Greg Cooper

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Jay ShendureProfessor of Genome Sciences, University of WashingtonEmail verificata su uw.edu
Richard M. MyersHudsonAlpha Institute for BiotechnologyEmail verificata su hudsonalpha.com
Daniela WittenProfessor of Statistics & Biostatistics, Dorothy Gilford Endowed Chair, University of WashingtonEmail verificata su u.washington.edu
Martin KircherBerlin Institute of Health, Charité - Universitätsmedizin BerlinEmail verificata su uw.edu
Deborah A. NickersonUniversity of WashingtonEmail verificata su uw.edu
Serafim BatzoglouSeerEmail verificata su seer.bio
Evan EichlerProfessor of Genome Sciences, University of WashingtonEmail verificata su gs.washington.edu
Heather C MeffordSt. Jude Children's Research HospitalEmail verificata su stjude.org
Eugene DavydovGoogleEmail verificata su google.com
Michael BrudnoProfessor of Computer Science, University of Toronto; Chief Data Scientist, UHNEmail verificata su cs.toronto.edu
David GoodeLaboratory Head, Biomedicine Discovery Institute, Monash UniversityEmail verificata su monash.edu
J. Nicholas (Nick) Cochran, Ph.D.Faculty Investigator, HudsonAlpha Institute for BiotechnologyEmail verificata su hudsonalpha.org
michael bamshaduniversity of washingtonEmail verificata su u.washington.edu
Nadav AhituvUCSFEmail verificata su ucsf.edu
Ian StanawayUniversity of WashingtonEmail verificata su uw.edu
Daniel SavicSt. Jude Children's Research HospitalEmail verificata su stjude.org
Paul M Ridker, MD, MPHEugene Braunwald Professor of Medicine, Harvard Medical SchoolEmail verificata su partners.org
Ronald M. KraussUCSFEmail verificata su ucsf.edu
Rikke S MøllerProfessor, Danish Epilepsy CentreEmail verificata su filadelfia.dk
Allan RettieUniversity of WashingtonEmail verificata su uw.edu

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Greg Cooper

Faculty Investigator, HudsonAlpha Institute for Biotechnology

Email verificata su hudsonalpha.org - Home page

Human Genetics and Genomics


Titolo Ordina per citazioni Ordina per anno Ordina per titolo	Citata da Citata da	Anno
A general framework for estimating the relative pathogenicity of human genetic variants M Kircher, DM Witten, P Jain, BJ O'roak, GM Cooper, J Shendure Nature genetics 46 (3), 310-315, 2014	6631	2014
Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project E Birney, JA Stamatoyannopoulos, A Dutta, R Guigó, TR Gingeras, ... Nature 447 (7146), 799-816, 2007	6114	2007
CADD: predicting the deleteriousness of variants throughout the human genome P Rentzsch, D Witten, GM Cooper, J Shendure, M Kircher Nucleic acids research 47 (D1), D886-D894, 2019	3315	2019
Genome sequence of the Brown Norway rat yields insights into mammalian evolution RA Gibbs, GM Weinstock, ML Metzker, DM Muzny, EJ Sodergren, ... Nature 428 (6982), 493-521, 2004	2589	2004
The ENCODE(ENCyclopedia Of DNA Elements) Project EA Feingold, PJ Good, MS Guyer, S Kamholz, L Liefer, K Wetterstrand, ... Science(Washington) 306 (5696), 636-40, 2004	2461	2004
Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia T Walsh, JM McClellan, SE McCarthy, AM Addington, SB Pierce, ... science 320 (5875), 539-543, 2008	2170	2008
Identifying a high fraction of the human genome to be under selective constraint using GERP++ EV Davydov, DL Goode, M Sirota, GM Cooper, A Sidow, S Batzoglou PLoS computational biology 6 (12), e1001025, 2010	1955	2010
Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome SB Ng, AW Bigham, KJ Buckingham, MC Hannibal, MJ McMillin, ... Nature genetics 42 (9), 790-793, 2010	1673	2010
Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans S Kathiresan, O Melander, C Guiducci, A Surti, NP Burtt, MJ Rieder, ... Nature genetics 40 (2), 189-197, 2008	1661	2008
Distribution and intensity of constraint in mammalian genomic sequence GM Cooper, EA Stone, G Asimenos, ED Green, S Batzoglou, A Sidow Genome research 15 (7), 901-913, 2005	1659	2005
A copy number variation morbidity map of developmental delay GM Cooper, BP Coe, S Girirajan, JA Rosenfeld, TH Vu, C Baker, ... Nature genetics 43 (9), 838-846, 2011	1496	2011
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
Mapping and sequencing of structural variation from eight human genomes JM Kidd, GM Cooper, WF Donahue, HS Hayden, N Sampas, T Graves, ... Nature 453 (7191), 56-64, 2008	1452	2008
LAGAN and Multi-LAGAN: efficient tools for large-scale multiple alignment of genomic DNA M Brudno, CB Do, GM Cooper, MF Kim, E Davydov, ED Green, A Sidow, ... Genome research 13 (4), 721-731, 2003	1385	2003
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways ET Cirulli, BN Lasseigne, S Petrovski, PC Sapp, PA Dion, CS Leblond, ... Science 347 (6229), 1436-1441, 2015	1061	2015
Population analysis of large copy number variants and hotspots of human genetic disease A Itsara, GM Cooper, C Baker, S Girirajan, J Li, D Absher, RM Krauss, ... The American Journal of Human Genetics 84 (2), 148-161, 2009	729	2009
Needles in stacks of needles: finding disease-causal variants in a wealth of genomic data GM Cooper, J Shendure Nature Reviews Genetics 12 (9), 628-640, 2011	723	2011
A recurrent 16p12. 1 microdeletion supports a two-hit model for severe developmental delay S Girirajan, JA Rosenfeld, GM Cooper, F Antonacci, P Siswara, A Itsara, ... Nature genetics 42 (3), 203-209, 2010	683	2010
A recurrent 15q13. 3 microdeletion syndrome associated with mental retardation and seizures AJ Sharp, HC Mefford, K Li, C Baker, C Skinner, RE Stevenson, ... Nature genetics 40 (3), 322-328, 2008	671	2008
Performance of ACMG-AMP variant-interpretation guidelines among nine laboratories in the clinical sequencing exploratory research consortium LM Amendola, GP Jarvik, MC Leo, HM McLaughlin, Y Akkari, MD Amaral, ... The American Journal of Human Genetics 98 (6), 1067-1076, 2016	645	2016

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