Aging. 21: 268. DOI: 10.1016/S0197-4580(00)83157-7 |
0.01 |
|
| 2000 |
Takao M, Hayakawa I, Ikeda E, Murrell JR, Piccardo P, Ghetti B, Koto A. Familial presenile dementia with Parkinsonism in a Japanese family Neurobiology of Aging. 21: 267. DOI: 10.1016/S0197-4580(00)83156-5 |
0.01 |
|
| 2000 |
Marcon G, Atzori C, Srinivasan AN, Okazawa H, Ghetti B, Migheli A. Caspase-3 is activated in Alzheimer disease but not in frontotemporal dementia Neurobiology of Aging. 21: 81. DOI: 10.1016/S0197-4580(00)82589-0 |
0.01 |
|
| 2000 |
Ghetti B. Neuropathology of hereditary tauopathies Neurobiology of Aging. 21: 69. DOI: 10.1016/S0197-4580(00)82530-0 |
0.01 |
|
| 2000 |
Yazaki M, Benson MD, Liepnieks JJ, Farlow MR, Piccardo P, Takao M, Murrell JR, Ghetti B. A S52R mutation in neuroserpin is associated with myoclonic epilepsy and dementia Neurobiology of Aging. 21: 66. DOI: 10.1016/S0197-4580(00)82517-8 |
0.01 |
|
| 2000 |
Farlow MR, Murrell JR, Hulette CM, Ghetti B. Hereditary lateral sclerosis and Alzheimer disease associated with mutation at codon 261 of the presenilin 1 (PS1) gene Neurobiology of Aging. 21: 62. DOI: 10.1016/S0197-4580(00)82502-6 |
0.01 |
|
| 2000 |
Hake AM, Murrell JR, Unverzagt FW, Ghetti B, Farlow MR. Clinical characteristics in a family with early-onset Alzheimer disease caused by a mutation (V717L) in the APP gene Neurobiology of Aging. 21: 59. DOI: 10.1016/S0197-4580(00)82488-4 |
0.01 |
|
| 2000 |
Parchi P, Brown P, Capellari S, Ghetti B, Gibbs CJ, Gambetti PL. Transmission to non-human primates indicates that kuru as well as the ataxic (VV2) or kuruplaque (MV2) variants of sporadic Creutzfeldt-Jakob disease are caused by the same strain of prions Neurobiology of Aging. 21: 57. DOI: 10.1016/S0197-4580(00)82481-1 |
0.01 |
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| 2000 |
Russo C, Saido TC, Hulette C, Price K, Ghetti B, Teller JK, Tabaton M, Schettini G, Gambetti PL. Increased presence of amino-terminally-truncated Aβ-peptides in presenilin 1 early-onset familial Alzheimer disease Neurobiology of Aging. 21: 194. DOI: 10.1016/S0197-4580(00)82214-9 |
0.01 |
|
| 1999 |
Ghetti B, Murrell J, Spillantini MG. Mutations in the Tau gene cause frontotemporal dementia. Brain Research Bulletin. 50: 471-2. PMID 10643489 DOI: 10.1016/S0361-9230(99)00139-2 |
0.01 |
|
| 1999 |
Bales KR, Verina T, Cummins DJ, Du Y, Dodel RC, Saura J, Fishman CE, DeLong CA, Piccardo P, Petegnief V, Ghetti B, Paul SM. Apolipoprotein E is essential for amyloid deposition in the APP(V717F) transgenic mouse model of Alzheimer's disease. Proceedings of the National Academy of Sciences of the United States of America. 96: 15233-8. PMID 10611368 DOI: 10.1073/Pnas.96.26.15233 |
0.01 |
|
| 1999 |
Murrell JR, Spillantini MG, Zolo P, Guazzelli M, Smith MJ, Hasegawa M, Redi F, Crowther RA, Pietrini P, Ghetti B, Goedert M. Tau gene mutation G389R causes a tauopathy with abundant pick body-like inclusions and axonal deposits. Journal of Neuropathology and Experimental Neurology. 58: 1207-26. PMID 10604746 DOI: 10.1097/00005072-199912000-00002 |
0.01 |
|
| 1999 |
Zhang W, Ghetti B, Yang XL, Lee W. Alteration of IGF system gene expression during the postnatal development of pcd mice. The Journal of Endocrinology. 163: 191-8. PMID 10556767 DOI: 10.1677/joe.0.1630191 |
0.01 |
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| 1999 |
Broome JD, Wills KV, Lapchak PA, Ghetti B, Camp LL, Bayer SA. Glial cell line-derived neurotrophic factor protects midbrain dopamine neurons from the lethal action of the weaver gene: a quantitative immunocytochemical study. Brain Research. Developmental Brain Research. 116: 1-7. PMID 10446341 DOI: 10.1016/S0165-3806(99)00065-6 |
0.01 |
|
| 1999 |
