Author

Anne‐Karin Kahlert

University Hospital Schleswig-HolsteinORCID 0000-0002-3201-2642Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Alejandro SifrimiD· 2 shared Anna WilsdoniD· 2 shared Enrique AudainiD· 2 shared Gregor DombrowskyiD· 2 shared Hashim Abdul‐KhaliqiD· 2 shared J. David BrookiD· 2 shared Jeroen BreckpotiD· 2 shared Yasset Pérez‐RiveroliD· 2 shared

Activity by Year

2021-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Alejandro SifrimORCID

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2 papers

Recent·Most cited

Genetic & Genomic Medicinenpj Genomic MedicinePeer-reviewedJun 2, 2026

Assessing the contribution of rare variants to congenital heart disease through a large-scale case-control exome study

Enrique Audain, Anna Wilsdon, Gregor Dombrowsky…·Marc‐Phillip Hitz

This study identifies rare variants and digenic interactions associated with congenital heart disease using a large-scale exome case-control analysis.

5 citations

humanwhole-exome sequencing

𝕏 PostBluesky

GeneticsPLoS GeneticsPeer-reviewedJul 29, 2021

Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease

Enrique Audain, Anna Wilsdon, Jeroen Breckpot…·MP Hitz

The paper identifies 21 candidate haploinsufficient genes associated with congenital heart disease through integrative analysis of CNVs and DNMs in CHD cases and controls.

35 citations

humanwhole-exome sequencing

𝕏 PostBluesky