| Year |
Citation |
Score |
| 2023 |
Hou X, Heckman MG, Fiesel FC, Koga S, Soto-Beasley AI, Watzlawik JO, Zhao J, Valentino RR, Johnson PW, White LJ, Quicksall ZS, Reddy JS, Bras J, Guerreiro R, Zhao N, et al. Genome-wide association study identifies and variants as mitophagy modifiers in Lewy body disease. Medrxiv : the Preprint Server For Health Sciences. PMID 37905059 DOI: 10.1101/2023.10.16.23297100 |
0.367 |
|
| 2023 |
Tunold JA, Tan MMX, Koga S, Geut H, Rozemuller AJM, Valentino R, Sekiya H, Martin NB, Heckman MG, Bras J, Guerreiro R, Dickson DW, Toft M, van de Berg W, Ross OA, et al. Lysosomal polygenic risk is associated with the severity of neuropathology in Lewy body disease. Brain : a Journal of Neurology. PMID 37247383 DOI: 10.1093/brain/awad183 |
0.459 |
|
| 2023 |
Sousa JA, Bernardes C, Bernardo-Castro S, Lino M, Albino I, Ferreira L, Brás J, Guerreiro R, Tábuas-Pereira M, Baldeiras I, Santana I, Sargento-Freitas J. Reconsidering the role of blood-brain barrier in Alzheimer's disease: From delivery to target. Frontiers in Aging Neuroscience. 15: 1102809. PMID 36875694 DOI: 10.3389/fnagi.2023.1102809 |
0.342 |
|
| 2022 |
Foddis M, Blumenau S, Holtgrewe M, Paquette K, Westra K, Alonso I, Macario MDC, Morgadinho AS, Velon AG, Santo G, Santana I, Mönkäre S, Kuuluvainen L, Schleutker J, Pöyhönen M, ... ... Guerreiro R, et al. TREX1 p.A129fs and p.Y305C variants in a large multi-ethnic cohort of CADASIL-like unrelated patients. Neurobiology of Aging. 123: 208-215. PMID 36586737 DOI: 10.1016/j.neurobiolaging.2022.11.013 |
0.379 |
|
| 2022 |
Holstege H, Hulsman M, Charbonnier C, Grenier-Boley B, Quenez O, Grozeva D, van Rooij JGJ, Sims R, Ahmad S, Amin N, Norsworthy PJ, Dols-Icardo O, Hummerich H, Kawalia A, Amouyel P, ... ... Guerreiro R, et al. Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer's disease. Nature Genetics. PMID 36411364 DOI: 10.1038/s41588-022-01208-7 |
0.631 |
|
| 2022 |
Khani M, Gibbons E, Bras J, Guerreiro R. Correction: Challenge accepted: Uncovering the role of rare genetic variants in Alzheimer's disease. Molecular Neurodegeneration. 17: 70. PMID 36320069 DOI: 10.1186/s13024-022-00575-3 |
0.437 |
|
| 2022 |
Tábuas-Pereira M, Guerreiro R, Kun-Rodrigues C, Almeida MR, Brás J, Santana I. Whole-exome sequencing reveals PSEN1 and ATP7B combined variants as a possible cause of early-onset Lewy body dementia: a case study of genotype-phenotype correlation. Neurogenetics. PMID 36114914 DOI: 10.1007/s10048-022-00699-0 |
0.461 |
|
| 2022 |
Gouveia C, Gibbons E, Dehghani N, Eapen J, Guerreiro R, Bras J. Genome-wide association of polygenic risk extremes for Alzheimer's disease in the UK Biobank. Scientific Reports. 12: 8404. PMID 35589863 DOI: 10.1038/s41598-022-12391-2 |
0.433 |
|
| 2022 |
Santos M, Damásio J, Carmona S, Neto JL, Dehghani N, Guedes LC, Barbot C, Barros J, Brás J, Sequeiros J, Guerreiro R. Molecular Characterization of Portuguese Patients with Hereditary Cerebellar Ataxia. Cells. 11. PMID 35326432 DOI: 10.3390/cells11060981 |
0.355 |
|
| 2022 |
Tábuas-Pereira M, Santana I, Almeida MR, Durães J, Lima M, Duro D, Kun-Rodrigues C, Bras J, Guerreiro R. Rare variants in TP73 in a frontotemporal dementia cohort link this gene with primary progressive aphasia phenotypes. European Journal of Neurology. PMID 35020242 DOI: 10.1111/ene.15248 |
0.323 |
|
| 2022 |
Khani M, Gibbons E, Bras J, Guerreiro R. Challenge accepted: uncovering the role of rare genetic variants in Alzheimer's disease. Molecular Neurodegeneration. 17: 3. PMID 35000612 DOI: 10.1186/s13024-021-00505-9 |
0.464 |
|
| 2021 |
Dehghani N, Guven G, Kun-Rodrigues C, Gouveia C, Foster K, Hanagasi H, Lohmann E, Samanci B, Gurvit H, Bilgic B, Bras J, Guerreiro R. A comprehensive analysis of copy number variation in a Turkish dementia cohort. Human Genomics. 15: 48. PMID 34321086 DOI: 10.1186/s40246-021-00346-z |
0.461 |
|
| 2021 |
Dehghani N, Bras J, Guerreiro R. Erratum to: How understudied populations have contributed to our understanding of Alzheimer's disease genetics. Brain : a Journal of Neurology. 144: e69. PMID 34015089 DOI: 10.1093/brain/awab180 |
0.378 |
|
| 2021 |
Samanci B, Bilgiç B, Gelişin Ö, Tepgeç F, Guven G, Tüfekçioğlu Z, Alaylıoğlu M, Hanagasi HA, Gürvit H, Guerreiro R, Hardy J, Emre M. TREM2 variants as a possible cause of frontotemporal dementia with distinct neuroimaging features. European Journal of Neurology. PMID 33969597 DOI: 10.1111/ene.14908 |
0.536 |
|
| 2021 |
Dehghani N, Bras J, Guerreiro R. How understudied populations have contributed to our understanding of Alzheimer's disease genetics. Brain : a Journal of Neurology. 144: 1067-1081. PMID 33889936 DOI: 10.1093/brain/awab028 |
0.394 |
|
| 2021 |
Najar J, van der Lee SJ, Joas E, Wetterberg H, Hardy J, Guerreiro R, Bras J, Waern M, Kern S, Zetterberg H, Blennow K, Skoog I, Zettergren A. Polygenic risk scores for Alzheimer's disease are related to dementia risk in APOE ɛ4 negatives. Alzheimer's & Dementia (Amsterdam, Netherlands). 13: e12142. PMID 33532541 DOI: 10.1002/dad2.12142 |
0.594 |
|
| 2021 |
Ly H, Verma N, Sharma S, Kotiya D, Despa S, Abner EL, Nelson PT, Jicha GA, Wilcock DM, Goldstein LB, Guerreiro R, Brás J, Hanson AJ, Craft S, Murray AJ, et al. The association of circulating amylin with β-amyloid in familial Alzheimer's disease. Alzheimer's & Dementia (New York, N. Y.). 7: e12130. PMID 33521236 DOI: 10.1002/trc2.12130 |
0.575 |
|
| 2021 |
Skoog I, Kern S, Najar J, Guerreiro R, Bras J, Waern M, Zetterberg H, Blennow K, Zettergren A. A Non-APOE Polygenic Risk Score for Alzheimer's Disease Is Associated With Cerebrospinal Fluid Neurofilament Light in a Representative Sample of Cognitively Unimpaired 70-Year Olds. The Journals of Gerontology. Series a, Biological Sciences and Medical Sciences. 76: 983-990. PMID 33512503 DOI: 10.1093/gerona/glab030 |
0.336 |
|
| 2020 |
Lawingco T, Chaudhury S, Brookes KJ, Guetta-Baranes T, Guerreiro R, Bras J, Hardy J, Francis P, Thomas A, Belbin O, Morgan K. Genetic variants in glutamate-, Aβ-, and tau-related pathways determine polygenic risk for Alzheimer's disease. Neurobiology of Aging. PMID 33303219 DOI: 10.1016/j.neurobiolaging.2020.11.009 |
0.554 |
|
| 2020 |
Mönkäre S, Kuuluvainen L, Kun-Rodrigues C, Carmona S, Schleutker J, Bras J, Pöyhönen M, Guerreiro R, Myllykangas L. Whole-exome sequencing of Finnish patients with vascular cognitive impairment. European Journal of Human Genetics : Ejhg. 29: 663-671. PMID 33268848 DOI: 10.1038/s41431-020-00775-9 |
0.364 |
|
| 2020 |
Balint B, Damasio J, Magrinelli F, Guerreiro R, Bras J, Bhatia KP. Psychiatric Manifestations of Mutations. Movement Disorders Clinical Practice. 7: 838-841. PMID 33033738 DOI: 10.1002/Mdc3.13034 |
0.416 |
|
| 2020 |
Faller KME, Ridyard AE, Gutierrez-Quintana R, Rupp A, Kun-Rodrigues C, Orme T, Tylee KL, Church HJ, Guerreiro R, Bras J. A deletion of IDUA exon 10 in a family of Golden Retriever dogs with an attenuated form of mucopolysaccharidosis type I. Journal of Veterinary Internal Medicine. PMID 32785987 DOI: 10.1111/Jvim.15868 |
0.35 |
|
| 2020 |
Brás J, Gibbons E, Guerreiro R. Genetics of synucleins in neurodegenerative diseases. Acta Neuropathologica. 1-20. PMID 32740728 DOI: 10.1007/S00401-020-02202-1 |
0.501 |
|
| 2020 |
Tábuas-Pereira M, Santana I, Kun-Rodrigues C, Bras J, Guerreiro R. CYLD variants in frontotemporal dementia associated with severe memory impairment in a Portuguese cohort Brain. 143. PMID 32666117 DOI: 10.1093/Brain/Awaa183 |
0.341 |
|
| 2020 |
Guerreiro R, Gibbons E, Tábuas-Pereira M, Kun-Rodrigues C, Santo GC, Bras J. Genetic architecture of common non-Alzheimer's disease dementias. Neurobiology of Disease. 142: 104946. PMID 32439597 DOI: 10.1016/J.Nbd.2020.104946 |