Parchi P, Giese A, Capellari S, Brown P, Schulz-Schaeffer W, Windl O, Zerr I, Budka H, Kopp N, Piccardo P, Poser S, Rojiani A, Streichemberger N, Julien J, Vital C, ... Ghetti B, et al. Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects. Annals of Neurology. 46: 224-33. PMID 10443888 DOI: 10.1002/1531-8249(199908)46:2<224::Aid-Ana12>3.0.Co;2-W |
0.01 |
|
| 1999 |
Migheli A, Piva R, Casolino S, Atzori C, Dlouhy SR, Ghetti B. A cell cycle alteration precedes apoptosis of granule cell precursors in the weaver mouse cerebellum. The American Journal of Pathology. 155: 365-73. PMID 10433930 DOI: 10.1016/S0002-9440(10)65133-4 |
0.01 |
|
| 1999 |
Delisle MB, Murrell JR, Richardson R, Trofatter JA, Rascol O, Soulages X, Mohr M, Calvas P, Ghetti B. A mutation at codon 279 (N279K) in exon 10 of the Tau gene causes a tauopathy with dementia and supranuclear palsy. Acta Neuropathologica. 98: 62-77. PMID 10412802 |
0.01 |
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| 1999 |
Varani L, Hasegawa M, Spillantini MG, Smith MJ, Murrell JR, Ghetti B, Klug A, Goedert M, Varani G. Structure of tau exon 10 splicing regulatory element RNA and destabilization by mutations of frontotemporal dementia and parkinsonism linked to chromosome 17. Proceedings of the National Academy of Sciences of the United States of America. 96: 8229-34. PMID 10393977 DOI: 10.1073/Pnas.96.14.8229 |
0.01 |
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| 1999 |
Bugiani O, Murrell JR, Giaccone G, Hasegawa M, Ghigo G, Tabaton M, Morbin M, Primavera A, Carella F, Solaro C, Grisoli M, Savoiardo M, Spillantini MG, Tagliavini F, Goedert M, ... Ghetti B, et al. Frontotemporal dementia and corticobasal degeneration in a family with a P301S mutation in tau. Journal of Neuropathology and Experimental Neurology. 58: 667-77. PMID 10374757 DOI: 10.1097/00005072-199906000-00011 |
0.01 |
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| 1999 |
Mirra SS, Murrell JR, Gearing M, Spillantini MG, Goedert M, Crowther RA, Levey AI, Jones R, Green J, Shoffner JM, Wainer BH, Schmidt ML, Trojanowski JQ, Ghetti B. Tau pathology in a family with dementia and a P301L mutation in tau. Journal of Neuropathology and Experimental Neurology. 58: 335-45. PMID 10218629 DOI: 10.1097/00005072-199904000-00004 |
0.01 |
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| 1999 |
Gambetti P, Petersen RB, Parchi P, Chen SG, Capellari S, Goldfarb L, Gabizon R, Montagna P, Lugaresi E, Piccardo P, Ghetti B. 13 Inherited Prion Diseases Cold Spring Harbor Monograph Archive. 38: 509-583. DOI: 10.1101/087969547.38.509 |
0.01 |
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| 1999 |
Migheli A, Piva R, Casolino S, Atzori C, Dlouhy SR, Ghetti B. A Cell Cycle Alteration Precedes Apoptosis Of Granule Cell Precursors In The Weaver Mouse Cerebellum Journal of Neuropathology and Experimental Neurology. 58: 556. DOI: 10.1097/00005072-199905000-00199 |
0.01 |
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| 1999 |
Gearing M, Schultz A, Ghetti B, Piccardo P, Mirra SS. Neuropathological Changes And Apolipoprotein E Genotype In AlzheimerʼS Disease (Ad) With Concomitant Lewy Bodies: An Alpha-Synuclein Immunohistochemical Study Journal of Neuropathology and Experimental Neurology. 58: 552. DOI: 10.1097/00005072-199905000-00185 |
0.01 |
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| 1999 |
Tarauto A, Piccardo P, Reich F, Sevlever G, Schultz M, Leuzzi A, Ruggiero M, Abecassis G, Engelmann M, Garcia AM, Capellari S, Lugaresi E, Gambetti P, Dlouhy SR, Ghetti B. INSOMNIA IN FAMILIAL CREUTZFELDT JAKOB DISEASE (FCJD), E200K, WITH THALAMIC INVOLVEMENT Journal of Neuropathology and Experimental Neurology. 58: 551. DOI: 10.1097/00005072-199905000-00179 |
0.01 |
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| 1999 |
