Ewa Zietkiewicz

professor

Institute of Human Genetics

Poland

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Articles (8)

Year:

2024

Year:

2023

Year:

2022

Year:

2022

Year:

2021

Year:

2021

Year:

2021

Year:

2020

Collaborators (14)

Anna Jander

Instytut Pomnik -Centrum Zdrowia Dziecka

POLAND

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Anna Moczulska

Assistant Professor

Uniwersytet Jagiellonski Collegium Medicum

POLAND

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Katarzyna Taranta-Janusz

Assoc. Prof.

Medical University of Białystok

POLAND

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Małgorzata Sobieszczańska

Head, Professor, MD PhD. ; kierownik, prof. dr hab.

Uniwersytet Medyczny im Piastów Śląskich we Wrocławiu

POLAND

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Kinga Musial

Prof.

Wroclaw Medical University

POLAND

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Claire Jackson

University of Southampton

UNITED KINGDOM

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Marta Kaczmarek-Ryś

Institute of Human Genetics Polish Academy of Sciences

POLAND

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Patrycja Daca-Roszak

Institute of Human Genetics

POLAND

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Anna Stanisławska-Sachadyn

Associate Professor

University of Gdańsk

POLAND

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Roman Jaksik

Assistant Professor

Silesian University of Technology

POLAND

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Tomasz Jurek

Head of department, associate professor

Medical University of Silesia

POLAND

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Zuzanna Bukowy-Bieryllo

IHG PAS Professor

Institute of Human Genetics

POLAND

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Szymon Hryhorowicz

Institute of Human Genetics Polish Academy of Sciences

POLAND

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Ploski R

POLAND

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Ewa Zietkiewicz

Research Interests

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Articles (8)

Estimation of the Age of the Kashubian-Specific Pathogenic NPHS2 Variant Responsible for Hereditary Steroid-Resistant Nephrotic Syndrome Points to Its Recent Local Origin

Schmidtea mediterranea as a Model Organism to Study the Molecular Background of Human Motile Ciliopathies

The hero of American and Polish nations: a molecular look at Thaddeus Kosciuszko’s cause of death suggests a contribution of endocarditis caused by Cutibacterium acnes infection

Genetic diversity in Kashubs: the regional increase in the frequency of several disease-causing variants

European context of the diversity and phylogenetic position of SARS-CoV-2 sequences from Polish COVID-19 patients

Mild X-linked Alport syndrome due to the COL4A5 G624D variant originating in the Middle Ages is predominant in Central/East Europe and causes kidney failure in midlife

Properties of Non-Aminoglycoside Compounds Used to Stimulate Translational Readthrough of PTC Mutations in Primary Ciliary Dyskinesia

Discrimination between human populations using a small number of differentially methylated CpG sites: a preliminary study using lymphoblastoid cell lines and peripheral blood samples of European and Chinese origin.

Collaborators (14)

Anna Jander

Anna Moczulska

Katarzyna Taranta-Janusz

Małgorzata Sobieszczańska

Kinga Musial

Claire Jackson

Marta Kaczmarek-Ryś

Patrycja Daca-Roszak

Anna Stanisławska-Sachadyn

Roman Jaksik

Tomasz Jurek

Zuzanna Bukowy-Bieryllo

Szymon Hryhorowicz

Ploski R

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