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Nature Genetics|June 21, 2016
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migrainePadhraig Gormley, Verneri Anttila, Bendik S Winsvold, et al.Human Genetics|May 21, 2011
Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriersKate M Im, Tomas Kirchhoff, Xianshu Wang, et al.Plos Genetics|November 10, 2010
Common genetic variants and modification of penetrance of BRCA2-associated breast cancerMia M Gaudet, Tomas Kirchhoff, Todd Green, et al.Nature Genetics|August 29, 2022
Large-scale sequencing identifies multiple genes and rare variants associated with Crohn's disease susceptibilityAleksejs Sazonovs, Christine R Stevens, Guhan R Venkataraman, et al.Nature|April 9, 2022
Rare coding variants in ten genes confer substantial risk for schizophreniaTarjinder Singh, Timothy Poterba, David Curtis, et al.Nature|October 19, 2007
Genome-wide detection and characterization of positive selection in human populationsPardis C Sabeti, Patrick Varilly, Ben Fry, et al.Nature|October 19, 2007
A second generation human haplotype map of over 3.1 million SNPs, Kelly A Frazer, Dennis G Ballinger, et al.Journal of the American College of Cardiology|October 12, 2010
Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studiesThemistocles L Assimes, Hilma Hólm, Sekar Kathiresan, et al.Nature|October 30, 2012
Pancreatic cancer genomes reveal aberrations in axon guidance pathway genesAndrew V Biankin, Nicola Waddell, Karin S Kassahn, et al.Lancet (London, England)|May 22, 2012
Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation studyBenjamin F Voight, Gina M Peloso, Marju Orho-Melander, et al.Pageof 163