| Year |
Citation |
Score |
| 2024 |
Winstone JK, Pathak KV, Winslow W, Piras IS, White J, Sharma R, Huentelman MJ, Pirrotte P, Velazquez R. Correction: Glyphosate infiltrates the brain and increases pro-inflammatory cytokine TNFα: implications for neurodegenerative disorders. Journal of Neuroinflammation. 21: 20. PMID 38233859 DOI: 10.1186/s12974-023-02990-9 |
0.544 |
|
| 2022 |
Winstone JK, Pathak KV, Winslow W, Piras IS, White J, Sharma R, Huentelman MJ, Pirrotte P, Velazquez R. Glyphosate infiltrates the brain and increases pro-inflammatory cytokine TNFα: implications for neurodegenerative disorders. Journal of Neuroinflammation. 19: 193. PMID 35897073 DOI: 10.1186/s12974-022-02544-5 |
0.572 |
|
| 2021 |
Dave N, Vural AS, Piras IS, Winslow W, Surendra L, Winstone JK, Beach TG, Huentelman MJ, Velazquez R. Identification of retinoblastoma binding protein 7 (Rbbp7) as a mediator against tau acetylation and subsequent neuronal loss in Alzheimer's disease and related tauopathies. Acta Neuropathologica. PMID 33978814 DOI: 10.1007/s00401-021-02323-1 |
0.576 |
|
| 2020 |
Ouellette AR, Neuner SM, Dumitrescu L, Anderson LC, Gatti DM, Mahoney ER, Bubier JA, Churchill G, Peters L, Huentelman MJ, Herskowitz JH, Yang HS, Smith AN, Reitz C, Kunkle BW, et al. Cross-Species Analyses Identify Dlgap2 as a Regulator of Age-Related Cognitive Decline and Alzheimer's Dementia. Cell Reports. 32: 108091. PMID 32877673 DOI: 10.1016/J.Celrep.2020.108091 |
0.343 |
|
| 2020 |
Piras IS, Bleul C, Schrauwen I, Talboom J, Llaci L, De Both MD, Naymik MA, Halliday G, Bettencourt C, Holton JL, Serrano GE, Sue LI, Beach TG, Stefanova N, Huentelman MJ. Transcriptional profiling of multiple system atrophy cerebellar tissue highlights differences between the parkinsonian and cerebellar sub-types of the disease. Acta Neuropathologica Communications. 8: 76. PMID 32493431 DOI: 10.1186/S40478-020-00950-5 |
0.37 |
|
| 2020 |
Piras IS, Bleul C, Siniard A, Wolfe AJ, De Both MD, Hernandez AG, Huentelman MJ. Association of Common Genetic Variants in the and Genes with Canine Idiopathic Pulmonary Fibrosis in the West Highland White Terrier. Genes. 11. PMID 32486318 DOI: 10.3390/Genes11060609 |
0.355 |
|
| 2020 |
Piras IS, Costa A, Tirindelli MC, Stoccoro A, Huentelman MJ, Sacco R, Coppedè F, Lintas C. Genetic and epigenetic gene variants in the mothers of attention-deficit/hyperactivity disorder affected children as possible risk factors for neurodevelopmental disorders. Epigenomics. PMID 32485115 DOI: 10.2217/Epi-2019-0356 |
0.315 |
|
| 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, 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 |
0.317 |
|
| 2019 |
Llaci L, Ramsey K, Belnap N, Claasen AM, Balak CD, Szelinger S, Jepsen WM, Siniard AL, Richholt R, Izat T, Naymik M, De Both M, Piras IS, Craig DW, Huentelman MJ, et al. Compound heterozygous mutations in SNAP29 is associated with Pelizaeus-Merzbacher-like disorder (PMLD). Human Genetics. 138: 1409-1417. PMID 31748968 DOI: 10.1007/S00439-019-02077-7 |
0.307 |
|
| 2019 |
Arboleda-Velasquez JF, Lopera F, O'Hare M, Delgado-Tirado S, Marino C, Chmielewska N, Saez-Torres KL, Amarnani D, Schultz AP, Sperling RA, Leyton-Cifuentes D, Chen K, Baena A, Aguillon D, Rios-Romenets S, ... ... Huentelman MJ, et al. Resistance to autosomal dominant Alzheimer's disease in an APOE3 Christchurch homozygote: a case report. Nature Medicine. PMID 31686034 DOI: 10.1038/S41591-019-0611-3 |
0.324 |
|
| 2019 |
McCullough CG, Szelinger S, Belnap N, Ramsey K, Schrauwen I, Claasen AM, Burke LW, Siniard AL, Huentelman MJ, Narayanan V, Craig DW. Utilizing RNA and Outlier Analysis to Identify an Intronic Splice-Altering Variant in AP4S1 in a Sibling Pair with Progressive Spastic Paraplegia. Human Mutation. PMID 31660686 DOI: 10.1002/Humu.23939 |
0.304 |
|
| 2019 |
Satizabal CL, Adams HHH, Hibar DP, White CC, Knol MJ, Stein JL, Scholz M, Sargurupremraj M, Jahanshad N, Roshchupkin GV, Smith AV, Bis JC, Jian X, Luciano M, Hofer E, ... ... Huentelman M, et al. Genetic architecture of subcortical brain structures in 38,851 individuals. Nature Genetics. PMID 31636452 DOI: 10.1038/S41588-019-0511-Y |
0.354 |
|
| 2019 |
Dumitrescu L, Barnes LL, Thambisetty M, Beecham G, Kunkle B, Bush WS, Gifford KA, Chibnik LB, Mukherjee S, De Jager PL, Kukull W, Crane PK, Resnick SM, Keene CD, Montine TJ, ... ... Huentelman M, et al. Sex differences in the genetic predictors of Alzheimer's pathology. Brain : a Journal of Neurology. 142: 2581-2589. PMID 31497858 DOI: 10.1093/Brain/Awz206 |
0.338 |
|
| 2019 |
Huentelman M, De Both M, Jepsen W, Piras IS, Talboom JS, Willeman M, Reiman EM, Hardy J, Myers AJ. Common BACE2 Polymorphisms are Associated with Altered Risk for Alzheimer's Disease and CSF Amyloid Biomarkers in APOE ε4 Non-Carriers. Scientific Reports. 9: 9640. PMID 31270419 DOI: 10.1038/S41598-019-45896-4 |
