PuSH - Publication Server of Helmholtz Zentrum München

121 Records found.
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61.
Gispert, S.* et al.: Loss of mitochondrial peptidase Clpp leads to infertility, hearing loss plus growth retardation via accumulation of CLPX, mtDNA, and inflammatory factors. Hum. Mol. Genet. 22, 4871-4887 (2013)
62.
Graff, M.* et al.: Genome-wide analysis of BMI in adolescents and young adults reveals additional insight into the effects of genetic loci over the life course. Hum. Mol. Genet. 22, 3597-3607 (2013)
63.
Guo, Y.* et al.: Gene-centric meta-analyses of 108912 individuals confirm known body mass index loci and reveal three novel signals. Hum. Mol. Genet. 22, 184-201 (2013)
64.
Holmans, P.* et al.: A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease. Hum. Mol. Genet. 22, 1039-1049 (2013)
65.
Kemter, E.* et al.: Type of uromodulin mutation and allelic status influence onset and severity of uromodulin-associated kidney disease in mice. Hum. Mol. Genet. 22, 4148-4163 (2013)
66.
Melka, M.G.* et al.: FTO, obesity and the adolescent brain. Hum. Mol. Genet. 22, 1050-1058 (2013)
67.
Reiner, A.P.* et al.: Genome-wide and gene-centric analyses of circulating myeloperoxidase levels in the charge and care consortia. Hum. Mol. Genet. 22, 3381-3393 (2013)
68.
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)
69.
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)
70.
Boraska, V.* et al.: Genome-wide meta-analysis of common variant differences between men and women. Hum. Mol. Genet. 21, 4805-4815 (2012)
71.
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)
72.
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)
73.
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)
74.
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)
75.
Petersen, A.-K. et al.: Genetic associations with lipoprotein subfractions provide information on their biological nature. Hum. Mol. Genet. 21, 1433-1443 (2012)
76.
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)
77.
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)
78.
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)
79.
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)
80.
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)