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Nature Genetics|June 15, 2007
Intra- and intercellular RNA interference in Arabidopsis thaliana requires components of the microRNA and heterochromatic silencing pathwaysPatrice Dunoyer, Christophe Himber, Virginia Ruiz-Ferrer, et al.Nature Genetics|June 15, 2007
Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndromeHeleen H Arts, Dan Doherty, Sylvia E C van Beersum, et al.Nature Genetics|June 15, 2007
A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21David A van Heel, Lude Franke, Karen A Hunt, et al.Nature Genetics|June 15, 2007
The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndromeMarion Delous, Lekbir Baala, Rémi Salomon, et al.Nature Genetics|July 3, 2007
Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetesJulius Gudmundsson, Patrick Sulem, Valgerdur Steinthorsdottir, et al.Nature Genetics|June 16, 2009
Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20Nature Genetics|June 16, 2009
Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune responseGillian I Rice, Jacquelyn Bond, Aruna Asipu, et al.Nature Genetics|September 8, 2009
Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's diseaseDenise Harold, Richard Abraham, Paul Hollingworth, et al.Nature Genetics|August 28, 2009
Inherited susceptibility to pediatric acute lymphoblastic leukemiaRoss L LevinePageof 744