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Nature Genetics|February 27, 2019
Identification of common genetic risk variants for autism spectrum disorderJakob Grove, Stephan Ripke, Thomas D Als, et al.Nature Genetics|February 27, 2019
S-CAP extends pathogenicity prediction to genetic variants that affect RNA splicingKarthik A Jagadeesh, Joseph M Paggi, James S Ye, et al.Nature Genetics|February 27, 2019
Biological and clinical insights from genetics of insomnia symptomsJacqueline M Lane, Samuel E Jones, Hassan S Dashti, et al.Nature Genetics|March 3, 2017
Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetranceAshley P L Marsh, Delphine Heron, Timothy J Edwards, et al.Nature Genetics|March 3, 2017
Diversity in non-repetitive human sequences not found in the reference genomeBirte Kehr, Anna Helgadottir, Pall Melsted, et al.Nature Genetics|April 30, 2014
RAF1 mutations in childhood-onset dilated cardiomyopathyPerundurai S Dhandapany, Md Abdur Razzaque, Uthiralingam Muthusami, et al.Nature Genetics|April 30, 2014
Heterotrimeric G proteins regulate nitrogen-use efficiency in riceHongying Sun, Qian Qian, Kun Wu, et al.Nature Genetics|April 30, 2014
Deep transcriptome profiling of mammalian stem cells supports a regulatory role for retrotransposons in pluripotency maintenanceAlexandre Fort, Kosuke Hashimoto, Daisuke Yamada, et al.Nature Genetics|May 6, 2014
A recurrent neomorphic mutation in MYOD1 defines a clinically aggressive subset of embryonal rhabdomyosarcoma associated with PI3K-AKT pathway mutationsShinji Kohsaka, Neerav Shukla, Nabahet Ameur, et al.Nature Genetics|November 22, 2016
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjectsChristian R Marshall, Daniel P Howrigan, Daniele Merico, et al.Pageof 743