Queen Mary University of London
324 papers found
Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility
An integrated epigenomic analysis for type 2 diabetes susceptibility loci in monozygotic twins
Habitual sleep duration is associated with BMI and macronutrient intake and may be modified by CLOCK genetic variants
Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins
Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption
Defining the role of common variation in the genomic and biological architecture of adult human height.
Cigarette smoking reduces DNA methylation levels at multiple genomic loci but the effect is partially reversible upon cessation
Epigenome-Wide DNA Methylation in Hearing Ability: New Mechanisms for an Old Problem
Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process
FTO genetic variants, dietary intake and body mass index: insights from 177 330 individuals
Cis and Trans Effects of Human Genomic Variants on Gene Expression
Effects of Long-Term Averaging of Quantitative Blood Pressure Traits on the Detection of Genetic Associations
Gene-Lifestyle Interaction and Type 2 Diabetes: The EPIC InterAct Case-Cohort Study
Low copy number of the salivary amylase gene predisposes to obesity
Repeated replication and meta-analysis of the association between chromosome 9p21.3 and coronary artery disease
Differential methylation of the TRPA1 promoter in pain sensitivity
A gene pathway analysis highlights the role of cellular adhesion molecules in multiple sclerosis susceptibility
Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease.
DNA methylation and body-mass index: A genome-wide analysis.
Obesity accelerates epigenetic aging of human liver
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