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Nature Genetics|October 7, 2008
Disruption of an AP-2alpha binding site in an IRF6 enhancer is associated with cleft lipFedik Rahimov, Mary L Marazita, Axel Visel, et al.Nature Genetics|October 7, 2008
EYS, encoding an ortholog of Drosophila spacemaker, is mutated in autosomal recessive retinitis pigmentosaMai M Abd El-Aziz, Isabel Barragan, Ciara A O'Driscoll, et al.Nature Genetics|October 7, 2008
Regulation of a remote Shh forebrain enhancer by the Six3 homeoproteinYongsu Jeong, Federico Coluccio Leskow, Kenia El-Jaick, et al.Nature Genetics|October 7, 2008
Sequence variants in IL10, ARPC2 and multiple other loci contribute to ulcerative colitis susceptibilityAndre Franke, Tobias Balschun, Tom H Karlsen, et al.Nature Genetics|September 23, 2008
Insights from retinitis pigmentosa into the roles of isocitrate dehydrogenases in the Krebs cycleDyonne T Hartong, Mayura Dange, Terri L McGee, et al.Nature Genetics|September 17, 2008
Common variants at CD40 and other loci confer risk of rheumatoid arthritisSoumya Raychaudhuri, Elaine F Remmers, Annette T Lee, et al.Nature Genetics|September 17, 2008
MYH9 is associated with nondiabetic end-stage renal disease in African AmericansW H Linda Kao, Michael J Klag, Lucy A Meoni, et al.Nature Genetics|August 12, 2009
Mutations in INPP5E, encoding inositol polyphosphate-5-phosphatase E, link phosphatidyl inositol signaling to the ciliopathiesStephanie L Bielas, Jennifer L Silhavy, Francesco Brancati, et al.Nature Genetics|August 25, 2009
Posterior malformations in Dact1 mutant mice arise through misregulated Vangl2 at the primitive streakRowena Suriben, Saul Kivimäe, Daniel A C Fisher, et al.Nature Genetics|July 7, 2009
Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibilityMargaret Wrensch, Robert B Jenkins, Jeffrey S Chang, et al.Pageof 745