Theo dõi
Philip Awadalla
Philip Awadalla
Professor of Molecular Genetics, University of Oxford
Email được xác minh tại ndph.ox.ac.uk - Trang chủ
Tiêu đề
Trích dẫn bởi
Trích dẫn bởi
Năm
A global reference for human genetic variation.
1000 Genomes Project Consortium
Nature 526 (7571), 68-74, 2015
165232015
The variant call format and VCFtools
P Danecek, A Auton, G Abecasis, CA Albers, E Banks, MA DePristo, ...
Bioinformatics 27 (15), 2156-2158, 2011
145942011
A map of human genome variation from population scale sequencing
GP Consortium
Nature 467 (7319), 1061-1073, 2010
9048*2010
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56, 2012
86332012
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
25642015
Pan-cancer analysis of whole genomes.
PCAWG Consortium
Nature 578 (7793), 82-93, 2020
2517*2020
A global reference for human genetic variation
TGP Consortium
Nature 526 (7571), 68-74, 2015
1533*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
14272012
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
13302011
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
1210*2021
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
8652018
Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes.
Consortium, eQTL
Nature Communications 9 (1), 2941, 2018
8122018
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
8102010
A coalescent-based method for detecting and estimating recombination from gene sequences
G McVean, P Awadalla, P Fearnhead
Genetics 160 (3), 1231-1241, 2002
7992002
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
7422011
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
7022011
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
7002019
Genomewide association studies: history, rationale, and prospects for psychiatric disorders
Psychiatric GWAS Consortium Coordinating Committee
American Journal of Psychiatry 166 (5), 540-556, 2009
6082009
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
5522011
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
5082018
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