Author

Heike Meiselbach

Friedrich-Alexander-Universität Erlangen-NürnbergORCID 0000-0001-5163-8264Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Assay:whole-exome sequencing· 2 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Assay:metabolomics· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Kai‐Uwe EckardtiD· 2 shared André ReisiD· 1 shared Anna KöttgeniD· 1 shared Arif Bülent EkiciiD· 1 shared Bernt PoppiD· 1 shared Cornelia S. KrausiD· 1 shared Daniel FässleriD· 1 shared Fabian Telkämper· 1 shared

Activity by Year

2022-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 25 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Kai‐Uwe EckardtORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintOct 17, 2023

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

Nora Scherer, Daniel Fässler, Oleg Borisov…·Anna Köttgen

The paper identifies gene-metabolite associations using exome sequencing and metabolomics, revealing graded effects of rare variants on traits and diseases.

2 citations

humanwhole-exome sequencing

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Genetic & Genomic MedicineEuropean Journal of Human GeneticsPeer-reviewedSep 13, 2022

Prevalence of hereditary tubulointerstitial kidney diseases in the German Chronic Kidney Disease study

Bernt Popp, Arif Bülent Ekici, Karl Xaver Knaup…·Michael Sean Wiesener

The paper identifies pathogenic variants in tubulointerstitial kidney disease genes in 12.5% of a CKD cohort using targeted sequencing and clinical criteria.

22 citations

humanwhole-exome sequencing

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