PuSH - Publication Server of Helmholtz Zentrum München

119 Records found.
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1.
Ahluwalia, T.S.* et al.: Genome-wide association study of circulating interleukin 6 levels identifies novel loci. Hum. Mol. Genet. 30, 393-409 (2021)
2.
Cai, N. ; Choi, K.W.* & Fried, E.I.*: Reviewing the genetics of heterogeneity in depression: Operationalizations, manifestations, and etiologies. Hum. Mol. Genet. 29, R10-R18 (2020)
3.
Nag, A.* et al.: Genome-wide scan identifies novel genetic loci regulating salivary metabolite levels. Hum. Mol. Genet. 29, 864-875 (2020)
4.
Bradfield, J.P.* et al.: A trans-ancestral meta-analysis of genome-wide association studies reveals loci associated with childhood obesity. Hum. Mol. Genet. 28, 3327-3338 (2019)
5.
Laaksonen, J.* et al.: Discovery of mitochondrial DNA variants associated with genome-wide blood cell gene expression: A population-based mtDNA sequencing study. Hum. Mol. Genet. 28, 1381-1391 (2019)
6.
Sharapov, S.Z.* et al.: Defining the genetic control of human blood plasma N-glycome using genome-wide association study. Hum. Mol. Genet. 28, 2062-2077 (2019)
7.
Sung, Y.J.* et al.: A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure. Hum. Mol. Genet. 28, 2615-2633 (2019)
8.
Brockmann, S.J.* et al.: CHCHD10 mutations p. R15L and p. G66V cause motoneuron disease by haploinsufficiency. Hum. Mol. Genet. 27, 706-715 (2018)
9.
Haworth, S.* et al.: Consortium-based genome-wide meta-analysis for childhood dental caries traits. Hum. Mol. Genet. 27, 3113-3127 (2018)
10.
Tönjes, A.* et al.: Genome-wide meta-analysis identifies novel determinants of circulating serum progranulin. Hum. Mol. Genet. 27, 546-558 (2018)
11.
Vogel, H.* et al.: A collective diabetes cross in combination with a computational framework to dissect the genetics of human obesity and Type 2 diabetes. Hum. Mol. Genet. 27, 3099-3112 (2018)
12.
Zaghlool, S.B.* et al.: Deep molecular phenotypes link complex disorders and physiological insult to CpG methylation. Hum. Mol. Genet. 27, 1106-1121 (2018)
13.
Cooper, H.M.* et al.: ATPase-deficient mitochondrial inner membrane protein ATAD3a disturbs mitochondrial dynamics in dominant hereditary spastic paraplegia. Hum. Mol. Genet. 26, 1432-1443 (2017)
14.
Dand, N.* et al.: Exome-wide association study reveals novel psoriasis susceptibility locus at TNFSF15 and rare protective alleles in genes contributing to type I IFN signalling. Hum. Mol. Genet. 26, 4301-4313 (2017)
15.
van den Berg, M.* et al.: Discovery of novel heart rate-associated loci using the Exome Chip. Hum. Mol. Genet. 26, 2346-2363 (2017)
16.
Bustamante, M.* et al.: A genome-wide association meta-analysis of diarrhoeal disease in young children identifies FUT2 locus and provides plausible biological pathways. Hum. Mol. Genet. 25, 4127-4142 (2016)
17.
Cornelis, M.C.* et al.: Genome-wide association study of caffeine metabolites provides new insights to caffeine metabolism and dietary caffeine-consumption behavior. Hum. Mol. Genet. 25, 5472-5482 (2016)
18.
de Vries, P.S.* et al.: A meta-analysis of 120,246 individuals identifies 18 new loci for fibrinogen concentration. Hum. Mol. Genet. 25, 358-370 (2016)
19.
Felix, J.F.* et al.: Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index. Hum. Mol. Genet. 25, 389-403 (2016)
20.
Huan, T.* et al.: A whole-blood transcriptome meta-analysis identifies gene expression signatures of cigarette smoking. Hum. Mol. Genet. 25, 4611-4623 (2016)