Queen Mary University of London
324 papers found
Large-scale association analysis identifies new risk loci for coronary artery disease.
Seventy-five genetic loci influencing the human red blood cell
A Comparison of the Whole Genome Approach of MeDIP-Seq to the Targeted Approach of the Infinium HumanMethylation450 BeadChip® for Methylome Profiling
Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity.
High density genetic mapping identifies new susceptibility loci for rheumatoid arthritis
Bayesian refinement of association signals for 14 loci in 3 common diseases
High Prevalence of Posterior Polymorphous Corneal Dystrophy in the Czech Republic; Linkage Disequilibrium Mapping and Dating an Ancestral Mutation
No evidence of an association between mitochondrial DNA variants and osteoarthritis in 7393 cases and 5122 controls
Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus.
Evaluation of the genetic overlap between osteoarthritis with body mass index and height using genome-wide association scan data
Mapping cis-and trans-regulatory effects across multiple tissues in twins
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes
Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways
The Metabochip, a Custom Genotyping Array for Genetic Studies of Metabolic, Cardiovascular, and Anthropometric Traits
Genetically Distinct Subsets within ANCA-Associated Vasculitis.
Six Novel Susceptibility Loci for Early-Onset Androgenetic Alopecia and Their Unexpected Association with Common Diseases
Patterns of Cis Regulatory Variation in Diverse Human Populations
Inheritance of coronary artery disease in men: An analysis of the role of the y chromosome
Compound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndrome.
Association of the GGCX (CAA)16/17 repeat polymorphism with higher warfarin dose requirements in African Americans
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