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Joseph Glessner
Joseph Glessner
Technical Director, Children's Hospital of Philadelphia
Verified email at email.chop.edu - Homepage
Title
Cited by
Cited by
Year
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
Nature 476 (7359), 214-219, 2011
26782011
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
21382010
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
18172007
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
14812009
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
10602009
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
8322013
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
6612010
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
6192007
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
5812010
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
5332009
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
4492009
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
4442008
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
4242010
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
4182009
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
4142009
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
4032012
Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease
S Kugathasan, RN Baldassano, JP Bradfield, P Sleiman, M Imielinski, ...
Nature genetics 40 (10), 1211-1215, 2008
3922008
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
3832012
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
3792010
Adjustment of genomic waves in signal intensities from whole-genome SNP genotyping platforms
SJ Diskin, M Li, C Hou, S Yang, J Glessner, H Hakonarson, M Bucan, ...
Nucleic acids research 36 (19), e126-e126, 2008
3592008
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