Published in Nat Genet on February 08, 2016
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Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis. Nat Genet (2017) 1.39
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A Splice Region Variant in LDLR Lowers Non-high Density Lipoprotein Cholesterol and Protects against Coronary Artery Disease. PLoS Genet (2015) 0.79
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A sequence variant associating with educational attainment also affects childhood cognition. Sci Rep (2016) 0.75
Identification of sequence variants influencing immunoglobulin levels. Nat Genet (2017) 0.75
A rare splice donor mutation in the haptoglobin gene associates with blood lipid levels and coronary artery disease. Hum Mol Genet (2017) 0.75
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Effect of sequence variants on variance in glucose levels predicts type 2 diabetes risk and accounts for heritability. Nat Genet (2017) 0.75