Author

Karen Schneider

Friedrich-Alexander-Universität Erlangen-Nürnberg

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

André ReisiD· 1 shared Arif Bülent EkiciiD· 1 shared Bernt PoppiD· 1 shared Cornelia S. KrausiD· 1 shared Heike MeiselbachiD· 1 shared Jonghun ParkiD· 1 shared Kai‐Uwe EckardtiD· 1 shared Karl Xaver KnaupiD· 1 shared

Activity by Year

2022-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

André ReisORCID

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1 paper

Recent·Most cited

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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