| Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis Nature 476 (7359), 214-219, 2011 | 2776 | 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 | 2206 | 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 | 1881 | 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 | 1539 | 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 | 1094 | 2009 |
| 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 | 879 | 2013 |
| 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 | 691 | 2010 |
| 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 | 625 | 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 | 594 | 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 | 546 | 2009 |
| Mapping the human genetic architecture of COVID-19 Writing group Writing group leaders Pathak Gita A. 6 Andrews Shea J. 7 Kanai ... Nature 600 (7889), 472-477, 2021 | 515 | 2021 |
| 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 | 465 | 2009 |
| Concept, design and implementation of a cardiovascular gene-centric 50 k SNP array for large-scale genomic association studies BJ Keating, S Tischfield, SS Murray, T Bhangale, TS Price, JT Glessner, ... PloS one 3 (10), e3583, 2008 | 452 | 2008 |
| Common variants at 5q22 associate with pediatric eosinophilic esophagitis ME Rothenberg, JM Spergel, JD Sherrill, K Annaiah, LJ Martin, ... Nature genetics 42 (4), 289-291, 2010 | 439 | 2010 |
| Copy number variation at 1q21. 1 associated with neuroblastoma SJ Diskin, C Hou, JT Glessner, EF Attiyeh, M Laudenslager, K Bosse, ... Nature 459 (7249), 987-991, 2009 | 434 | 2009 |
| Individual common variants exert weak effects on the risk for autism spectrum disorders R Anney, L Klei, D Pinto, J Almeida, E Bacchelli, G Baird, N Bolshakova, ... Human molecular genetics 21 (21), 4781-4792, 2012 | 429 | 2012 |
| High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications TH Shaikh, X Gai, JC Perin, JT Glessner, H Xie, K Murphy, R O'Hara, ... Genome research 19 (9), 1682-1690, 2009 | 426 | 2009 |
| Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease S Kugathasan, RN Baldassano, JP Bradfield, PMA Sleiman, M Imielinski, ... Nature genetics 40 (10), 1211-1215, 2008 | 402 | 2008 |
| Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder J Elia, JT Glessner, K Wang, N Takahashi, CJ Shtir, D Hadley, ... Nature genetics 44 (1), 78-84, 2012 | 397 | 2012 |
| Variants of DENND1B Associated with Asthma in Children PMA Sleiman, J Flory, M Imielinski, JP Bradfield, K Annaiah, ... New England journal of medicine 362 (1), 36-44, 2010 | 396 | 2010 |
Hakon HakonarsonDirector, Center for Applied Genomics, CHOP, UPENNVerified email at email.chop.edu
