Margaux F. Keller, PhD
Margaux F. Keller, PhD
Research Coordinator, HJF
Verified email at - Homepage
Cited by
Cited by
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease
MA Nalls, N Pankratz, CM Lill, CB Do, DG Hernandez, M Saad, ...
Nature genetics 46 (9), 989-993, 2014
A multicenter study of glucocerebrosidase mutations in dementia with Lewy bodies
MA Nalls, R Duran, G Lopez, M Kurzawa-Akanbi, IG McKeith, ...
JAMA neurology 70 (6), 727-735, 2013
Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair
FR Day, KS Ruth, DJ Thompson, KL Lunetta, N Pervjakova, DI Chasman, ...
Nature genetics 47 (11), 1294-1303, 2015
Using genome-wide complex trait analysis to quantify ‘missing heritability’in Parkinson's disease
MF Keller, M Saad, J Bras, F Bettella, N Nicolaou, J Simón-Sánchez, ...
Human molecular genetics 21 (22), 4996-5009, 2012
Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations
N Franceschini, E Fox, Z Zhang, TL Edwards, MA Nalls, YJ Sung, ...
The American Journal of Human Genetics 93 (3), 545-554, 2013
Diagnosis of Parkinson's disease on the basis of clinical and genetic classification: a population-based modelling study
MA Nalls, CY McLean, J Rick, S Eberly, SJ Hutten, K Gwinn, M Sutherland, ...
The Lancet Neurology 14 (10), 1002-1009, 2015
Serum iron levels and the risk of Parkinson disease: a Mendelian randomization study
I Pichler, F Del Greco M, M Gögele, CM Lill, L Bertram, CB Do, N Eriksson, ...
PLoS medicine 10 (6), e1001462, 2013
Cardiometabolic effects of genetic upregulation of the interleukin 1 receptor antagonist: a Mendelian randomisation analysis
Interleukin 1 Genetics Consortium
The Lancet Diabetes & Endocrinology 3 (4), 243-253, 2015
NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases
MA Nalls, J Bras, DG Hernandez, MF Keller, E Majounie, AE Renton, ...
Neurobiology of aging 36 (3), 1605. e7-1605. e12, 2015
Gain-of-function lipoprotein lipase variant rs13702 modulates lipid traits through disruption of a microRNA-410 seed site
K Richardson, JA Nettleton, N Rotllan, T Tanaka, CE Smith, CQ Lai, ...
The American Journal of Human Genetics 92 (1), 5-14, 2013
Genetic risk and age in Parkinson's disease: continuum not stratum
MA Nalls, V Escott‐Price, NM Williams, S Lubbe, MF Keller, HR Morris, ...
Movement Disorders 30 (6), 850-854, 2015
Analysis of genome-wide association studies of Alzheimer disease and of Parkinson disease to determine if these 2 diseases share a common genetic risk
V Moskvina, D Harold, GC Russo, A Vedernikov, M Sharma, M Saad, ...
JAMA neurology 70 (10), 1268-1276, 2013
Genome-wide association analysis of red blood cell traits in African Americans: the COGENT Network
Z Chen, H Tang, R Qayyum, UM Schick, MA Nalls, R Handsaker, J Li, ...
Human molecular genetics 22 (12), 2529-2538, 2013
Genome-wide analysis of the heritability of amyotrophic lateral sclerosis
MF Keller, L Ferrucci, AB Singleton, PJ Tienari, H Laaksovirta, ...
JAMA neurology 71 (9), 1123-1134, 2014
Genetic comorbidities in Parkinson's disease
MA Nalls, M Saad, AJ Noyce, MF Keller, A Schrag, JP Bestwick, ...
Human molecular genetics 23 (3), 831-841, 2014
Large C9orf72 repeat expansions are not a common cause of Parkinson's disease
E Majounie, Y Abramzon, AE Renton, MF Keller, BJ Traynor, AB Singleton
Neurobiology of aging 33 (10), 2527. e1-2527. e2, 2012
Consumption of meat is associated with higher fasting glucose and insulin concentrations regardless of glucose and insulin genetic risk scores: a meta-analysis of 50,345 Caucasians
AM Fretts, JL Follis, JA Nettleton, RN Lemaitre, JS Ngwa, MK Wojczynski, ...
The American journal of clinical nutrition 102 (5), 1266-1278, 2015
Baseline genetic associations in the Parkinson's Progression Markers Initiative (PPMI)
MA Nalls, MF Keller, DG Hernandez, L Chen, DJ Stone, AB Singleton, ...
Movement Disorders 31 (1), 79-85, 2016
Use of support vector machines for disease risk prediction in genome‐wide association studies: Concerns and opportunities
F Mittag, F Büchel, M Saad, A Jahn, C Schulte, Z Bochdanovits, ...
Human mutation 33 (12), 1708-1718, 2012
Trans-ethnic meta-analysis and functional annotation illuminates the genetic architecture of fasting glucose and insulin
CT Liu, S Raghavan, N Maruthur, EK Kabagambe, J Hong, MCY Ng, ...
The American Journal of Human Genetics 99 (1), 56-75, 2016
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