Kai Wang

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Hakon HakonarsonDirector, Center for Applied Genomics, CHOP, UPENNVerificeret mail på email.chop.edu
Mingyao LiProfessor of Biostatistics, University of Pennsylvania School of MedicineVerificeret mail på mail.med.upenn.edu
Jonathan BradfieldPresident, Quantinuum Research LLCVerificeret mail på quantinuumresearch.com
Gholson LyonInstitute for Basic Research in Developmental DisabilitiesVerificeret mail på opwdd.ny.gov
Patrick SleimanDirector, GeneticsVerificeret mail på rhythmtx.com
Ram SamudralaProfessor and Chief, Division of Bioinformatics, University at BuffaloVerificeret mail på compbio.org
Xiao ChangChildren's hospital of philadelphiaVerificeret mail på email.chop.edu
Zhi WeiProf of Comp Sci and Statistics, NJIT; Adjunct Prof. at UPenn.Verificeret mail på njit.edu
Prof. Dr. med., Dipl. Phys. Peter KrawitzInstitute for Genomic Statistics and BioinformaticsVerificeret mail på uni-bonn.de
Peter RobinsonBerlin Institute of Health, Charité - Universitätsmedizin, Berlin, GermanyVerificeret mail på bih-charite.de
Reid Robison, MD MBABoard-certified Psychiatrist. Co-Founded Genomics (acquired 2016), Polizzi Free Clinic. Board ChairVerificeret mail på utahresearch.org
Samuel P. DicksonPentara CorporationVerificeret mail på stat-smart.com
Huiqi QuChildren's Hospital of PhiladelphiaVerificeret mail på email.chop.edu
Marcin ImielinskiWeill Cornell Medicine, New York Genome CenterVerificeret mail på med.cornell.edu
Dexter HadleyChief of AI, University of Central Florida, College of MedicineVerificeret mail på ucf.edu
Damian SmedleyQueen Mary University of LondonVerificeret mail på qmul.ac.uk
W. Evan JohnsonProfessor of MedicineVerificeret mail på rutgers.edu
John M MarisProfessor Pediatrics, Children's Hospital of Philadelphia and University of PennsylvaniaVerificeret mail på chop.edu
Andrew SingletonNational Institute on AgingVerificeret mail på mail.nih.gov
Paul ScheetUniversity of Texas MD Anderson Cancer CenterVerificeret mail på mdanderson.org

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Kai Wang

Children's Hospital of Philadelphia

Verificeret mail på email.chop.edu - Startside

genomics bioinformatics GWAS CNV NGS


Titel Sortér efter henvisninger Sortér efter årstal Sortér efter titel	Citeret af Citeret af	År
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	14100	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, ...	3095*	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	2732	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	2384	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	2063	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	1641	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	1191	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	978	2017
Analysing biological pathways in genome-wide association studies K Wang, M Li, H Hakonarson Nature Reviews Genetics 11 (12), 843-854, 2010	940	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	908	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	897	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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