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| 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 | 2059 | 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 | 1635 | 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 | 1176 | 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), e1000294, 2010 | 1052 | 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 | 1048 | 2007 |
| De novo mutations in histone-modifying genes in congenital heart disease S Zaidi, M Choi, H Wakimoto, L Ma, J Jiang, JD Overton, ... Nature 498 (7453), 220-223, 2013 | 997 | 2013 |
| 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 | 965 | 2017 |
| Analysing biological pathways in genome-wide association studies K Wang, M Li, H Hakonarson Nature Reviews Genetics 11 (12), 843-854, 2010 | 936 | 2010 |
| Genomic variant annotation and prioritization with ANNOVAR and wANNOVAR H Yang, K Wang Nature protocols 10 (10), 1556-1566, 2015 | 882 | 2015 |
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| A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene H Hakonarson, SFA Grant, JP Bradfield, L Marchand, CE Kim, ... Nature 448 (7153), 591-594, 2007 | 653 | 2007 |
| Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes J Elia, X Gai, HM Xie, JC Perin, E Geiger, JT Glessner, M D'arcy, ... Molecular psychiatry 15 (6), 637-646, 2010 | 643 | 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 | 585 | 2009 |
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| Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications DF Levinson, J Duan, S Oh, K Wang, AR Sanders, J Shi, N Zhang, ... American Journal of Psychiatry 168 (3), 302-316, 2011 | 506 | 2011 |
| Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes M Bucan, BS Abrahams, K Wang, JT Glessner, EI Herman, LI Sonnenblick, ... PLoS genetics 5 (6), e1000536, 2009 | 496 | 2009 |
| wANNOVAR: annotating genetic variants for personal genomes via the web X Chang, K Wang Journal of medical genetics 49 (7), 433-436, 2012 | 483 | 2012 |
