Author

Michaela A. H. Hofrichter

Universitätsklinikum Würzburg

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· 2

Signature Assays, Organisms & Methods

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Research Focus:gene regulatory network inference· 2 Organism:human· 2 Approach:statistical model· 2 Organism:mouse· 1 Organism:zebrafish· 1

Frequent Co-Authors

Barbara VonaiD· 2 shared Thomas HaafiD· 2 shared Amanda M. LaueriD· 1 shared Anahid Hemmatpour· 1 shared Christian VogliD· 1 shared Cordula Neuner· 1 shared Daniel Bengl· 1 shared Daniel LiedtkeiD· 1 shared

Activity by Year

2026-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Barbara VonaORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicineEuropean Journal of Human GeneticsPeer-reviewedJul 29, 2026

PALM3 and hearing loss: a potential dual diagnosis interfering with novel gene discovery

Paria Najarzadeh Torbati, Lukas Hallbrucker, Michaela A. H. Hofrichter…·Barbara Vona

The paper identifies a homozygous splice-site variant in PALM3 and a missense variant in OTOA in a family with autosomal recessive hearing loss, supporting PALM3 as a candidate gene through functional and comparative analysis.

1 citation

humanstatistical model

𝕏 PostBluesky

Genetic & Genomic MedicinemedRxivPreprintMar 30, 2026

FRMPD4, a causal gene for intellectual disability and epilepsy, is associated with X-linked non-syndromic hearing loss

Daniel Liedtke, K Rak, Katrina M. Schrode…·Barbara Vona

The paper identifies FRMPD4 as a causal gene for X-linked non-syndromic hearing loss through genetic analysis and cross-species functional studies.

DOI 10.64898/2026.03.27.26349271

humanmouse

𝕏 PostBluesky