0.346 |
|
| 2019 |
Piras IS, Krate J, Delvaux E, Nolz J, Mastroeni DF, Persico AM, Jepsen WM, Beach TG, Huentelman MJ, Coleman PD. Transcriptome Changes in the Alzheimer's Disease Middle Temporal Gyrus: Importance of RNA Metabolism and Mitochondria-Associated Membrane Genes. Journal of Alzheimer's Disease : Jad. PMID 31256118 DOI: 10.3233/Jad-181113 |
0.331 |
|
| 2019 |
Talboom JS, Håberg AK, De Both MD, Naymik MA, Schrauwen I, Lewis CR, Bertinelli SF, Hammersland C, Fritz MA, Myers AJ, Hay M, Barnes CA, Glisky E, Ryan L, Huentelman MJ. Family history of Alzheimer's disease alters cognition and is modified by medical and genetic factors. Elife. 8. PMID 31210642 DOI: 10.7554/Elife.46179 |
0.327 |
|
| 2019 |
Piras IS, Krate J, Delvaux E, Nolz J, De Both MD, Mastroeni DF, Serrano GE, Sue LI, Beach TG, Coleman PD, Huentelman MJ. Association of AEBP1 and NRN1 RNA expression with Alzheimer's disease and neurofibrillary tangle density in middle temporal gyrus. Brain Research. 1719: 217-224. PMID 31176712 DOI: 10.1016/J.Brainres.2019.06.004 |
0.318 |
|
| 2019 |
Peter B, Dinu V, Liu L, Huentelman M, Naymik M, Lancaster H, Vose C, Schrauwen I. Exome Sequencing of Two Siblings with Sporadic Autism Spectrum Disorder and Severe Speech Sound Disorder Suggests Pleiotropic and Complex Effects. Behavior Genetics. PMID 30949922 DOI: 10.1007/S10519-019-09957-8 |
0.305 |
|
| 2019 |
Escott-Price V, Baker E, Shoai M, Leonenko G, Myers AJ, Huentelman M, Hardy J. Genetic analysis suggests high misassignment rates in clinical Alzheimer's cases and controls. Neurobiology of Aging. 77: 178-182. PMID 30851568 DOI: 10.1016/J.Neurobiolaging.2018.12.002 |
0.304 |
|
| 2019 |
Lewis CR, Henderson-Smith A, Breitenstein RS, Sowards HA, Piras IS, Huentelman MJ, Doane LD, Lemery-Chalfant K. Dopaminergic Gene Methylation is Associated with Cognitive Performance in a Childhood Monozygotic Twin Study. Epigenetics. PMID 30806146 DOI: 10.1080/15592294.2019.1583032 |
0.309 |
|
| 2019 |
Velazquez R, Ferreira E, Winslow W, Dave N, Piras IS, Naymik M, Huentelman MJ, Tran A, Caccamo A, Oddo S. Maternal choline supplementation ameliorates Alzheimer's disease pathology by reducing brain homocysteine levels across multiple generations. Molecular Psychiatry. PMID 30622336 DOI: 10.1038/S41380-018-0322-Z |
0.603 |
|
| 2018 |
Neuner SM, Heuer SE, Huentelman MJ, O'Connell KMS, Kaczorowski CC. Harnessing Genetic Complexity to Enhance Translatability of Alzheimer's Disease Mouse Models: A Path toward Precision Medicine. Neuron. PMID 30595332 DOI: 10.1016/J.Neuron.2018.11.040 |
0.329 |
|
| 2018 |
Piras IS, Manchia M, Huentelman MJ, Pinna F, Zai CC, Kennedy JL, Carpiniello B. Peripheral biomarkers in schizophrenia: A meta-analysis of microarray gene-expression datasets. The International Journal of Neuropsychopharmacology. PMID 30576541 DOI: 10.1093/Ijnp/Pyy103 |
0.321 |
|
| 2018 |
Petyuk VA, Chang R, Ramirez-Restrepo M, Beckmann ND, Henrion MYR, Piehowski PD, Zhu K, Wang S, Clarke J, Huentelman MJ, Xie F, Andreev V, Engel A, Guettoche T, Navarro L, et al. The human brainome: network analysis identifies HSPA2 as a novel Alzheimer's disease target. Brain : a Journal of Neurology. PMID 30137212 DOI: 10.1093/Brain/Awy215 |
0.356 |
|
| 2018 |
Ho H, Both M, Siniard A, Sharma S, Notwell JH, Wallace M, Leone DP, Nguyen A, Zhao E, Lee H, Zwilling D, Thompson KR, Braithwaite SP, Huentelman M, Portmann T. A Guide to Single-Cell Transcriptomics in Adult Rodent Brain: The Medium Spiny Neuron Transcriptome Revisited. Frontiers in Cellular Neuroscience. 12: 159. PMID 29970990 DOI: 10.3389/Fncel.2018.00159 |
0.32 |
|
| 2018 |
Gerald B, Ramsey K, Belnap N, Szelinger S, Siniard AL, Balak C, Russell M, Richholt R, De Both M, Claasen AM, Schrauwen I, Huentelman MJ, Craig DW, Rangasamy S, Narayanan V. Neonatal epileptic encephalopathy caused by de novo GNAO1 mutation misdiagnosed as atypical Rett syndrome: Cautions in interpretation of genomic test results. Seminars in Pediatric Neurology. 26: 28-32. PMID 29961512 DOI: 10.1016/J.Spen.2017.08.008 |
0.334 |
|
| 2018 |
Huentelman MJ, Piras IS, Siniard AL, De Both MD, Richholt RF, Balak CD, Jamshidi P, Bigio EH, Weintraub S, Loyer ET, Mesulam MM, Geula C, Rogalski EJ. Associations of Gene Variants With Superior Memory in SuperAgers. Frontiers in Aging Neuroscience. 10: 155. PMID 29896098 DOI: 10.3389/Fnagi.2018.00155 |
0.366 |
|
| 2018 |
Caselli RJ, Woodruff BK, Lindor NM, Wieben ED, Piras I, Huentelman MJ, Liu L. P3-098: Reduced Genomic Diversity As A Risk Factor For Nonfamilial Young Onset Alzheimer'S Disease Alzheimers & Dementia. 14. DOI: 10.1016/J.Jalz.2018.06.1454 |
