Asgeir Sigurdsson

Author PubWeight™ 12.15‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Large-scale whole-genome sequencing of the Icelandic population. Nat Genet 2015 4.54
2 Identification of a large set of rare complete human knockouts. Nat Genet 2015 2.28
3 Identification of low-frequency and rare sequence variants associated with elevated or reduced risk of type 2 diabetes. Nat Genet 2014 1.92
4 Variants with large effects on blood lipids and the role of cholesterol and triglycerides in coronary disease. Nat Genet 2016 1.71
5 Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis. Nat Genet 2017 1.39
6 A Splice Region Variant in LDLR Lowers Non-high Density Lipoprotein Cholesterol and Protects against Coronary Artery Disease. PLoS Genet 2015 0.79
7 Diversity in non-repetitive human sequences not found in the reference genome. Nat Genet 2017 0.75
8 Identification of sequence variants influencing immunoglobulin levels. Nat Genet 2017 0.75
9 A rare splice donor mutation in the haptoglobin gene associates with blood lipid levels and coronary artery disease. Hum Mol Genet 2017 0.75