Justyna A Karolak

ORCID

Publication Activity (10 Years)

Years Active: 2020-2023
Publications (10 Years): 11

Top Venues

Genes

PeerJ

American journal of respiratory and critical care medicine

Molecular genetics & genomic medicine

Baylor College of Medicine

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

Affiliation History

Baylor College of Medicine

United States

Postdoctoral Associate :: Department of Molecular and Human Genetics

Publications

Katarzyna Bzdęga, Anna Kutkowska-Kaźmierczak, Gail H Deutsch, Izabela Plaskota, Marta Smyk, Magdalena Niemiec, Artur Barczyk, Ewa Obersztyn, Jan Modzelewski, Iwona Lipska, Paweł Stankiewicz, Marzena Gajecka, Małgorzata Rydzanicz, Rafał Płoski, Tomasz Szczapa, Justyna A Karolak
Prenatal Detection of a FOXF1 Deletion in a Fetus with ACDMPV and Hydronephrosis. Genes 14 (3) (2023)
Katarzyna Bzdęga, Anna Kutkowska-Kaźmierczak, Gail H Deutsch, Izabela Plaskota, Marta Smyk, Magdalena Niemiec, Artur Barczyk, Ewa Obersztyn, Jan Modzelewski, Iwona Lipska, Paweł Stankiewicz, Marzena Gajecka, Małgorzata Rydzanicz, Rafał Płoski, Tomasz Szczapa, Justyna A Karolak
Prenatal Detection of a FOXF1 Deletion in a Fetus with ACDMPV and Hydronephrosis. Genes 14 (3) (2023)
Minzhe Guo, Kathryn A Wikenheiser-Brokamp, Joseph A Kitzmiller, Cheng Jiang, Guolun Wang, Allen Wang, Sebastian Preissl, Xiaomeng Hou, Justin Buchanan, Justyna A Karolak, Yifei Miao, David B Frank, William J Zacharias, Xin Sun, Yan Xu, Mingxia Gu, Paweł Stankiewicz, Vladimir V Kalinichenko, Jennifer A Wambach, Jeffrey A Whitsett
Single Cell Multiomics Identifies Cells and Genetic Networks Underlying Alveolar Capillary Dysplasia. American journal of respiratory and critical care medicine (2023)
Katarzyna Bzdęga, Anna Kutkowska-Kaźmierczak, Gail H Deutsch, Izabela Plaskota, Marta Smyk, Magdalena Niemiec, Artur Barczyk, Ewa Obersztyn, Jan Modzelewski, Iwona Lipska, Paweł Stankiewicz, Marzena Gajecka, Małgorzata Rydzanicz, Rafał Płoski, Tomasz Szczapa, Justyna A Karolak
Prenatal Detection of a FOXF1 Deletion in a Fetus with ACDMPV and Hydronephrosis. Genes 14 (3) (2023)
Katarzyna Bzdęga, Mateusz Biela, Gail H Deutsch, Joseph A Kitzmiller, Małgorzata Rydzanicz, Ploski Rafal, Jeffrey A Whitsett, Robert Śmigiel, Justyna A Karolak
A novel non-recurrent CNV deletion involving TBX4 and leaving TBX2 intact causes congenital alveolar dysplasia. Clinical genetics (2023)
Barbara Poszewiecka, Krzysztof Gogolewski, Justyna A Karolak, Przemyslaw Szafranski, Anna Gambin
PhaseDancer: a novel targeted assembler of segmental duplications unravels the complexity of the human chromosome 2 fusion going from 48 to 46 chromosomes in hominin evolution. Genome biology 24 (1) (2023)
Esra Yıldız-Bölükbaşı, Justyna A Karolak, Przemyslaw Szafranski, Tomasz Gambin, Omer Murik, David A Zeevi, Gheona Altarescu, Przemyslaw Szafranski
Exacerbation of mild lung disorders to lethal pulmonary hypoplasia by a noncoding hypomorphic SNV in a lung-specific enhancer in trans to the frameshifting TBX4 variant. American journal of medical genetics. Part A 188 (5) (2022)
Esra Yıldız-Bölükbaşı, Justyna A Karolak, Przemyslaw Szafranski, Tomasz Gambin, Nicholas Willard, Steven H Abman, Csaba Galambos, John P Kinsella, Przemyslaw Szafranski
High-level gonosomal mosaicism for a pathogenic non-coding CNV deletion of the lung-specific FOXF1 enhancer in an unaffected mother of an infant with ACDMPV. Molecular genetics & genomic medicine 10 (11) (2022)
Justyna A Karolak, Carrie L Welch, Christian Mosimann, Katarzyna Bzdega, James D West, I David Montani, Mélanie Eyries, Mary P Mullen, Steven H Abman, Matina Prapa, Stefan Gräf, Nicholas W Morrell, Anna R Hemnes, Frédéric Perros, Rizwan Hamid, Malcolm P O Logan, Jeffrey Whitsett, Csaba Galambos, Paweł Stankiewicz, Wendy K Chung, Eric D Austin, null null
Molecular Function and Contribution of TBX4 in Development and Disease. American journal of respiratory and critical care medicine (2022)
Justyna A Karolak, Tomasz Gambin, Malgorzata Rydzanicz, Piotr Polakowski, Ploski Rafal, Jacek P Szaflik, Marzena Gajecka
Accumulation of sequence variants in genes of Wnt signaling and focal adhesion pathways in human corneas further explains their involvement in keratoconus. PeerJ 8 (2020)
Justyna A Karolak, Barbara Ginter-Matuszewska, Katarzyna Tomela, Michal Kabza, Dorota M Nowak-Malczewska, Malgorzata Rydzanicz, Piotr Polakowski, Jacek P Szaflik, Marzena Gajecka
Further evaluation of differential expression of keratoconus candidate genes in human corneas. PeerJ 8 (2020)

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Publication Activity (10 Years)

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Justyna A Karolak