Theo dõi
Struan Grant
Struan Grant
Professor of Genetics and Pediatrics
Email được xác minh tại pennmedicine.upenn.edu - Trang chủ
Tiêu đề
Trích dẫn bởi
Trích dẫn bởi
Năm
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
Nature 476 (7359), 214-219, 2011
31082011
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
29092006
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
20662007
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
16532009
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
12352004
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
11422009
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
9311996
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
6632007
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
6582007
The power of genetic diversity in genome-wide association studies of lipids
SE Graham, SL Clarke, KHH Wu, S Kanoni, GJM Zajac, S Ramdas, ...
Nature 600 (7890), 675-679, 2021
6572021
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
6572001
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
6462010
A saturated map of common genetic variants associated with human height
L Yengo, S Vedantam, E Marouli, J Sidorenko, E Bartell, S Sakaue, ...
Nature 610 (7933), 704-712, 2022
6002022
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
5862009
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
5801998
Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors
NM Warrington, RN Beaumont, M Horikoshi, FR Day, Ø Helgeland, ...
Nature genetics 51 (5), 804-814, 2019
5322019
The time is right for a new classification system for diabetes: rationale and implications of the β-cell–centric classification schema
SS Schwartz, S Epstein, BE Corkey, SFA Grant, JR Gavin III, RB Aguilar
Diabetes care 39 (2), 179-186, 2016
5322016
A genome-wide association meta-analysis identifies new childhood obesity loci
Nature genetics 44 (5), 526-531, 2012
5292012
Genome-wide associations for birth weight and correlations with adult disease
M Horikoshi, RN Beaumont, FR Day, NM Warrington, MN Kooijman, ...
Nature 538 (7624), 248-252, 2016
4982016
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
4982009
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