Kai Wang

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	Hepsi	2016 yılından bugüne
Alıntılar	42315	23998
h-endeksi	71	57
i10-endeksi	167	149

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20082009201020112012201320142015201620172018201920202021160 455 1163 2111 2937 3258 3769 3888 4063 4138 4150 4453 4677 2504

Genel erişim

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Finansman sağlayan kuruluşun getirdiği zorunluluğa dayalı olarak

Katkıda bulunan yazarlar

Hakon HakonarsonDirector, Center for Applied Genomics, CHOP, UPENNemail.chop.edu üzerinde doğrulanmış e-posta adresine sahip
Mingyao LiProfessor of Biostatistics, University of Pennsylvania School of Medicinemail.med.upenn.edu üzerinde doğrulanmış e-posta adresine sahip
Jonathan BradfieldPresident, Quantinuum Research LLCquantinuumresearch.com üzerinde doğrulanmış e-posta adresine sahip
Gholson LyonInstitute for Basic Research in Developmental Disabilitiesopwdd.ny.gov üzerinde doğrulanmış e-posta adresine sahip
Patrick SleimanAssociate Professor of Geneticsemail.chop.edu üzerinde doğrulanmış e-posta adresine sahip
Ram SamudralaProfessor and Chief, Division of Bioinformatics, University at Buffalocompbio.org üzerinde doğrulanmış e-posta adresine sahip
Chang XiaoChildren's hospital of philadelphiaemail.chop.edu üzerinde doğrulanmış e-posta adresine sahip
Zhi WeiProf of Comp Sci and Statistics, NJIT; Adjunct Prof. at UPenn.njit.edu üzerinde doğrulanmış e-posta adresine sahip
Peter RobinsonProfessor of Computational Biology, The Jackson Laboratory for Genomic Medicinejax.org üzerinde doğrulanmış e-posta adresine sahip
Samuel P. DicksonSocial & Scientific Systemsstat-smart.com üzerinde doğrulanmış e-posta adresine sahip
Wei WangPh.D. in Computer Science, New Jersey Institute of Technologynjit.edu üzerinde doğrulanmış e-posta adresine sahip
Reid Robison, MD MBABoard-certified Psychiatrist. Co-Founded Genomics (acquired 2016), Polizzi Free Clinic. Board Chairutahresearch.org üzerinde doğrulanmış e-posta adresine sahip
Jason O'Rawecshl.edu üzerinde doğrulanmış e-posta adresine sahip
Marcin ImielinskiWeill Cornell Medicine, New York Genome Centermed.cornell.edu üzerinde doğrulanmış e-posta adresine sahip
Dexter HadleyChief of AI, University of Central Florida, College of Medicineucf.edu üzerinde doğrulanmış e-posta adresine sahip
Damian SmedleyQueen Mary University of Londonqmul.ac.uk üzerinde doğrulanmış e-posta adresine sahip
Prof. Dr. med., Dipl. Phys. Peter KrawitzInstitute for Genomic Statistics and Bioinformaticsuni-bonn.de üzerinde doğrulanmış e-posta adresine sahip
W. Evan JohnsonAssociate Professor of Medicine and Biostatisticsbu.edu üzerinde doğrulanmış e-posta adresine sahip
Huiqi QuChildren's Hospital of Philadelphiaemail.chop.edu üzerinde doğrulanmış e-posta adresine sahip
John M MarisProfessor Pediatrics, Children's Hospital of Philadelphia and University of Pennsylvaniachop.edu üzerinde doğrulanmış e-posta adresine sahip

Kai Wang

Children's Hospital of Philadelphia

email.chop.edu üzerinde doğrulanmış e-posta adresine sahip - Ana Sayfa

genomics bioinformatics GWAS CNV NGS


Başlık Alıntılara göre sırala Yıla göre sırala Başlığa göre sırala	Alıntı yapanlar Alıntı yapanlar	Yıl
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	8217	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	2643	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, ...	2400	2011
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	1983	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	1684	2007
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	1393	2015
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	1387	2009
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	996	2009
Rare variants create synthetic genome-wide associations SP Dickson, K Wang, I Krantz, H Hakonarson, DB Goldstein PLoS biology 8 (1), 34, 2010	965	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	943	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	920	2008
Analysing biological pathways in genome-wide association studies K Wang, M Li, H Hakonarson Nature Reviews Genetics 11 (12), 843-854, 2010	840	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	730	2011
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	643	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	604	2010
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	542	2016
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	503	2009
Proteins encoded in genomic regions associated with immune-mediated disease physically interact and suggest underlying biology EJ Rossin, K Lage, S Raychaudhuri, RJ Xavier, D Tatar, Y Benita, ... PLoS Genet 7 (1), e1001273, 2011	491	2011
Genomic variant annotation and prioritization with ANNOVAR and wANNOVAR H Yang, K Wang Nature protocols 10 (10), 1556-1566, 2015	489	2015
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	474	2013

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