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Struan Grant
Struan Grant
Professor of Pediatrics
Verified email at mail.med.upenn.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
26612011
Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes
SFA Grant, G Thorleifsson, I Reynisdottir, R Benediktsson, A Manolescu, ...
Nature genetics 38 (3), 320-323, 2006
26252006
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
17992007
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
14682009
The gene encoding 5-lipoxygenase activating protein confers risk of myocardial infarction and stroke
A Helgadottir, A Manolescu, G Thorleifsson, S Gretarsdottir, H Jonsdottir, ...
Nature genetics 36 (3), 233-239, 2004
11632004
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
10552009
Reduced bone density and osteoporosis associated with a polymorphic Sp1 binding site in the collagen type I α 1 gene
SFA Grant, DM Reid, G Blake, R Herd, I Fogelman, SH Ralston
Nature genetics 14 (2), 203-205, 1996
8881996
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
6182007
Refining the impact of TCF7L2 gene variants on type 2 diabetes and adaptive evolution
A Helgason, S Pálsson, G Thorleifsson, SFA Grant, V Emilsson, ...
Nature genetics 39 (2), 218-225, 2007
6082007
A COL1A1 Sp1 binding site polymorphism predisposes to osteoporotic fracture by affecting bone density and quality
V Mann, EE Hobson, B Li, TL Stewart, SFA Grant, SP Robins, RM Aspden, ...
The Journal of clinical investigation 107 (7), 899-907, 2001
5902001
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
5782010
Relation of alleles of the collagen type Iα1 gene to bone density and the risk of osteoporotic fractures in postmenopausal women
AG Uitterlinden, H Burger, Q Huang, F Yue, FEA McGuigan, SFA Grant, ...
New England Journal of Medicine 338 (15), 1016-1021, 1998
5551998
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
5292009
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
4482009
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
4432008
A genome-wide association meta-analysis identifies new childhood obesity loci
Nature genetics 44 (5), 526-531, 2012
4422012
A variant of the gene encoding leukotriene A4 hydrolase confers ethnicity-specific risk of myocardial infarction
A Helgadottir, A Manolescu, A Helgason, G Thorleifsson, ...
Nature genetics 38 (1), 68-74, 2006
4292006
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
4192010
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
4152009
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
4132009
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