Articles with public access mandates - Philip AwadallaLearn more
Not available anywhere: 4
Review
Recombination affects accumulation of damaging and disease-associated mutations in human populations
JG Hussin, A Hodgkinson, Y Idaghdour, JC Grenier, JP Goulet, E Gbeha, ...
Nature genetics 47 (4), 400-404, 2015
Mandates: Fonds de recherche du Québec - Santé, Genome Canada
Review
Next-generation sequencing approaches for genetic mapping of complex diseases
F Casals, Y Idaghdour, J Hussin, P Awadalla
Journal of neuroimmunology 248 (1-2), 10-22, 2012
Mandates: Genome Canada
Review
Lifestyle factors and lung cancer risk among never smokers in the Canadian Partnership for Tomorrow’s Health (CanPath)
RA Murphy, M Darvishian, J Qi, Y Chen, Q Chu, J Vena, TJB Dummer, ...
Cancer Causes & Control 33 (6), 913-918, 2022
Mandates: Canadian Institutes of Health Research, Genome Canada, Michael Smith …
Review
Score tests for scale effects, with application to genomic analysis
D Soave, JF Lawless, P Awadalla
Statistics in Medicine 40 (16), 3808-3822, 2021
Mandates: Canadian Institutes of Health Research, Natural Sciences and Engineering …
Available somewhere: 121
Review
A global reference for human genetic variation.
1000 Genomes Project Consortium
Nature 526 (7571), 68-74, 2015
Mandates: US National Institutes of Health, Howard Hughes Medical Institute, Canadian …
Review
The variant call format and VCFtools
P Danecek, A Auton, G Abecasis, CA Albers, E Banks, MA DePristo, ...
Bioinformatics 27 (15), 2156-2158, 2011
Mandates: US National Institutes of Health, British Heart Foundation
Review
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56, 2012
Mandates: Swiss National Science Foundation, US National Institutes of Health, Howard …
Review
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
Mandates: US National Institutes of Health, German Research Foundation, European …
Review
Pan-cancer analysis of whole genomes.
PCAWG Consortium
Nature 578 (7793), 82-93, 2020
Mandates: US National Institutes of Health, Cancer Research UK, UK Medical Research …
Review
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
Mandates: Swiss National Science Foundation, US National Institutes of Health, British …
Review
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
Mandates: US National Institutes of Health, German Research Foundation
Review
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
Mandates: US National Institutes of Health, Canadian Cancer Society, Canadian …
Review
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
Mandates: US National Institutes of Health, Howard Hughes Medical Institute
Review
Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes.
Consortium, eQTL
Nature Communications 9 (1), 2941, 2018
Mandates: US National Institutes of Health, Australian Research Council, National …
Review
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
Mandates: US National Institutes of Health
Review
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
Mandates: US National Institutes of Health, Genome Canada
Review
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
Mandates: US National Institutes of Health, Genome Canada, Social Sciences and …
Review
Genomewide association studies: history, rationale, and prospects for psychiatric disorders
Psychiatric GWAS Consortium Coordinating Committee
American Journal of Psychiatry 166 (5), 540-556, 2009
Mandates: US National Institutes of Health
Review
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
Mandates: US National Institutes of Health, Howard Hughes Medical Institute
Review
Unraveling the polygenic architecture of complex traits using blood eQTL metaanalysis
U Võsa, A Claringbould, HJ Westra, MJ Bonder, P Deelen, B Zeng, ...
BioRxiv, 447367, 2018
Mandates: Netherlands Organisation for Scientific Research, European Commission
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