Amy L. Williams
Cited by
Cited by
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56, 2012
National Institutes of Health consensus development conference panel statement: Management of hepatitis C
DW Powell, BZ Abramson, JA Balint, S Belle, JR Bloomer, AK Diehl, ...
Hepatology 26 (3 SUPPL.), 2S-10S, 1997
Sequence variants in SLC16A11 are a common risk factor for type 2 diabetes in Mexico
SIGMA Type 2 Diabetes Consortium
Nature 506 (7486), 97, 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
Static deadlock detection for Java libraries
A Williams, W Thies, MD Ernst
European conference on object-oriented programming, 602-629, 2005
An efficient and robust ray-box intersection algorithm
A Williams, S Barrus, RK Morley, P Shirley
ACM SIGGRAPH 2005 Courses, 9-es, 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
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
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
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
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
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
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
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
Rapid haplotype inference for nuclear families
AL Williams, DE Housman, MC Rinard, DK Gifford
Genome biology 11 (10), 1-17, 2010
Sequence variants in SLC16A11 are a common risk factor for type 2 diabetes in Mexico
STD Consortium, AL Williams, SB Jacobs, H Moreno-Macias, ...
Nature 506 (7486), 97-101, 2014
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
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
Static detection of deadlock for Java libraries
AL Williams
Massachusetts Institute of Technology, 2005
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
The system can't perform the operation now. Try again later.
Articles 1–20