0.314 |
|
| 2017 |
Ianov L, De Both M, Chawla MK, Rani A, Kennedy AJ, Piras I, Day JJ, Siniard A, Kumar A, Sweatt JD, Barnes CA, Huentelman MJ, Foster TC. Hippocampal Transcriptomic Profiles: Subfield Vulnerability to Age and Cognitive Impairment. Frontiers in Aging Neuroscience. 9: 383. PMID 29276487 DOI: 10.3389/Fnagi.2017.00383 |
0.304 |
|
| 2017 |
Caccamo A, Branca C, Piras IS, Ferreira E, Huentelman MJ, Liang WS, Readhead B, Dudley JT, Spangenberg EE, Green KN, Belfiore R, Winslow W, Oddo S. Necroptosis activation in Alzheimer's disease. Nature Neuroscience. PMID 28758999 DOI: 10.1038/Nn.4608 |
0.323 |
|
| 2017 |
Manchia M, Piras IS, Huentelman MJ, Pinna F, Zai CC, Kennedy JL, Carpiniello B. Pattern of gene expression in different stages of schizophrenia: Down-regulation of NPTX2 gene revealed by a meta-analysis of microarray datasets. European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology. PMID 28732597 DOI: 10.1016/J.Euroneuro.2017.07.002 |
0.345 |
|
| 2017 |
Escott-Price V, Myers AJ, Huentelman M, Hardy J. Polygenic Risk Score Analysis of Pathologically Confirmed Alzheimer's Disease. Annals of Neurology. PMID 28727176 DOI: 10.1002/Ana.24999 |
0.307 |
|
| 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, ... ... Huentelman MJ, 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 |
0.355 |
|
| 2017 |
Piras IS, Krate J, Schrauwen I, Corneveaux JJ, Serrano GE, Sue L, Beach TG, Huentelman MJ. Whole transcriptome profiling of the human hippocampus suggests an involvement of the KIBRA rs17070145 polymorphism in differential activation of the MAPK signaling pathway. Hippocampus. PMID 28380666 DOI: 10.1002/Hipo.22731 |
0.335 |
|
| 2017 |
Hibar DP, Adams HH, Jahanshad N, Chauhan G, Stein JL, Hofer E, Renteria ME, Bis JC, Arias-Vasquez A, Ikram MK, Desrivières S, Vernooij MW, Abramovic L, Alhusaini S, Amin N, ... ... Huentelman M, et al. Novel genetic loci associated with hippocampal volume. Nature Communications. 8: 13624. PMID 28098162 DOI: 10.1038/Ncomms13624 |
0.36 |
|
| 2017 |
Huentelman MJ, Piras I, Siniard A, De Both M, Richholt R, Bigio EH, Weintraub S, Loyer E, Mesulam M, Geula C, Rogalski EJ. [P4-081]: ASSOCIATION OF MAP2K3
GENE VARIATION AND THE SUPERAGING PHENOTYPE DETECTED BY WHOLE EXOME SEQUENCING Alzheimer's & Dementia. 13: P1290-P1290. DOI: 10.1016/J.Jalz.2017.06.1946 |
0.306 |
|
| 2016 |
Henderson-Smith A, Corneveaux JJ, De Both M, Cuyugan L, Liang WS, Huentelman M, Adler C, Driver-Dunckley E, Beach TG, Dunckley TL. Next-generation profiling to identify the molecular etiology of Parkinson dementia. Neurology. Genetics. 2: e75. PMID 27275011 DOI: 10.1212/Nxg.0000000000000075 |
0.307 |
|
| 2016 |
Sommen M, Schrauwen I, Vandeweyer G, Boeckx N, Corneveaux JJ, van den Ende J, Boudewyns A, De Leenheer E, Janssens S, Claes K, Verstreken M, Strenzke N, Predöhl F, Wuyts W, Mortier G, ... ... Huentelman MJ, et al. DNA Diagnostics of Hereditary Hearing Loss: A Targeted Resequencing Approach Combined With a Mutation Classification System. Human Mutation. PMID 27068579 DOI: 10.1002/Humu.22999 |
0.333 |
|
| 2015 |
Turk MN, Huentelman MJ. Nucleic acid-based risk factors and biomarkers: a future perspective on their use and development in Alzheimer's disease. Personalized Medicine. 12: 475-482. PMID 29749892 DOI: 10.2217/Pme.15.18 |
0.33 |
|
| 2015 |
Lalli MA, Bettcher BM, Arcila ML, Garcia G, Guzman C, Madrigal L, Ramirez L, Acosta-Uribe J, Baena A, Wojta KJ, Coppola G, Fitch R, de Both MD, Huentelman MJ, Reiman EM, et al. Whole-genome sequencing suggests a chemokine gene cluster that modifies age at onset in familial Alzheimer's disease. Molecular Psychiatry. PMID 26324103 DOI: 10.1038/Mp.2015.131 |
0.392 |
|
| 2015 |
Hunter JM, Ahearn ME, Balak CD, Liang WS, Kurdoglu A, Corneveaux JJ, Russell M, Huentelman MJ, Craig DW, Carpten J, Coons SW, DeMello DE, Hall JG, Bernes SM, Baumbach-Reardon L. Novel pathogenic variants and genes for myopathies identified by whole exome sequencing. Molecular Genetics & Genomic Medicine. 3: 283-301. PMID 26247046 DOI: 10.1002/Mgg3.142 |
0.312 |
|
| 2015 |
Chen CH, Peng Q, Schork AJ, Lo MT, Fan CC, Wang Y, Desikan RS, Bettella F, Hagler DJ, Westlye LT, Kremen WS, Jernigan TL, Hellard SL, ... ... Huentelman M, et al. Large-scale genomics unveil polygenic architecture of human cortical surface area. Nature Communications. 6: 7549. PMID 26189703 DOI: 10.1038/Ncomms8549 |
0.303 |
|
| 2015 |
Schrauwen I, Szelinger S, Siniard AL, Kurdoglu A, Corneveaux JJ, Malenica I, Richholt R, Van Camp G, De Both M, Swaminathan S, Turk M, Ramsey K, Craig DW, Narayanan V, Huentelman MJ. A Frame-Shift Mutation in CAV1 Is Associated with a Severe Neonatal Progeroid and Lipodystrophy Syndrome. Plos One. 10: e0131797. PMID 26176221 DOI: 10.1371/Journal.Pone.0131797 |
