Kai Wang

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Hakon HakonarsonDirector, Center for Applied Genomics, CHOP, UPENNE-mailová adresa ověřena na: email.chop.edu
Mingyao LiProfessor of Biostatistics, University of Pennsylvania School of MedicineE-mailová adresa ověřena na: mail.med.upenn.edu
Jonathan BradfieldPresident, Quantinuum Research LLCE-mailová adresa ověřena na: quantinuumresearch.com
Gholson LyonInstitute for Basic Research in Developmental DisabilitiesE-mailová adresa ověřena na: opwdd.ny.gov
Patrick SleimanDirector, GeneticsE-mailová adresa ověřena na: rhythmtx.com
Ram SamudralaProfessor and Chief, Division of Bioinformatics, University at BuffaloE-mailová adresa ověřena na: compbio.org
Xiao ChangChildren's hospital of philadelphiaE-mailová adresa ověřena na: email.chop.edu
Zhi WeiProf of Comp Sci and Statistics, NJIT; Adjunct Prof. at UPenn.E-mailová adresa ověřena na: njit.edu
Prof. Dr. med., Dipl. Phys. Peter KrawitzInstitute for Genomic Statistics and BioinformaticsE-mailová adresa ověřena na: uni-bonn.de
Peter RobinsonBerlin Institute of Health, Charité - Universitätsmedizin, Berlin, GermanyE-mailová adresa ověřena na: bih-charite.de
Reid Robison, MD MBABoard-certified Psychiatrist. Co-Founded Genomics (acquired 2016), Polizzi Free Clinic. Board ChairE-mailová adresa ověřena na: utahresearch.org
Samuel P. DicksonPentara CorporationE-mailová adresa ověřena na: stat-smart.com
Huiqi QuChildren's Hospital of PhiladelphiaE-mailová adresa ověřena na: email.chop.edu
Marcin ImielinskiWeill Cornell Medicine, New York Genome CenterE-mailová adresa ověřena na: med.cornell.edu
Dexter HadleyChief of AI, University of Central Florida, College of MedicineE-mailová adresa ověřena na: ucf.edu
Damian SmedleyQueen Mary University of LondonE-mailová adresa ověřena na: qmul.ac.uk
W. Evan JohnsonProfessor of MedicineE-mailová adresa ověřena na: rutgers.edu
John M MarisProfessor Pediatrics, Children's Hospital of Philadelphia and University of PennsylvaniaE-mailová adresa ověřena na: chop.edu
Andrew SingletonNational Institute on AgingE-mailová adresa ověřena na: mail.nih.gov
Paul ScheetUniversity of Texas MD Anderson Cancer CenterE-mailová adresa ověřena na: mdanderson.org

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Kai Wang

Children's Hospital of Philadelphia

E-mailová adresa ověřena na: email.chop.edu - Domovská stránka

genomics bioinformatics GWAS CNV NGS


Název Seřadit podle citací Seřadit podle roku Seřadit podle názvu	Citace Citace	Rok
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	14117	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	3242	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, ...	3097*	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	2740	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	2388	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	1642	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	1194	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	1052	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	1041	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	980	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	899	2016
Genomic variant annotation and prioritization with ANNOVAR and wANNOVAR H Yang, K Wang Nature protocols 10 (10), 1556-1566, 2015	890	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	557	2013

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