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Nature Genetics|January 15, 2013
Recurrent mutations at codon 625 of the splicing factor SF3B1 in uveal melanomaJ William Harbour, Elisha D O Roberson, Hima Anbunathan, et al.Nature Genetics|January 15, 2013
Loss-of-function mutations in MGME1 impair mtDNA replication and cause multisystemic mitochondrial diseaseCornelia Kornblum, Thomas J Nicholls, Tobias B Haack, et al.Nature Genetics|December 25, 2012
Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretionJeroen R Huyghe, Anne U Jackson, Marie P Fogarty, et al.Nature Genetics|February 27, 2013
Interpreting the role of de novo protein-coding mutations in neuropsychiatric diseaseJacob Gratten, Peter M Visscher, Bryan J Mowry, et al.Nature Genetics|April 23, 2013
Dense genotyping of immune-related disease regions identifies 14 new susceptibility loci for juvenile idiopathic arthritisAnne Hinks, Joanna Cobb, Miranda C Marion, et al.Nature Genetics|April 23, 2013
Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephalyKarine Poirier, Nicolas Lebrun, Loic Broix, et al.Nature Genetics|May 28, 2013
A genome-wide association study identifies two risk loci for congenital heart malformations in Han Chinese populationsZhibin Hu, Yongyong Shi, Xuming Mo, et al.Nature Genetics|June 18, 2013
Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemiaSonja I Berndt, Christine F Skibola, Vijai Joseph, et al.Nature Genetics|July 16, 2013
Evidence for APOBEC3B mutagenesis in multiple human cancersMichael B Burns, Nuri A Temiz, Reuben S HarrisNature Genetics|July 16, 2013
An APOBEC cytidine deaminase mutagenesis pattern is widespread in human cancersSteven A Roberts, Michael S Lawrence, Leszek J Klimczak, et al.Pageof 744