Wellcome Trust Sanger Institute
138 papers found
Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility
The African Genome Variation Project shapes medical genetics in Africa
Genetic characterization of Greek population isolates reveals strong genetic drift at missense and trait-associated variants
Using genetically isolated populations to understand the genomic basis of disease
A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans
Using population isolates in genetic association studies
Effects of Long-Term Averaging of Quantitative Blood Pressure Traits on the Detection of Genetic Associations
Whole exome re-sequencing implicates CCDC38 and cilia structure and function in resistance to smoking related airflow obstruction
Using ancestry-informative markers to identify fine structure across 15 populations of European origin
Functional annotation of noncoding sequence variants
Revisiting the thrifty gene hypothesis via 65 loci associated with susceptibility to type 2 diabetes
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility.
Leveraging cross-species transcription factor binding site patterns: From diabetes risk loci to disease mechanisms.
A rare functional cardioprotective APOC3 variant has risen in frequency in distinct population isolates
PW01-038 – Genomewide association study of Still’s disease
In search of low-frequency and rare variants affecting complex traits
Advances in osteoarthritis genetics: Table 1
Genome-wide association study for osteoarthritis – Authors' reply
Rare and Low Frequency Variant Stratification in the UK Population: Description and Impact on Association Tests
No evidence of an association between mitochondrial DNA variants and osteoarthritis in 7393 cases and 5122 controls
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