David Wesley Craig

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Matthew HuentelmanAssociate Professor of Neurogenomics, TGenVerified email at tgen.org
Dietrich A. StephanProfessor and Chairman, Human Genetics Department, University of PittsburghVerified email at pitt.edu
john v pearsonQIMR Berghofer MRIVerified email at qimrberghofer.edu.au
John R KelsoeUniversity of California San DiegoVerified email at ucsd.edu
Jason J. CorneveauxBioinformatician II, Translational Genomics Research InstituteVerified email at tgen.org
Shripad SinariThe University of ArizonaVerified email at arizona.edu
Victoria ZismannLaboratory Manager, TGenVerified email at tgen.org
Rebecca HalperinTranslational Genomics Research InstituteVerified email at asu.edu
Klaus SchultenProfessor of Physics, University of Illinois at Urbana-ChampaignVerified email at ks.uiuc.edu
Alexis ChristoforidesVerified email at tgen.org
Daniel Von HoffChief Scientific Officer US Oncology, Chief Scientific Officer TGen, Distinguished Professor MayoVerified email at tgen.org
Eric ReimanBanner Alzheimer's InstituteVerified email at bannerhealth.com
Andrew SaykinIndiana University School of MedicineVerified email at iu.edu
Li ShenProfessor of Informatics and Radiology, University of Pennsylvania Perelman School of MedicineVerified email at pennmedicine.upenn.edu
Nils HomerFulcrum GenomicsVerified email at fulcrumgenomics.com
Angela S BakerTGenVerified email at tgen.org
Jonathan J KeatsAssistant Professor, Translational Genomics Research InstituteVerified email at tgen.org
Jennifer A. WebsterRWE Scientist, PfizerVerified email at pfizer.com
Andreas PapassotiropoulosTransfaculty Research Platform Molecular and Cognitive NeuroscienceVerified email at unibas.ch
Sungeun KimState University of New YorkVerified email at oswego.edu

David Wesley Craig

Chair of Integrated Translational Sciences, City of Hope

Verified email at coh.org - Homepage

genomics Bioinformatics


Title Sort by citations Sort by year Sort by title	Cited by Cited by	Year
A global reference for human genetic variation 1000 Genomes Project Consortium Nature 526 (7571), 68, 2015	15886	2015
A map of human genome variation from population scale sequencing 1000 Genomes Project Consortium Nature 467 (7319), 1061, 2010	8904	2010
An integrated map of genetic variation from 1,092 human genomes 1000 Genomes Project Consortium Nature 491 (7422), 56, 2012	8541	2012
Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis Cross-Disorder Group of the Psychiatric Genomics Consortium The Lancet 381 (9875), 1371-1379, 2013	3089	2013
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs B Devlin, JR Kelsoe, P Sklar, MJ Daly, MC O'Donovan, N Craddock, ... Nature genetics 45 (9), 984-994, 2013	2403	2013
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies MA Nalls, C Blauwendraat, CL Vallerga, K Heilbron, S Bandres-Ciga, ... The Lancet Neurology 18 (12), 1091-1102, 2019	1836	2019
Resolving individuals contributing trace amounts of DNA to highly complex mixtures using high-density SNP genotyping microarrays N Homer, S Szelinger, M Redman, D Duggan, W Tembe, J Muehling, ... PLoS genetics 4 (8), e1000167, 2008	1532	2008
Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4 Nature genetics 43 (10), 977-983, 2011	1519	2011
Genome-wide association study identifies 30 loci associated with bipolar disorder EA Stahl, G Breen, AJ Forstner, A McQuillin, S Ripke, V Trubetskoy, ... Nature genetics 51 (5), 793-803, 2019	1470	2019
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	1315	2011
Germline mutations in HOXB13 and prostate-cancer risk CM Ewing, AM Ray, EM Lange, KA Zuhlke, CM Robbins, WD Tembe, ... New England Journal of Medicine 366 (2), 141-149, 2012	828	2012
Detection of chromosomal alterations in the circulation of cancer patients with whole-genome sequencing RJ Leary, M Sausen, I Kinde, N Papadopoulos, JD Carpten, D Craig, ... Science translational medicine 4 (162), 162ra154-162ra154, 2012	826	2012
Diversity of human copy number variation and multicopy genes PH Sudmant, JO Kitzman, F Antonacci, C Alkan, M Malig, A Tsalenko, ... Science 330 (6004), 641-646, 2010	820	2010
Translating RNA sequencing into clinical diagnostics: opportunities and challenges SA Byron, KR Van Keuren-Jensen, DM Engelthaler, JD Carpten, ... Nature Reviews Genetics 17 (5), 257-271, 2016	768	2016
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	735	2011
A high-density whole-genome association study reveals that APOE is the major susceptibility gene for sporadic late-onset Alzheimer's disease KD Coon, AJ Myers, DW Craig, JA Webster, JV Pearson, DH Lince, ... Journal of Clinical Psychiatry 68 (4), 613, 2007	735	2007
Variation in genome-wide mutation rates within and between human families Nature genetics 43 (7), 712-714, 2011	696	2011
GAB2 alleles modify Alzheimer's risk in APOE ɛ4 carriers EM Reiman, JA Webster, AJ Myers, J Hardy, T Dunckley, VL Zismann, ... Neuron 54 (5), 713-720, 2007	584	2007
A survey of genetic human cortical gene expression AJ Myers, JR Gibbs, JA Webster, K Rohrer, A Zhao, L Marlowe, M Kaleem, ... Nature genetics 39 (12), 1494-1499, 2007	575	2007
Genomic dissection of bipolar disorder and schizophrenia, including 28 subphenotypes DM Ruderfer, S Ripke, A McQuillin, J Boocock, EA Stahl, JMW Pavlides, ... Cell 173 (7), 1705-1715. e16, 2018	559	2018

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