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61.
Reinthaler, E.M.* et al.: 16p11.2 600 kb duplications confer risk for typical and atypical Rolandic epilepsy. Hum. Mol. Genet. 23, 6069-6080 (2014)
62.
Ried, J.S. et al.: Novel genetic associations with serum level metabolites identified by phenotype set enrichment analyses. Hum. Mol. Genet. 23, 5847-5857 (2014)
63.
Yan, X. et al.: Peroxidasin is essential for eye development in the mouse. Hum. Mol. Genet. 23, 5597-5614 (2014)
64.
Yoneyama, S.* et al.: Gene-centric meta-analyses for central adiposity traits in up to 57412 individuals of European descent confirm known loci and reveal several novel associations. Hum. Mol. Genet. 23, 2498-2510 (2014)
65.
Cousminer, D.L.* et al.: Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity. Hum. Mol. Genet. 22, 2735-2747 (2013)
66.
Enciso-Mora, V.* et al.: Deciphering the 8q24.21 association for glioma. Hum. Mol. Genet. 22, 2293-2302 (2013)
67.
Ganesh, S.K.* et al.: Loci influencing blood pressure identified using a cardiovascular gene-centric array. Hum. Mol. Genet. 22, 1663-1678 (2013)
68.
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)
69.
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)
70.
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)
71.
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)
72.
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)
73.
Melka, M.G.* et al.: FTO, obesity and the adolescent brain. Hum. Mol. Genet. 22, 1050-1058 (2013)
74.
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)
75.
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)
76.
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)
77.
Boraska, V.* et al.: Genome-wide meta-analysis of common variant differences between men and women. Hum. Mol. Genet. 21, 4805-4815 (2012)
78.
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)
79.
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)
80.
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)