Wellcome Trust Sanger Institute
138 papers found
An Evaluation of Power to Detect Low-Frequency Variant Associations Using Allele-Matching Tests That Account for Uncertainty
Testing for rare variant associations in complex diseases
Synthetic Associations Are Unlikely to Account for Many Common Disease Genome-Wide Association Signals
Rare Variant Association Analysis Methods for Complex Traits
Reply to Dlouha et al.
Synthetic associations in the context of genome-wide association scan signals
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis
Large-scale association analysis of TNF/LTA gene region polymorphisms in type 2 diabetes
Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls
CCRaVAT and QuTie - enabling analysis of rare variants in large-scale case control and quantitative trait association studies
A Powerful Approach to Sub-Phenotype Analysis in Population-Based Genetic Association Studies
Type 2 diabetes
Parental origin of sequence variants associated with complex diseases
Genetic evidence that raised sex hormone binding globulin (SHBG) levels reduce the risk of type 2 diabetes.
Replication in Genome-Wide Association Studies
An Evaluation of Statistical Approaches to Rare Variant Analysis in Genetic Association Studies
Ranking of genome-wide association scan signals by different measures
Lack of Significant Effects of the Type 2 Diabetes Susceptibility LociJAZF1,CDC123/CAMK1D,NOTCH2,ADAMTS9,THADA, andTSPAN8/LGR5on Diabetes and Quantitative Metabolic Traits
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