M C Y Ng
Overview
Explore the profile of M C Y Ng including associated specialties, affiliations and a list of published articles.
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19
Citations
370
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Recent Articles
1.
Ma R, Hu C, Tam C, Zhang R, Kwan P, Leung T, et al.
Diabetologia
. 2013 Mar;
56(6):1291-305.
PMID: 23532257
Aims/hypothesis: Most genetic variants identified for type 2 diabetes have been discovered in European populations. We performed genome-wide association studies (GWAS) in a Chinese population with the aim of identifying...
2.
Liu C, Ng M, Rybin D, Adeyemo A, Bielinski S, Boerwinkle E, et al.
Diabetologia
. 2012 Aug;
55(11):2970-84.
PMID: 22893027
Aims/hypothesis: Hyperglycaemia disproportionately affects African-Americans (AfAs). We tested the transferability of 18 single-nucleotide polymorphisms (SNPs) associated with glycaemic traits identified in European ancestry (EuA) populations in 5,984 non-diabetic AfAs. Methods:...
3.
Hester J, Wing M, Li J, Palmer N, Xu J, Hicks P, et al.
Int J Obes (Lond)
. 2011 Jul;
36(3):465-73.
PMID: 21750520
Objective: Recent genome-wide association studies (GWAS) have identified multiple novel loci associated with adiposity in European-derived study populations. Limited study of these loci has been reported in African Americans. Here...
4.
Ng M, Lam V, Tam C, Chan A, So W, Ma R, et al.
Diabet Med
. 2010 Nov;
27(12):1443-9.
PMID: 21059098
Aims: POU class 2 homeobox 1 (POU2F1), also known as octamer-binding transcription factor-1 (OCT-1), is a ubiquitous transcription factor that plays a key role in the regulation of genes related...
5.
Wang Y, Luk A, Ma R, So W, Tam C, Ng M, et al.
Diabet Med
. 2010 Jun;
27(4):376-83.
PMID: 20536507
Aims: To examine the independent and joint effects of multiple genetic variants on a cardiac end-point in an 8-year prospective study of a Chinese diabetic cohort. Methods: Seventy-seven single nucleotide...
6.
Mong J, Ng M, Guldan G, Tam C, Lee H, Ma R, et al.
Int J Obes (Lond)
. 2009 Sep;
33(12):1446-53.
PMID: 19786971
Objective: Childhood obesity is a growing global epidemic. Recent studies indicate that obesity and related metabolic traits are highly heritable. Increasing evidence suggests that growth hormone (GH) and the insulin-like...
7.
Song X, Lee S, Ma R, So W, Cai J, Tam C, et al.
Diabetologia
. 2009 May;
52(8):1543-53.
PMID: 19479237
Aims/hypothesis: Cardiovascular and renal diseases share common risk factors. We used structural equation modelling (SEM) to evaluate the independent and combined effects of phenotypes and genotypes implicated in cardiovascular diseases...
8.
Leung T, Sy H, Ng M, Chan I, Wong G, Tang N, et al.
Allergy
. 2009 Jan;
64(4):621-8.
PMID: 19175592
Background: Single-nucleotide polymorphism (SNP)-based genome-wide association study revealed that markers on chromosome 17q21 were linked to childhood asthma but not atopy in Caucasians, with the strongest signal being detected for...
9.
Tong P, Kong A, So W, Yang X, Ng M, Ho C, et al.
Diabet Med
. 2007 Apr;
24(7):741-6.
PMID: 17403120
Aims: To examine the effect of albuminuria and retinopathy on the risk of cardiovascular and renal events, and all-cause mortality in patients with Type 2 diabetes. Methods: A post-hoc analysis...
10.
Ng M, Baum L, So W, Lam V, Wang Y, Poon E, et al.
Clin Genet
. 2006 Jul;
70(1):20-8.
PMID: 16813599
Diabetic nephropathy (DN) is the leading cause of end-stage renal disease. In DN patients, triglyceride (TG) level is elevated and lipoprotein lipase (LPL) activity, which hydrolyzes TG, is decreased. The...