0.565 |
|
| 2020 |
Santos M, Damásio J, Kun-Rodrigues C, Barbot C, Sequeiros J, Brás J, Alonso I, Guerreiro R. Novel Variant Causes Cerebellar Ataxia with Oculomotor Apraxia: Molecular Basis and Expanded Clinical Phenotype. Journal of Clinical Medicine. 9. PMID 32340215 DOI: 10.3390/Jcm9041212 |
0.411 |
|
| 2020 |
Balint B, Guerreiro R, Carmona S, Dehghani N, Latorre A, Cordivari C, Bhatia KP, Bras J. KCNN2 mutation in autosomal-dominant tremulous myoclonus-dystonia. European Journal of Neurology. PMID 32212350 DOI: 10.1111/Ene.14228 |
0.392 |
|
| 2020 |
Orme T, Hernandez D, Ross OA, Kun-Rodrigues C, Darwent L, Shepherd CE, Parkkinen L, Ansorge O, Clark L, Honig LS, Marder K, Lemstra A, Rogaeva E, St George-Hyslop P, Londos E, ... ... Guerreiro R, et al. Analysis of neurodegenerative disease-causing genes in dementia with Lewy bodies. Acta Neuropathologica Communications. 8: 5. PMID 31996268 DOI: 10.1186/S40478-020-0879-Z |
0.807 |
|
| 2020 |
Tábuas-Pereira M, Santana I, Guerreiro R, Brás J. Alzheimer’s Disease Genetics: Review of Novel Loci Associated with Disease Current Genetic Medicine Reports. 8: 1-16. DOI: 10.1007/S40142-020-00182-Y |
0.551 |
|
| 2019 |
Piers TM, Cosker K, Mallach A, Johnson GT, Guerreiro R, Hardy J, Pocock JM. A locked immunometabolic switch underlies TREM2 R47H loss of function in human iPSC-derived microglia. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. PMID 31907987 DOI: 10.1096/Fj.201902447R |
0.58 |
|
| 2019 |
Shafei R, Woollacott IOC, Mummery CJ, Bocchetta M, Guerreiro R, Bras J, Warren JD, Lashley T, Jaunmuktane Z, Rohrer JD. Two pathologically confirmed cases of novel mutations in the MAPT gene causing frontotemporal dementia. Neurobiology of Aging. PMID 31870644 DOI: 10.1016/J.Neurobiolaging.2019.11.009 |
0.496 |
|
| 2019 |
Moore KM, Nicholas J, Grossman M, McMillan CT, Irwin DJ, Massimo L, Van Deerlin VM, Warren JD, Fox NC, Rossor MN, Mead S, Bocchetta M, Boeve BF, Knopman DS, Graff-Radford NR, ... ... Guerreiro R, et al. Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study. The Lancet. Neurology. PMID 31810826 DOI: 10.1016/S1474-4422(19)30394-1 |
0.473 |
|
| 2019 |
Sundal C, Carmona S, Yhr M, Almström O, Ljungberg M, Hardy J, Hedberg-Oldfors C, Fred Å, Brás J, Oldfors A, Andersen O, Guerreiro R. An AARS variant as the likely cause of Swedish type hereditary diffuse leukoencephalopathy with spheroids. Acta Neuropathologica Communications. 7: 188. PMID 31775912 DOI: 10.1186/S40478-019-0843-Y |
0.644 |
|
| 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, ... ... Guerreiro R, 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 |
0.804 |
|
| 2019 |
Chaudhury S, Brookes KJ, Patel T, Fallows A, Guetta-Baranes T, Turton JC, Guerreiro R, Bras J, Hardy J, Francis PT, Croucher R, Holmes C, Morgan K. Correction: Alzheimer's disease polygenic risk score as a predictor of conversion from mild-cognitive impairment. Translational Psychiatry. 9: 167. PMID 31186402 DOI: 10.1038/s41398-019-0503-9 |
0.529 |
|
| 2019 |
Chaudhury S, Brookes KJ, Patel T, Fallows A, Guetta-Baranes T, Turton JC, Guerreiro R, Bras J, Hardy J, Francis PT, Croucher R, Holmes C, Morgan K. Alzheimer's disease polygenic risk score as a predictor of conversion from mild-cognitive impairment. Translational Psychiatry. 9: 154. PMID 31127079 DOI: 10.1038/S41398-019-0485-7 |
0.598 |
|
| 2019 |
Guerreiro R, Escott-Price V, Hernandez DG, Kun-Rodrigues C, Ross OA, Orme T, Neto JL, Carmona S, Dehghani N, Eicher JD, Shepherd C, Parkkinen L, Darwent L, Heckman MG, Scholz SW, et al. Heritability and genetic variance of dementia with Lewy bodies. Neurobiology of Disease. PMID 30953760 DOI: 10.1016/J.Nbd.2019.04.004 |
0.766 |
|
| 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, ... ... Guerreiro R, 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 |
0.825 |
|
| 2019 |
Santo GC, Baldeiras I, Guerreiro R, Ribeiro JA, Cunha R, Youngstein T, Nanthapisal S, Leitão J, Fernandes C, Caramelo F, Almeida MDR, Brás J, Santana I. Adenosine Deaminase Two and Immunoglobulin M Accurately Differentiate Adult Sneddon's Syndrome of Unknown Cause. Cerebrovascular Diseases (Basel, Switzerland). 46: 257-264. PMID 30645994 DOI: 10.1159/000495794 |
0.383 |
|
| 2018 |
Guven G, Bilgic B, Tufekcioglu Z, Erginel Unaltuna N, Hanagasi H, Gurvit H, Singleton A, Hardy J, Emre M, Gulec C, Bras J, Guerreiro R, Lohmann E. Peripheral GRN mRNA and Serum Progranulin Levels as a Potential Indicator for Both the Presence of Splice Site Mutations and Individuals at Risk for Frontotemporal Dementia. Journal of Alzheimer's Disease : Jad. PMID 30475763 DOI: 10.3233/Jad-180599 |
0.703 |
|
| 2018 |
Kun-Rodrigues C, Orme T, Carmona S, Hernandez DG, Ross OA, Eicher JD, Shepherd C, Parkkinen L, Darwent L, Heckman MG, Scholz SW, Troncoso JC, Pletnikova O, Dawson T, Rosenthal L, ... ... Guerreiro R, et al. A comprehensive screening of copy number variability in dementia with Lewy bodies. Neurobiology of Aging. PMID 30448004 DOI: 10.1016/J.Neurobiolaging.2018.10.019 |
0.755 |
|
| 2018 |
Carmona S, Marecos C, Amorim M, Ferreira AC, Conceição C, Brás J, Duarte ST, Guerreiro R. splice-site mutation in a case of spastic paraplegia type 52 with polymicrogyria. Neurology. Genetics. 4: e273. PMID 30283821 DOI: 10.1212/Nxg.0000000000000273 |
0.444 |
|
| 2018 |
Guerreiro R, Orme T, Naj AC, Kuzma AB, Schellenberg GD, Bras J. Is APOE ε4 required for Alzheimer's disease to develop in TREM2 p.R47H variant carriers? Neuropathology and Applied Neurobiology. PMID 30229991 DOI: 10.1111/Nan.12517 |
0.521 |
|
| 2018 |
Orme T, Guerreiro R, Bras J. The Genetics of Dementia with Lewy Bodies: Current Understanding and Future Directions. Current Neurology and Neuroscience Reports. 18: 67. PMID 30097731 DOI: 10.1007/S11910-018-0874-Y |
0.515 |
|
| 2018 |
Blauwendraat C, Reed X, Kia DA, Gan-Or Z, Lesage S, Pihlstrøm L, Guerreiro R, Gibbs JR, Sabir M, Ahmed S, Ding J, Alcalay RN, Hassin-Baer S, Pittman AM, Brooks J, et al. Frequency of Loss of Function Variants in LRRK2 in Parkinson Disease. Jama Neurology. PMID 30039155 DOI: 10.1001/Jamaneurol.2018.1885 |
0.717 |
|
| 2018 |
Carmona S, Zahs K, Wu E, Dakin K, Bras J, Guerreiro R. The role of TREM2 in Alzheimer's disease and other neurodegenerative disorders. The Lancet. Neurology. 17: 721-730. PMID 30033062 DOI: 10.1016/S1474-4422(18)30232-1 |
0.549 |
|
| 2018 |
Hartl D, May P, Gu W, Mayhaus M, Pichler S, Spaniol C, Glaab E, Bobbili DR, Antony P, Koegelsberger S, Kurz A, Grimmer T, Morgan K, Vardarajan BN, Reitz C, ... ... Guerreiro R, et al. A rare loss-of-function variant of ADAM17 is associated with late-onset familial Alzheimer disease. Molecular Psychiatry. PMID 29988083 DOI: 10.1038/S41380-018-0091-8 |
0.688 |
|
| 2018 |
Anttila V, Bulik-Sullivan B, Finucane HK, Walters RK, Bras J, Duncan L, Escott-Price V, Falcone GJ, Gormley P, Malik R, Patsopoulos NA, Ripke S, Wei Z, Yu D, ... ... Guerreiro R, et al. Analysis of shared heritability in common disorders of the brain. Science (New York, N.Y.). 360. PMID 29930110 DOI: 10.1126/Science.Aap8757 |
0.554 |
|
| 2018 |
Brookes KJ, McConnell G, Williams K, Chaudhury S, Madhan G, Patel T, Turley C, Guetta-Baranes T, Bras J, Guerreiro R, Hardy J, Francis PT, Morgan K. Genotyping of the Alzheimer's Disease Genome-Wide Association Study Index Single Nucleotide Polymorphisms in the Brains for Dementia Research Cohort. Journal of Alzheimer's Disease : Jad. PMID 29914034 DOI: 10.3233/Jad-180191 |
0.615 |
|
| 2018 |
