Monika Ołdak

25PUBLICATIONS
255CO-AUTHORS
Gene mappingOptical technologySensory systemsEpidemiological modellingGene expression (incl. microarray and other genome-wide approaches)
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Publications (25)

|Jun 29, 2026
Integrative genetic and functional analysis of autosomal dominant hearing loss in 108 multigenerational families.

|Jun 26, 2026
Analysis of genetic risk factors for Leber hereditary optic neuropathy in the Polish population.

|Jan 09, 2026
De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa.

Mathieu Quinodoz, Kim Rodenburg, Zuzana Cvackova

|Oct 16, 2025
The Derkay Scale as a Predictor of Voice Dysfunction in Recurrent Respiratory Papillomatosis: Correlations Between Acoustic and Patient-Reported Outcomes.

Beata Miaśkiewicz, Elżbieta Gos, Aleksandra Panasiewicz

|Feb 11, 2025
Characterization of a novel GRHL2 mutation reveals molecular mechanisms underlying autosomal dominant hearing loss (DFNA28): insights from structural and functional studies.

Dominika Oziębło, Natalia Bałdyga, Marcin L Leja

|Jan 20, 2025
De novo and inherited dominant variants in U4 and U6 snRNAs cause retinitis pigmentosa.

Mathieu Quinodoz, Kim Rodenburg, Zuzana Cvackova

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Frequent Collaborators

16 joint publications

Dominika Oziębło

11 joint publications

Henryk Skarżyński

7 joint publications

Marcin Ludwik Leja

5 joint publications

Susanne Roosing