Anselm S. Hoppmann

Freiburg, BW, Germany

Last Updated: 09/26/2026

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Found 17 publications

Synonymous and non-synonymous variants at splice junctions can disrupt splicing and are frequently linked to disease associated loss of function genes.

Synonymous and non-synonymous variants at splice junctions can disrupt splicing and are frequently linked to disease associated loss of function genes.

Journal: BMC genomics

Published: August 15, 2025

Coupling metabolomics and exome sequencing reveals graded effects of rare damaging heterozygous variants on gene function and human traits.

Coupling metabolomics and exome sequencing reveals graded effects of rare damaging heterozygous variants on gene function and human traits.

Journal: Nature genetics

Published: October 27, 2023

X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements.

X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements.

Journal: Nature communications

Published: May 01, 2023

Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals.

Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals.

Journal: Communications biology

Published: December 16, 2021

Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies.

Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies.

Journal: Kidney international

Published: October 15, 2021

Ttc30a affects tubulin modifications in a model for ciliary chondrodysplasia with polycystic kidney disease.

Ttc30a affects tubulin modifications in a model for ciliary chondrodysplasia with polycystic kidney disease.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: August 04, 2021

Meta-analyses identify DNA methylation associated with kidney function and damage.

Meta-analyses identify DNA methylation associated with kidney function and damage.

Journal: Nature communications

Published: March 25, 2021

Epigenome-wide association study of serum urate reveals insights into urate co-regulation and the SLC2A9 locus.

Epigenome-wide association study of serum urate reveals insights into urate co-regulation and the SLC2A9 locus.

Journal: Nature communications

Published: March 17, 2021

Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline.

Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline.

Journal: Kidney international

Published: June 04, 2020

Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels.

Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels.

Journal: Nature genetics

Published: January 17, 2019

Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria.

Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria.

Journal: Nature communications

Published: December 07, 2018

A catalog of genetic loci associated with kidney function from analyses of a million individuals.

A catalog of genetic loci associated with kidney function from analyses of a million individuals.

Journal: Nature genetics

Published: September 16, 2018

Showing 1-12 of 17

Last Updated: 09/26/2026