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241.
Lewis, M.A.* et al.: An ENU-induced mutation of miR-96 associated with progressive hearing loss in mice. Nat. Genet. 41, 614-618 (2009)
242.
Newton-Cheh, C.* et al.: Genome-wide association study identifies eight loci associated with blood pressure. Nat. Genet. 41, 666-676 (2009)
243.
Pfeufer, A. et al.: Common variants at ten loci modulate the QT interval duration in the QTSCD Study. Nat. Genet. 41, 407-414 (2009)
244.
Prokopenko, I.* et al.: Variants in MTNR1B influence fasting glucose levels. Nat. Genet. 41, 77-81 (2009)
245.
Simon-Sanchez, J.* et al.: Genome-wide association study reveals genetic risk underlying Parkinson's disease. Nat. Genet. 41, 1308-1314 (2009)
246.
Soranzo, N.* et al.: A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. Nat. Genet. 41, 1182-1190 (2009)
247.
Tregouet, D.A.* et al.: Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease. Nat. Genet. 41, 283-285 (2009)
248.
van Es, M.A.* et al.: Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis. Nat. Genet. 41, 1083-1087 (2009)
249.
Willer, C.J.* et al.: Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. Nat. Genet. 41, 25-34 (2009)
250.
Döring, A. et al.: SLC2A9 influences uric acid concentrations with pronounced sex-specific effects. Nat. Genet. 40, 430-436 (2008)
251.
Lettre, G.* et al.: Identification of ten loci associated with height highlights new biological pathways in human growth. Nat. Genet. 40, 584-591 (2008)
252.
Loos, R.J.* et al.: Common variants near MC4R are associated with fat mass, weight and risk of obesity. Nat. Genet. 40, 768-775 (2008)
253.
McGowan, K.A. et al.: Ribosomal mutations cause p53-mediated dark skin and pleiotropic effects. Nat. Genet. 40, 963-970 (2008)
254.
Schormair, B. et al.: PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome. Nat. Genet. 40, 946-948 (2008)
255.
Zeggini, E.* et al.: Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. Nat. Genet. 40, 638-645 (2008)
256.
den Hollander, A.I.* et al.: Mutations in LCA5, encoding the ciliary protein lebercilin, cause Leber congenital amaurosis. Nat. Genet. 39, 889-895 (2007)
257.
Horn, C.* et al.: Splinkerette PCR for more efficient characterization of gene trap events. Nat. Genet. 39, 933-935 (2007)
258.
Winkelmann, J. et al.: Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions. Nat. Genet. 39, 1000-1006 (2007)
259.
Arking, D.E.* et al.: A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization. Nat. Genet. 38, 644-651 (2006)
260.
Consonni, C.* et al.: Conserved requirement for a plant host cell protein in powdery mildew pathogenesis. Nat. Genet. 38, 716-720 (2006)
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