Author

Lukas Hallbrucker

Innsbruck Medical University

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

Frequent Co-Authors

Anahid Hemmatpour· 1 shared Barbara VonaiD· 1 shared Christian VogliD· 1 shared Daniel OwrangiD· 1 shared Ehsan Ghayoor KarimianiiD· 1 shared Jonas SetzkeiD· 1 shared Manfred W. KilimanniD· 1 shared Michaela A. H. Hofrichter· 1 shared

Activity by Year

2026-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Anahid Hemmatpour

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1 paper

Recent·Most cited

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

Paria Najarzadeh Torbati, Lukas Hallbrucker, Michaela A. H. Hofrichter, Daniel Owrang, Jonas Setzke, Manfred W. Kilimann, Anahid Hemmatpour, Mohsen Rajati, Ehsan Ghayoor Karimiani, Thomas Haaf, Christian Vogl, 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.

European Journal of Human Genetics · Jul 29, 2026Peer-reviewedGenetic & Genomic Medicine