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Homuth, G.
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Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications
Gene-educational attainment interactions in a multi-population genome-wide meta-analysis identify novel lipid loci
Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus
Epigenome-wide association study reveals CpG sites associated with thyroid function and regulatory effects on KLF9
Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals
DNA methylation signature of chronic low-grade inflammation and its role in cardio-respiratory diseases
Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways
Association of Thyroid dysfunction with cognitive function an individual participant data analysis
Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression
Genome-wide association study of circulating interleukin 6 levels identifies novel loci
Genetic studies of leptin concentrations implicate leptin in the regulation of early adiposity
An individual participant data analysis of prospective cohort studies on the association between subclinical thyroid dysfunction and depressive symptoms
Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci
The genetic architecture of the human cerebral cortex
Classical human leukocyte antigen alleles and C4 haplotypes are not significantly associated with depression
Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank
Genetic architecture of subcortical brain structures in 38,851 individuals
Associations of autozygosity with a broad range of human phenotypes
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels
World Health Organization cardiovascular disease risk charts: revised models to estimate risk in 21 global regions
Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria
Subclinical thyroid dysfunction and depressive symptoms: protocol for a systematic review and individual participant data meta-analysis of prospective cohort studies
Mendelian randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traits
A catalog of genetic loci associated with kidney function from analyses of a million individuals
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