Natalia Bałdyga

5PUBLICATIONS
16CO-AUTHORS
Gene mappingGene expression (incl. microarray and other genome-wide approaches)Medical devicesPhonetics and speech science
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Publications (5)

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

|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

|Feb 25, 2023
The Genetic Background of Hearing Loss in Patients with EVA and Cochlear Malformation.

Natalia Bałdyga, Dominika Oziębło, Nina Gan

|Jun 10, 2022
Searching for the Molecular Basis of Partial Deafness.

Dominika Oziębło, Natalia Bałdyga, Marcin L Leja

|Mar 07, 2022
Update on CD164 and LMX1A genes to strengthen their causative role in autosomal dominant hearing loss.

Dominika Oziębło, Sang-Yeon Lee, Marcin Ludwik Leja

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Frequent Collaborators

5 joint publications

Dominika Oziębło

5 joint publications

Marcin Ludwik Leja

5 joint publications

Henryk Skarżyński

5 joint publications

Monika Ołdak