Sassi C, Nalls MA, Ridge PG, Gibbs JR, Lupton MK, Troakes C, Lunnon K, Al-Sarraj S, Brown KS, Medway C, Lord J, Turton J, Bras J, Blumenau S, ... ... Guerreiro R, et al. Mendelian adult-onset leukodystrophy genes in Alzheimer's disease: critical influence of CSF1R and NOTCH3. Neurobiology of Aging. PMID 29544907 DOI: 10.1016/j.neurobiolaging.2018.01.015 |
0.783 |
|
| 2018 |
Carmona S, Hardy J, Guerreiro R. The genetic landscape of Alzheimer disease. Handbook of Clinical Neurology. 148: 395-408. PMID 29478590 DOI: 10.1016/B978-0-444-64076-5.00026-0 |
0.708 |
|
| 2018 |
Pasanen P, Myllykangas L, Pöyhönen M, Kiviharju A, Siitonen M, Hardy J, Bras J, Paetau A, Tienari PJ, Guerreiro R, Verkkoniemi-Ahola A. Genetics of dementia in a Finnish cohort. European Journal of Human Genetics : Ejhg. PMID 29476165 DOI: 10.1038/S41431-018-0117-3 |
0.688 |
|
| 2018 |
Camargos S, Guerreiro R, Bras J, Mageste LS. Late-onset and acute presentation of Brown-Vialetto-Van Laere syndrome in a Brazilian family Neurology Genetics. 4. PMID 29473049 DOI: 10.1212/Nxg.0000000000000215 |
0.345 |
|
| 2018 |
Rusbridge C, Salguero FJ, David MA, Faller KME, Bras JT, Guerreiro RJ, Richard-Londt AC, Grainger D, Head E, Brandner SGP, Summers B, Hardy J, Tayebi M. An Aged Canid with Behavioral Deficits Exhibits Blood and Cerebrospinal Fluid Amyloid Beta Oligomers. Frontiers in Aging Neuroscience. 10: 7. PMID 29441010 DOI: 10.3389/Fnagi.2018.00007 |
0.566 |
|
| 2018 |
Ridge PG, Karch CM, Hsu S, Arano I, Teerlink CC, Ebbert MTW, Murcia JDG, Farnham JM, Damato AR, Allen M, Wang X, Harari O, Fernandez VM, Guerreiro R, Bras J, et al. Correction to: Linkage, whole genome sequence, and biological data implicate variants in RAB10 in Alzheimer's disease resilience. Genome Medicine. 10: 4. PMID 29329552 DOI: 10.1186/S13073-018-0516-7 |
0.78 |
|
| 2018 |
Guerreiro R, Ross OA, Kun-Rodrigues C, Hernandez DG, Orme T, Eicher JD, Shepherd CE, Parkkinen L, Darwent L, Heckman MG, Scholz SW, Troncoso JC, Pletnikova O, Ansorge O, Clarimon J, et al. Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association study. The Lancet. Neurology. 17: 64-74. PMID 29263008 DOI: 10.1016/S1474-4422(17)30400-3 |
0.748 |
|
| 2018 |
Khan RR, Altmann A, Napolioni V, Kim Y, Guerreiro R, Bras JT, Carmona S, Pereira M, Santana I, Hardy J, Mead S, Cruchaga C, Fernandez MV, Holstege H, Flier WMVd, et al. P4-240: Stop-Gain Variant In Microglia-Expressed Gene Gmip Is Associated With Early-Onset Alzheimer'S Disease Alzheimers & Dementia. 14. DOI: 10.1016/J.Jalz.2018.07.061 |
0.662 |
|
| 2018 |
Patel T, Brookes KJ, Guetta-Baranes T, Chaudhury SR, Turton J, Hernandez D, Singleton A, Hardy J, Guerreiro R, Francis PT, Bras JT, Morgan K. P1-168: Linking Polygenic Risk Scores To Alzheimer'S Disease Genes Alzheimers & Dementia. 14. DOI: 10.1016/J.Jalz.2018.06.172 |
0.74 |
|
| 2018 |
Chaudhury SR, Patel T, Fallows A, Brookes KJ, Guetta-Baranes T, Turton J, Sussams R, Guerreiro R, Bras JT, Hardy J, Francis PT, Holmes C, Morgan K. P3-077: Alzheimer'S Disease (Ad) Polygenic Risk Score (Prs) As A Predictor Of Conversion From Mild Cognitive Impairment (Mci) Alzheimers & Dementia. 14. DOI: 10.1016/J.Jalz.2018.06.1433 |
0.61 |
|
| 2017 |
Ridge PG, Karch CM, Hsu S, Arano I, Teerlink CC, Ebbert MTW, Gonzalez Murcia JD, Farnham JM, Damato AR, Allen M, Wang X, Harari O, Fernandez VM, Guerreiro R, Bras J, et al. Linkage, whole genome sequence, and biological data implicate variants in RAB10 in Alzheimer's disease resilience. Genome Medicine. 9: 100. PMID 29183403 DOI: 10.1186/S13073-017-0486-1 |
0.776 |
|
| 2017 |
Patel T, Brookes KJ, Turton J, Chaudhury S, Guetta-Baranes T, Guerreiro R, Bras J, Hernandez D, Singleton A, Francis PT, Hardy J, Morgan K. Whole-exome sequencing of the BDR cohort: Evidence to support the role of the PILRA gene in Alzheimer's disease. Neuropathology and Applied Neurobiology. PMID 29181857 DOI: 10.1111/Nan.12452 |
0.794 |
|
| 2017 |
Chaudhury S, Patel T, Barber IS, Guetta-Baranes T, Brookes KJ, Chappell S, Turton J, Guerreiro R, Bras J, Hernandez D, Singleton A, Hardy J, Mann D, Morgan K. Polygenic risk score in postmortem diagnosed sporadic early-onset Alzheimer's disease. Neurobiology of Aging. PMID 29103623 DOI: 10.1016/J.Neurobiolaging.2017.09.035 |
0.775 |
|
| 2017 |
Darwent L, Carmona S, Lohmann E, Guven G, Kun-Rodrigues C, Bilgic B, Hanagasi H, Gurvit H, Erginel-Unaltuna N, Pak M, Hardy J, Singleton A, Brás J, Guerreiro R. Mutations in TYROBP are not a common cause of dementia in a Turkish cohort. Neurobiology of Aging. PMID 28716534 DOI: 10.1016/J.Neurobiolaging.2017.06.019 |
0.77 |
|
| 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, ... ... Guerreiro R, 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 |
0.788 |
|
| 2017 |
Blauwendraat C, Faghri F, Pihlstrom L, Geiger JT, Elbaz A, Lesage S, Corvol JC, May P, Nicolas A, Abramzon Y, Murphy NA, Gibbs JR, Ryten M, Ferrari R, Bras J, ... Guerreiro R, et al. NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseases. Neurobiology of Aging. PMID 28602509 DOI: 10.1016/J.Neurobiolaging.2017.05.009 |
0.767 |
|
| 2017 |
Siitonen M, Börjesson-Hanson A, Pöyhönen M, Ora A, Pasanen P, Bras J, Kern S, Kern J, Andersen O, Stanescu H, Kleta R, Baumann M, Kalaria R, Kalimo H, Singleton A, ... ... Guerreiro R, et al. Multi-infarct dementia of Swedish type is caused by a 3'UTR mutation of COL4A1. Brain : a Journal of Neurology. PMID 28369186 DOI: 10.1093/Brain/Awx062 |
0.569 |
|
| 2017 |
Beesley C, Guerreiro RJ, Bras JT, Williams RE, Taratuto AL, Eltze C, Mole SE. CLN8 disease caused by large genomic deletions. Molecular Genetics & Genomic Medicine. 5: 85-91. PMID 28116333 DOI: 10.1002/Mgg3.263 |
0.494 |
|
| 2017 |
Pasanen P, Mäkinen J, Myllykangas L, Guerreiro R, Bras J, Valori M, Viitanen M, Baumann M, Tienari PJ, Pöyhönen M, Baumann P. Primary familial brain calcification linked to deletion of 5' noncoding region of SLC20A2 Acta Neurologica Scandinavica. 136: 59-63. PMID 27726124 DOI: 10.1111/Ane.12697 |
0.462 |
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| 2017 |
Paquete A, Alarcão J, Fiorentino F, Guerreiro R, Miguel LS, Borges M. Acute Lymphoblastic Leukaemia’s Burden Of Disease In Portugal Value in Health. 20. DOI: 10.1016/J.Jval.2017.08.400 |
0.35 |
|
| 2017 |
Carmona S, Guven G, Lohmann E, Singleton A, Hardy J, Bras JT, Guerreiro R. Genetic Characterization Of A Turkish Dementia Cohort: Focus On Tyrobp Alzheimers & Dementia. 13. DOI: 10.1016/J.Jalz.2017.07.576 |
0.717 |
|
| 2017 |
Patel T, Brookes KJ, Guetta-Baranes T, Chappell S, Guerreiro R, Bras JT, Hardy J, Francis PT, Morgan K. Investigating Genetic Variation In Alzheimer’S Disease Using Whole-Exome Sequencing Alzheimers & Dementia. 13: 977. DOI: 10.1016/J.Jalz.2017.06.1323 |
0.617 |
|
| 2017 |
Orme T, Guerreiro R, Santana I, Bras JT. Novel Candidate Genes For Dementia With Lewy Bodies Alzheimers & Dementia. 13: 977. DOI: 10.1016/J.Jalz.2017.06.1322 |
0.351 |
|
| 2017 |
Siitonen M, Hanson AB, Pasanen P, Bras JT, Kern S, Kern J, Andersen O, Stanescu H, Kleta R, Baumann M, Kalaria RN, Kalimo H, Singleton A, Hardy J, Myllykangas L, ... ... Guerreiro R, et al. Multi-Infarct Dementia Of Swedish Type Is Caused By 3’Utr Col4A1 Mutation Alzheimers & Dementia. 13: 973. DOI: 10.1016/J.Jalz.2017.06.1312 |
0.692 |
|
| 2016 |
Ryan NS, Nicholas JM, Weston PS, Liang Y, Lashley T, Guerreiro R, Adamson G, Kenny J, Beck J, Chavez-Gutierrez L, de Strooper B, Revesz T, Holton J, Mead S, Rossor MN, et al. Clinical phenotype and genetic associations in autosomal dominant familial Alzheimer's disease: a case series. The Lancet. Neurology. PMID 27777022 DOI: 10.1016/S1474-4422(16)30193-4 |
