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Nature Genetics|February 12, 2013
Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencingAndrew Kirby, Andreas Gnirke, David B Jaffe, et al.Nature Genetics|February 12, 2013
Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopiaVirginie J M Verhoeven, Pirro G Hysi, Robert Wojciechowski, et al.Nature Genetics|February 12, 2013
RNF212 is a dosage-sensitive regulator of crossing-over during mammalian meiosisApril Reynolds, Huanyu Qiao, Ye Yang, et al.Nature Genetics|February 12, 2013
Identification of multiple independent susceptibility loci in the HLA region in Behçet's diseaseTravis Hughes, Patrick Coit, Adam Adler, et al.Nature Genetics|February 19, 2013
Sequencing ancient calcified dental plaque shows changes in oral microbiota with dietary shifts of the Neolithic and Industrial revolutionsChristina J Adler, Keith Dobney, Laura S Weyrich, et al.Nature Genetics|February 5, 2013
Oomycete pathogens encode RNA silencing suppressorsYongli Qiao, Lin Liu, Qin Xiong, et al.Nature Genetics|January 29, 2013
Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosisVikram P Sharma, Aimée L Fenwick, Mia S Brockop, et al.Nature Genetics|January 29, 2013
Recurrent somatic mutation of FAT1 in multiple human cancers leads to aberrant Wnt activationLuc G T Morris, Andrew M Kaufman, Yongxing Gong, et al.Nature Genetics|February 26, 2013
De novo mutations in the autophagy gene WDR45 cause static encephalopathy of childhood with neurodegeneration in adulthoodHirotomo Saitsu, Taki Nishimura, Kazuhiro Muramatsu, et al.Nature Genetics|April 10, 2012
Bayesian method to predict individual SNP genotypes from gene expression dataEric E Schadt, Sangsoon Woo, Ke HaoPageof 743