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Nature Genetics|November 4, 2008
Expression of 24,426 human alternative splicing events and predicted cis regulation in 48 tissues and cell linesJohn C Castle, Chaolin Zhang, Jyoti K Shah, et al.Nature Genetics|November 4, 2008
Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk lociJason D Cooper, Deborah J Smyth, Adam M Smiles, et al.Nature Genetics|June 5, 2007
Mutations in X-linked PORCN, a putative regulator of Wnt signaling, cause focal dermal hypoplasiaXiaoling Wang, V Reid Sutton, J Omar Peraza-Llanes, et al.Nature Genetics|May 9, 2007
Mutation of RRM2B, encoding p53-controlled ribonucleotide reductase (p53R2), causes severe mitochondrial DNA depletionAlice Bourdon, Limor Minai, Valérie Serre, et al.Nature Genetics|July 24, 2007
Axonal loss and neuroinflammation caused by peroxisome-deficient oligodendrocytesCelia M Kassmann, Corinna Lappe-Siefke, Myriam Baes, et al.Nature Genetics|September 5, 2007
Mutational and selective effects on copy-number variants in the human genomeGregory M Cooper, Deborah A Nickerson, Evan E EichlerNature Genetics|September 5, 2007
Major changes in our DNA lead to major changes in our thinkingJonathan SebatNature Genetics|September 5, 2007
The population genetics of structural variationDonald F Conrad, Matthew E HurlesNature Genetics|July 17, 2007
A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone diseaseStephan Buch, Clemens Schafmayer, Henry Völzke, et al.Nature Genetics|July 17, 2007
Mutations in RNF135, a gene within the NF1 microdeletion region, cause phenotypic abnormalities including overgrowthJenny Douglas, Deirdre Cilliers, Kim Coleman, et al.Pageof 744