0.555 |
|
| 2016 |
Barber IS, Braae A, Clement N, Patel T, Guetta-Baranes T, Brookes K, Medway C, Chappell S, Guerreiro R, Bras J, Hernandez D, Singleton A, Hardy J, Mann DM, et al. Mutation analysis of sporadic early-onset Alzheimer's disease using the NeuroX array. Neurobiology of Aging. PMID 27776828 DOI: 10.1016/J.Neurobiolaging.2016.09.008 |
0.773 |
|
| 2016 |
Kun-Rodrigues C, Ross OA, Orme T, Shepherd C, Parkkinen L, Darwent L, Hernandez D, Ansorge O, Clark LN, Honig LS, Marder K, Lemstra A, Scheltens P, van der Flier W, Louwersheimer E, ... ... Guerreiro R, et al. Analysis of C9orf72 repeat expansions in a large international cohort of dementia with Lewy bodies. Neurobiology of Aging. PMID 27666590 DOI: 10.1016/J.Neurobiolaging.2016.08.023 |
0.644 |
|
| 2016 |
Pottier C, Ravenscroft TA, Brown PH, Finch NA, Baker M, Parsons M, Asmann YW, Ren Y, Christopher E, Levitch D, van Blitterswijk M, Cruchaga C, Campion D, Nicolas G, Richard AC, ... Guerreiro R, et al. TYROBP genetic variants in early-onset Alzheimer's disease. Neurobiology of Aging. PMID 27658901 DOI: 10.1016/J.Neurobiolaging.2016.07.028 |
0.572 |
|
| 2016 |
Guven G, Lohmann E, Bras J, Gibbs JR, Gurvit H, Bilgic B, Hanagasi H, Rizzu P, Heutink P, Emre M, Erginel-Unaltuna N, Just W, Hardy J, Singleton A, Guerreiro R. Mutation Frequency of the Major Frontotemporal Dementia Genes, MAPT, GRN and C9ORF72 in a Turkish Cohort of Dementia Patients. Plos One. 11: e0162592. PMID 27632209 DOI: 10.1371/Journal.Pone.0162592 |
0.739 |
|
| 2016 |
Bras J, Djaldetti R, Alves AM, Mead S, Darwent L, Lleo A, Molinuevo JL, Blesa R, Singleton A, Hardy J, Clarimon J, Guerreiro R. Exome sequencing in a consanguineous family clinically diagnosed with early-onset Alzheimer's disease identifies a homozygous CTSF mutation. Neurobiology of Aging. PMID 27524508 DOI: 10.1016/J.Neurobiolaging.2016.06.018 |
0.794 |
|
| 2016 |
Guerreiro R, Brás J, Batista S, Pires P, Ribeiro H, Almeida R, Oliveira C, Hardy J, Santana I. Pseudohypoparathyroidism Type I-b with neurological involvement is associated with a homozygous PTH1R mutation. Genes, Brain, and Behavior. PMID 27415614 DOI: 10.1111/Gbb.12308 |
0.492 |
|
| 2016 |
Sassi C, Nalls MA, Ridge PG, Gibbs JR, Ding J, Lupton MK, Troakes C, Lunnon K, Al-Sarraj S, Brown KS, Medway C, Clement N, Lord J, Turton J, Bras J, ... ... Guerreiro R, et al. ABCA7 p.G215S as potential protective factor for Alzheimer's disease. Neurobiology of Aging. PMID 27289440 DOI: 10.1016/J.Neurobiolaging.2016.04.004 |
0.79 |
|
| 2016 |
Guerreiro RJ, Brown R, Dian D, de Goede C, Bras J, Mole SE. Mutation of TBCK causes a rare recessive developmental disorder. Neurology. Genetics. 2: e76. PMID 27275012 DOI: 10.1212/Nxg.0000000000000076 |
0.361 |
|
| 2016 |
Sassi C, Ridge PG, Nalls MA, Gibbs R, Ding J, Lupton MK, Troakes C, Lunnon K, Al-Sarraj S, Brown KS, Medway C, Lord J, Turton J, Morgan K, ... ... Guerreiro R, et al. Influence of Coding Variability in APP-Aβ Metabolism Genes in Sporadic Alzheimer's Disease. Plos One. 11: e0150079. PMID 27249223 DOI: 10.1371/Journal.Pone.0150079 |
0.771 |
|
| 2016 |
Ngoh A, Bras J, Guerreiro R, Meyer E, McTague A, Dawson E, Mankad K, Gunny R, Clayton P, Mills PB, Thornton R, Lai M, Forsyth R, Kurian MA. RARS2 mutations in a sibship with infantile spasms. Epilepsia. PMID 27061686 DOI: 10.1111/Epi.13358 |
0.358 |
|
| 2016 |
Almeida MR, Letra L, Pires P, Santos A, Rebelo O, Guerreiro R, van der Zee J, Van Broeckhoven C, Santana I. Characterization of an FTLD-PDB family with the coexistence of SQSTM1 mutation and hexanucleotide (G4C2) repeat expansion in C9orf72 gene. Neurobiology of Aging. 40: 191.e1-8. PMID 26839080 DOI: 10.1016/J.Neurobiolaging.2015.12.015 |
0.484 |
|
| 2016 |
Faller KM, Bras J, Sharpe SJ, Anderson GW, Darwent L, Kun-Rodrigues C, Alroy J, Penderis J, Mole SE, Gutierrez-Quintana R, Guerreiro RJ. The Chihuahua dog: A new animal model for neuronal ceroid lipofuscinosis CLN7 disease? Journal of Neuroscience Research. PMID 26762174 DOI: 10.1002/Jnr.23710 |
0.419 |
|
| 2016 |
Patel T, Clement NS, Barber I, Braae A, Brookes KJ, Guetta-Baranes T, Chappell S, Guerreiro R, Bras JT, Singleton A, Hardy J, Morgan K. Investigating Sarm1 Variants In Alzheimer’S Disease Cohorts Alzheimers & Dementia. 12: 855. DOI: 10.1016/J.Jalz.2016.06.1750 |
0.744 |
|
| 2016 |
Kauwe K, Arano I, Bras JT, Cannon-Albright L, Cruchaga C, Goate AM, Murcia JDG, Guerreiro R, Hardy J, Hsu S, Karch C, Munger RG, Norton MC, Ridge PG, Sassi C, et al. Linkage And Whole Genome Sequence Analysis Of Alzheimer'S Disease Resilience And Risk Alzheimers & Dementia. 12: 675. DOI: 10.1016/J.Jalz.2016.06.1325 |
0.768 |
|
| 2015 |
Lesage S, Bras J, Cormier-Dequaire F, Condroyer C, Nicolas A, Darwent L, Guerreiro R, Majounie E, Federoff M, Heutink P, Wood NW, Gasser T, Hardy J, Tison F, Singleton A, et al. Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson disease. Neurology. Genetics. 1: e9. PMID 27066548 DOI: 10.1212/Nxg.0000000000000009 |
0.721 |
|
| 2015 |
Barber IS, García-Cárdenas JM, Sakdapanichkul C, Deacon C, Zapata Erazo G, Guerreiro R, Bras J, Hernandez D, Singleton A, Guetta-Baranes T, Braae A, Clement N, Patel T, Brookes K, Medway C, et al. Screening exons 16 and 17 of the amyloid precursor protein gene in sporadic early-onset Alzheimer's disease. Neurobiology of Aging. PMID 26803359 DOI: 10.1016/J.Neurobiolaging.2015.12.011 |
0.692 |
|
| 2015 |
Guerreiro R, Escott-Price V, Darwent L, Parkkinen L, Ansorge O, Hernandez DG, Nalls MA, Clark L, Honig L, Marder K, van der Flier W, Holstege H, Louwersheimer E, Lemstra A, Scheltens P, et al. Genome-wide analysis of genetic correlation in dementia with Lewy bodies, Parkinson's and Alzheimer's diseases. Neurobiology of Aging. PMID 26643944 DOI: 10.1016/J.Neurobiolaging.2015.10.028 |
0.762 |
|
| 2015 |
Guerreiro R, Bras J. The age factor in Alzheimer's disease. Genome Medicine. 7: 106. PMID 26482651 DOI: 10.1186/s13073-015-0232-5 |
0.433 |
|
| 2015 |
Marshall CR, Guerreiro R, Thust S, Fletcher P, Rohrer JD, Fox NC. A Novel MAPT Mutation Causing Corticobasal Syndrome Led by Progressive Apraxia of Speech. Journal of Alzheimer's Disease : Jad. 48: 923-6. PMID 26402116 DOI: 10.3233/Jad-150477 |
0.369 |
|
| 2015 |
Kun-Rodrigues C, Ganos C, Guerreiro R, Schneider SA, Schulte C, Lesage S, Darwent L, Holmans P, Singleton A, Bhatia K, Bras J. A systematic screening to identify de novo mutations causing sporadic early-onset Parkinson's disease. Human Molecular Genetics. PMID 26362251 DOI: 10.1093/Hmg/Ddv376 |
0.678 |
|
| 2015 |
Bras J, Alonso I, Barbot C, Costa MM, Darwent L, Orme T, Sequeiros J, Hardy J, Coutinho P, Guerreiro R. Mutations in PNKP cause recessive ataxia with oculomotor apraxia type 4. American Journal of Human Genetics. 96: 474-9. PMID 25728773 DOI: 10.1016/J.Ajhg.2015.01.005 |
0.615 |
|
| 2015 |
Guerreiro R, Brás J, Hardy J. SnapShot: Genetics of ALS and FTD. Cell. 160: 798.e1. PMID 25679767 DOI: 10.1016/J.Cell.2015.01.052 |
0.583 |
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| 2015 |
Guerreiro R, Bras J, Toombs J, Heslegrave A, Hardy J, Zetterberg H. Genetic Variants and Related Biomarkers in Sporadic Alzheimer's Disease. Current Genetic Medicine Reports. 3: 19-25. PMID 25664224 DOI: 10.1007/S40142-014-0062-6 |
0.675 |
|
| 2015 |
Brás J, Guerreiro R, Hardy J. SnapShot: Genetics of Parkinson's disease. Cell. 160: 570-570.e1. PMID 25635463 DOI: 10.1016/J.Cell.2015.01.019 |
0.635 |
|
| 2015 |
