Publications by authors named "Anselm Hoppmann"

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Synonymous and non-synonymous variants at splice junctions can disrupt splicing and are frequently linked to disease associated loss of function genes.
Sruthi Srinivasan, Swetha Subramanian, Hui Zhou, Anselm Hoppmann, Patrick Metzger

BMC Genomics· December 2025

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Coupling metabolomics and exome sequencing reveals graded effects of rare damaging heterozygous variants on gene function and human traits.
Nora Scherer, Daniel Fässler, Oleg Borisov, Yurong Cheng, Pascal Schlosser, Anselm Hoppmann

Nat Genet· January 2025

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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.
Markus Scholz, Katrin Horn, Janne Pott, Matthias Wuttke, Andreas Kühnapfel, Anselm Hoppmann

Nat Commun· January 2024

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Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies.
Mathias Gorski, Humaira Rasheed, Alexander Teumer, Laurent F Thomas, Sarah E Graham, Anselm Hoppmann

Kidney Int· September 2022

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Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals.
Thomas W Winkler, Humaira Rasheed, Alexander Teumer, Mathias Gorski, Bryce X Rowan, Anselm Hoppmann

Commun Biol· June 2022

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Epigenome-wide association study of serum urate reveals insights into urate co-regulation and the SLC2A9 locus.
Adrienne Tin, Pascal Schlosser, Pamela R Matias-Garcia, Chris H L Thio, Roby Joehanes, Anselm Hoppmann

Nat Commun· December 2021

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Meta-analyses identify DNA methylation associated with kidney function and damage.
Pascal Schlosser, Adrienne Tin, Pamela R Matias-Garcia, Chris H L Thio, Roby Joehanes, Anselm Hoppmann

Nat Commun· December 2021

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Ttc30a affects tubulin modifications in a model for ciliary chondrodysplasia with polycystic kidney disease.
Maike Getwan, Anselm Hoppmann, Pascal Schlosser, Kelli Grand, Weiting Song

Proc Natl Acad Sci U S A· September 2021

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Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline.
Mathias Gorski, Bettina Jung, Yong Li, Pamela R Matias-Garcia, Matthias Wuttke, Anselm Hoppmann

Kidney Int· April 2021

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Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels.
Adrienne Tin, Jonathan Marten, Victoria L Halperin Kuhns, Yong Li, Matthias Wuttke, Anselm Hoppmann

Nat Genet· October 2019

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Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria.
Alexander Teumer, Yong Li, Sahar Ghasemi, Bram P Prins, Matthias Wuttke, Anselm Hoppmann

Nat Commun· September 2019

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A catalog of genetic loci associated with kidney function from analyses of a million individuals.
Matthias Wuttke, Yong Li, Man Li, Karsten B Sieber, Mary F Feitosa, Anselm Hoppmann

Nat Genet· June 2019

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A novel LMNA nonsense mutation causes two distinct phenotypes of cardiomyopathy with high risk of sudden cardiac death in a large five-generation family.
Christina R Glöcklhofer, Johannes Steinfurt, Gerlind Franke, Anselm Hoppmann, Theresa Glantschnig

Europace· December 2018

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A common pathomechanism in GMAP-210- and LBR-related diseases.
Anika Wehrle, Tomasz M Witkos, Judith C Schneider, Anselm Hoppmann, Sidney Behringer

JCI Insight· December 2018

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GenToS: Use of Orthologous Gene Information to Prioritize Signals from Human GWAS.
Anselm S Hoppmann, Pascal Schlosser, Rolf Backofen, Ekkehart Lausch, Anna Köttgen

PLoS One· August 2017

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Combination of mouse models and genomewide association studies highlights novel genes associated with human kidney function.
Jiaojiao Jing, Cristian Pattaro, Anselm Hoppmann, Yukinori Okada,

Kidney Int· October 2016

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Genetic loci associated with renal function measures and chronic kidney disease in children: the Pediatric Investigation for Genetic Factors Linked with Renal Progression Consortium.
Matthias Wuttke, Craig S Wong, Elke Wühl, Daniel Epting, Li Luo, Anselm Hoppmann

Nephrol Dial Transplant· February 2016

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