Piccardo P, Dlouhy SR, Young K, William A, Feng Y, Ouinn B, Canto MD, Sufit R, Ghetti B. Creutzfeldt Jakob Disease (Cjd) With Prion Protein Gene (Prnp) V2101 Mutation Journal of Neuropathology and Experimental Neurology. 58: 550. DOI: 10.1097/00005072-199905000-00177 |
0.01 |
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| 1999 |
Dlouhy S, Feng Y, Young K, Bird T, DeCarli C, Hodes ME, Piccardo P, Ghetti B. AN INTRON MUTATION IN THE PRION PROTEIN GENE (PRNP) Journal of Neuropathology and Experimental Neurology. 58: 550. DOI: 10.1097/00005072-199905000-00176 |
0.01 |
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| 1999 |
Zolo P, Spillantini MG, Crowter T, Redi F, Guazzelli M, Murrell J, Ghetti B. Pick Disease With Glial Tau Inclusions In The White Matter Journal of Neuropathology and Experimental Neurology. 58: 546. DOI: 10.1097/00005072-199905000-00159 |
0.01 |
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| 1999 |
Ghetti B, Gambetti P. Chapter 5 Human Prion Diseases Advances in Cell Aging and Gerontology. 3: 135-187. DOI: 10.1016/S1566-3124(08)60025-5 |
0.01 |
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| 1998 |
Chiesa R, Piccardo P, Ghetti B, Harris DA. Neurological illness in transgenic mice expressing a prion protein with an insertional mutation. Neuron. 21: 1339-51. PMID 9883727 DOI: 10.1016/S0896-6273(00)80653-4 |
0.01 |
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| 1998 |
Schwartz NB, Szabo M, Verina T, Wei J, Dlouhy SR, Won L, Heller A, Hodes ME, Ghetti B. Hypothalamic-pituitary-gonadal axis in the mutant weaver mouse. Neuroendocrinology. 68: 374-85. PMID 9873201 DOI: 10.1159/000054387 |
0.01 |
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| 1998 |
Fox AP, Dlouhy S, Ghetti B, Hurley JH, Nucifora PG, Nelson DJ, Won L, Heller A. Altered responses to potassium in cerebellar neurons from weaver heterozygote mice. Experimental Brain Research. 123: 298-306. PMID 9860268 DOI: 10.1007/S002210050572 |
0.01 |
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| 1998 |
Jiménez-Huete A, Lievens PM, Vidal R, Piccardo P, Ghetti B, Tagliavini F, Frangione B, Prelli F. Endogenous proteolytic cleavage of normal and disease-associated isoforms of the human prion protein in neural and non-neural tissues. The American Journal of Pathology. 153: 1561-72. PMID 9811348 DOI: 10.1016/S0002-9440(10)65744-6 |
0.01 |
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| 1998 |
Lippa CF, Fujiwara H, Mann DM, Giasson B, Baba M, Schmidt ML, Nee LE, O'Connell B, Pollen DA, St George-Hyslop P, Ghetti B, Nochlin D, Bird TD, Cairns NJ, Lee VM, et al. Lewy bodies contain altered alpha-synuclein in brains of many familial Alzheimer's disease patients with mutations in presenilin and amyloid precursor protein genes. The American Journal of Pathology. 153: 1365-70. PMID 9811326 DOI: 10.1016/S0002-9440(10)65722-7 |
0.01 |
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| 1998 |
Piccardo P, Dlouhy SR, Lievens PM, Young K, Bird TD, Nochlin D, Dickson DW, Vinters HV, Zimmerman TR, Mackenzie IR, Kish SJ, Ang LC, De Carli C, Pocchiari M, Brown P, ... ... Ghetti B, et al. Phenotypic variability of Gerstmann-Sträussler-Scheinker disease is associated with prion protein heterogeneity. Journal of Neuropathology and Experimental Neurology. 57: 979-88. PMID 9786248 DOI: 10.1097/00005072-199810000-00010 |
0.01 |
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| 1998 |
Wei J, Hodes ME, Piva R, Feng Y, Wang Y, Ghetti B, Dlouhy SR. Characterization of murine Girk2 transcript isoforms: structure and differential expression. Genomics. 51: 379-90. PMID 9721208 DOI: 10.1006/Geno.1998.5369 |
0.01 |
|
| 1998 |
Spillantini MG, Murrell JR, Goedert M, Farlow MR, Klug A, Ghetti B. Mutation in the tau gene in familial multiple system tauopathy with presenile dementia. Proceedings of the National Academy of Sciences of the United States of America. 95: 7737-41. PMID 9636220 DOI: 10.1073/Pnas.95.13.7737 |