0.328 |
|
| 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, ... ... Huentelman MJ, 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 |
0.345 |
|
| 2015 |
Fransen E, Bonneux S, Corneveaux JJ, Schrauwen I, Di Berardino F, White CH, Ohmen JD, Van de Heyning P, Ambrosetti U, Huentelman MJ, Van Camp G, Friedman RA. Genome-wide association analysis demonstrates the highly polygenic character of age-related hearing impairment. European Journal of Human Genetics : Ejhg. 23: 110-5. PMID 24939585 DOI: 10.1038/Ejhg.2014.56 |
0.361 |
|
| 2015 |
Neuner SM, Wilmott L, DeBoth M, Shapaker T, Ingels J, Lu L, Williams R, Kempermann G, Huentelman M, Kaczorowski CC. Multi-scale study of normal aging predicts novel late-onset Alzheimer's disease risk variants Bmc Bioinformatics. 16: P11. DOI: 10.1186/1471-2105-16-S15-P11 |
0.308 |
|
| 2014 |
Schrauwen I, Barber RM, Schatzberg SJ, Siniard AL, Corneveaux JJ, Porter BF, Vernau KM, Keesler RI, Matiasek K, Flegel T, Miller AD, Southard T, Mariani CL, Johnson GC, Huentelman MJ. Identification of novel genetic risk loci in Maltese dogs with necrotizing meningoencephalitis and evidence of a shared genetic risk across toy dog breeds. Plos One. 9: e112755. PMID 25393235 DOI: 10.1371/Journal.Pone.0112755 |
0.317 |
|
| 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, 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 |
0.329 |
|
| 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, 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 |
0.339 |
|
| 2014 |
Escott-Price V, Bellenguez C, Wang LS, Choi SH, Harold D, Jones L, Holmans P, Gerrish A, Vedernikov A, Richards A, DeStefano AL, Lambert JC, Ibrahim-Verbaas CA, Naj AC, Sims R, ... ... Huentelman MJ, et al. Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease. Plos One. 9: e94661. PMID 24922517 DOI: 10.1371/Journal.Pone.0094661 |
0.398 |
|
| 2014 |
Zhang K, Huentelman MJ, Rao F, Sun EI, Corneveaux JJ, Schork AJ, Wei Z, Waalen J, Miramontes-Gonzalez JP, Hightower CM, Maihofer AX, Mahata M, Pastinen T, Ehret GB, et al. Genetic implication of a novel thiamine transporter in human hypertension. Journal of the American College of Cardiology. 63: 1542-55. PMID 24509276 DOI: 10.1016/J.Jacc.2014.01.007 |
0.341 |
|
| 2014 |
Dean DC, Jerskey BA, Chen K, Protas H, Thiyyagura P, Roontiva A, O'Muircheartaigh J, Dirks H, Waskiewicz N, Lehman K, Siniard AL, Turk MN, Hua X, Madsen SK, Thompson PM, ... ... Huentelman MJ, et al. Brain differences in infants at differential genetic risk for late-onset Alzheimer disease: a cross-sectional imaging study. Jama Neurology. 71: 11-22. PMID 24276092 DOI: 10.1001/Jamaneurol.2013.4544 |
0.309 |
|
| 2014 |
Shen L, Thompson PM, Potkin SG, Bertram L, Farrer LA, Foroud TM, Green RC, Hu X, Huentelman MJ, Kim S, Kauwe JS, Li Q, Liu E, Macciardi F, Moore JH, et al. Genetic analysis of quantitative phenotypes in AD and MCI: imaging, cognition and biomarkers. Brain Imaging and Behavior. 8: 183-207. PMID 24092460 DOI: 10.1007/S11682-013-9262-Z |
0.364 |
|
| 2014 |
Ramanan VK, Risacher SL, Nho K, Kim S, Swaminathan S, Shen L, Foroud TM, Hakonarson H, Huentelman MJ, Aisen PS, Petersen RC, Green RC, Jack CR, Koeppe RA, Jagust WJ, et al. APOE and BCHE as modulators of cerebral amyloid deposition: a florbetapir PET genome-wide association study. Molecular Psychiatry. 19: 351-7. PMID 23419831 DOI: 10.1038/Mp.2013.19 |
0.357 |
|
| 2014 |
Hendricks WP, Zismann V, Button B, Legendre C, Tembe W, Yin H, Bittner M, Berry D, Huentelman M, Khanna C, LoRusso P, Breen M, Sekulic A, Trent J. Abstract 3417: The genomic landscape of canine melanoma reveals broad mutational heterogeneity and recurrent patterns of structural variation Cancer Research. 74: 3417-3417. DOI: 10.1158/1538-7445.Am2014-3417 |
0.32 |
|
| 2014 |
Ramanan VK, Nho K, Risacher SL, Kim S, Shen L, Swaminathan S, Foroud TM, Aisen P, Hakonarson H, Huentelman M, Jack C, Jagust W, Petersen RC, Potkin S, Shaw L, et al. P3-024: NEXT-GENERATION SEQUENCING OF THE BCHE LOCUS IDENTIFIES A FUNCTIONAL SNP ASSOCIATED WITH ALZHEIMER'S DISEASE BIOMARKERS AND AGE OF ONSET Alzheimer's & Dementia. 10: P636-P636. DOI: 10.1016/J.Jalz.2014.05.1111 |
0.383 |
|
| 2013 |
Shulman JM, Chen K, Keenan BT, Chibnik LB, Fleisher A, Thiyyagura P, Roontiva A, McCabe C, Patsopoulos NA, Corneveaux JJ, Yu L, Huentelman MJ, Evans DA, Schneider JA, Reiman EM, et al. Genetic susceptibility for Alzheimer disease neuritic plaque pathology. Jama Neurology. 70: 1150-7. PMID 23836404 DOI: 10.1001/Jamaneurol.2013.2815 |
0.372 |
|