Erro R, Hersheson J, Ganos C, Mencacci NE, Stamelou M, Batla A, Thust SC, Bras JM, Guerreiro RJ, Hardy J, Quinn NP, Houlden H, Bhatia KP. H-ABC syndrome and DYT4: Variable expressivity or pleiotropy of TUBB4 mutations? Movement Disorders : Official Journal of the Movement Disorder Society. 30: 828-33. PMID 25545912 DOI: 10.1002/Mds.26129 |
0.576 |
|
| 2015 |
Nalls MA, Bras J, Hernandez DG, Keller MF, Majounie E, Renton AE, Saad M, Jansen I, Guerreiro R, Lubbe S, Plagnol V, Gibbs JR, Schulte C, Pankratz N, Sutherland M, et al. NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases. Neurobiology of Aging. 36: 1605.e7-12. PMID 25444595 DOI: 10.1016/J.Neurobiolaging.2014.07.028 |
0.749 |
|
| 2015 |
Boutoleau-Bretonnière C, Camuzat A, Le Ber I, Bouya-Ahmed K, Guerreiro R, Deruet AL, Evrard C, Bras J, Lamy E, Auffray-Calvier E, Pallardy A, Hardy J, Brice A, Derkinderen P, Vercelletto M. A phenotype of atypical apraxia of speech in a family carrying SQSTM1 mutation. Journal of Alzheimer's Disease : Jad. 43: 625-30. PMID 25114083 DOI: 10.3233/Jad-141512 |
0.622 |
|
| 2015 |
Guerreiro R, Bras J. The age factor in Alzheimer's disease Genome Medicine. 7: 1-3. DOI: 10.1186/S13073-015-0232-5 |
0.497 |
|
| 2015 |
Gurvit H, Bilgic B, Hanagasi H, Guven G, Guerreiro R, Hardy J. PSEN1 mutation presenting as posterior cortical atrophy Journal of the Neurological Sciences. 357. DOI: 10.1016/J.Jns.2015.08.409 |
0.541 |
|
| 2014 |
Bras JM, Guerreiro RJ, Teo JTH, Darwent L, Vaughan J, Molloy S, Hardy J, Schneider SA. Atypical Parkinsonism-Dystonia Syndrome Caused by a Novel DJ1 Mutation. Movement Disorders Clinical Practice. 1: 45-49. PMID 30363821 DOI: 10.1002/Mdc3.12008 |
0.606 |
|
| 2014 |
Slattery CF, Beck JA, Harper L, Adamson G, Abdi Z, Uphill J, Campbell T, Druyeh R, Mahoney CJ, Rohrer JD, Kenny J, Lowe J, Leung KK, Barnes J, Clegg SL, ... ... Guerreiro RJ, et al. R47H TREM2 variant increases risk of typical early-onset Alzheimer's disease but not of prion or frontotemporal dementia. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. 10: 602-608.e4. PMID 25160042 DOI: 10.1016/J.Jalz.2014.05.1751 |
0.656 |
|
| 2014 |
Guerreiro R, Hardy J. Genetics of Alzheimer's disease. Neurotherapeutics : the Journal of the American Society For Experimental Neurotherapeutics. 11: 732-7. PMID 25113539 DOI: 10.1007/S13311-014-0295-9 |
0.69 |
|
| 2014 |
Sassi C, Guerreiro R, Gibbs R, Ding J, Lupton MK, Troakes C, Al-Sarraj S, Niblock M, Gallo JM, Adnan J, Killick R, Brown KS, Medway C, Lord J, Turton J, et al. Investigating the role of rare coding variability in Mendelian dementia genes (APP, PSEN1, PSEN2, GRN, MAPT, and PRNP) in late-onset Alzheimer's disease. Neurobiology of Aging. 35: 2881.e1-6. PMID 25104557 DOI: 10.1016/J.Neurobiolaging.2014.06.002 |
0.794 |
|
| 2014 |
Bras J, Guerreiro R, Darwent L, Parkkinen L, Ansorge O, Escott-Price V, Hernandez DG, Nalls MA, Clark LN, Honig LS, Marder K, Van Der Flier WM, Lemstra A, Scheltens P, Rogaeva E, et al. Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies. Human Molecular Genetics. 23: 6139-46. PMID 24973356 DOI: 10.1093/Hmg/Ddu334 |
0.768 |
|
| 2014 |
Guerreiro R, Brás J, Wojtas A, Rademakers R, Hardy J, Graff-Radford N. A nonsense mutation in PRNP associated with clinical Alzheimer's disease. Neurobiology of Aging. 35: 2656.e13-6. PMID 24958194 DOI: 10.1016/J.Neurobiolaging.2014.05.013 |
0.647 |
|
| 2014 |
Le Ber I, De Septenville A, Guerreiro R, Bras J, Camuzat A, Caroppo P, Lattante S, Couarch P, Kabashi E, Bouya-Ahmed K, Dubois B, Brice A. Homozygous TREM2 mutation in a family with atypical frontotemporal dementia Neurobiology of Aging. 35: 2419e23-2419e25. PMID 24910390 DOI: 10.1016/J.Neurobiolaging.2014.04.010 |
0.423 |
|
| 2014 |
Sassi C, Guerreiro R, Gibbs R, Ding J, Lupton MK, Troakes C, Lunnon K, Al-Sarraj S, Brown KS, Medway C, Lord J, Turton J, Mann D, Snowden J, Neary D, et al. Exome sequencing identifies 2 novel presenilin 1 mutations (p.L166V and p.S230R) in British early-onset Alzheimer's disease. Neurobiology of Aging. 35: 2422.e13-6. PMID 24880964 DOI: 10.1016/J.Neurobiolaging.2014.04.026 |
0.789 |
|
| 2014 |
Guerreiro R, Brás J, Hardy J, Singleton A. Next generation sequencing techniques in neurological diseases: redefining clinical and molecular associations. Human Molecular Genetics. 23: R47-53. PMID 24794858 DOI: 10.1093/Hmg/Ddu203 |
0.737 |
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| 2014 |
Benitez BA, Jin SC, Guerreiro R, Graham R, Lord J, Harold D, Sims R, Lambert JC, Gibbs JR, Bras J, Sassi C, Harari O, Bertelsen S, Lupton MK, Powell J, et al. Missense variant in TREML2 protects against Alzheimer's disease. Neurobiology of Aging. 35: 1510.e19-26. PMID 24439484 DOI: 10.1016/J.Neurobiolaging.2013.12.010 |
0.792 |
|
| 2014 |
Cruchaga C, Karch CM, Jin SC, Benitez BA, Cai Y, Guerreiro R, Harari O, Norton J, Budde J, Bertelsen S, Jeng AT, Cooper B, Skorupa T, Carrell D, Levitch D, et al. Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer's disease. Nature. 505: 550-4. PMID 24336208 DOI: 10.1038/Nature12825 |
0.794 |
|
| 2014 |
Holmans P, Moskvina V, Jones L, Sharma M, Vedernikov A, Buchel F, Saad M, Bras JM, Bettella F, Nicolaou N, Simón-Sánchez J, Mittag F, Gibbs JR, Schulte C, Durr A, ... Guerreiro R, et al. A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease [Human Molecular Genetics 22, 5, 2013, 1039-1049] doi:10.1093/hmg/dds492 Human Molecular Genetics. 23: 562. DOI: 10.1093/Hmg/Ddt554 |
0.721 |
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| 2014 |
Gurvit H, Lohmann E, Guerreiro R. Mapt Mutation Causing Right Temporal Variant Semantic Dementia Alzheimers & Dementia. 10: 882. DOI: 10.1016/J.Jalz.2014.07.036 |
0.408 |
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| 2014 |
Bilgic B, Gelisin O, Guerreiro R, Lohmann E, Hanagasi HA, Gurvit H, Emre M. P1-287: NEUROIMAGING FINDINGS OF NASU-HAKOLA DISEASE Alzheimer's & Dementia. 10: P415-P415. DOI: 10.1016/J.Jalz.2014.05.527 |
0.396 |
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| 2014 |
Cruchaga C, Brkanac Z, Jin SC, Benitez BA, Rehker J, Ridge P, Kauwe J, Hardy J, Bras J, Guerreiro R, Singleton A, Goate A. O1-04-02: EXOME-SEQUENCING IN LATE-ONSET FAMILIES IDENTIFIED ADDITIONAL CANDIDATES GENES FOR ALZHEIMER'S DISEASE Alzheimer's & Dementia. 10: P135-P135. DOI: 10.1016/J.Jalz.2014.04.075 |
0.769 |
|
| 2013 |
Guerreiro R, Brás J, Hardy J. SnapShot: genetics of Alzheimer's disease. Cell. 155: 968-968.e1. PMID 24209629 DOI: 10.1016/J.Cell.2013.10.037 |
0.558 |
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| 2013 |
Guerreiro R, Hardy J. TREM2 and neurodegenerative disease. The New England Journal of Medicine. 369: 1569-70. PMID 24143816 DOI: 10.1056/Nejmc1306509 |
0.608 |
|
| 2013 |
Ross OA, Soto-Ortolaza AI, Heckman MG, Verbeeck C, Serie DJ, Rayaprolu S, Rich SS, Nalls MA, Singleton A, Guerreiro R, Kinsella E, Wszolek ZK, Brott TG, Brown RD, Worrall BB, et al. NOTCH3 variants and risk of ischemic stroke. Plos One. 8: e75035. PMID 24086431 DOI: 10.1371/Journal.Pone.0075035 |
0.582 |
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| 2013 |
Le Ber I, Camuzat A, Guerreiro R, Bouya-Ahmed K, Bras J, Nicolas G, Gabelle A, Didic M, De Septenville A, Millecamps S, Lenglet T, Latouche M, Kabashi E, Campion D, Hannequin D, et al. SQSTM1 mutations in French patients with frontotemporal dementia or frontotemporal dementia with amyotrophic lateral sclerosis. Jama Neurology. 70: 1403-10. PMID 24042580 DOI: 10.1001/Jamaneurol.2013.3849 |
0.61 |
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| 2013 |
