Kai Wang

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223 articles

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Hakon HakonarsonDirector, Center for Applied Genomics, CHOP, UPENNCorreu electrònic verificat a email.chop.edu
Mingyao LiProfessor of Biostatistics, University of Pennsylvania School of MedicineCorreu electrònic verificat a mail.med.upenn.edu
Jonathan BradfieldPresident, Quantinuum Research LLCCorreu electrònic verificat a quantinuumresearch.com
Gholson LyonInstitute for Basic Research in Developmental DisabilitiesCorreu electrònic verificat a opwdd.ny.gov
Patrick SleimanDirector, GeneticsCorreu electrònic verificat a rhythmtx.com
Ram SamudralaProfessor and Chief, Division of Bioinformatics, University at BuffaloCorreu electrònic verificat a compbio.org
Xiao ChangChildren's hospital of philadelphiaCorreu electrònic verificat a email.chop.edu
Zhi WeiProf of Comp Sci and Statistics, NJIT; Adjunct Prof. at UPenn.Correu electrònic verificat a njit.edu
Prof. Dr. med., Dipl. Phys. Peter KrawitzInstitute for Genomic Statistics and BioinformaticsCorreu electrònic verificat a uni-bonn.de
Peter RobinsonBerlin Institute of Health, Charité - Universitätsmedizin, Berlin, GermanyCorreu electrònic verificat a bih-charite.de
Reid Robison, MD MBABoard-certified Psychiatrist. Co-Founded Genomics (acquired 2016), Polizzi Free Clinic. Board ChairCorreu electrònic verificat a utahresearch.org
Samuel P. DicksonPentara CorporationCorreu electrònic verificat a stat-smart.com
Huiqi QuChildren's Hospital of PhiladelphiaCorreu electrònic verificat a email.chop.edu
Marcin ImielinskiWeill Cornell Medicine, New York Genome CenterCorreu electrònic verificat a med.cornell.edu
Dexter HadleyChief of AI, University of Central Florida, College of MedicineCorreu electrònic verificat a ucf.edu
Damian SmedleyQueen Mary University of LondonCorreu electrònic verificat a qmul.ac.uk
W. Evan JohnsonProfessor of MedicineCorreu electrònic verificat a rutgers.edu
John M MarisProfessor Pediatrics, Children's Hospital of Philadelphia and University of PennsylvaniaCorreu electrònic verificat a chop.edu
Andrew SingletonNational Institute on AgingCorreu electrònic verificat a mail.nih.gov
Paul ScheetUniversity of Texas MD Anderson Cancer CenterCorreu electrònic verificat a mdanderson.org

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Kai Wang

Children's Hospital of Philadelphia

Correu electrònic verificat a email.chop.edu - Pàgina d'inici

genomics bioinformatics GWAS CNV NGS


Títol Ordena per cites Ordena per any Ordena per títol	Citada per Citada per	Any
ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data K Wang, M Li, H Hakonarson Nucleic acids research 38 (16), e164-e164, 2010	14094	2010
Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci A Franke, DPB McGovern, JC Barrett, K Wang, GL Radford-Smith, ... Nature genetics 42 (12), 1118-1125, 2010	3239	2010
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis S Sawcer, G Hellenthal, M Pirinen, CC Spencer, NA Patsopoulos, ...	3094*	2011
Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations JZ Liu, S van Sommeren, H Huang, SC Ng, R Alberts, A Takahashi, ... Nature genetics 47 (9), 979-986, 2015	2730	2015
Functional impact of global rare copy number variation in autism spectrum disorders D Pinto, AT Pagnamenta, L Klei, R Anney, D Merico, R Regan, J Conroy, ... Nature 466 (7304), 368-372, 2010	2383	2010
PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data K Wang, M Li, D Hadley, R Liu, J Glessner, SFA Grant, H Hakonarson, ... Genome research 17 (11), 1665-1674, 2007	2064	2007
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes JT Glessner, K Wang, G Cai, O Korvatska, CE Kim, S Wood, H Zhang, ... Nature 459 (7246), 569-573, 2009	1639	2009
Comparison and integration of deleteriousness prediction methods for nonsynonymous SNVs in whole exome sequencing studies C Dong, P Wei, X Jian, R Gibbs, E Boerwinkle, K Wang, X Liu Human molecular genetics 24 (8), 2125-2137, 2015	1190	2015
Common genetic variants on 5p14. 1 associate with autism spectrum disorders K Wang, H Zhang, D Ma, M Bucan, JT Glessner, BS Abrahams, ... Nature 459 (7246), 528-533, 2009	1149	2009
Rare variants create synthetic genome-wide associations SP Dickson, K Wang, I Krantz, H Hakonarson, DB Goldstein PLoS biology 8 (1), 34, 2010	1057	2010
Pathway-based approaches for analysis of genomewide association studies K Wang, M Li, M Bucan The American Journal of Human Genetics 81 (6), 1278-1283, 2007	1053	2007
Genotype, haplotype and copy-number variation in worldwide human populations M Jakobsson, SW Scholz, P Scheet, JR Gibbs, JM VanLiere, HC Fung, ... Nature 451 (7181), 998-1003, 2008	1043	2008
InterVar: Clinical interpretation of genetic variants by the 2015 ACMG-AMP guidelines Q Li, K Wang The American Journal of Human Genetics 100 (2), 267-280, 2017	976	2017
Analysing biological pathways in genome-wide association studies K Wang, M Li, H Hakonarson Nature Reviews Genetics 11 (12), 843-854, 2010	939	2010
Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease MA Rivas, M Beaudoin, A Gardet, C Stevens, Y Sharma, CK Zhang, ... Nature genetics 43 (11), 1066-1073, 2011	907	2011
Inherited determinants of Crohn's disease and ulcerative colitis phenotypes: a genetic association study I Cleynen, G Boucher, L Jostins, LP Schumm, S Zeissig, T Ahmad, ... The Lancet 387 (10014), 156-167, 2016	895	2016
Genomic variant annotation and prioritization with ANNOVAR and wANNOVAR H Yang, K Wang Nature protocols 10 (10), 1556-1566, 2015	889	2015
A genome-wide scan for common alleles affecting risk for autism R Anney, L Klei, D Pinto, R Regan, J Conroy, TR Magalhaes, C Correia, ... Human molecular genetics 19 (20), 4072-4082, 2010	741	2010
Common variants at five new loci associated with early-onset inflammatory bowel disease M Imielinski, RN Baldassano, A Griffiths, RK Russell, V Annese, ... Nature genetics 41 (12), 1335-1340, 2009	589	2009
Low concordance of multiple variant-calling pipelines: practical implications for exome and genome sequencing J O'Rawe, T Jiang, G Sun, Y Wu, W Wang, J Hu, P Bodily, L Tian, ... Genome medicine 5 (3), 28, 2013	556	2013

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