Deborah A. Nickerson

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Jay ShendureProfessor of Genome Sciences, University of WashingtonEmail verificata su uw.edu
Evan EichlerProfessor of Genome Sciences, University of WashingtonEmail verificata su gs.washington.edu
Leonid KruglyakUCLAEmail verificata su ucla.edu
Ronald M. KraussUCSFEmail verificata su ucsf.edu
Raphael BernierUniversity of WashingtonEmail verificata su u.washington.edu
Greg CooperFaculty Investigator, HudsonAlpha Institute for BiotechnologyEmail verificata su hudsonalpha.org
Paul M Ridker, MD, MPHEugene Braunwald Professor of Medicine, Harvard Medical SchoolEmail verificata su partners.org
Niklas KrummUniversity of Washington - Department of Laboratory MedicineEmail verificata su uw.edu
Stephanie Malia FullertonUniversity of Washington School of MedicineEmail verificata su uw.edu
Joshua AkeyProfessor of Ecology and Evolutionary Biology and Lewis Sigler Institute, Princeton UniversityEmail verificata su princeton.edu
Emre KarakocPrincipal Bioinformatician, Wellcome Sanger InstituteEmail verificata su sanger.ac.uk
Allan RettieUniversity of WashingtonEmail verificata su uw.edu
Matthew StephensUniversity of ChicagoEmail verificata su uchicago.edu
Goncalo AbecasisUniversity of Michigan School of Public HealthEmail verificata su umich.edu
Pui-Yan KwokHenry Bachrach Distinguished Professor, University of California, San FranciscoEmail verificata su ucsf.edu
Richard M. MyersHudsonAlpha Institute for BiotechnologyEmail verificata su hudsonalpha.com
Hyun Min KangProfessor of Biostatistics, University of Michigan, Ann ArborEmail verificata su umich.edu
Tushar BhangaleGenentech IncEmail verificata su gene.com

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Deborah A. Nickerson

University of Washington

Email verificata su uw.edu

Human Genetics Genomics


Titolo Ordina per citazioni Ordina per anno Ordina per titolo	Citata da Citata da	Anno
Heart disease and stroke statistics—2016 update: a report from the American Heart Association D Mozaffarian, EJ Benjamin, AS Go, DK Arnett, MJ Blaha, M Cushman, ... circulation 133 (4), e38-e360, 2016	74554*	2016
A map of human genome variation from population scale sequencing 1000 Genomes Project Consortium Nature 467 (7319), 1061, 2010	8735	2010
An integrated map of genetic variation from 1,092 human genomes 1000 Genomes Project Consortium Nature 491 (7422), 56, 2012	8228	2012
The international HapMap project RA Gibbs, JW Belmont, P Hardenbol, TD Willis, FL Yu, HM Yang, ... Nature Publishing Group, 2003	6188	2003
Biological, clinical and population relevance of 95 loci for blood lipids TM Teslovich, K Musunuru, AV Smith, AC Edmondson, IM Stylianou, ... Nature 466 (7307), 707-713, 2010	4022	2010
A reference panel of 64,976 haplotypes for genotype imputation Nature genetics 48 (10), 1279-1283, 2016	2821	2016
Targeted capture and massively parallel sequencing of 12 human exomes SB Ng, EH Turner, PD Robertson, SD Flygare, AW Bigham, C Lee, ... Nature 461 (7261), 272-276, 2009	2630	2009
The contribution of de novo coding mutations to autism spectrum disorder I Iossifov, BJ O’roak, SJ Sanders, M Ronemus, N Krumm, D Levy, ... Nature 515 (7526), 216-221, 2014	2540	2014
Exome sequencing identifies the cause of a mendelian disorder SB Ng, KJ Buckingham, C Lee, AW Bigham, HK Tabor, KM Dent, CD Huff, ... Nature genetics 42 (1), 30-35, 2010	2519	2010
Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations BJ O’Roak, L Vives, S Girirajan, E Karakoc, N Krumm, BP Coe, R Levy, ... Nature 485 (7397), 246-250, 2012	2384	2012
Exome sequencing as a tool for Mendelian disease gene discovery MJ Bamshad, SB Ng, AW Bigham, HK Tabor, MJ Emond, DA Nickerson, ... Nature Reviews Genetics 12 (11), 745-755, 2011	2152	2011
Evolution and functional impact of rare coding variation from deep sequencing of human exomes JA Tennessen, AW Bigham, TD O’connor, W Fu, EE Kenny, S Gravel, ... science 337 (6090), 64-69, 2012	1877	2012
Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium CS Carlson, MA Eberle, MJ Rieder, Q Yi, L Kruglyak, DA Nickerson The American Journal of Human Genetics 74 (1), 106-120, 2004	1852	2004
Effect of VKORC1 haplotypes on transcriptional regulation and warfarin dose MJ Rieder, AP Reiner, BF Gage, DA Nickerson, CS Eby, HL McLeod, ... New England Journal of Medicine 352 (22), 2285-2293, 2005	1818	2005
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	1607	2010
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	1424	2008
Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations BJ O'Roak, P Deriziotis, C Lee, L Vives, JJ Schwartz, S Girirajan, ... Nature genetics 43 (6), 585-589, 2011	1403	2011
Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders BJ O’Roak, L Vives, W Fu, JD Egertson, IB Stanaway, IG Phelps, G Carvill, ... Science 338 (6114), 1619-1622, 2012	1392	2012
Variation is the spice of life L Kruglyak, DA Nickerson Nature genetics 27 (3), 234-236, 2001	1365	2001
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program D Taliun, DN Harris, MD Kessler, J Carlson, ZA Szpiech, R Torres, ... Nature 590 (7845), 290-299, 2021	1302	2021

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