Pawel Gawlinski
9PUBLICATIONS
64CO-AUTHORS
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Publications (9)
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|Dec 19, 2025
DE NOVO VARIANTS IN THE POLY(RC)-BINDING PROTEIN GENE PCBP1 CAUSE A NEURODEVELOPMENTAL DISORDER.Wallid Deb, Thomas Besnard, Florence Desprez
|Aug 20, 2023
Congenital coenzyme Q5-linked pathology: causal genetic association, core phenotype, and molecular mechanism.Mateusz Dawidziuk, Aleksandra Podwysocka, Marta Jurek
|Sep 09, 2022
A Zebrafish/Drosophila Dual System Model for Investigating Human Microcephaly.Slawomir Bartoszewski, Mateusz Dawidziuk, Natalia Kasica
|Jan 21, 2022
De Novo ACTG1 Variant Expands the Phenotype and Genotype of Partial Deafness and Baraitser-Winter Syndrome.Mateusz Dawidziuk, Anna Kutkowska-Kazmierczak, Ewelina Bukowska-Olech
|Dec 24, 2021
Exome Sequencing Reveals Novel Variants and Expands the Genetic Landscape for Congenital Microcephaly.Mateusz Dawidziuk, Tomasz Gambin, Ewelina Bukowska-Olech
|Jun 27, 2021
Clinical and molecular characterization of craniofrontonasal syndrome: new symptoms and novel pathogenic variants in the EFNB1 gene.Ewelina Bukowska-Olech, Paweł Gawliński, Anna Jakubiuk-Tomaszuk
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Frequent Collaborators
5 joint publications
Mateusz Dawidziuk
3 joint publications
Ewelina Bukowska-Olech
3 joint publications
Monika Bekiesińska-Figatowska
3 joint publications
Anna Kutkowska-Kaźmierczak
2 joint publications
Sylwia Rzonca
2 joint publications
Wojciech Wiszniewski
2 joint publications
James R. Lupski
1 joint publications
Joanna Oswiecimska
1 joint publications
Tomasz Gambin
1 joint publications
Marta Marek
