Steven Wiltshire
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Explore the profile of Steven Wiltshire including associated specialties, affiliations and a list of published articles.
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31
Citations
2462
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Recent Articles
1.
Horikoshi M, Pasquali L, Wiltshire S, Huyghe J, Mahajan A, Asimit J, et al.
Hum Mol Genet
. 2016 Feb;
25(10):2070-2081.
PMID: 26911676
To gain insight into potential regulatory mechanisms through which the effects of variants at four established type 2 diabetes (T2D) susceptibility loci (CDKAL1, CDKN2A-B, IGF2BP2 and KCNQ1) are mediated, we...
2.
Gaulton K, Ferreira T, Lee Y, Raimondo A, Magi R, Reschen M, et al.
Nat Genet
. 2015 Nov;
47(12):1415-25.
PMID: 26551672
We performed fine mapping of 39 established type 2 diabetes (T2D) loci in 27,206 cases and 57,574 controls of European ancestry. We identified 49 distinct association signals at these loci,...
3.
Discovery and Fine-Mapping of Glycaemic and Obesity-Related Trait Loci Using High-Density Imputation
Horikoshi M, Mgi R, van de Bunt M, Surakka I, Sarin A, Mahajan A, et al.
PLoS Genet
. 2015 Jul;
11(7):e1005230.
PMID: 26132169
Reference panels from the 1000 Genomes (1000G) Project Consortium provide near complete coverage of common and low-frequency genetic variation with minor allele frequency ≥0.5% across European ancestry populations. Within the...
4.
Mahajan A, Go M, Zhang W, Below J, Gaulton K, Ferreira T, et al.
Nat Genet
. 2014 Feb;
46(3):234-44.
PMID: 24509480
To further understanding of the genetic basis of type 2 diabetes (T2D) susceptibility, we aggregated published meta-analyses of genome-wide association studies (GWAS), including 26,488 cases and 83,964 controls of European,...
5.
Peters K, Beilby J, Cadby G, Warrington N, Bruce D, Davis W, et al.
BMC Med Genet
. 2013 Jan;
14:15.
PMID: 23351195
Background: Low levels of serum adiponectin have been linked to central obesity, insulin resistance, metabolic syndrome, and type 2 diabetes. Variants in ADIPOQ, the gene encoding adiponectin, have been shown...
6.
Morris A, Voight B, Teslovich T, Ferreira T, V Segre A, Steinthorsdottir V, et al.
Nat Genet
. 2012 Aug;
44(9):981-90.
PMID: 22885922
To extend understanding of the genetic architecture and molecular basis of type 2 diabetes (T2D), we conducted a meta-analysis of genetic variants on the Metabochip, including 34,840 cases and 114,981...
7.
Verbrugghe P, Bouwer S, Wiltshire S, Carter K, Chandler D, Cooper M, et al.
Am J Med Genet B Neuropsychiatr Genet
. 2012 Mar;
159B(4):392-404.
PMID: 22419519
Our previous neurocognitive studies of schizophrenia outlined two clusters of affected subjects--cognitively spared (CS) and cognitive deficit (CD), the latter's characteristics pointing to developmental origins and impaired synaptic plasticity. Here...
8.
Powell B, Wiltshire S, Arscott G, McCaskie P, Hung J, McQuillan B, et al.
Hum Genet
. 2008 Sep;
124(3):263-70.
PMID: 18758826
PARL (presenilin-associated rhomboid-like) is a mitochondrial protein involved in mitochondrial membrane remodelling, and maps to a quantitative trait locus (3q27) associated with metabolic traits. Recently the rs3732581 (Leu262Val) variant was...
9.
Carter K, Hung J, Powell B, Wiltshire S, Foo B, Leow Y, et al.
Hum Genet
. 2008 Aug;
124(3):199-206.
PMID: 18716798
The objective of this study was to determine whether single nucleotide polymorphisms (SNPs) in the Interleukin-1 (IL-1) gene family are associated with central obesity and metabolic syndrome in a coronary...
10.
Franks S, Webber L, Goh M, Valentine A, White D, Conway G, et al.
J Clin Endocrinol Metab
. 2008 Jun;
93(9):3396-402.
PMID: 18559912
Context: Polycystic ovary syndrome (PCOS) is a common endocrinopathy of uncertain etiology but with strong evidence for a genetic contribution. Objective: The objective of the study was to test the...