| 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, ... ... Huentelman MJ, 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 |
0.332 |
|
| 2013 |
Giraldo M, Lopera F, Siniard AL, Corneveaux JJ, Schrauwen I, Carvajal J, Muñoz C, Ramirez-Restrepo M, Gaiteri C, Myers AJ, Caselli RJ, Kosik KS, Reiman EM, Huentelman MJ. Variants in triggering receptor expressed on myeloid cells 2 are associated with both behavioral variant frontotemporal lobar degeneration and Alzheimer's disease. Neurobiology of Aging. 34: 2077.e11-8. PMID 23582655 DOI: 10.1016/J.Neurobiolaging.2013.02.016 |
0.379 |
|
| 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, ... ... Huentelman MJ, 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 |
0.36 |
|
| 2012 |
Swaminathan S, Huentelman MJ, Corneveaux JJ, Myers AJ, Faber KM, Foroud T, Mayeux R, Shen L, Kim S, Turk M, Hardy J, Reiman EM, Saykin AJ. Analysis of copy number variation in Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individuals. Plos One. 7: e50640. PMID 23227193 DOI: 10.1371/Journal.Pone.0050640 |
0.4 |
|
| 2012 |
Fleisher AS, Chen K, Quiroz YT, Jakimovich LJ, Gomez MG, Langois CM, Langbaum JB, Ayutyanont N, Roontiva A, Thiyyagura P, Lee W, Mo H, Lopez L, Moreno S, Acosta-Baena N, ... ... Huentelman MJ, et al. Florbetapir PET analysis of amyloid-β deposition in the presenilin 1 E280A autosomal dominant Alzheimer's disease kindred: a cross-sectional study. The Lancet. Neurology. 11: 1057-65. PMID 23137949 DOI: 10.1016/S1474-4422(12)70227-2 |
0.31 |
|
| 2012 |
Reiman EM, Quiroz YT, Fleisher AS, Chen K, Velez-Pardo C, Jimenez-Del-Rio M, Fagan AM, Shah AR, Alvarez S, Arbelaez A, Giraldo M, Acosta-Baena N, Sperling RA, Dickerson B, Stern CE, ... ... Huentelman MJ, et al. Brain imaging and fluid biomarker analysis in young adults at genetic risk for autosomal dominant Alzheimer's disease in the presenilin 1 E280A kindred: a case-control study. The Lancet. Neurology. 11: 1048-56. PMID 23137948 DOI: 10.1016/S1474-4422(12)70228-4 |
0.344 |
|
| 2012 |
Keenan BT, Shulman JM, Chibnik LB, Raj T, Tran D, Sabuncu MR, Allen AN, Corneveaux JJ, Hardy JA, Huentelman MJ, Lemere CA, Myers AJ, Nicholson-Weller A, Reiman EM, et al. A coding variant in CR1 interacts with APOE-ε4 to influence cognitive decline. Human Molecular Genetics. 21: 2377-88. PMID 22343410 DOI: 10.1093/Hmg/Dds054 |
0.314 |
|
| 2012 |
De Jager PL, Shulman JM, Chibnik LB, Keenan BT, Raj T, Wilson RS, Yu L, Leurgans SE, Tran D, Aubin C, Anderson CD, Biffi A, Corneveaux JJ, Huentelman MJ, et al. A genome-wide scan for common variants affecting the rate of age-related cognitive decline. Neurobiology of Aging. 33: 1017.e1-15. PMID 22054870 DOI: 10.1016/J.Neurobiolaging.2011.09.033 |
0.336 |
|
| 2012 |
Swaminathan S, Shen L, Risacher SL, Yoder KK, West JD, Kim S, Nho K, Foroud T, Inlow M, Potkin SG, Huentelman MJ, Craig DW, Jagust WJ, Koeppe RA, Mathis CA, et al. Amyloid pathway-based candidate gene analysis of [(11)C]PiB-PET in the Alzheimer's Disease Neuroimaging Initiative (ADNI) cohort. Brain Imaging and Behavior. 6: 1-15. PMID 21901424 DOI: 10.1007/S11682-011-9136-1 |
0.371 |
|
| 2012 |
Nho K, Corneveaux J, Kim S, Lin H, Risacher S, Shen L, Liu Y, Foroud T, Inlow M, Siniard A, Reiman R, Green R, Jack C, Weiner M, Huentelman M, et al. Integrating whole-exome sequencing and imaging genetics to identify single-nucleotide variants associated with rate of hippocampal neurodegeneration in APOE-ε3/ε3 males with mild cognitive impairment Alzheimers & Dementia. 8. DOI: 10.1016/J.Jalz.2013.08.116 |
0.302 |
|
| 2011 |
Barber RM, Schatzberg SJ, Corneveaux JJ, Allen AN, Porter BF, Pruzin JJ, Platt SR, Kent M, Huentelman MJ. Identification of risk loci for necrotizing meningoencephalitis in Pug dogs. The Journal of Heredity. 102: S40-6. PMID 21846746 DOI: 10.1093/Jhered/Esr048 |
0.335 |
|
| 2011 |
Swaminathan S, Kim S, Shen L, Risacher SL, Foroud T, Pankratz N, Potkin SG, Huentelman MJ, Craig DW, Weiner MW, Saykin AJ, The Alzheimer's Disease Neuroimaging Initiative Adni. Genomic Copy Number Analysis in Alzheimer's Disease and Mild Cognitive Impairment: An ADNI Study. International Journal of Alzheimer's Disease. 2011: 729478. PMID 21660214 DOI: 10.4061/2011/729478 |
0.382 |
|
| 2011 |
Hibar DP, Stein JL, Kohannim O, Jahanshad N, Saykin AJ, Shen L, Kim S, Pankratz N, Foroud T, Huentelman MJ, Potkin SG, Jack CR, Weiner MW, Toga AW, Thompson PM, et al. Voxelwise gene-wide association study (vGeneWAS): multivariate gene-based association testing in 731 elderly subjects. Neuroimage. 56: 1875-91. PMID 21497199 DOI: 10.1016/J.Neuroimage.2011.03.077 |
0.386 |
|
| 2011 |