Moskvina V, Harold D, Russo G, Vedernikov A, Sharma M, Saad M, Holmans P, Bras JM, Bettella F, Keller MF, Nicolaou N, Simón-Sánchez J, Gibbs JR, Schulte C, Durr A, ... Guerreiro R, et al. Analysis of genome-wide association studies of Alzheimer disease and of Parkinson disease to determine if these 2 diseases share a common genetic risk. Jama Neurology. 70: 1268-76. PMID 23921447 DOI: 10.1001/Jamaneurol.2013.448 |
0.764 |
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| 2013 |
Guerreiro R, Bilgic B, Guven G, Brás J, Rohrer J, Lohmann E, Hanagasi H, Gurvit H, Emre M. Novel compound heterozygous mutation in TREM2 found in a Turkish frontotemporal dementia-like family. Neurobiology of Aging. 34: 2890.e1-5. PMID 23870839 DOI: 10.1016/J.Neurobiolaging.2013.06.005 |
0.426 |
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| 2013 |
Forabosco P, Ramasamy A, Trabzuni D, Walker R, Smith C, Bras J, Levine AP, Hardy J, Pocock JM, Guerreiro R, Weale ME, Ryten M. Insights into TREM2 biology by network analysis of human brain gene expression data. Neurobiology of Aging. 34: 2699-714. PMID 23855984 DOI: 10.1016/J.Neurobiolaging.2013.05.001 |
0.609 |
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| 2013 |
Ahmed R, Guerreiro R, Rohrer JD, Guven G, Rossor MN, Hardy J, Fox NC. A novel A781V mutation in the CSF1R gene causes hereditary diffuse leucoencephalopathy with axonal spheroids. Journal of the Neurological Sciences. 332: 141-4. PMID 23816250 DOI: 10.1016/J.Jns.2013.06.007 |
0.574 |
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| 2013 |
Guerreiro R, Bras JT, Vieira M, Warrier V, Agrawal S, Stewart H, Anderson G, Mole SE. CLN6 disease caused by the same mutation originating in Pakistan has varying pathology. European Journal of Paediatric Neurology : Ejpn : Official Journal of the European Paediatric Neurology Society. 17: 657-60. PMID 23735787 DOI: 10.1016/J.Ejpn.2013.04.011 |
0.482 |
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| 2013 |
Guerreiro R, Kara E, Le Ber I, Bras J, Rohrer JD, Taipa R, Lashley T, Dupuits C, Gurunlian N, Mochel F, Warren JD, Hannequin D, Sedel F, Depienne C, Camuzat A, et al. Genetic analysis of inherited leukodystrophies: genotype-phenotype correlations in the CSF1R gene. Jama Neurology. 70: 875-82. PMID 23649896 DOI: 10.1001/Jamaneurol.2013.698 |
0.629 |
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| 2013 |
Holton P, Ryten M, Nalls M, Trabzuni D, Weale ME, Hernandez D, Crehan H, Gibbs JR, Mayeux R, Haines JL, Farrer LA, Pericak-Vance MA, Schellenberg GD, Ramirez-Restrepo M, ... ... Guerreiro R, et al. Initial assessment of the pathogenic mechanisms of the recently identified Alzheimer risk Loci. Annals of Human Genetics. 77: 85-105. PMID 23360175 DOI: 10.1111/Ahg.12000 |
0.794 |
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| 2013 |
Guerreiro RJ, Lohmann E, Brás JM, Gibbs JR, Rohrer JD, Gurunlian N, Dursun B, Bilgic B, Hanagasi H, Gurvit H, Emre M, Singleton A, Hardy J. Using exome sequencing to reveal mutations in TREM2 presenting as a frontotemporal dementia-like syndrome without bone involvement. Jama Neurology. 70: 78-84. PMID 23318515 DOI: 10.1001/Jamaneurol.2013.579 |
0.757 |
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| 2013 |
Holmans P, Moskvina V, Jones L, Sharma M, Vedernikov A, Buchel F, Saad M, Sadd M, Bras JM, Bettella F, Nicolaou N, Simón-Sánchez J, Mittag F, Gibbs JR, ... ... Guerreiro R, et al. A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease. Human Molecular Genetics. 22: 1039-49. PMID 23223016 DOI: 10.1093/Hmg/Dds492 |
0.714 |
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| 2013 |
Guerreiro R, Wojtas A, Bras J, Carrasquillo M, Rogaeva E, Majounie E, Cruchaga C, Sassi C, Kauwe JS, Younkin S, Hazrati L, Collinge J, Pocock J, Lashley T, Williams J, et al. TREM2 variants in Alzheimer's disease. The New England Journal of Medicine. 368: 117-27. PMID 23150934 DOI: 10.1056/Nejmoa1211851 |
0.834 |
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| 2013 |
Keller MF, Saad M, Bras J, Bettella F, Nicolaou N, Simón-Sánchez J, Mittag F, Büchel F, Sharma M, Gibbs JR, Schulte C, Moskvina V, Durr A, Holmans P, Kilarski LL, ... Guerreiro R, et al. Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease Human Molecular Genetics. 22: 2973. DOI: 10.1093/hmg/ddt199 |
0.311 |
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| 2013 |
Keller MF, Saad M, Bras J, Bettella F, Nicolaou N, Siḿn-śnchez J, Mittag F, B̈chel F, Sharma M, Gibbs JR, Schulte C, Moskvina V, Durr A, Holmans P, Kilarski LL, ... Guerreiro R, et al. Corrigendum to Using genome-wide complex trait analysis to quantify 'missing heritability' in parkinson's disease [Human Molecular Genetics, 21:22 (2012) 4996-5009] doi: 10.1093/hmg/dds335] Human Molecular Genetics. 22: 1696. DOI: 10.1093/Hmg/Ddt030 |
0.724 |
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| 2013 |
Harold D, Abraham R, Hollingworth P, Sims R, Gerrish A, Hamshere ML, Pahwa JS, Moskvina V, Dowzell K, Williams A, Jones N, Thomas C, Stretton A, Morgan AR, Lovestone S, ... ... Guerreiro R, et al. Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease Nature Genetics. 45: 712-712. DOI: 10.1038/Ng0613-712A |
0.819 |
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| 2013 |
Gurvit H, Bilgic B, Hanagasi H, Guerreiro R, Hardy J. Homozygous TREM2 mutations: Another addition to the list of genetic causes of familial frontotemporal dementia Alzheimers & Dementia. 9: 860. DOI: 10.1016/J.Jalz.2013.08.183 |
0.626 |
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| 2012 |
Keller MF, Saad M, Bras J, Bettella F, Nicolaou N, Simón-Sánchez J, Mittag F, Büchel F, Sharma M, Gibbs JR, Schulte C, Moskvina V, Durr A, Holmans P, Kilarski LL, ... Guerreiro R, et al. Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease. Human Molecular Genetics. 21: 4996-5009. PMID 22892372 DOI: 10.1093/Hmg/Dds335 |
0.723 |
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| 2012 |
Guerreiro RJ, Hardy J. TOMM40 association with Alzheimer disease: tales of APOE and linkage disequilibrium. Archives of Neurology. 69: 1243-4. PMID 22869030 DOI: 10.1001/Archneurol.2012.1935 |
0.667 |
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| 2012 |
Bras J, Guerreiro R, Hardy J. Use of next-generation sequencing and other whole-genome strategies to dissect neurological disease. Nature Reviews. Neuroscience. 13: 453-64. PMID 22714018 DOI: 10.1038/Nrn3271 |
0.648 |
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| 2012 |
Lohmann E, Guerreiro RJ, Erginel-Unaltuna N, Gurunlian N, Bilgic B, Gurvit H, Hanagasi HA, Luu N, Emre M, Singleton A. Identification of PSEN1 and PSEN2 gene mutations and variants in Turkish dementia patients. Neurobiology of Aging. 33: 1850.e17-27. PMID 22503161 DOI: 10.1016/J.Neurobiolaging.2012.02.020 |
0.722 |
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| 2012 |
Bras J, Verloes A, Schneider SA, Mole SE, Guerreiro RJ. Mutation of the parkinsonism gene ATP13A2 causes neuronal ceroid-lipofuscinosis. Human Molecular Genetics. 21: 2646-50. PMID 22388936 DOI: 10.1093/Hmg/Dds089 |
0.496 |
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| 2012 |
Matsuki T, Zaka M, Guerreiro R, van der Brug MP, Cooper JA, Cookson MR, Hardy JA, Howell BW. Identification of Stk25 as a genetic modifier of Tau phosphorylation in Dab1-mutant mice. Plos One. 7: e31152. PMID 22355340 DOI: 10.1371/Journal.Pone.0031152 |
0.667 |
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| 2012 |
Dobricic V, Stefanova E, Jankovic M, Gurunlian N, Novakovic I, Hardy J, Kostic V, Guerreiro R. Genetic testing in familial and young-onset Alzheimer's disease: mutation spectrum in a Serbian cohort. Neurobiology of Aging. 33: 1481.e7-12. PMID 22221884 DOI: 10.1016/J.Neurobiolaging.2011.12.007 |
