Kai Wang

Alıntı yapanlar

	Hepsi	2017 yılından bugüne
Alıntılar	47903	25335
h-endeksi	74	58
i10-endeksi	183	158

6000

3000

1500

4500

200820092010201120122013201420152016201720182019202020212022162 447 1162 2139 2947 3298 3819 3873 4075 4169 4226 4514 4640 5143 2634

Genel erişim

Tümünü görüntüle

189 makale

3 makale

genel erişime açık olanlar

genel erişime açık olmayanlar

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
Reid Robison, MD MBABoard-certified Psychiatrist. Co-Founded Genomics (acquired 2016), Polizzi Free Clinic. Board Chairutahresearch.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
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
Huiqi QuChildren's Hospital of Philadelphiaemail.chop.edu üzerinde doğrulanmış e-posta adresine sahip
W. Evan JohnsonAssociate Professor of Medicine and Biostatisticsbu.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

Takip et

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	9891	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	2841	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, ...	2642*	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	2105	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	1792	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	1726	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	1457	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	1050	2009
Rare variants create synthetic genome-wide associations SP Dickson, K Wang, I Krantz, H Hakonarson, DB Goldstein PLoS biology 8 (1), 34, 2010	1001	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	984	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	948	2008
Analysing biological pathways in genome-wide association studies K Wang, M Li, H Hakonarson Nature Reviews Genetics 11 (12), 843-854, 2010	883	2010
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	848	2015
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	792	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	654	2016
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	648	2010
Genomic variant annotation and prioritization with ANNOVAR and wANNOVAR H Yang, K Wang Nature protocols 10 (10), 1556-1566, 2015	618	2015
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	561	2017
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	526	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	500	2013

Sistem, işlemi şu anda gerçekleştiremiyor. Daha sonra yeniden deneyin.

Makaleler 1–20

Yıllık alıntı sayısı

Mükerrer alıntılar

Birleştirilmiş alıntılar

Katkıda bulunan yazar ekleKatkıda bulunan yazarlar

Bu yazarı takip edin

Alıntı yapanlar

Katkıda bulunan yazarlar