| 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 | 5100 | 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 | 2126 | 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 | 817 | 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 | 774 | 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 | 598 | 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 | 596 | 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 | 472 | 2014 |
| 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 | 449 | 2022 |
| 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 | 445 | 1998 |
| 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 | 397 | 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 | 313 | 2008 |
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| 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 | 237 | 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 | 235 | 2015 |
| 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 | 235 | 2000 |
| 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 | 211 | 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 | 191 | 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 | 181 | 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 | 146 | 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 | 130 | 2016 |