Joseph Glessner

Alıntı yapanlar

	Hepsi	2020 yılından bugüne
Alıntılar	33365	10736
h-endeksi	80	52
i10-endeksi	161	134

2700

1350

675

2025

200820092010201120122013201420152016201720182019202020212022202320242025191 482 1258 1916 2232 2570 2640 2418 2365 2191 2074 1955 2078 2057 2179 2103 2060 242

Genel erişim

Tümünü görüntüle

163 makale

6 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
Struan GrantProfessor of Genetics and Pediatricspennmedicine.upenn.edu üzerinde doğrulanmış e-posta adresine sahip
Patrick SleimanDirector, Geneticsrhythmtx.com üzerinde doğrulanmış e-posta adresine sahip
Jonathan BradfieldPresident, Quantinuum Research LLCquantinuumresearch.com üzerinde doğrulanmış e-posta adresine sahip
Huiqi QuChildren's Hospital of Philadelphiaemail.chop.edu üzerinde doğrulanmış e-posta adresine sahip
Kai WangChildren's Hospital of Philadelphiaemail.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
Xiao ChangChildren's hospital of philadelphiaemail.chop.edu üzerinde doğrulanmış e-posta adresine sahip
haitao zhangMITsunovion.com üzerinde doğrulanmış e-posta adresine sahip
Yichuan Edward LiuThe Children's Hospital of Philadelphia, Center for Applied Genomicsemail.chop.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
Constantin PolychronakosMcGill Universitymcgill.ca üzerinde doğrulanmış e-posta adresine sahip
Lifeng TianThe Children's Hospital of Philadelphiaemail.chop.edu üzerinde doğrulanmış e-posta adresine sahip
Marcin ImielinskiWeill Cornell Medicine, New York Genome Centermed.cornell.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
Sharon J. DiskinChildren's Hospital of Philadelphia and University of Pennsylvaniaemail.chop.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
Brendan KeatingNew York University, Langone Healthmail.med.upenn.edu üzerinde doğrulanmış e-posta adresine sahip
Tamim H. ShaikhProfessor of Pediatrics and Biochemistry & Molecular Genetics, University of Colorado Denver, Schoolucdenver.edu üzerinde doğrulanmış e-posta adresine sahip
Xiaowu GaiMedical College of Wisconsinmcw.edu üzerinde doğrulanmış e-posta adresine sahip

Takip et

Joseph Glessner

Technical Director, Children's Hospital of Philadelphia

email.chop.edu üzerinde doğrulanmış e-posta adresine sahip - Ana Sayfa

Computational Biology


Başlık Alıntılara göre sırala Yıla göre sırala Başlığa göre sırala	Alıntı yapanlar Alıntı yapanlar	Yıl
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis Nature 476 (7359), 214-219, 2011	3080	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	2383	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	2063	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	1639	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	1148	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	1003	2013
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	839	2021
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	741	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	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	644	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	588	2009
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	499	2009
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	486	2010
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	461	2012
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	455	2008
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	450	2009
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	437	2009
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	432	2012
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	426	2008
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	415	2010

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