scispace - formally typeset
M

Meng May Chee

Researcher at University of Glasgow

Publications -  13
Citations -  1036

Meng May Chee is an academic researcher from University of Glasgow. The author has contributed to research in topics: Genome-wide association study & Single-nucleotide polymorphism. The author has an hindex of 12, co-authored 13 publications receiving 956 citations. Previous affiliations of Meng May Chee include Glasgow Royal Infirmary.

Papers
More filters
Journal ArticleDOI

Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus

Timothy R D J Radstake, +63 more
- 01 May 2010 - 
TL;DR: The first genome-wide association study in a population of European ancestry including a total of 2,296 individuals with SSc and 5,171 controls identified a new susceptibility locus for systemic sclerosis at CD247 (1q22–23, rs2056626).
Journal ArticleDOI

Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy

Olga Y. Gorlova, +69 more
- 14 Jul 2011 - 
TL;DR: The aim of this study was to determine the genetic components contributing to different clinical sub-phenotypes of systemic sclerosis (SSc), and to identify three new non-HLA genes associated with SSc clinical and auto-antibody subgroups.
Journal ArticleDOI

A systemic sclerosis and systemic lupus erythematosus pan-meta-GWAS reveals new shared susceptibility loci

TL;DR: A pan-meta-analysis of two genome-wide association studies together with a replication stage including additional SSc and SLE cohorts increased the sample size to a total of 21,109 and validated KIAA0319L, PXK and JAZF1 as novel susceptibility loci for SSc or SLE, increasing significantly the knowledge of the genetic basis of autoimmunity.
Journal ArticleDOI

Identification of CSK as a systemic sclerosis genetic risk factor through Genome Wide Association Study follow-up

TL;DR: This study significantly increases the number of known putative genetic risk factors for SSc, including the genes CSK, PSD3 and NFKB1, and further confirms six previously described ones.
Journal ArticleDOI

A replication study confirms the association of TNFSF4 (OX40L) polymorphisms with systemic sclerosis in a large European cohort

Lara Bossini-Castillo, +57 more
TL;DR: The data confirm the influence of TNFSF4 polymorphisms in SSc genetic susceptibility, especially in subsets of patients positive for lcSSc and ACA positive subgroups, and revealed a new risk haplotype associated with the same groups of patients.