| An integrated map of genetic variation from 1,092 human genomes 1000 Genomes Project Consortium Nature 491 (7422), 56, 2012 | 8491 | 2012 |
| Sequence variants in SLC16A11 are a common risk factor for type 2 diabetes in Mexico AL Williams, SBR Jacobs, H Moreno-Macías, A Huerta-Chagoya, ... Nature 506 (7486), 97-101, 2014 | 570 | 2014 |
| Association of a low-frequency variant in HNF1A with type 2 diabetes in a Latino population K Estrada, I Aukrust, L Bjørkhaug, NP Burtt, JM Mercader, H García-Ortiz, ... Jama 311 (22), 2305-2314, 2014 | 295 | 2014 |
| An efficient and robust ray-box intersection algorithm A Williams, S Barrus, RK Morley, P Shirley ACM SIGGRAPH 2005 Courses, 9-es, 2005 | 217 | 2005 |
| Rare variants in PPARG with decreased activity in adipocyte differentiation are associated with increased risk of type 2 diabetes AR Majithia, J Flannick, P Shahinian, M Guo, MA Bray, P Fontanillas, ... Proceedings of the National Academy of Sciences 111 (36), 13127-13132, 2014 | 192 | 2014 |
| Static deadlock detection for Java libraries A Williams, W Thies, MD Ernst ECOOP 2005-Object-Oriented Programming: 19th European Conference, Glasgow …, 2005 | 191 | 2005 |
| Phasing of many thousands of genotyped samples AL Williams, N Patterson, J Glessner, H Hakonarson, D Reich The American Journal of Human Genetics 91 (2), 238-251, 2012 | 154 | 2012 |
| Non-crossover gene conversions show strong GC bias and unexpected clustering in humans AL Williams, G Genovese, T Dyer, N Altemose, K Truax, G Jun, ... Elife 4, e04637, 2015 | 126 | 2015 |
| Mapping gene flow between ancient hominins through demography-aware inference of the ancestral recombination graph MJ Hubisz, AL Williams, A Siepel PLoS genetics 16 (8), e1008895, 2020 | 123 | 2020 |
| Genetic variants associated with quantitative glucose homeostasis traits translate to type 2 diabetes in Mexican Americans: the GUARDIAN (Genetics Underlying Diabetes in … ND Palmer, MO Goodarzi, CD Langefeld, N Wang, X Guo, KD Taylor, ... Diabetes, DB_140732, 2014 | 103 | 2014 |
| Benchmarking relatedness inference methods with genome-wide data from thousands of relatives MD Ramstetter, TD Dyer, DM Lehman, JE Curran, R Duggirala, ... Genetics 207 (1), 75-82, 2017 | 87 | 2017 |
| Admixture mapping identifies a locus on 6q25 associated with breast cancer risk in US Latinas L Fejerman, GK Chen, C Eng, S Huntsman, D Hu, A Williams, B Pasaniuc, ... Human molecular genetics 21 (8), 1907-1917, 2012 | 84 | 2012 |
| Crossover interference and sex-specific genetic maps shape identical by descent sharing in close relatives M Caballero, DN Seidman, Y Qiao, J Sannerud, TD Dyer, DM Lehman, ... PLoS Genetics 15 (12), e1007979, 2019 | 77 | 2019 |
| A Loss-of-Function Splice Acceptor Variant in IGF2 Is Protective for Type 2 Diabetes JM Mercader, RG Liao, AD Bell, Z Dymek, K Estrada, T Tukiainen, ... Diabetes 66 (11), 2903-2914, 2017 | 64 | 2017 |
| Rapid, phase-free detection of long identity-by-descent segments enables effective relationship classification DN Seidman, SA Shenoy, M Kim, R Babu, IG Woods, TD Dyer, ... The American Journal of Human Genetics 106 (4), 453-466, 2020 | 55 | 2020 |
| Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease D Harold, R Abraham, P Hollingworth, R Sims, A Gerrish, ML Hamshere, ... Nature Genetics 41 (10), 1156-1156, 2009 | 50 | 2009 |
| Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees G Jun, A Manning, M Almeida, M Zawistowski, AR Wood, TM Teslovich, ... Proceedings of the National Academy of Sciences 115 (2), 379-384, 2018 | 42 | 2018 |
| Inferring identical-by-descent sharing of sample ancestors promotes high-resolution relative detection MD Ramstetter, SA Shenoy, TD Dyer, DM Lehman, JE Curran, ... The American Journal of Human Genetics 103 (1), 30-44, 2018 | 40 | 2018 |
| Rapid haplotype inference for nuclear families AL Williams, DE Housman, MC Rinard, DK Gifford Genome biology 11, 1-17, 2010 | 29 | 2010 |
| Distinguishing pedigree relationships via multi-way identity by descent sharing and sex-specific genetic maps Y Qiao, JG Sannerud, S Basu-Roy, C Hayward, AL Williams The American Journal of Human Genetics 108 (1), 68-83, 2021 | 22* | 2021 |