Theo dõi
Kai Wang
Kai Wang
Children's Hospital of Philadelphia
Email được xác minh tại email.chop.edu - Trang chủ
Tiêu đề
Trích dẫn bởi
Trích dẫn bởi
Năm
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
141842010
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
32122010
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
S Sawcer, G Hellenthal, M Pirinen, CC Spencer, NA Patsopoulos, ...
3108*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
27472015
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
24162010
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
20662007
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
16532009
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
12032015
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
11422009
Rare variants create synthetic genome-wide associations
SP Dickson, K Wang, I Krantz, H Hakonarson, DB Goldstein
PLoS biology 8 (1), 34, 2010
10542010
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
10512007
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
10412008
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
9972017
Analysing biological pathways in genome-wide association studies
K Wang, M Li, H Hakonarson
Nature Reviews Genetics 11 (12), 843-854, 2010
9382010
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
9152011
Genomic variant annotation and prioritization with ANNOVAR and wANNOVAR
H Yang, K Wang
Nature protocols 10 (10), 1556-1566, 2015
8992015
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
8962016
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
7352010
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
5862009
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
5602013
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