Katarzyna Niepokój

5PUBLICATIONS
16CO-AUTHORS
NeurogeneticsInfant and child healthGene mappingDevelopmental genetics (incl. sex determination)Optical technology
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Publications (5)

|Aug 12, 2025
NGS sequencing reveals the cause of hearing loss in a group of Polish patients with an isolated, non-DFNB1 hearing loss.

Katarzyna Niepokój, Agnieszka Magdalena Rygiel, Katarzyna Wertheim-Tysarowska

|Nov 22, 2023
Use of Fibrin Glue in the Treatment of Persistent Pneumothorax in Premature Infants at the Limit of Viability: Ethical Issues and Two and A Half Years Follow-Up.

Magdalena Rutkowska, Martyna Woynarowska, Iwona Terczyńska

|Jun 10, 2023
The Epidermal Transcriptome Analysis of a Novel c.639_642dup LORICRIN Variant-Delineation of the Loricrin Keratoderma Pathology.

Katarzyna Wertheim-Tysarowska, Katarzyna Osipowicz, Bartłomiej Gielniewski

|Aug 27, 2021
Wide Fontanels, Delayed Speech Development and Hoarse Voice as Useful Signs in the Diagnosis of KBG Syndrome: A Clinical Description of 23 Cases with Pathogenic Variants Involving the ANKRD11 Gene or Submicroscopic Chromosomal Rearrangements of 16q24.3.

Anna Kutkowska-Kaźmierczak, Maria Boczar, Ewa Kalka

|Nov 20, 2017
Hearing impairment caused by mutations in two different genes responsible for nonsyndromic and syndromic hearing loss within a single family.

Katarzyna Niepokój, Agnieszka M Rygiel, Piotr Jurczak

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Frequent Collaborators

1 joint publications

Anna Kutkowska-Kaźmierczak

1 joint publications

Katarzyna Kowalczyk

1 joint publications

Mateusz Dawidziuk

1 joint publications

Krzysztof Szczałuba