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Nature Genetics|February 10, 2009
New susceptibility locus for coronary artery disease on chromosome 3q22.3Jeanette Erdmann, Anika Grosshennig, Peter S Braund, et al.Nature Genetics|February 10, 2009
Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populationsJulius Gudmundsson, Patrick Sulem, Daniel F Gudbjartsson, et al.Nature Genetics|March 24, 2009
Common variants at ten loci influence QT interval duration in the QTGEN StudyChristopher Newton-Cheh, Mark Eijgelsheim, Kenneth M Rice, et al.Nature Genetics|October 28, 2008
Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humansZubair M Ahmed, Saber Masmoudi, Ersan Kalay, et al.Nature Genetics|August 20, 2008
SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populationsHiroyuki Unoki, Atsushi Takahashi, Takahisa Kawaguchi, et al.Nature Genetics|August 20, 2008
tRNA splicing endonuclease mutations cause pontocerebellar hypoplasiaBirgit S Budde, Yasmin Namavar, Peter G Barth, et al.Nature Genetics|September 9, 2008
Integrated detection and population-genetic analysis of SNPs and copy number variationSteven A McCarroll, Finny G Kuruvilla, Joshua M Korn, et al.Nature Genetics|September 9, 2008
Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVsJoshua M Korn, Finny G Kuruvilla, Steven A McCarroll, et al.Nature Genetics|September 2, 2008
A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemiaMaria Chiara Di Bernardo, Dalemari Crowther-Swanepoel, Peter Broderick, et al.Nature Genetics|December 17, 2013
Meta-analysis of gene-level tests for rare variant associationDajiang J Liu, Gina M Peloso, Xiaowei Zhan, et al.Pageof 744