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130 Records found.
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1.
Aboulmaouahib, B.* et al.: First mitochondrial genome wide association study with metabolomics. Hum. Mol. Genet. 31, 3367-3376 (2022)
2.
Brunet, T. et al.: Clonal hematopoiesis as a pitfall in germline variant interpretation in the context of Mendelian disorders. Hum. Mol. Genet. 31, 2386-2395 (2022)
3.
Castaneda, A.B.* et al.: Associations of carotid intima media thickness with gene expression in whole blood and genetically predicted gene expression across 48 tissues. Hum. Mol. Genet. 31, 1171-1182 (2022)
4.
Cruz, R.* et al.: Novel genes and sex differences in COVID-19 severity. Hum. Mol. Genet., DOI: 10.1093/hmg/ddac132 (2022)
5.
Katsoula G. et al.: A molecular map of long non-coding RNA expression, isoform switching and alternative splicing in osteoarthritis. Hum. Mol. Genet. 31, 2090-2105 (2022)
6.
Pervjakova, N.* et al.: Multi-ancestry genome-wide association study of gestational diabetes mellitus highlights genetic links with type 2 diabetes. Hum. Mol. Genet., DOI: 10.1093/hmg/ddac050 (2022)
7.
Portilla-Fernandez, E.* et al.: Genetic and clinical determinants of abdominal aortic diameter: Genome-wide association studies, exome array data and Mendelian randomization study. Hum. Mol. Genet., DOI: 10.1093/hmg/ddac051 (2022)
8.
Riedhammer, K.M.* et al.: Suleiman-El-Hattab syndrome: A histone modification disorder caused by TASP1 deficiency. Hum. Mol. Genet. 31, 3083-3094 (2022)
9.
Ahluwalia, T.S.* et al.: Genome-wide association study of circulating interleukin 6 levels identifies novel loci. Hum. Mol. Genet. 30, 393-409 (2021)
10.
Gergei, I.* et al.: GWAS META-analysis followed by MENDELIAN randomisation revealed potential control mechanisms for circulating α-klotho levels. Hum. Mol. Genet., DOI: 10.1093/hmg/ddab263 (2021)
11.
Lam, D. et al.: Intronic elements associated with insomnia and restless legs syndrome exhibit cell type-specific epigenetic features contributing to MEIS1 regulation. Hum. Mol. Genet. 31, 1733-1746 (2021)
12.
Pott, J.* et al.: Meta-GWAS of PCSK9 levels detects two novel loci at APOB and TM6SF2. Hum. Mol. Genet. 31, 999-1011 (2021)
13.
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)
14.
Nag, A.* et al.: Genome-wide scan identifies novel genetic loci regulating salivary metabolite levels. Hum. Mol. Genet. 29, 864-875 (2020)
15.
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)
16.
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)
17.
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)
18.
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)
19.
Brockmann, S.J.* et al.: CHCHD10 mutations p. R15L and p. G66V cause motoneuron disease by haploinsufficiency. Hum. Mol. Genet. 27, 706-715 (2018)
20.
Haworth, S.* et al.: Consortium-based genome-wide meta-analysis for childhood dental caries traits. Hum. Mol. Genet. 27, 3113-3127 (2018)