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Philip Awadalla
Philip Awadalla
Professor, Ontario Institute for Cancer Research, University of Toronto
Verified email at utoronto.ca - Homepage
Title
Cited by
Cited by
Year
A global reference for human genetic variation.
1000 Genomes Project Consortium
Nature 526 (7571), 68-74, 2015
114972015
The variant call format and VCFtools
P Danecek, A Auton, G Abecasis, CA Albers, E Banks, MA DePristo, ...
Bioinformatics 27 (15), 2156-2158, 2011
95402011
A map of human genome variation from population scale sequencing
GP Consortium
Nature 467 (7319), 1061-1073, 2010
8215*2010
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium Corresponding Author McVean Gil A. mcvean ...
Nature 491 (7422), 56-65, 2012
7692*2012
An integrated map of structural variation in 2,504 human genomes.
PH Sudmant, T Rausch, EJ Gardner, RE Handsaker, A Abyzov, ...
Nature 526 (7571), 75-81, 2015
19422015
A systematic survey of loss-of-function variants in human protein-coding genes
DG MacArthur, S Balasubrmanian, A Frankish, N Huang, J Morris, ...
Science 335 (6070), 823-828, 2012
12362012
Mapping copy number variation by population-scale genome sequencing
RE Mills, K Walter, C Stewart, RE Handsaker, K Chen, C Alkan, A Abyzov, ...
Nature 470 (7332), 59-65, 2011
11962011
Pan-cancer analysis of whole genomes.
PCAWG Consortium
Nature 578 (7793), 82-93, 2020
1102*2020
A global reference for human genetic variation
TGP Consortium
Nature 526 (7571), 68-74, 2015
1097*2015
A coalescent-based method for detecting and estimating recombination from gene sequences
G McVean, P Awadalla, P Fearnhead
Genetics 160 (3), 1231-1241, 2002
7662002
Diversity of human copy number variation and multicopy genes
PH Sudmant, JO Kitzman, F Antonacci, C Alkan, M Malig, A Tsalenko, ...
Science 330 (6004), 641-646, 2010
7192010
Demographic history and rare allele sharing among human populations
S Gravel, BM Henn, RN Gutenkunst, AR Indap, GT Marth, AG Clark, F Yu, ...
Proceedings of the National Academy of Sciences 108 (29), 11983-11988, 2011
6522011
Variation in genome-wide mutation rates within and between human families
DF Conrad, JEM Keebler, MA DePristo, SJ Lindsay, Y Zhang, F Casals, ...
Nature Genetics 43 (7), 712-714, 2011
6412011
Prediction of acute myeloid leukaemia risk in healthy individuals
S Abelson, G Collord, SWK Ng, O Weissbrod, N Mendelson Cohen, ...
Nature 559 (7714), 400-404, 2018
5742018
Genomewide association studies: history, rationale, and prospects for psychiatric disorders
Psychiatric GWAS Consortium Coordinating Committee
American Journal of Psychiatry 166 (5), 540-556, 2009
5692009
Classic selective sweeps were rare in recent human evolution
RD Hernandez, JL Kelley, E Elyashiv, S Melton, A Auton, G McVean, ...
Science 331 (6019), 920-924, 2011
4882011
Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes.
Consortium, eQTL
Nature Communications 9 (1), 2941, 2018
458*2018
Genome-Wide Association Study in Asian Populations Identifies Variants in ETS1 and WDFY4 Associated with Systemic Lupus Erythematosus
W Yang, N Shen, DQ Ye, Q Liu, Y Zhang, XX Qian, N Hirankarn, D Ying, ...
PLoS genetics 6 (2), e1000841, 2010
4412010
Linkage disequilibrium and recombination in hominid mitochondrial DNA
P Awadalla, A Eyre-Walker, JM Smith
Science 286 (5449), 2524-2525, 1999
4301999
Unraveling the polygenic architecture of complex traits using blood eQTL metaanalysis
U Vősa, A Claringbould, HJ Westra, MJ Bonder, P Deelen, B Zeng, ...
BioRxiv, 447367, 2018
4282018
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