Chibnik LB, Shulman JM, Leurgans SE, Schneider JA, Wilson RS, Tran D, Aubin C, Buchman AS, Heward CB, Myers AJ, Hardy JA, Huentelman MJ, Corneveaux JJ, Reiman EM, Evans DA, et al. CR1 is associated with amyloid plaque burden and age-related cognitive decline. Annals of Neurology. 69: 560-9. PMID 21391232 DOI: 10.1002/Ana.22277 |
0.329 |
|
| 2011 |
Pawlowski TL, Huentelman MJ. Identification of a common variant affecting human episodic memory performance using a pooled genome-wide association approach: a case study of disease gene identification. Methods in Molecular Biology (Clifton, N.J.). 700: 261-9. PMID 21204039 DOI: 10.1007/978-1-61737-954-3_17 |
0.355 |
|
| 2011 |
Kim S, Swaminathan S, Shen L, Risacher SL, Nho K, Foroud T, Shaw LM, Trojanowski JQ, Potkin SG, Huentelman MJ, Craig DW, DeChairo BM, Aisen PS, Petersen RC, Weiner MW, et al. Genome-wide association study of CSF biomarkers Abeta1-42, t-tau, and p-tau181p in the ADNI cohort. Neurology. 76: 69-79. PMID 21123754 DOI: 10.1212/Wnl.0B013E318204A397 |
0.369 |
|
| 2011 |
Liang WS, Chen K, Lee W, Sidhar K, Corneveaux JJ, Allen AN, Myers A, Villa S, Meechoovet B, Pruzin J, Bandy D, Fleisher AS, Langbaum JB, Huentelman MJ, Jensen K, et al. Association between GAB2 haplotype and higher glucose metabolism in Alzheimer's disease-affected brain regions in cognitively normal APOEε4 carriers. Neuroimage. 54: 1896-902. PMID 20888920 DOI: 10.1016/J.Neuroimage.2010.09.066 |
0.356 |
|
| 2011 |
Shulman J, Chipendo P, Chibnik L, Keenan B, Tran D, Aubin C, Corneveaux J, Huentelman M, Kramer P, Reiman E, Schneider J, Evans D, Bennett D, Feany M, Jager PD. Integrating genome-wide association and functional validation to understand susceptibility for Alzheimer's pathology Alzheimers & Dementia. 7. DOI: 10.1016/J.Jalz.2011.05.2390 |
0.32 |
|
| 2010 |
Valla J, Yaari R, Wolf AB, Kusne Y, Beach TG, Roher AE, Corneveaux JJ, Huentelman MJ, Caselli RJ, Reiman EM. Reduced posterior cingulate mitochondrial activity in expired young adult carriers of the APOE ε4 allele, the major late-onset Alzheimer's susceptibility gene. Journal of Alzheimer's Disease : Jad. 22: 307-13. PMID 20847408 DOI: 10.3233/Jad-2010-100129 |
0.305 |
|
| 2010 |
Schneider A, Huentelman MJ, Kremerskothen J, Duning K, Spoelgen R, Nikolich K. KIBRA: A New Gateway to Learning and Memory? Frontiers in Aging Neuroscience. 2: 4. PMID 20552044 DOI: 10.3389/Neuro.24.004.2010 |
0.33 |
|
| 2010 |
Corneveaux JJ, Myers AJ, Allen AN, Pruzin JJ, Ramirez M, Engel A, Nalls MA, Chen K, Lee W, Chewning K, Villa SE, Meechoovet HB, Gerber JD, Frost D, Benson HL, ... ... Huentelman MJ, et al. Association of CR1, CLU and PICALM with Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individuals. Human Molecular Genetics. 19: 3295-301. PMID 20534741 DOI: 10.1093/Hmg/Ddq221 |
0.348 |
|
| 2010 |
Saykin AJ, Shen L, Foroud TM, Potkin SG, Swaminathan S, Kim S, Risacher SL, Nho K, Huentelman MJ, Craig DW, Thompson PM, Stein JL, Moore JH, Farrer LA, Green RC, et al. Alzheimer's Disease Neuroimaging Initiative biomarkers as quantitative phenotypes: Genetics core aims, progress, and plans. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. 6: 265-73. PMID 20451875 DOI: 10.1016/J.Jalz.2010.03.013 |
0.353 |
|
| 2010 |
Stein JL, Hua X, Morra JH, Lee S, Hibar DP, Ho AJ, Leow AD, Toga AW, Sul JH, Kang HM, Eskin E, Saykin AJ, Shen L, Foroud T, Pankratz N, ... Huentelman MJ, et al. Genome-wide analysis reveals novel genes influencing temporal lobe structure with relevance to neurodegeneration in Alzheimer's disease. Neuroimage. 51: 542-54. PMID 20197096 DOI: 10.1016/J.Neuroimage.2010.02.068 |
0.379 |
|
| 2010 |
Stein JL, Hua X, Lee S, Ho AJ, Leow AD, Toga AW, Saykin AJ, Shen L, Foroud T, Pankratz N, Huentelman MJ, Craig DW, Gerber JD, Allen AN, Corneveaux JJ, et al. Voxelwise genome-wide association study (vGWAS). Neuroimage. 53: 1160-74. PMID 20171287 DOI: 10.1016/J.Neuroimage.2010.02.032 |
0.371 |
|
| 2010 |
Shen L, Kim S, Risacher SL, Nho K, Swaminathan S, West JD, Foroud T, Pankratz N, Moore JH, Sloan CD, Huentelman MJ, Craig DW, Dechairo BM, Potkin SG, Jack CR, et al. Whole genome association study of brain-wide imaging phenotypes for identifying quantitative trait loci in MCI and AD: A study of the ADNI cohort. Neuroimage. 53: 1051-63. PMID 20100581 DOI: 10.1016/J.Neuroimage.2010.01.042 |
0.379 |
|
| 2010 |
Van Laer L, Huyghe JR, Hannula S, Van Eyken E, Stephan DA, Mäki-Torkko E, Aikio P, Fransen E, Lysholm-Bernacchi A, Sorri M, Huentelman MJ, Van Camp G. A genome-wide association study for age-related hearing impairment in the Saami. European Journal of Human Genetics : Ejhg. 18: 685-93. PMID 20068591 DOI: 10.1038/Ejhg.2009.234 |
0.35 |
|
| 2010 |