0.691 |
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| 2012 |
Charlesworth G, Gandhi S, Bras JM, Barker RA, Burn DJ, Chinnery PF, Gentleman SM, Guerreiro R, Hardy J, Holton JL, Lees A, Morrison K, Sheerin UM, Williams N, Morris H, et al. Tau acts as an independent genetic risk factor in pathologically proven PD. Neurobiology of Aging. 33: 838.e7-11. PMID 22221882 DOI: 10.1016/J.Neurobiolaging.2011.11.001 |
0.558 |
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| 2012 |
Sheerin UM, Charlesworth G, Bras J, Guerreiro R, Bhatia K, Foltynie T, Limousin P, Silveira-Moriyama L, Lees A, Wood N. Screening for VPS35 mutations in Parkinson's disease Neurobiology of Aging. 33: 838.e1-838.e5. PMID 22154191 DOI: 10.1016/J.Neurobiolaging.2011.10.032 |
0.45 |
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| 2012 |
Guerreiro RJ, Lohmann E, Kinsella E, Brás JM, Luu N, Gurunlian N, Dursun B, Bilgic B, Santana I, Hanagasi H, Gurvit H, Gibbs JR, Oliveira C, Emre M, Singleton A. Exome sequencing reveals an unexpected genetic cause of disease: NOTCH3 mutation in a Turkish family with Alzheimer's disease. Neurobiology of Aging. 33: 1008.e17-23. PMID 22153900 DOI: 10.1016/J.Neurobiolaging.2011.10.009 |
0.732 |
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| 2012 |
Gerrish A, Russo G, Richards A, Moskvina V, Ivanov D, Harold D, Sims R, Abraham R, Hollingworth P, Chapman J, Hamshere M, Pahwa JS, Dowzell K, Williams A, Jones N, ... ... Guerreiro R, et al. The role of variation at AβPP, PSEN1, PSEN2, and MAPT in late onset Alzheimer's disease. Journal of Alzheimer's Disease : Jad. 28: 377-87. PMID 22027014 DOI: 10.3233/Jad-2011-110824 |
0.852 |
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| 2012 |
Crehan H, Holton P, Wray S, Pocock J, Guerreiro R, Hardy J. Complement receptor 1 (CR1) and Alzheimer's disease. Immunobiology. 217: 244-50. PMID 21840620 DOI: 10.1016/J.Imbio.2011.07.017 |
0.738 |
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| 2012 |
McNaughton D, Knight W, Guerreiro R, Ryan N, Lowe J, Poulter M, Nicholl DJ, Hardy J, Revesz T, Lowe J, Rossor M, Collinge J, Mead S. Duplication of amyloid precursor protein (APP), but not prion protein (PRNP) gene is a significant cause of early onset dementia in a large UK series. Neurobiology of Aging. 33: 426.e13-21. PMID 21193246 DOI: 10.1016/J.Neurobiolaging.2010.10.010 |
0.723 |
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| 2012 |
Guerreiro RJ, Gustafson DR, Hardy J. The genetic architecture of Alzheimer's disease: beyond APP, PSENs and APOE. Neurobiology of Aging. 33: 437-56. PMID 20594621 DOI: 10.1016/J.Neurobiolaging.2010.03.025 |
0.69 |
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| 2012 |
Guerreiro R. Exome sequencing in Alzheimer's disease: Do rare variants play a role in risk? Alzheimers & Dementia. 8: 78. DOI: 10.1016/J.Jalz.2012.05.184 |
0.481 |
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| 2011 |
Hardy J, Guerreiro R, Lovestone S. Clusterin as an Alzheimer biomarker. Archives of Neurology. 68: 1459-60. PMID 22084130 DOI: 10.1001/Archneurol.2011.1000 |
0.591 |
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| 2011 |
Renton AE, Majounie E, Waite A, Simón-Sánchez J, Rollinson S, Gibbs JR, Schymick JC, Laaksovirta H, van Swieten JC, Myllykangas L, Kalimo H, Paetau A, Abramzon Y, Remes AM, Kaganovich A, ... ... Guerreiro RJ, et al. A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD. Neuron. 72: 257-68. PMID 21944779 DOI: 10.1016/J.Neuron.2011.09.010 |
0.815 |
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| 2011 |
Guerreiro RJ, Hardy J. Alzheimer's disease genetics: lessons to improve disease modelling. Biochemical Society Transactions. 39: 910-6. PMID 21787322 DOI: 10.1042/Bst0390910 |
0.666 |
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| 2011 |
Hardy J, Guerreiro R. A new way APP mismetabolism can lead to Alzheimer's disease Embo Molecular Medicine. 3: 247-248. PMID 21523909 DOI: 10.1002/Emmm.201100139 |
0.611 |
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| 2011 |
Hollingworth P, Harold D, Sims R, Gerrish A, Lambert JC, Carrasquillo MM, Abraham R, Hamshere ML, Pahwa JS, Moskvina V, Dowzell K, Jones N, Stretton A, Thomas C, Richards A, ... ... Guerreiro R, et al. Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease. Nature Genetics. 43: 429-35. PMID 21460840 DOI: 10.1038/Ng.803 |
0.79 |
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| 2011 |
Pearson JP, Williams NM, Majounie E, Waite A, Stott J, Newsway V, Murray A, Hernandez D, Guerreiro R, Singleton AB, Neal J, Morris HR. Familial frontotemporal dementia with amyotrophic lateral sclerosis and a shared haplotype on chromosome 9p. Journal of Neurology. 258: 647-55. PMID 21072532 DOI: 10.1007/S00415-010-5815-X |
0.654 |
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| 2011 |
Hardy J, Guerreiro R, Wray S, Ferrari R, Momeni P. The genetics of Alzheimer's disease and other tauopathies Journal of Alzheimer's Disease. 23: S33-S39. DOI: 10.3233/Jad-2011-001433 |
0.612 |
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| 2011 |
Jones L, Holmans PA, Hamshere ML, Harold D, Moskvina V, Ivanov D, Pocklington A, Abraham R, Hollingworth P, Sims R, Gerrish A, Pahwa JS, Jones N, Stretton A, Morgan AR, ... ... Guerreiro R, et al. Correction: Genetic Evidence Implicates the Immune System and Cholesterol Metabolism in the Aetiology of Alzheimer's Disease Plos One. 6. DOI: 10.1371/annotation/a0bb886d-d345-4a20-a82e-adce9b047798 |
0.771 |
|
| 2010 |
Jones L, Holmans PA, Hamshere ML, Harold D, Moskvina V, Ivanov D, Pocklington A, Abraham R, Hollingworth P, Sims R, Gerrish A, Pahwa JS, Jones N, Stretton A, Morgan AR, ... ... Guerreiro R, et al. Genetic evidence implicates the immune system and cholesterol metabolism in the aetiology of Alzheimer's disease. Plos One. 5: e13950. PMID 21085570 DOI: 10.1371/Journal.Pone.0013950 |
0.807 |
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| 2010 |
Beck JA, Poulter M, Campbell TA, Adamson G, Uphill JB, Guerreiro R, Jackson GS, Stevens JC, Manji H, Collinge J, Mead S. PRNP allelic series from 19 years of prion protein gene sequencing at the MRC Prion Unit. Human Mutation. 31: E1551-63. PMID 20583301 DOI: 10.1002/Humu.21281 |
0.616 |
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| 2010 |
Guerreiro RJ, Beck J, Gibbs JR, Santana I, Rossor MN, Schott JM, Nalls MA, Ribeiro H, Santiago B, Fox NC, Oliveira C, Collinge J, Mead S, Singleton A, Hardy J. Genetic variability in CLU and its association with Alzheimer's disease. Plos One. 5: e9510. PMID 20209083 DOI: 10.1371/Journal.Pone.0009510 |
0.798 |
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| 2010 |
Guerreiro RJ, Washecka N, Hardy J, Singleton A. A thorough assessment of benign genetic variability in GRN and MAPT. Human Mutation. 31: E1126-40. PMID 20020531 DOI: 10.1002/Humu.21152 |
0.75 |
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| 2010 |
Guerreiro RJ, Baquero M, Blesa R, Boada M, Brás JM, Bullido MJ, Calado A, Crook R, Ferreira C, Frank A, Gómez-Isla T, Hernández I, Lleó A, Machado A, MartÃnez-Lage P, et al. Genetic screening of Alzheimer's disease genes in Iberian and African samples yields novel mutations in presenilins and APP. Neurobiology of Aging. 31: 725-31. PMID 18667258 DOI: 10.1016/J.Neurobiolaging.2008.06.012 |
0.757 |
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| 2009 |
Rohrer JD, Guerreiro R, Vandrovcova J, Uphill J, Reiman D, Beck J, Isaacs AM, Authier A, Ferrari R, Fox NC, Mackenzie IR, Warren JD, de Silva R, Holton J, Revesz T, et al. The heritability and genetics of frontotemporal lobar degeneration. Neurology. 73: 1451-6. PMID 19884572 DOI: 10.1212/Wnl.0B013E3181Bf997A |
