PuSH - Publication Server of Helmholtz Zentrum München

121 Records found.
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81.
Winkelmann, J. et al.: Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy. Hum. Mol. Genet. 21, 2205-2210 (2012)
82.
Wu, X.* et al.: A genome-wide association study identifies a novel susceptibility locus for renal cell carcinoma on 12p11.23. Hum. Mol. Genet. 21, 456-462 (2012)
83.
Chapman, G.* ; Sparrow, D.B.* ; Kremmer, E. & Dunwoodie, S.L.*: Notch inhibition by the ligand Delta-Like 3 defines the mechanism of abnormal vertebral segmentation in spondylocostal dysostosis. Hum. Mol. Genet. 20, 905-916 (2011)
84.
Coene, K.L.* et al.: The ciliopathy-associated protein homologs RPGRIP1 and RPGRIP1L are linked to cilium integrity through interaction with Nek4 serine/threonine kinase. Hum. Mol. Genet. 20, 3592-3605 (2011)
85.
Cross, S.H.* et al.: The Opdc missense mutation of Pax2 has a milder than loss-of-function phenotype. Hum. Mol. Genet. 20, 223-234 (2011)
86.
Del Greco, M, F.* et al.: Genome-wide association analysis and fine mapping of NT-proBNP level provide novel insight into the role of the MTHFR-CLCN6-NPPA-NPPB gene cluster. Hum. Mol. Genet. 20, 1660-1671 (2011)
87.
Duering, M.* et al.: Co-aggregate formation of CADASIL-mutant NOTCH3: A single-particle analysis. Hum. Mol. Genet. 20, 3256-3265 (2011)
88.
Fox, E.R.* et al.: Association of genetic variation with systolic and diastolic blood pressure among African Americans: The Candidate Gene Association Resource study. Hum. Mol. Genet. 20, 2273-2284 (2011)
89.
Kaplan, R.C.* et al.: A genome-wide association study identifies novel loci associated with circulating IGF-I and IGFBP-3. Hum. Mol. Genet. 20, 1241-1251 (2011)
90.
Oexle, K.* et al.: Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels. Hum. Mol. Genet. 20, 1042-1047 (2011)
91.
Sanson, M.* et al.: Chromosome 7p11.2 (EGFR) variation influences glioma risk. Hum. Mol. Genet. 20, 2897-2904 (2011)
92.
Barbalic, M.* et al.: Large-scale genomic studies reveal central role of ABO in sP-selectin and sICAM-1 levels. Hum. Mol. Genet. 19, 1863-1872 (2010)
93.
Burbulla, L.F.* et al.: Dissecting the role of the mitochondrial chaperone mortalin in Parkinson's disease: Functional impact of disease-related variants on mitochondrial homeostasis. Hum. Mol. Genet. 19, 4437-4452 (2010)
94.
Eijgelsheim, M.* et al.: Genome-wide association analysis identifies multiple loci related to resting heart rate. Hum. Mol. Genet. 19, 3885-3894 (2010)
95.
Kettunen, J.* et al.: European lactase persistence genotype shows evidence of association with increase in body mass index. Hum. Mol. Genet. 19, 1129-1136 (2010)
96.
Perry, J.R.B.* et al.: Genetic evidence that raised sex hormone binding globulin (SHBG) levels reduce the risk of type 2 diabetes. Hum. Mol. Genet. 19, 535-544 (2010)
97.
Qi, L.* et al.: Genetic variants at 2q24 are associated with susceptibility to type 2 diabetes. Hum. Mol. Genet. 19, 2706-2715 (2010)
98.
Chio, A.* et al.: A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis. Hum. Mol. Genet. 18, 1524-1532 (2009)
99.
Deplazes, J.* et al.: Rac1 and Rho contribute to the migratory and invasive phenotype associated with somatic E-cadherin mutation. Hum. Mol. Genet. 18, 3632-3644 (2009)
100.
Johansson, A.* et al.: Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysis. Hum. Mol. Genet. 18, 373-380 (2009)