Roses AD, Lutz MW, Amrine-Madsen H, Saunders AM, Crenshaw DG, Sundseth SS, Huentelman MJ, Welsh-Bohmer KA, Reiman EM. A TOMM40 variable-length polymorphism predicts the age of late-onset Alzheimer's disease. The Pharmacogenomics Journal. 10: 375-84. PMID 20029386 DOI: 10.1038/Tpj.2009.69 |
0.329 |
|
| 2010 |
Huyghe JR, Fransen E, Hannula S, Van Laer L, Van Eyken E, Mäki-Torkko E, Lysholm-Bernacchi A, Aikio P, Stephan DA, Sorri M, Huentelman MJ, Van Camp G. Genome-wide SNP analysis reveals no gain in power for association studies of common variants in the Finnish Saami. European Journal of Human Genetics : Ejhg. 18: 569-74. PMID 19935831 DOI: 10.1038/Ejhg.2009.210 |
0.326 |
|
| 2010 |
Corneveaux JJ, Liang WS, Reiman EM, Webster JA, Myers AJ, Zismann VL, Joshipura KD, Pearson JV, Hu-Lince D, Craig DW, Coon KD, Dunckley T, Bandy D, Lee W, Chen K, ... ... Huentelman MJ, et al. Evidence for an association between KIBRA and late-onset Alzheimer's disease. Neurobiology of Aging. 31: 901-9. PMID 18789830 DOI: 10.1016/J.Neurobiolaging.2008.07.014 |
0.369 |
|
| 2010 |
Huentelman M, Corneveaux J, Myers A, Allen A, Pruzin J, Nalls M, Chibnik L, Singleton A, Craig D, Van Keuren-Jensen K, Dunckley T, Bennett D, DeJager P, Hardy J, Reiman E. S4-03-02: Genome-Wide Association Study for Alzheimer's Disease Risk in a Large Cohort Of Clinically Characterized And Neuropathologically Verified Subjects Alzheimer's & Dementia. 6: e13-e13. DOI: 10.1016/J.Jalz.2010.08.041 |
0.319 |
|
| 2009 |
Webster JA, Gibbs JR, Clarke J, Ray M, Zhang W, Holmans P, Rohrer K, Zhao A, Marlowe L, Kaleem M, McCorquodale DS, Cuello C, Leung D, Bryden L, Nath P, ... ... Huentelman MJ, et al. Genetic control of human brain transcript expression in Alzheimer disease. American Journal of Human Genetics. 84: 445-58. PMID 19361613 DOI: 10.1016/J.Ajhg.2009.03.011 |
0.36 |
|
| 2009 |
Schrauwen I, Ealy M, Huentelman MJ, Thys M, Homer N, Vanderstraeten K, Fransen E, Corneveaux JJ, Craig DW, Claustres M, Cremers CW, Dhooge I, Van de Heyning P, Vincent R, Offeciers E, et al. A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosis. American Journal of Human Genetics. 84: 328-38. PMID 19230858 DOI: 10.1016/J.Ajhg.2009.01.023 |
0.352 |
|
| 2009 |
Pawlowski TL, Bellush LL, Wright AW, Walker JP, Colvin RA, Huentelman MJ. Hippocampal gene expression changes during age-related cognitive decline Brain Research. 1256: 101-110. PMID 19133237 DOI: 10.1016/J.Brainres.2008.12.039 |
0.321 |
|
| 2009 |
Friedman RA, Van Laer L, Huentelman MJ, Sheth SS, Van Eyken E, Corneveaux JJ, Tembe WD, Halperin RF, Thorburn AQ, Thys S, Bonneux S, Fransen E, Huyghe J, Pyykkö I, Cremers CW, et al. GRM7 variants confer susceptibility to age-related hearing impairment. Human Molecular Genetics. 18: 785-96. PMID 19047183 DOI: 10.1093/Hmg/Ddn402 |
0.33 |
|
| 2009 |
Hilgert N, Huentelman MJ, Thorburn AQ, Fransen E, Dieltjens N, Mueller-Malesinska M, Pollak A, Skorka A, Waligora J, Ploski R, Castorina P, Primignani P, Ambrosetti U, Murgia A, Orzan E, et al. Phenotypic variability of patients homozygous for the GJB2 mutation 35delG cannot be explained by the influence of one major modifier gene. European Journal of Human Genetics : Ejhg. 17: 517-24. PMID 18985073 DOI: 10.1038/Ejhg.2008.201 |
0.337 |
|
| 2008 |
Webster JA, Myers AJ, Pearson JV, Craig DW, Hu-Lince D, Coon KD, Zismann VL, Beach T, Leung D, Bryden L, Halperin RF, Marlowe L, Kaleem M, Huentelman MJ, Joshipura K, et al. Sorl1 as an Alzheimer's disease predisposition gene? Neuro-Degenerative Diseases. 5: 60-4. PMID 17975299 DOI: 10.1159/000110789 |
0.379 |
|
| 2007 |
Myers AJ, Gibbs JR, Webster JA, Rohrer K, Zhao A, Marlowe L, Kaleem M, Leung D, Bryden L, Nath P, Zismann VL, Joshipura K, Huentelman MJ, Hu-Lince D, Coon KD, et al. A survey of genetic human cortical gene expression. Nature Genetics. 39: 1494-9. PMID 17982457 DOI: 10.1038/Ng.2007.16 |
0.344 |
|
| 2007 |
Dunckley T, Huentelman MJ, Craig DW, Pearson JV, Szelinger S, Joshipura K, Halperin RF, Stamper C, Jensen KR, Letizia D, Hesterlee SE, Pestronk A, Levine T, Bertorini T, Graves MC, et al. Whole-genome analysis of sporadic amyotrophic lateral sclerosis. The New England Journal of Medicine. 357: 775-88. PMID 17671248 DOI: 10.1056/Nejmoa070174 |
0.321 |
|
| 2007 |
Huentelman MJ, Papassotiropoulos A, Craig DW, Hoerndli FJ, Pearson JV, Huynh KD, Corneveaux J, Hänggi J, Mondadori CR, Buchmann A, Reiman EM, Henke K, de Quervain DJ, Stephan DA. Calmodulin-binding transcription activator 1 (CAMTA1) alleles predispose human episodic memory performance. Human Molecular Genetics. 16: 1469-77. PMID 17470457 DOI: 10.1093/Hmg/Ddm097 |
0.313 |
|
| 2007 |
Melquist S, Craig DW, Huentelman MJ, Crook R, Pearson JV, Baker M, Zismann VL, Gass J, Adamson J, Szelinger S, Corneveaux J, Cannon A, Coon KD, Lincoln S, Adler C, et al. Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphisms. American Journal of Human Genetics. 80: 769-78. PMID 17357082 DOI: 10.1086/513320 |