0.65 |
|
| 2009 |
Harold D, Abraham R, Hollingworth P, Sims R, Gerrish A, Hamshere ML, Pahwa JS, Moskvina V, Dowzell K, Williams A, Jones N, Thomas C, Stretton A, Morgan AR, Lovestone S, ... ... Guerreiro R, et al. Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease. Nature Genetics. 41: 1088-93. PMID 19734902 DOI: 10.1038/Ng.440 |
0.805 |
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| 2009 |
Guerreiro RJ, Vaskov T, Crews C, Singleton A, Hardy J. A case of dementia with PRNP D178Ncis-129M and no insomnia. Alzheimer Disease and Associated Disorders. 23: 415-7. PMID 19571725 DOI: 10.1097/Wad.0B013E3181Ae3A76 |
0.748 |
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| 2009 |
Neumann J, Bras J, Deas E, O'Sullivan SS, Parkkinen L, Lachmann RH, Li A, Holton J, Guerreiro R, Paudel R, Segarane B, Singleton A, Lees A, Hardy J, Houlden H, et al. Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's disease. Brain : a Journal of Neurology. 132: 1783-94. PMID 19286695 DOI: 10.1093/Brain/Awp044 |
0.761 |
|
| 2009 |
Nalls MA, Guerreiro RJ, Simon-Sanchez J, Bras JT, Traynor BJ, Gibbs JR, Launer L, Hardy J, Singleton AB. Extended tracts of homozygosity identify novel candidate genes associated with late-onset Alzheimer's disease. Neurogenetics. 10: 183-90. PMID 19271249 DOI: 10.1007/S10048-009-0182-4 |
0.752 |
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| 2009 |
Rollinson S, Rizzu P, Sikkink S, Baker M, Halliwell N, Snowden J, Traynor BJ, Ruano D, Cairns N, Rohrer JD, Mead S, Collinge J, Rossor M, Akay E, Guerreiro R, et al. Ubiquitin associated protein 1 is a risk factor for frontotemporal lobar degeneration. Neurobiology of Aging. 30: 656-65. PMID 19217189 DOI: 10.1016/J.Neurobiolaging.2009.01.009 |
0.585 |
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| 2009 |
Clarimón J, Djaldetti R, Lleó A, Guerreiro RJ, Molinuevo JL, Paisán-Ruiz C, Gómez-Isla T, Blesa R, Singleton A, Hardy J. Whole genome analysis in a consanguineous family with early onset Alzheimer's disease. Neurobiology of Aging. 30: 1986-91. PMID 18387709 DOI: 10.1016/J.Neurobiolaging.2008.02.008 |
0.781 |
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| 2009 |
Bras J, Paisan-Ruiz C, Guerreiro R, Ribeiro MH, Morgadinho A, Januario C, Sidransky E, Oliveira C, Singleton A. Complete screening for glucocerebrosidase mutations in Parkinson disease patients from Portugal. Neurobiology of Aging. 30: 1515-7. PMID 18160183 DOI: 10.1016/J.Neurobiolaging.2007.11.016 |
0.672 |
|
| 2009 |
Harold D, Abraham R, Hollingworth P, Sims R, Gerrish A, Hamshere ML, Pahwa JS, Moskvina V, Dowzell K, Williams A, Jones N, Thomas C, Stretton A, Morgan AR, Lovestone S, ... ... Guerreiro R, et al. Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease Nature Genetics. 41: 1156-1156. DOI: 10.1038/Ng1009-1156D |
0.807 |
|
| 2009 |
Ryan N, McNaughton D, Knight W, Guerreiro R, Poulter M, Nicholl D, Hardy J, Rossor M, Collinge J, Mead S. Duplications of APP—but not PRNP—are a significant cause of early-onset dementia in a large UK referral series Alzheimers & Dementia. 5: 460. DOI: 10.1016/J.Jalz.2009.04.869 |
0.665 |
|
| 2008 |
Guerreiro RJ, Schymick JC, Crews C, Singleton A, Hardy J, Traynor BJ. TDP-43 is not a common cause of sporadic amyotrophic lateral sclerosis. Plos One. 3: e2450. PMID 18545701 DOI: 10.1371/Journal.Pone.0002450 |
0.825 |
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| 2008 |
Guerreiro RJ, Santana I, Bras JM, Revesz T, Rebelo O, Ribeiro MH, Santiago B, Oliveira CR, Singleton A, Hardy J. Novel progranulin mutation: screening for PGRN mutations in a Portuguese series of FTD/CBS cases. Movement Disorders : Official Journal of the Movement Disorder Society. 23: 1269-73. PMID 18464284 DOI: 10.1002/Mds.22078 |
0.726 |
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| 2008 |
Jakobsson M, Scholz SW, Scheet P, Gibbs JR, VanLiere JM, Fung HC, Szpiech ZA, Degnan JH, Wang K, Guerreiro R, Bras JM, Schymick JC, Hernandez DG, Traynor BJ, Simon-Sanchez J, et al. Genotype, haplotype and copy-number variation in worldwide human populations. Nature. 451: 998-1003. PMID 18288195 DOI: 10.1038/Nature06742 |
0.778 |
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| 2008 |
Camargos S, Scholz S, Simón-Sánchez J, Paisán-Ruiz C, Lewis P, Hernandez D, Ding J, Gibbs JR, Cookson MR, Bras J, Guerreiro R, Oliveira CR, Lees A, Hardy J, Cardoso F, et al. DYT16, a novel young-onset dystonia-parkinsonism disorder: identification of a segregating mutation in the stress-response protein PRKRA. The Lancet. Neurology. 7: 207-15. PMID 18243799 DOI: 10.1016/S1474-4422(08)70022-X |
0.792 |
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| 2008 |
Bras J, Guerreiro R, Ribeiro M, Morgadinho A, Januario C, Dias M, Calado A, Semedo C, Oliveira C, Hardy J, Singleton A. Analysis of Parkinson disease patients from Portugal for mutations in SNCA, PRKN, PINK1 and LRRK2. Bmc Neurology. 8: 1. PMID 18211709 DOI: 10.1186/1471-2377-8-1 |
0.745 |
|
| 2008 |
Clarimón J, Guerreiro R, Lleó A, Guardia C, Blesa R, Gómez-Isla T, Boada M, Bullido M, Ferrer I, Martínez-Lage P, Masdeu J, Molina L, Molinuevo JL, Pastor P, Pérez-Tur J, et al. P3-213: Genetic screening in a large cohort of early-onset Alzheimer's disease patients from Spain: Novel mutations in the amyloid precursor protein and presenilines Alzheimers & Dementia. 4. DOI: 10.1016/J.Jalz.2008.05.1780 |
0.831 |
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| 2007 |
Guerreiro RJ, Santana I, Brás JM, Santiago B, Paiva A, Oliveira C. Peripheral inflammatory cytokines as biomarkers in Alzheimer's disease and mild cognitive impairment. Neuro-Degenerative Diseases. 4: 406-12. PMID 17934323 DOI: 10.1159/000107700 |
0.332 |
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| 2006 |
Guerreiro RJ, Bras JM, Santana I, Januario C, Santiago B, Morgadinho AS, Ribeiro MH, Hardy J, Singleton A, Oliveira C. Association of HFE common mutations with Parkinson's disease, Alzheimer's disease and mild cognitive impairment in a Portuguese cohort. Bmc Neurology. 6: 24. PMID 16824219 DOI: 10.1186/1471-2377-6-24 |
0.755 |
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| 2006 |
Guerreiro RJ, Bras JM, Santana I, Santiago B, Ribeiro MH, Momeni P, Rogaeva E, Oliveira C, Hardy J. P1-349: Genetic analysis of Portuguese patients with Alzheimer's disease and frontotemporal dementia Alzheimer's & Dementia. 2: S199-S200. DOI: 10.1016/J.Jalz.2006.05.727 |
0.671 |
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| 2006 |
Santana I, Sá A, Guerreiro R, Brás J, Hardy J, Rogaeva E, Oliveira C. P1-348: Early onset familial Alzheimer's disease: First Portuguese cases Alzheimer's & Dementia. 2: S199-S199. DOI: 10.1016/J.Jalz.2006.05.726 |
0.637 |
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| 2005 |
Bras JM, Guerreiro RJ, Ribeiro MH, Januario C, Morgadinho A, Oliveira CR, Cunha L, Hardy J, Singleton A. G2019S dardarin substitution is a common cause of Parkinson's disease in a Portuguese cohort. Movement Disorders : Official Journal of the Movement Disorder Society. 20: 1653-5. PMID 16149095 DOI: 10.1002/Mds.20682 |
0.745 |
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| 2004 |
Santana I, Guerreiro R, Paiva A, Sarmento A, Santiago B, Barbosa V, Oliveira C. P4-208 Inflammation in mild cognitive impairment and mild Alzheimer's disease Neurobiology of Aging. 25: S534. DOI: 10.1016/S0197-4580(04)81766-4 |
0.395 |
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