PuSH - Publication Server of Helmholtz Zentrum München

Journal browsing

135 Records found.
Zum Exportieren der Ergebnisse bitte einloggen.
▮◀ ◀◀ 1 ... 2 ... 3 ... 4 ... 5 ... 6 ... 7 ... ▶▶ ▶▮
Lay all publications on this page into basket
1.
Kreitmaier, P. et al.: Epigenomic profiling of the infrapatellar fat pad in osteoarthritis. Hum. Mol. Genet. 33:ddad198 (2023)
2.
Lucienne, M.* et al.: Insights into energy balance dysregulation from a mouse model of methylmalonic aciduria. Hum. Mol. Genet. 32, 2717-2734 (2023)
3.
Thareja, G.* et al.: Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Hum. Mol. Genet. 32, 907–916 (2023)
4.
Aboulmaouahib, B.* et al.: First mitochondrial genome wide association study with metabolomics. Hum. Mol. Genet. 31, 3367-3376 (2022)
5.
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)
6.
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)
7.
Cruz, R.* et al.: Novel genes and sex differences in COVID-19 severity. Hum. Mol. Genet. 31, 3789-3806 (2022)
8.
Gergei, I.* et al.: GWAS META-analysis followed by MENDELIAN randomisation revealed potential control mechanisms for circulating α-klotho levels. Hum. Mol. Genet. 31, 792-802 (2022)
9.
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)
10.
Kuhn, T.* et al.: Comparative genomic analyses of multiple backcross mouse populations suggest SGCG as a novel potential obesity-modifier gene. Hum. Mol. Genet. 31, 4019-4033 (2022)
11.
Pervjakova, N.* et al.: Multi-ancestry genome-wide association study of gestational diabetes mellitus highlights genetic links with type 2 diabetes. Hum. Mol. Genet. 31, 3377–3391 (2022)
12.
Png, G. et al.: Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Hum. Mol. Genet. 32, 1266-1275 (2022)
13.
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. 31, 3566-3579 (2022)
14.
Riedhammer, K.M.* et al.: Suleiman-El-Hattab syndrome: A histone modification disorder caused by TASP1 deficiency. Hum. Mol. Genet. 31, 3083-3094 (2022)
15.
Ahluwalia, T.S.* et al.: Genome-wide association study of circulating interleukin 6 levels identifies novel loci. Hum. Mol. Genet. 30, 393-409 (2021)
16.
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)
17.
Pott, J.* et al.: Meta-GWAS of PCSK9 levels detects two novel loci at APOB and TM6SF2. Hum. Mol. Genet. 31, 999-1011 (2021)
18.
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)
19.
Nag, A.* et al.: Genome-wide scan identifies novel genetic loci regulating salivary metabolite levels. Hum. Mol. Genet. 29, 864-875 (2020)
20.
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)
▮◀ ◀◀ 1 ... 2 ... 3 ... 4 ... 5 ... 6 ... 7 ... ▶▶ ▶▮