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Nature Genetics|February 7, 2012
Differential confounding of rare and common variants in spatially structured populationsIain Mathieson, Gil McVeanNature Genetics|February 7, 2012
Germline mutations in DIS3L2 cause the Perlman syndrome of overgrowth and Wilms tumor susceptibilityDewi Astuti, Mark R Morris, Wendy N Cooper, et al.Nature Genetics|February 14, 2012
Mutations in SLC20A2 link familial idiopathic basal ganglia calcification with phosphate homeostasisCheng Wang, Yulei Li, Lei Shi, et al.Nature Genetics|November 22, 2011
Mutations in MEGF10, a regulator of satellite cell myogenesis, cause early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD)Clare V Logan, Barbara Lucke, Caroline Pottinger, et al.Nature Genetics|March 13, 2012
Generation of functional insulin-producing cells in the gut by Foxo1 ablationChutima Talchai, Shouhong Xuan, Tadahiro Kitamura, et al.Nature Genetics|November 11, 2014
Identification of enterotoxigenic Escherichia coli (ETEC) clades with long-term global distributionAstrid von Mentzer, Thomas R Connor, Lothar H Wieler, et al.Nature Genetics|October 27, 2014
RNF43 is frequently mutated in colorectal and endometrial cancersMarios Giannakis, Eran Hodis, Xinmeng Jasmine Mu, et al.Nature Genetics|October 27, 2014
Mutations in PLK4, encoding a master regulator of centriole biogenesis, cause microcephaly, growth failure and retinopathyCarol-Anne Martin, Ilyas Ahmad, Anna Klingseisen, et al.Nature Genetics|November 3, 2014
A multiscale statistical mechanical framework integrates biophysical and genomic data to assemble cancer networksMohammed AlQuraishi, Grigoriy Koytiger, Anne Jenney, et al.Pageof 743