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Nature Genetics|August 30, 2008
MYO5B mutations cause microvillus inclusion disease and disrupt epithelial cell polarityThomas Müller, Michael W Hess, Natalia Schiefermeier, et al.Nature Genetics|July 16, 2008
Common variants in DVWA on chromosome 3p24.3 are associated with susceptibility to knee osteoarthritisYoshinari Miyamoto, Dongquan Shi, Masahiro Nakajima, et al.Nature Genetics|September 26, 2007
The imprinted gene Magel2 regulates normal circadian outputSerguei V Kozlov, James W Bogenpohl, Maureen P Howell, et al.Nature Genetics|September 28, 2007
The NCBI dbGaP database of genotypes and phenotypesMatthew D Mailman, Michael Feolo, Yumi Jin, et al.Nature Genetics|July 22, 2008
Ribosomal mutations cause p53-mediated dark skin and pleiotropic effectsKelly A McGowan, Jun Z Li, Christopher Y Park, et al.Nature Genetics|July 29, 2008
High-throughput sequencing provides insights into genome variation and evolution in Salmonella TyphiKathryn E Holt, Julian Parkhill, Camila J Mazzoni, et al.Nature Genetics|July 29, 2008
PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndromeBarbara Schormair, David Kemlink, Darina Roeske, et al.Nature Genetics|July 31, 2008
Putting science over supposition in the arena of personalized genomicsColleen M McBride, Sharon Hensley Alford, Robert J Reid, et al.Nature Genetics|November 11, 2008
Gerodermia osteodysplastica is caused by mutations in SCYL1BP1, a Rab-6 interacting golginHans Christian Hennies, Uwe Kornak, Haikuo Zhang, et al.Nature Genetics|November 11, 2008
Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosisYurii S Aulchenko, Ilse A Hoppenbrouwers, Sreeram V Ramagopalan, et al.Pageof 742