0.01 |
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| 1998 |
Piccardo P, Langeveld JP, Hill AF, Dlouhy SR, Young K, Giaccone G, Rossi G, Bugiani M, Bugiani O, Meloen RH, Collinge J, Tagliavini F, Ghetti B. An antibody raised against a conserved sequence of the prion protein recognizes pathological isoforms in human and animal prion diseases, including Creutzfeldt-Jakob disease and bovine spongiform encephalopathy. The American Journal of Pathology. 152: 1415-20. PMID 9626045 |
0.01 |
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| 1998 |
Spillantini MG, Bird TD, Ghetti B. Frontotemporal dementia and Parkinsonism linked to chromosome 17: a new group of tauopathies. Brain Pathology (Zurich, Switzerland). 8: 387-402. PMID 9546295 DOI: 10.1111/J.1750-3639.1998.Tb00162.X |
0.01 |
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| 1998 |
Salanova V, Markand O, Worth R, Smith R, Wellman H, Hutchins G, Park H, Ghetti B, Azzarelli B. FDG-PET and MRI in temporal lobe epilepsy: relationship to febrile seizures, hippocampal sclerosis and outcome. Acta Neurologica Scandinavica. 97: 146-53. PMID 9531429 DOI: 10.1111/J.1600-0404.1998.TB00628.X |
0.01 |
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| 1998 |
Brown P, Cervenáková L, McShane L, Goldfarb LG, Bishop K, Bastian F, Kirkpatrick J, Piccardo P, Ghetti B, Gajdusek DC. Creutzfeldt-Jakob disease in a husband and wife. Neurology. 50: 684-8. PMID 9521256 DOI: 10.1212/WNL.50.3.684 |
0.01 |
|
| 1998 |
Piccardo P, Kish SJ, Ang LC, Young K, Bugiani O, Tagliavini F, Dlouhy SR, Ghetti B. PRION PROTEIN ISOFORMS IN THE NEW VARIANT OF GERSTMAN-STRÄUSSLER-SCHEINKER DISEASE Q212P Journal of Neuropathology and Experimental Neurology. 57: 518. DOI: 10.1097/00005072-199805000-00214 |
0.01 |
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| 1998 |
Young K, Piccardo P, Kish SJ, Ang LC, Dlouhy S, Ghetti B. GERSTMANN-STRÄUSSLER-SCHEINKER DISEASE (GSS) WITH A MUTATION AT PRION PROTEIN (PrP) RESIDUE 212 Journal of Neuropathology and Experimental Neurology. 57: 518. DOI: 10.1097/00005072-199805000-00213 |
0.01 |
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| 1998 |
-J. Lievens PM, Ouaglio E, Piccardo P, Tranchant C, Warter JM, Bird T, Bugiani O, Ghetti B, Tagliavini F. DISTINCTIVE PrP ISOFOMS IN GERSTMANN-STRÄUSSLER-SCHEINKER DISEASE WITH TANGLES Journal of Neuropathology and Experimental Neurology. 57: 517. DOI: 10.1097/00005072-199805000-00212 |
0.01 |
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| 1998 |
Verina T, Bales K, Dodel RC, Du Y, Altstiel L, Bender M, Hyslop P, Johnstone EM, Little SP, Cummins DJ, Piccardo P, Paul S, Ghetti B. LACK OF apoE GENE REDUCES AMYLOID FORMATION IN TRANSGENIC MICE OVEREXPRESSING APPV717F Journal of Neuropathology and Experimental Neurology. 57: 512. DOI: 10.1097/00005072-199805000-00191 |
0.01 |
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| 1998 |
Wei JJ, Hodes ME, Feng Y, Ghetti B, Dlouhy SR. GENOMIC ORGANIZATION OF Girk2, A POTASSIUM CHANNEL GENE IN MICE Journal of Neuropathology and Experimental Neurology. 57: 486. DOI: 10.1097/00005072-199805000-00078 |
0.01 |
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| 1997 |
Migheli A, Piva R, Wei J, Attanasio A, Casolino S, Hodes ME, Dlouhy SR, Bayer SA, Ghetti B. Diverse cell death pathways result from a single missense mutation in weaver mouse. The American Journal of Pathology. 151: 1629-38. PMID 9403713 |
0.01 |
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| 1997 |
Bales KR, Verina T, Dodel RC, Du Y, Altstiel L, Bender M, Hyslop P, Johnstone EM, Little SP, Cummins DJ, Piccardo P, Ghetti B, Paul SM. Lack of apolipoprotein E dramatically reduces amyloid beta-peptide deposition. Nature Genetics. 17: 263-4. PMID 9354781 DOI: 10.1038/Ng1197-263 |
