Don Conrad

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Matthew HurlesDirector, Senior Group Leader in Human Genetics, Wellcome Sanger InstituteVerifisert e-postadresse på sanger.ac.uk
Jonathan K PritchardStanford UniversityVerifisert e-postadresse på stanford.edu
Noah RosenbergStanford UniversityVerifisert e-postadresse på stanford.edu
Stephen B MontgomeryProfessor, Pathology, Genetics and Biomedical Data Science, Stanford UniversityVerifisert e-postadresse på stanford.edu
Dan AndrewsAustralian National UniversityVerifisert e-postadresse på anu.edu.au
Charles Lee, PhD, DSc, FACMG, FRSCThe Jackson Laboratory for Genomic MedicineVerifisert e-postadresse på jax.org
Graham CoopEvolution and Ecology, UC DavisVerifisert e-postadresse på ucdavis.edu
Lars FeukProfessor, Uppsala UniversityVerifisert e-postadresse på igp.uu.se
Dalila PintoAssociate Professor, Icahn School of Medicine at Mount Sinai, NYVerifisert e-postadresse på mssm.edu
Reed A. CartwrightAssociate Professor of Genomics, Evolution, and Bioinformatics, Arizona State UniversityVerifisert e-postadresse på asu.edu
Ravinesh A. KumarDirector of Research, The University of ChicagoVerifisert e-postadresse på uchicago.edu
Xiaoquan WenUniversity of MichiganVerifisert e-postadresse på umich.edu
Scherer, Stephen W.The Hospital for Sick Children, Genetics and Genome Biology Program, University of TorontoVerifisert e-postadresse på sickkids.ca
Chris P BarnesUniversity College LondonVerifisert e-postadresse på ucl.ac.uk
Daniel J WilsonUniversity of OxfordVerifisert e-postadresse på bdi.ox.ac.uk
Xavier DidelotUniversity of WarwickVerifisert e-postadresse på warwick.ac.uk
Daniel FalushShanghai Institute of Immunity and InfectionVerifisert e-postadresse på ips.ac.cn
Philip AwadallaProfessor of Molecular Genetics, University of OxfordVerifisert e-postadresse på ndph.ox.ac.uk
Mark DalyDirector, Institute for Molecular Medicine Finland (FIMM) & Chief, ATGU, MGH & Broad InstituteVerifisert e-postadresse på atgu.mgh.harvard.edu
Mark DePristoBigHat BiosciencesVerifisert e-postadresse på bighatbio.com

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Don Conrad

Professor, Oregon Health & Science University

Verifisert e-postadresse på ohsu.edu - Startside

Human Genetics and Genomics Statistical Genetics Infertility


Tittel Sorter etter sitater Sorter etter år Sorter etter tittel	Sitert av Sitert av	År
A map of human genome variation from population scale sequencing 1000 Genomes Project Consortium Nature 467 (7319), 1061, 2010	9045	2010
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	5517	2006
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	3592	2017
The GTEx Consortium atlas of genetic regulatory effects across human tissues GTEx Consortium Science 369 (6509), 1318-1330, 2020	3422	2020
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	2304	2010
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	1449	2014
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	1427	2012
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	1330	2011
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	941	2010
The impact of sex on gene expression across human tissues M Oliva, M Muñoz-Aguirre, S Kim-Hellmuth, V Wucher, ADH Gewirtz, ... Science 369 (6509), eaba3066, 2020	883	2020
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	876	2006
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	845	2008
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	742	2011
Variation in genome-wide mutation rates within and between human families Nature genetics 43 (7), 712-714, 2011	702	2011
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	621	2006
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	613	2017
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	449	2017
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	410	2010
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	382	2020
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	365	2015

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