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Don Conrad
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A map of human genome variation from population scale sequencing
1000 Genomes Project Consortium
Nature 467 (7319), 1061, 2010
87382010
Global variation in copy number in the human genome
R Redon, S Ishikawa, KR Fitch, L Feuk, GH Perry, TD Andrews, H Fiegler, ...
nature 444 (7118), 444-454, 2006
53982006
Genetic effects on gene expression across human tissues
GTEx Consortium Lead analysts: Aguet François 1 Brown Andrew A. 2 3 4 Castel ...
Nature 550 (7675), 204-213, 2017
32602017
The GTEx Consortium atlas of genetic regulatory effects across human tissues
GTEx Consortium
Science 369 (6509), 1318-1330, 2020
24352020
Origins and functional impact of copy number variation in the human genome
DF Conrad, D Pinto, R Redon, L Feuk, O Gokcumen, Y Zhang, J Aerts, ...
Nature 464 (7289), 704-712, 2010
22392010
Guidelines for investigating causality of sequence variants in human disease
DG MacArthur, TA Manolio, DP Dimmock, HL Rehm, J Shendure, ...
Nature 508 (7497), 469-476, 2014
13822014
A systematic survey of loss-of-function variants in human protein-coding genes
DG MacArthur, S Balasubramanian, A Frankish, N Huang, J Morris, ...
Science 335 (6070), 823-828, 2012
13572012
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
12722011
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls
Nature 464 (7289), 713-720, 2010
9312010
A high-resolution survey of deletion polymorphism in the human genome
DF Conrad, TD Andrews, NP Carter, ME Hurles, JK Pritchard
Nature genetics 38 (1), 75-81, 2006
8692006
Recurrent 16p11. 2 microdeletions in autism
RA Kumar, S KaraMohamed, J Sudi, DF Conrad, C Brune, JA Badner, ...
Human molecular genetics 17 (4), 628-638, 2008
8152008
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
Variation in genome-wide mutation rates within and between human families
Nature genetics 43 (7), 712-714, 2011
6842011
A worldwide survey of haplotype variation and linkage disequilibrium in the human genome
DF Conrad, M Jakobsson, G Coop, X Wen, JD Wall, NA Rosenberg, ...
Nature genetics 38 (11), 1251-1260, 2006
6122006
Dynamic landscape and regulation of RNA editing in mammals
MH Tan, Q Li, R Shanmugam, R Piskol, J Kohler, AN Young, KI Liu, ...
Nature 550 (7675), 249-254, 2017
5292017
The impact of structural variation on human gene expression
C Chiang, AJ Scott, JR Davis, EK Tsang, X Li, Y Kim, T Hadzic, ...
Nature genetics 49 (5), 692-699, 2017
4002017
Towards a comprehensive structural variation map of an individual human genome
AW Pang, JR MacDonald, D Pinto, J Wei, MA Rafiq, DF Conrad, H Park, ...
Genome biology 11, 1-14, 2010
3922010
Effect of predicted protein-truncating genetic variants on the human transcriptome
MA Rivas, M Pirinen, DF Conrad, M Lek, EK Tsang, KJ Karczewski, ...
Science 348 (6235), 666-669, 2015
3412015
A quantitative proteome map of the human body
L Jiang, M Wang, S Lin, R Jian, X Li, J Chan, G Dong, H Fang, ...
Cell 183 (1), 269-283. e19, 2020
2852020
Mutation spectrum revealed by breakpoint sequencing of human germline CNVs
DF Conrad, C Bird, B Blackburne, S Lindsay, L Mamanova, C Lee, ...
Nature genetics 42 (5), 385-391, 2010
2772010
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