Margaret (Meg) Gelder Ehm
Margaret (Meg) Gelder Ehm
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Linkage disequilibrium mapping identifies a 390 kb region associated with CYP2D6 poor drug metabolising activity
LK Hosking, PR Boyd, CF Xu, M Nissum, K Cantone, IJ Purvis, R Khakhar, ...
The Pharmacogenomics Journal 2 (3), 165-175, 2002
FinnGen provides genetic insights from a well-phenotyped isolated population
MI Kurki, J Karjalainen, P Palta, TP Sipilä, K Kristiansson, KM Donner, ...
Nature 613 (7944), 508-518, 2023
An abundance of rare functional variants in 202 drug target genes sequenced in 14,002 people
MR Nelson, D Wegmann, MG Ehm, D Kessner, P St. Jean, C Verzilli, ...
Science 337 (6090), 100-104, 2012
Testing association of statistically inferred haplotypes with discrete and continuous traits in samples of unrelated individuals
DV Zaykin, PH Westfall, SS Young, MA Karnoub, MJ Wagner, MG Ehm
Human Heredity 53 (2), 79-91, 2002
Candidate single-nucleotide polymorphisms from a genomewide association study of Alzheimer disease
H Li, S Wetten, L Li, PLS Jean, R Upmanyu, L Surh, D Hosford, ...
Archives of neurology 65 (1), 45-53, 2008
An autosomal genomic scan for loci linked to type II diabetes mellitus and body-mass index in Pima Indians
RL Hanson, MG Ehm, DJ Pettitt, M Prochazka, DB Thompson, ...
The American Journal of Human Genetics 63 (4), 1130-1138, 1998
HIBAG—HLA genotype imputation with attribute bagging
X Zheng, J Shen, C Cox, JC Wakefield, MG Ehm, MR Nelson, BS Weir
The pharmacogenomics journal 14 (2), 192-200, 2014
Detecting marker-disease association by testing for Hardy-Weinberg disequilibrium at a marker locus
BSW Dahlia M Nielsen, Margaret G Ehm
American Journal of Human Genetics 63 (5), 1531-1540, 1998
FinnGen: Unique genetic insights from combining isolated population and national health register data
MI Kurki, J Karjalainen, P Palta, TP Sipilä, K Kristiansson, K Donner, ...
medrxiv, 2022.03. 03.22271360, 2022
Rare Variants in APP, PSEN1 and PSEN2 Increase Risk for AD in Late-Onset Alzheimer's Disease Families
C Cruchaga, S Chakraverty, K Mayo, FLM Vallania, RD Mitra, K Faber, ...
PloS one 7 (2), e31039, 2012
The Population Reference Sample, POPRES: a resource for population, disease, and pharmacological genetics research
MR Nelson, K Bryc, KS King, A Indap, AR Boyko, J Novembre, LP Briley, ...
The American Journal of Human Genetics 83 (3), 347-358, 2008
An autosomal genomic scan for loci linked to prediabetic phenotypes in Pima Indians.
RE Pratley, DB Thompson, M Prochazka, L Baier, D Mott, E Ravussin, ...
The Journal of clinical investigation 101 (8), 1757-1764, 1998
Genomewide search for type 2 diabetes susceptibility genes in four American populations
MG Ehm, MC Karnoub, H Sakul, K Gottschalk, DC Holt, JL Weber, ...
The American Journal of Human Genetics 66 (6), 1871-1881, 2000
Autosomal genomic scan for loci linked to obesity and energy metabolism in Pima Indians
RA Norman, PA Tataranni, R Pratley, DB Thompson, RL Hanson, ...
The American Journal of Human Genetics 62 (3), 659-668, 1998
Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility
J Wessel, AY Chu, SM Willems, S Wang, H Yaghootkar, JA Brody, ...
Nature communications 6 (1), 5897, 2015
Diabetes in the Old Order Amish: characterization and heritability analysis of the Amish Family Diabetes Study.
WC Hsueh, BD Mitchell, R Aburomia, T Pollin, H Sakul, M Gelder Ehm, ...
Diabetes care 23 (5), 595-601, 2000
Selection of genetic markers for association analyses, using linkage disequilibrium and haplotypes
Z Meng, DV Zaykin, CF Xu, M Wagner, MG Ehm
The American Journal of Human Genetics 73 (1), 115-130, 2003
Genome-wide and fine-mapping linkage studies of type 2 diabetes and glucose traits in the Old Order Amish: evidence for a new diabetes locus on chromosome 14q11 and …
WC Hsueh, PL St. Jean, BD Mitchell, TI Pollin, WC Knowler, MG Ehm, ...
Diabetes 52 (2), 550-557, 2003
A 3.9-centimorgan-resolution human single-nucleotide polymorphism linkage map and screening set
TC Matise, R Sachidanandam, AG Clark, L Kruglyak, E Wijsman, J Kakol, ...
The American Journal of Human Genetics 73 (2), 271-284, 2003
A genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart disease
RA Scott, DF Freitag, L Li, AY Chu, P Surendran, R Young, N Grarup, ...
Science translational medicine 8 (341), 341ra76-341ra76, 2016
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