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81.
Stambolian, D.* et al.: Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error. Hum. Mol. Genet. 22, 2754-2764 (2013)
82.
Weidinger, S.* et al.: A genome-wide association study of atopic dermatitis identifies loci with overlapping effects on asthma and psoriasis. Hum. Mol. Genet. 22, 4841-4856 (2013)
83.
Boraska, V.* et al.: Genome-wide meta-analysis of common variant differences between men and women. Hum. Mol. Genet. 21, 4805-4815 (2012)
84.
Chasman, D.I.* et al.: Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function. Hum. Mol. Genet. 21, 5329-5343 (2012)
85.
Imamura, M.* et al.: A single-nucleotide polymorphism in ANK1 is associated with susceptibility to type 2 diabetes in Japanese populations. Hum. Mol. Genet. 21, 3042-3049 (2012)
86.
Keller, M.F.* et al.: Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease. Hum. Mol. Genet. 21, 4996-5009 (2012)
87.
Mead, S.* et al.: Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP. Hum. Mol. Genet. 21, 1897-1906 (2012)
88.
Petersen, A.-K. et al.: Genetic associations with lipoprotein subfractions provide information on their biological nature. Hum. Mol. Genet. 21, 1433-1443 (2012)
89.
Rawal, R. et al.: Meta-analysis of two genome-wide association studies identifies four genetic loci associated with thyroid function. Hum. Mol. Genet. 21, 3275-3282 (2012)
90.
Siddiq, A.* et al.: A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11. Hum. Mol. Genet. 21, 5373-5384 (2012)
91.
Steffens, M.* et al.: Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32. Hum. Mol. Genet. 21, 5359-5372 (2012)
92.
Thiele, F. et al.: Cardiopulmonary dysfunction in the osteogenesis imperfecta mouse model Aga2 and human patients are caused by bone-independent mechanisms. Hum. Mol. Genet. 21, 3535-3545 (2012)
93.
Timofeeva, M.N.* et al.: Influence of common genetic variation on lung cancer risk: Meta-analysis of 14900 cases and 29485 controls. Hum. Mol. Genet. 21, 4980-4995 (2012)
94.
Winkelmann, J. et al.: Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy. Hum. Mol. Genet. 21, 2205-2210 (2012)
95.
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)
96.
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)
97.
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)
98.
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)
99.
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)
100.
Duering, M.* et al.: Co-aggregate formation of CADASIL-mutant NOTCH3: A single-particle analysis. Hum. Mol. Genet. 20, 3256-3265 (2011)