0.334 |
|
| 2007 |
Pearson JV, Huentelman MJ, Halperin RF, Tembe WD, Melquist S, Homer N, Brun M, Szelinger S, Coon KD, Zismann VL, Webster JA, Beach T, Sando SB, Aasly JO, Heun R, et al. Identification of the genetic basis for complex disorders by use of pooling-based genomewide single-nucleotide-polymorphism association studies. American Journal of Human Genetics. 80: 126-39. PMID 17160900 DOI: 10.1086/510686 |
0.346 |
|
| 2006 |
Der Sarkissian S, Huentelman MJ, Stewart J, Katovich MJ, Raizada MK. ACE2: A novel therapeutic target for cardiovascular diseases. Progress in Biophysics and Molecular Biology. 91: 163-98. PMID 16009403 DOI: 10.1016/J.Pbiomolbio.2005.05.011 |
0.507 |
|
| 2006 |
Escott-Price V, Baker EA, Myers A, Huentelman MJ, Hardy J. P2-307: GENETIC ANALYSIS SUGGESTS HIGH MISASSIGNMENT RATE IN BOTH ALZHEIMER'S DISEASE CASES AND CONTROLS Alzheimer's & Dementia. 14: P800-P800. DOI: 10.1016/J.Jalz.2018.06.997 |
0.308 |
|
| 2006 |
Neuner SM, Philip V, Huentelman MJ, Kaczorowski CC. P4-048: IDENTIFYING PRESYMPTOMATIC GENE SIGNATURES PREDICTIVE OF RESILIENCE TO ALZHEIMER'S Alzheimer's & Dementia. 14: P1451-P1452. DOI: 10.1016/J.Jalz.2018.06.2450 |
0.306 |
|
| 2006 |
Melquist S, Huentelman MJ, Craig DW, Baker M, Crook R, Pearson JV, Zisman VL, Gass J, Adamson J, Szelinger S, Cournevaux JJ, Cannon A, Coon KD, Dickson DW, Stephan D, et al. P3-163: Identification of a novel risk gene for progressive supranuclear palsy by a genome-wide scan of 500,288 SNPs Alzheimer's & Dementia. 2: S422-S422. DOI: 10.1016/J.Jalz.2006.05.1431 |
0.333 |
|
| 2005 |
Craig DW, Huentelman MJ, Hu-Lince D, Zismann VL, Kruer MC, Lee AM, Puffenberger EG, Pearson JM, Stephan DA. Identification of disease causing loci using an array-based genotyping approach on pooled DNA. Bmc Genomics. 6: 138. PMID 16197552 DOI: 10.1186/1471-2164-6-138 |
0.322 |
|
| 2005 |
Hu-Lince D, Craig DW, Huentelman MJ, Stephan DA. The Autism Genome Project: goals and strategies. American Journal of Pharmacogenomics : Genomics-Related Research in Drug Development and Clinical Practice. 5: 233-46. PMID 16078860 DOI: 10.2165/00129785-200505040-00004 |
0.336 |
|
| 2005 |
Huentelman MJ, Grobe JL, Vazquez J, Stewart JM, Mecca AP, Katovich MJ, Ferrario CM, Raizada MK. Protection from angiotensin II-induced cardiac hypertrophy and fibrosis by systemic lentiviral delivery of ACE2 in rats. Experimental Physiology. 90: 783-90. PMID 16049057 DOI: 10.1113/Expphysiol.2005.031096 |
0.48 |
|
| 2005 |
Katovich MJ, Grobe JL, Huentelman M, Raizada MK. Angiotensin-converting enzyme 2 as a novel target for gene therapy for hypertension. Experimental Physiology. 90: 299-305. PMID 15640278 DOI: 10.1113/Expphysiol.2004.028522 |
0.529 |
|
| 2004 |
Huentelman MJ, Zubcevic J, Hernández Prada JA, Xiao X, Dimitrov DS, Raizada MK, Ostrov DA. Structure-based discovery of a novel angiotensin-converting enzyme 2 inhibitor. Hypertension. 44: 903-6. PMID 15492138 DOI: 10.1161/01.Hyp.0000146120.29648.36 |
0.466 |
|
| 2004 |
Huentelman MJ, Zubcevic J, Katovich MJ, Raizada MK. Cloning and characterization of a secreted form of angiotensin-converting enzyme 2. Regulatory Peptides. 122: 61-7. PMID 15380922 DOI: 10.1016/J.Regpep.2004.05.003 |
0.398 |
|
| 2004 |
Metcalfe BL, Huentelman MJ, Parilak LD, Taylor DG, Katovich MJ, Knot HJ, Sumners C, Raizada MK. Prevention of cardiac hypertrophy by angiotensin II type-2 receptor gene transfer. Hypertension. 43: 1233-8. PMID 15166182 DOI: 10.1161/01.Hyp.0000127563.14064.Fd |
0.724 |
|
| 2003 |
Coleman JE, Huentelman MJ, Kasparov S, Metcalfe BL, Paton JF, Katovich MJ, Semple-Rowland SL, Raizada MK. Efficient large-scale production and concentration of HIV-1-based lentiviral vectors for use in vivo. Physiological Genomics. 12: 221-8. PMID 12488511 DOI: 10.1152/Physiolgenomics.00135.2002 |
0.715 |
|
| 2002 |
Huentelman MJ, Reaves PY, Katovich MJ, Raizada MK. Large-scale production of retroviral vectors for systemic gene delivery. Methods in Enzymology. 346: 562-73. PMID 11883091 DOI: 10.1016/S0076-6879(02)46077-6 |
0.477 |
|
| 2001 |
Metcalfe BL, Sellers KW, Jeng MJ, Huentelman MJ, Katovich MJ, Raizada MK. Gene therapy for cardiovascular disorders: is there a future? Annals of the New York Academy of Sciences. 953: 31-42. PMID 11795421 DOI: 10.1111/J.1749-6632.2001.Tb11358.X |
0.693 |
|
| 2001 |
Pachori AS, Huentelman MJ, Francis SC, Gelband CH, Katovich MJ, Raizada MK. The future of hypertension therapy: sense, antisense, or nonsense? Hypertension. 37: 357-64. PMID 11230300 DOI: 10.1161/01.Hyp.37.2.357 |
0.455 |
|
| Show low-probability matches. |