Don Conrad

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Matthew HurlesDirector, Senior Group Leader in Human Genetics, Wellcome Sanger InstituteEmail verificata su sanger.ac.uk
Jonathan K PritchardStanford UniversityEmail verificata su stanford.edu
Noah RosenbergStanford UniversityEmail verificata su stanford.edu
Stephen B MontgomeryProfessor, Pathology, Genetics and Biomedical Data Science, Stanford UniversityEmail verificata su stanford.edu
Charles Lee, Ph.D., FACMGThe Jackson Laboratory for Genomic MedicineEmail verificata su jax.org
Graham CoopEvolution and Ecology, UC DavisEmail verificata su ucdavis.edu
Reed A. CartwrightAssociate Professor of Genomics, Evolution, and Bioinformatics, Arizona State UniversityEmail verificata su asu.edu
Dan AndrewsAustralian National UniversityEmail verificata su anu.edu.au
Ravinesh A. KumarDirector of Research, The University of ChicagoEmail verificata su uchicago.edu
Xiaoquan WenUniversity of MichiganEmail verificata su umich.edu
Lars FeukProfessor, Uppsala UniversityEmail verificata su igp.uu.se
Scherer, Stephen W.The Hospital for Sick Children, Genetics and Genome Biology Program, University of TorontoEmail verificata su sickkids.ca
Dalila PintoAssociate Professor, Icahn School of Medicine at Mount Sinai, NYEmail verificata su mssm.edu
Chris P BarnesUniversity College LondonEmail verificata su ucl.ac.uk
Daniel J WilsonUniversity of OxfordEmail verificata su bdi.ox.ac.uk
Xavier DidelotUniversity of WarwickEmail verificata su warwick.ac.uk
Daniel FalushShanghai Institute of Immunity and InfectionEmail verificata su ips.ac.cn
Philip AwadallaProfessor of Molecular Genetics, University of OxfordEmail verificata su ndph.ox.ac.uk
Mark DalyDirector, Institute for Molecular Medicine Finland (FIMM) & Chief, ATGU, MGH & Broad InstituteEmail verificata su atgu.mgh.harvard.edu
Mark DePristoBigHat BiosciencesEmail verificata su bighatbio.com

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Don Conrad

Professor, Oregon Health & Science University

Email verificata su ohsu.edu - Home page

Human Genetics and Genomics Statistical Genetics Infertility


Titolo Ordina per citazioni Ordina per anno Ordina per titolo	Citata da Citata da	Anno
A map of human genome variation from population scale sequencing 1000 Genomes Project Consortium Nature 467 (7319), 1061, 2010	8987	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	5539	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	3601	2017
The GTEx Consortium atlas of genetic regulatory effects across human tissues GTEx Consortium Science 369 (6509), 1318-1330, 2020	3319	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	2309	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	1455	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	1428	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	1321	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	948	2010
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	882	2006
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	864	2020
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	847	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	738	2011
Variation in genome-wide mutation rates within and between human families Nature genetics 43 (7), 712-714, 2011	703	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	622	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	607	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	451	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	412	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	375	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	372	2015

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