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Nature Genetics|April 22, 2014
De novo mutations in HCN1 cause early infantile epileptic encephalopathyCaroline Nava, Carine Dalle, Agnès Rastetter, et al.Nature Genetics|April 22, 2014
Recurrent activating mutation in PRKACA in cortisol-producing adrenal tumorsGerald Goh, Ute I Scholl, James M Healy, et al.Nature Genetics|May 6, 2014
Dystrophin is a tumor suppressor in human cancers with myogenic programsYuexiang Wang, Adrian Marino-Enriquez, Richard R Bennett, et al.Nature Genetics|May 6, 2014
Pan-cancer genetic analysis identifies PARK2 as a master regulator of G1/S cyclinsYongxing Gong, Travis Ian Zack, Luc G T Morris, et al.Nature Genetics|April 2, 2014
Rare missense variants in POT1 predispose to familial cutaneous malignant melanomaJianxin Shi, Xiaohong R Yang, Bari Ballew, et al.Nature Genetics|April 2, 2014
Gain-of-function mutations in IFIH1 cause a spectrum of human disease phenotypes associated with upregulated type I interferon signalingGillian I Rice, Yoandris Del Toro Duany, Emma M Jenkinson, et al.Nature Genetics|April 2, 2014
Low copy number of the salivary amylase gene predisposes to obesityMario Falchi, Julia Sarah El-Sayed Moustafa, Petros Takousis, et al.Nature Genetics|April 8, 2014
De novo CCND2 mutations leading to stabilization of cyclin D2 cause megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndromeGhayda Mirzaa, David A Parry, Andrew E Fry, et al.Nature Genetics|April 15, 2014
Heritability and genomics of gene expression in peripheral bloodFred A Wright, Patrick F Sullivan, Andrew I Brooks, et al.Nature Genetics|March 18, 2014
Ancestry estimation and control of population stratification for sequence-based association studiesChaolong Wang, Xiaowei Zhan, Jennifer Bragg-Gresham, et al.Pageof 745