| Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease JC Lambert, CA Ibrahim-Verbaas, D Harold, AC Naj, R Sims, ... Nature genetics 45 (12), 1452-1458, 2013 | 2821 | 2013 |
| Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease AC Naj, G Jun, GW Beecham, LS Wang, BN Vardarajan, J Buros, ... Nature genetics 43 (5), 436-441, 2011 | 1641 | 2011 |
| A test for linkage and association in general pedigrees: the pedigree disequilibrium test ER Martin, SA Monks, LL Warren, NL Kaplan The American Journal of Human Genetics 67 (1), 146-154, 2000 | 694 | 2000 |
| Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing BW Kunkle, B Grenier-Boley, R Sims, JC Bis, V Damotte, AC Naj, ... Nature genetics 51 (3), 414-430, 2019 | 592 | 2019 |
| Mitochondrial polymorphisms significantly reduce the risk of Parkinson disease JM Van Der Walt, KK Nicodemus, ER Martin, WK Scott, MA Nance, ... The American Journal of Human Genetics 72 (4), 804-811, 2003 | 578 | 2003 |
| A multiple testing correction method for genetic association studies using correlated single nucleotide polymorphisms X Gao, J Starmer, ER Martin Genetic Epidemiology: The Official Publication of the International Genetic …, 2008 | 547 | 2008 |
| Variation in the miRNA-433 binding site of FGF20 confers risk for Parkinson disease by overexpression of α-synuclein G Wang, JM van der Walt, G Mayhew, YJ Li, S Züchner, WK Scott, ... The American Journal of Human Genetics 82 (2), 283-289, 2008 | 501 | 2008 |
| Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database CM Lill, JT Roehr, MB McQueen, FK Kavvoura, S Bagade, BMM Schjeide, ... PLoS Genet 8 (3), e1002548, 2012 | 499 | 2012 |
| No gene is an island: the flip-flop phenomenon PI Lin, JM Vance, MA Pericak-Vance, ER Martin The American Journal of Human Genetics 80 (3), 531-538, 2007 | 476 | 2007 |
| Genome‐Wide Association Study Confirms SNPs in SNCA and the MAPT Region as Common Risk Factors for Parkinson Disease TL Edwards, WK Scott, C Almonte, A Burt, EH Powell, GW Beecham, ... Annals of human genetics 74 (2), 97-109, 2010 | 466 | 2010 |
| Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease R Sims, SJ Van Der Lee, AC Naj, C Bellenguez, N Badarinarayan, ... Nature genetics 49 (9), 1373-1384, 2017 | 447 | 2017 |
| SNPing away at complex diseases: analysis of single-nucleotide polymorphisms around APOE in Alzheimer disease ER Martin, EH Lai, JR Gilbert, AR Rogala, AJ Afshari, J Riley, KL Finch, ... The American Journal of Human Genetics 67 (2), 383-394, 2000 | 424 | 2000 |
| Meta-analysis confirms CR1, CLU, and PICALM as alzheimer disease risk loci and reveals interactions with APOE genotypes G Jun, AC Naj, GW Beecham, LS Wang, J Buros, PJ Gallins, JD Buxbaum, ... Archives of neurology 67 (12), 1473-1484, 2010 | 390 | 2010 |
| Identification of significant association and gene-gene interaction of GABA receptor subunit genes in autism DQ Ma, PL Whitehead, MM Menold, ER Martin, AE Ashley-Koch, H Mei, ... The American Journal of Human Genetics 77 (3), 377-388, 2005 | 361 | 2005 |
| Linkage of the MHC to familial multiple sclerosis suggests genetic heterogeneity Multiple Sclerosis Genetics Group, JL Haines, HA Terwedow, K Burgess, ... Human molecular genetics 7 (8), 1229-1234, 1998 | 329 | 1998 |
| HLA-DR2 dose effect on susceptibility to multiple sclerosis and influence on disease course LF Barcellos, JR Oksenberg, AB Begovich, ER Martin, S Schmidt, ... The American Journal of Human Genetics 72 (3), 710-716, 2003 | 325 | 2003 |
| Genome-wide studies of copy number variation and exome sequencing identify rare variants in BAG3 as a cause of dilated cardiomyopathy N Norton, D Li, MJ Rieder, JD Siegfried, E Rampersaud, S Züchner, ... The American Journal of Human Genetics 88 (3), 273-282, 2011 | 311 | 2011 |
| Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum G Stevanin, FM Santorelli, H Azzedine, P Coutinho, J Chomilier, ... Nature genetics 39 (3), 366-372, 2007 | 311 | 2007 |
| Pesticide exposure and risk of Parkinson's disease: a family-based case-control study DB Hancock, ER Martin, GM Mayhew, JM Stajich, R Jewett, MA Stacy, ... BMC neurology 8 (1), 1-12, 2008 | 309 | 2008 |
| Analysis of European mitochondrial haplogroups with Alzheimer disease risk JM Van Der Walt, YA Dementieva, ER Martin, WK Scott, KK Nicodemus, ... Neuroscience letters 365 (1), 28-32, 2004 | 290 | 2004 |
William K. ScottProfessor of Human Genetics, University of MiamiVerified email at med.miami.edu
