Dominika Oziębło

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 19

Top Topics

High Throughput Sequencing

Autism Spectrum Disorder

Top Venues

International journal of molecular sciences

Journal of translational medicine

Audiology research

This page only lists publications with an associated author ORCID identifier.

Publications

Monika Matusiak, Dominika Oziębło, Monika Ołdak, Emilia Rejmak, Leszek Kaczmarek, Henryk Skarzynski
Longitudinal Changes in BDNF and MMP-9 Protein Plasma Levels in Children after Cochlear Implantation. International journal of molecular sciences 24 (4) (2023)
Laurence Jonard, Davide Brotto, Miguel Angel Moreno-Pelayo, Ignacio Del Castillo, Hannie Kremer, Ronald J E Pennings, Helena Caria, Graça Fialho, An Boudewyns, Guy Van Camp, Monika Ołdak, Dominika Oziębło, Naïma Deggouj, Romolo Daniele De Siati, Paolo Gasparini, Giorgia Girotto, Margriet Verstreken, Silvia Dossena, Sebastian Roesch, Saba Battelino, Katarina Trebušak Podkrajšek, Athanasia Warnecke, Thomas Lenarz, Anke Lesinski-Schiedat, Michel Mondain, Anne-Françoise Roux, Françoise Denoyelle, Natalie Loundon, Margaux Serey-Gaut, Patrizia Trevisi, Elisa Rubinato, Alessandro Martini, Sandrine Marlin
Genetic Evaluation of Prelingual Hearing Impairment: Recommendations of an European Network for Genetic Hearing Impairment. Audiology research 13 (3) (2023)
Monika Matusiak, Dominika Oziębło, Monika Ołdak, Emilia Rejmak, Leszek Kaczmarek, Henryk Skarzynski
Longitudinal Changes in BDNF and MMP-9 Protein Plasma Levels in Children after Cochlear Implantation. International journal of molecular sciences 24 (4) (2023)
Natalia Bałdyga, Dominika Oziębło, Nina Gan, Mariusz Furmanek, Marcin Ludwik Leja, Henryk Skarzynski, Monika Ołdak
The Genetic Background of Hearing Loss in Patients with EVA and Cochlear Malformation. Genes 14 (2) (2023)
Monika Matusiak, Dominika Oziębło, Monika Ołdak, Emilia Rejmak, Leszek Kaczmarek, Henryk Skarzynski
Longitudinal Changes in BDNF and MMP-9 Protein Plasma Levels in Children after Cochlear Implantation. International journal of molecular sciences 24 (4) (2023)
Natalia Bałdyga, Dominika Oziębło, Nina Gan, Mariusz Furmanek, Marcin Ludwik Leja, Henryk Skarzynski, Monika Ołdak
The Genetic Background of Hearing Loss in Patients with EVA and Cochlear Malformation. Genes 14 (2) (2023)
Monika Matusiak, Dominika Oziębło, Monika Ołdak, Emilia Rejmak, Leszek Kaczmarek, Henryk Skarzynski
Longitudinal Changes in BDNF and MMP-9 Protein Plasma Levels in Children after Cochlear Implantation. International journal of molecular sciences 24 (4) (2023)
Natalia Bałdyga, Dominika Oziębło, Nina Gan, Mariusz Furmanek, Marcin Ludwik Leja, Henryk Skarzynski, Monika Ołdak
The Genetic Background of Hearing Loss in Patients with EVA and Cochlear Malformation. Genes 14 (2) (2023)
Monika Matusiak, Dominika Oziębło, Monika Ołdak, Emilia Rejmak, Leszek Kaczmarek, Dominik Dobek, Henryk Skarżyński
MMP-9 plasma level as biomarker of cochlear implantation outcome in cohort study of deaf children. European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery (2023)
Natalia Bałdyga, Dominika Oziębło, Nina Gan, Mariusz Furmanek, Marcin Ludwik Leja, Henryk Skarzynski, Monika Ołdak
The Genetic Background of Hearing Loss in Patients with EVA and Cochlear Malformation. Genes 14 (2) (2023)
Dominika Oziębło, Natalia Bałdyga, Marcin Ludwik Leja, Henryk Skarzynski, Monika Ołdak
Searching for the Molecular Basis of Partial Deafness. International journal of molecular sciences 23 (11) (2022)
Monika Matusiak, Dominika Oziębło, Monika Ołdak, Emilia Rejmak, Leszek Kaczmarek, Piotr Henryk Skarzynski, Henryk Skarzynski
Prospective cohort study reveals MMP-9, a neuroplasticity regulator, as a prediction marker of cochlear implantation outcome in prelingual deafness treatment. Molecular neurobiology 59 (4) (2022)
Dominika Oziębło, Sang Yeon Lee, Marcin Ludwik Leja, Anna Sarosiak, Natalia Bałdyga, Henryk Skarzynski, Yehree Kim, Jin-Hee Han, Hyo Soon Yoo, Min-Hyun Park, Byung Yoon Choi, Monika Ołdak
Update on CD164 and LMX1A genes to strengthen their causative role in autosomal dominant hearing loss. Human genetics 141 (3-4) (2022)
Janine Reurink, Adrian Dockery, Dominika Oziębło, Gwyneth Jane Farrar, Monika Ołdak, Jacoline B Ten Brink, Arthur A Bergen, Tuula Rinne, Helger G Yntema, Ronald J E Pennings, L Ingeborgh van den Born, Marco Aben, Jaap Oostrik, Hanka Venselaar, Astrid S Plomp, M Imran Khan, Erwin van Wijk, Frans P M Cremers, Susanne Roosing, Hannie Kremer
Molecular Inversion Probe-Based Sequencing of USH2A Exons and Splice Sites as a Cost-Effective Screening Tool in USH2 and arRP Cases. International journal of molecular sciences 22 (12) (2021)
Dominika Oziębło, Marcin Ludwik Leja, Michal Lazniewski, Anna Sarosiak, Grażyna Tacikowska, Krzysztof Kochanek, Dariusz Plewczyński, Henryk Skarzynski, Monika Ołdak
TBC1D24 emerges as an important contributor to progressive postlingual dominant hearing loss. Scientific reports 11 (1) (2021)
Anna Sarosiak, Dominika Oziębło, Monika Udziela, Cees Vermeer, Jacek Malejczyk, Jacek Paweł Szaflik, Monika Ołdak
High expression of Matrix Gla Protein in Schnyder corneal dystrophy patients points to an active role of vitamin K in corneal health. Acta ophthalmologica 99 (2) (2020)
Dominika Oziębło, Joanna Pazik, Iwona Stępniak, Henryk Skarzynski, Monika Ołdak
Two Novel Pathogenic Variants Confirm RMND1 Causative Role in Perrault Syndrome with Renal Involvement. Genes 11 (9) (2020)
Dominika Oziębło, Anna Sarosiak, Marcin Ludwik Leja, Birgit S Budde, Grażyna Tacikowska, Nataliya Di Donato, Hanno J Bolz, Peter Nürnberg, Henryk Skarzynski, Monika Ołdak
First confirmatory study on PTPRQ as an autosomal dominant non-syndromic hearing loss gene. Journal of translational medicine 17 (1) (2019)
Monika Ołdak, Urszula Lechowicz, Agnieszka Pollak, Dominika Oziębło, Henryk Skarzynski
Overinterpretation of high throughput sequencing data in medical genetics: first evidence against TMPRSS3/GJB2 digenic inheritance of hearing loss. Journal of translational medicine 17 (1) (2019)