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Nature Genetics|January 23, 1999
Overt nephrogenic diabetes insipidus in mice lacking the CLC-K1 chloride channelY Matsumura, S Uchida, Y Kondo, et al.Nature Genetics|January 23, 1999
Synergy of demethylation and histone deacetylase inhibition in the re-expression of genes silenced in cancerE E Cameron, K E Bachman, S Myöhänen, et al.Nature Genetics|February 12, 2002
BRCA1 regulates the G2/M checkpoint by activating Chk1 kinase upon DNA damageRonit I Yarden, Sherly Pardo-Reoyo, Magda Sgagias, et al.Nature Genetics|December 20, 2016
A genome-wide CRISPR screen identifies a restricted set of HIV host dependency factorsRyan J Park, Tim Wang, Dylan Koundakjian, et al.Nature Genetics|January 10, 2017
Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel diseaseKatrina M de Lange, Loukas Moutsianas, James C Lee, et al.Nature Genetics|January 10, 2017
SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndromeNatalie D Shaw, Harrison Brand, Zachary A Kupchinsky, et al.Nature Genetics|January 10, 2017
De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal developmentChristopher T Gordon, Shifeng Xue, Gökhan Yigit, et al.Nature Genetics|January 10, 2017
Genome-wide association study identifies distinct genetic contributions to prognosis and susceptibility in Crohn's diseaseJames C Lee, Daniele Biasci, Rebecca Roberts, et al.Nature Genetics|April 22, 2014
Mutations in CCNO result in congenital mucociliary clearance disorder with reduced generation of multiple motile ciliaJulia Wallmeier, Dalal A Al-Mutairi, Chun-Ting Chen, et al.Pageof 745