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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
14723*2015
The variant call format and VCFtools
P Danecek, A Auton, G Abecasis, CA Albers, E Banks, MA DePristo, ...
Bioinformatics 27 (15), 2156-2158, 2011
126982011
A map of human genome variation from population scale sequencing
GP Consortium
Nature 467 (7319), 1061-1073, 2010
8781*2010
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56, 2012
82732012
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
23632015
Pan-cancer analysis of whole genomes.
PCAWG Consortium
Nature 578 (7793), 82-93, 2020
1721*2020
A global reference for human genetic variation
TGP Consortium
Nature 526 (7571), 68-74, 2015
1406*2015
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
13672012
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
12762011
A coalescent-based method for detecting and estimating recombination from gene sequences
G McVean, P Awadalla, P Fearnhead
Genetics 160 (3), 1231-1241, 2002
7892002
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
7862010
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
7842018
Large-scale cis-and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression
QTL consortium
Nature Genetics, 1-11, 2021
750*2021
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
7072011
Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes.
Consortium, eQTL
Nature Communications 9 (1), 2941, 2018
7012018
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
6882011
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences
MR Team, QTL Consortium, IC Consortium
Nature Genetics, 2019
5972019
Genomewide association studies: history, rationale, and prospects for psychiatric disorders
Psychiatric GWAS Consortium Coordinating Committee
American Journal of Psychiatry 166 (5), 540-556, 2009
5932009
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
5392011
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
4912018
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