Struan Grant

Alıntı yapanlar

	Hepsi	2020 yılından bugüne
Alıntılar	46378	15653
h-endeksi	100	66
i10-endeksi	266	203

3500

1750

875

2625

199920002001200220032004200520062007200820092010201120122013201420152016201720182019202020212022202320242025144 192 282 246 278 307 444 494 814 982 1181 1861 2196 2462 2715 2670 2532 2583 2459 2566 2669 2676 2907 2850 3055 3436 721

Genel erişim

Tümünü görüntüle

259 makale

9 makale

genel erişime açık olanlar

genel erişime açık olmayanlar

Finansman sağlayan kuruluşun getirdiği zorunluluğa dayalı olarak

Katkıda bulunan yazarlar

Jonathan BradfieldPresident, Quantinuum Research LLCquantinuumresearch.com üzerinde doğrulanmış e-posta adresine sahip
Alessandra ChesiUniversity of Pennsylvaniapennmedicine.upenn.edu üzerinde doğrulanmış e-posta adresine sahip
Kai WangChildren's Hospital of Philadelphiaemail.chop.edu üzerinde doğrulanmış e-posta adresine sahip
Andrew WellsUniversity of Pennsylvaniapennmedicine.upenn.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
Diana L CousminerGSKgsk.com üzerinde doğrulanmış e-posta adresine sahip
Jonathan MitchellAssociate Professor, Children's Hospital of Philadelphia / University of Pennsylvaniachop.edu üzerinde doğrulanmış e-posta adresine sahip
Kenyaita M. HodgePostdoctoral Fellow, Morehouse School of Medicinemsm.edu üzerinde doğrulanmış e-posta adresine sahip
Chun SuScientist, Amgenamgen.com üzerinde doğrulanmış e-posta adresine sahip
Kurt HankensonProfessor of Orthopaedic Surgery, University of Michiganumich.edu üzerinde doğrulanmış e-posta adresine sahip
Matthew C. PahlChildren's Hospital of Philadelphiachop.edu üzerinde doğrulanmış e-posta adresine sahip
Yadav WagleyUniversity of Michiganmed.umich.edu üzerinde doğrulanmış e-posta adresine sahip
Christopher D BrownAssociate Professor of Genetics, University of Pennsylvaniapennmedicine.upenn.edu üzerinde doğrulanmış e-posta adresine sahip
Sheridan LittletonResearch Associatecam.ac.uk üzerinde doğrulanmış e-posta adresine sahip
Benjamin F. VoightAssociate Professor, Dept. of Systems Pharmacology and Translational Therapeutics, Dept. of Geneticspennmedicine.upenn.edu üzerinde doğrulanmış e-posta adresine sahip
KH KaestnerDepartment of Genetics and Institute for Diabetes, Obesity and Metabolism, Perelman School ofmail.med.upenn.edu üzerinde doğrulanmış e-posta adresine sahip
Rajashree MishraUniversity of Pennsylvaniapennmedicine.upenn.edu üzerinde doğrulanmış e-posta adresine sahip
Fusun Doldur BalliUniversity of Pennsylvaniapennmedicine.upenn.edu üzerinde doğrulanmış e-posta adresine sahip
Philip GehrmanUniversity of Pennsylvaniaupenn.edu üzerinde doğrulanmış e-posta adresine sahip
Alex KeeneProfessor and Head of Biology, Texas A&Mbio.tamu.edu üzerinde doğrulanmış e-posta adresine sahip

Takip et

Struan Grant

Professor of Genetics and Pediatrics

pennmedicine.upenn.edu üzerinde doğrulanmış e-posta adresine sahip - Ana Sayfa

bone obesity/diabetes sleep genetics genomics


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	3108	2011
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	2909	2006
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	2066	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	1653	2009
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	1235	2004
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	1142	2009
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	931	1996
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	663	2007
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	658	2007
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	657	2021
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	657	2001
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	646	2010
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	600	2022
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	586	2009
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	580	1998
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	532	2019
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	532	2016
A genome-wide association meta-analysis identifies new childhood obesity loci Nature genetics 44 (5), 526-531, 2012	529	2012
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	498	2016
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	498	2009

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