Eden Martin
Eden Martin
Professor of Human Genetics, University of Miami
Verified email at med.miami.edu
Cited by
Cited by
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
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
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
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
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
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
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
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 genetics 8 (3), e1002548, 2012
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
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
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
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
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
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
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
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
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
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
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
Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis
DC Whitcomb, J LaRusch, AM Krasinskas, L Klei, JP Smith, RE Brand, ...
Nature genetics 44 (12), 1349-1354, 2012
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