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Nature Genetics|October 9, 2012
CSK regulatory polymorphism is associated with systemic lupus erythematosus and influences B-cell signaling and activationNataly Manjarrez-Orduño, Emiliano Marasco, Sharon A Chung, et al.Nature Genetics|August 7, 2012
Genome-wide association study identifies a susceptibility locus for thyrotoxic periodic paralysis at 17q24.3Ching-Lung Cheung, Kam-Shing Lau, Andrew Y Y Ho, et al.Nature Genetics|August 7, 2012
Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk lociKerstin U Ludwig, Elisabeth Mangold, Stefan Herms, et al.Nature Genetics|August 28, 2012
A direct characterization of human mutation based on microsatellitesJames X Sun, Agnar Helgason, Gisli Masson, et al.Nature Genetics|August 28, 2012
Mutations in ABCD4 cause a new inborn error of vitamin B12 metabolismDavid Coelho, Jaeseung C Kim, Isabelle R Miousse, et al.Nature Genetics|August 28, 2012
Genome-wide association analyses identify three new susceptibility loci for primary angle closure glaucomaEranga N Vithana, Chiea-Chuen Khor, Chunyan Qiao, et al.Nature Genetics|August 28, 2012
The draft genome of a diploid cotton Gossypium raimondiiKunbo Wang, Zhiwen Wang, Fuguang Li, et al.Nature Genetics|July 31, 2012
Exome sequencing identifies recurrent somatic RAC1 mutations in melanomaMichael Krauthammer, Yong Kong, Byung Hak Ha, et al.Nature Genetics|July 31, 2012
Exome sequencing identifies NMNAT1 mutations as a cause of Leber congenital amaurosisPei-Wen Chiang, Juan Wang, Yang Chen, et al.Nature Genetics|August 21, 2012
Mouse ooplasm confers context-specific reprogramming capacityMichelle M Chan, Zachary D Smith, Dieter Egli, et al.Pageof 744