0.01 |
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| 1997 |
Murrell JR, Koller D, Foroud T, Goedert M, Spillantini MG, Edenberg HJ, Farlow MR, Ghetti B. Familial multiple-system tauopathy with presenile dementia is localized to chromosome 17. American Journal of Human Genetics. 61: 1131-8. PMID 9345089 DOI: 10.1086/301594 |
0.01 |
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| 1997 |
Won L, Ghetti B, Heller B, Heller A. In vitro evidence that the reduction in mesencephalic dopaminergic neurons in the weaver heterozygote is not due to a failure in target cell interaction. Experimental Brain Research. 115: 174-9. PMID 9224846 DOI: 10.1007/Pl00005679 |
0.01 |
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| 1997 |
Wei J, Dlouhy SR, Bayer S, Piva R, Verina T, Wang Y, Feng Y, Dupree B, Hodes ME, Ghetti B. In situ hybridization analysis of Girk2 expression in the developing central nervous system in normal and weaver mice. Journal of Neuropathology and Experimental Neurology. 56: 762-71. PMID 9210872 |
0.01 |
|
| 1997 |
Simon JR, Bare DJ, Ghetti B, Richter JA. A possible role for tyrosine kinases in the regulation of the neuronal dopamine transporter in mouse striatum. Neuroscience Letters. 224: 201-5. PMID 9131671 DOI: 10.1016/S0304-3940(97)13479-6 |
0.01 |
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| 1997 |
Unverzagt FW, Farlow MR, Norton J, Dlouhy SR, Young K, Ghetti B. Neuropsychological function in patients with Gerstmann-Sträussler-Scheinker disease from the Indiana kindred (F198S). Journal of the International Neuropsychological Society : Jins. 3: 169-78. PMID 9126858 DOI: 10.1017/S1355617797001690 |
0.01 |
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| 1997 |
Park DW, Boldt HC, Massicotte SJ, Akang EE, Roos KL, Bodnar A, Pless J, Ghetti B, Pascuzzi RM. Subacute sclerosing panencephalitis manifesting as viral retinitis: clinical and histopathologic findings. American Journal of Ophthalmology. 123: 533-42. PMID 9124250 DOI: 10.1016/S0002-9394(14)70179-5 |
0.01 |
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| 1997 |
Spillantini MG, Goedert M, Crowther RA, Murrell JR, Farlow MR, Ghetti B. Familial multiple system tauopathy with presenile dementia: a disease with abundant neuronal and glial tau filaments. Proceedings of the National Academy of Sciences of the United States of America. 94: 4113-8. PMID 9108114 DOI: 10.1073/Pnas.94.8.4113 |
0.01 |
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| 1997 |
Zhang W, Ghetti B, Lee WH. Decreased IGF-I gene expression during the apoptosis of Purkinje cells in pcd mice. Brain Research. Developmental Brain Research. 98: 164-76. PMID 9051257 DOI: 10.1016/S0165-3806(96)00168-X |
0.01 |
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| 1997 |
Young K, Clark HB, Piccardo P, Dlouhy SR, Ghetti B. Gerstmann-Sträussler-Scheinker disease with the PRNP P102L mutation and valine at codon 129. Brain Research. Molecular Brain Research. 44: 147-50. PMID 9030710 DOI: 10.1016/S0169-328X(96)00251-3 |
0.01 |
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| 1997 |
Verina T, Norton JA, Sorbel JJ, Triarhou LC, Laferty D, Richter JA, Simon JR, Ghetti B. Atrophy and loss of dopaminergic mesencephalic neurons in heterozygous weaver mice. Experimental Brain Research. 113: 5-12. PMID 9028770 DOI: 10.1007/Bf02454137 |
0.01 |
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| 1997 |
Wei J, Dlouhy SR, Bayer S, Piva R, Verina T, Wang Y, Feng Y, Dupree B, Hodes ME, Ghetti B. In Situ Hybridization Analysis of Girk2 Expression in the Developing Central Nervous System in Normal and Weaver Mice Journal of Neuropathology and Experimental Neurology. 56: 762-771. DOI: 10.1097/00005072-199756070-00002 |
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