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Nature Genetics|July 1, 2008
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's diseaseJeffrey C Barrett, Sarah Hansoul, Dan L Nicolae, et al.Nature Genetics|July 1, 2008
Conservation of the H19 noncoding RNA and H19-IGF2 imprinting mechanism in theriansGuillaume Smits, Andrew J Mungall, Sam Griffiths-Jones, et al.Nature Genetics|July 1, 2008
Identification of renal Cd36 as a determinant of blood pressure and risk for hypertensionMichal Pravenec, Paul C Churchill, Monique C Churchill, et al.Nature Genetics|August 7, 2007
Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathyAnne-Sophie Nicot, Anne Toussaint, Valérie Tosch, et al.Nature Genetics|November 18, 2008
The forkhead protein Foxj1 specifies node-like cilia in Xenopus and zebrafish embryosJennifer L Stubbs, Isao Oishi, Juan Carlos Izpisúa Belmonte, et al.Nature Genetics|November 18, 2008
Foxj1 transcription factors are master regulators of the motile ciliogenic programXianwen Yu, Chee Peng Ng, Hermann Habacher, et al.Nature Genetics|December 9, 2008
Common variants at 30 loci contribute to polygenic dyslipidemiaSekar Kathiresan, Cristen J Willer, Gina M Peloso, et al.Nature Genetics|December 9, 2008
Variants in MTNR1B influence fasting glucose levelsInga Prokopenko, Claudia Langenberg, Jose C Florez, et al.Nature Genetics|December 9, 2008
A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes riskNabila Bouatia-Naji, Amélie Bonnefond, Christine Cavalcanti-Proença, et al.Nature Genetics|December 2, 2008
Human adenylate kinase 2 deficiency causes a profound hematopoietic defect associated with sensorineural deafnessChantal Lagresle-Peyrou, Emmanuelle M Six, Capucine Picard, et al.Pageof 744