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M. Kurkowiak · SciRah

Researcher profile · Semantic Scholar

M. Kurkowiak

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M. Kurkowiak — researcher profile on SciRah

h-index: 9
Works: 18
Citations: 698

Most-cited papers

ZMYND10 is mutated in primary ciliary dyskinesia and interacts with LRRC6.
M. Zariwala, H. Gee, M. Kurkowiak, D. A. Al-Mutairi +54 more
2013American Journal of Human Genetics195 citations Open access
Semantic Scholar
CCDC151 Mutations Cause Primary Ciliary Dyskinesia by Disruption of the Outer Dynein Arm Docking Complex Formation
R. Hjeij, A. Onoufriadis, C. Watson, Christopher E. Slagle +31 more
2014American Journal of Human Genetics158 citations Open access
Semantic Scholar
Recent advances in primary ciliary dyskinesia genetics
M. Kurkowiak, E. Ziętkiewicz, M. Witt
2014Journal of Medical Genetics101 citations Open access
Semantic Scholar
Autoimmunity and Cancer—Two Sides of the Same Coin
J. Sakowska, Łukasz Arcimowicz, M. Jankowiak, Ines Papak +8 more
2022Frontiers in Immunology69 citations Open access
Semantic Scholar
Adoptive Cell Therapy—Harnessing Antigen-Specific T Cells to Target Solid Tumours
Elżbieta Chruściel, Zuzanna Urban-Wójciuk, Łukasz Arcimowicz, M. Kurkowiak +9 more
2020Cancers42 citations Open access
Semantic Scholar
Triple Combination of Ascorbate, Menadione and the Inhibition of Peroxiredoxin-1 Produces Synergistic Cytotoxic Effects in Triple-Negative Breast Cancer Cells
Malgorzata Bajor, Agnieszka Graczyk-Jarzynka, Katsiaryna Marhelava, M. Kurkowiak +8 more
2020Antioxidants34 citations Open access
Semantic Scholar
The effects of RNA editing in cancer tissue at different stages in carcinogenesis
M. Kurkowiak, Łukasz Arcimowicz, Elżbieta Chruściel, Zuzanna Urban-Wójciuk +6 more
2021RNA Biology23 citations Open access
Semantic Scholar
Altered Levels of Proteins and Phosphoproteins, in the Absence of Early Causative Transcriptional Changes, Shape the Molecular Pathogenesis in the Brain of Young Presymptomatic Ki91 SCA3/MJD Mouse
Kalina Wiatr, P. Piasecki, Ł. Marczak, Pawel Wojciechowski +8 more
2019Molecular Neurobiology18 citations Open access
Semantic Scholar
ZMYND10 - Mutation Analysis in Slavic Patients with Primary Ciliary Dyskinesia
M. Kurkowiak, E. Ziętkiewicz, Agnieszka Greber, K. Voelkel +3 more
2016PLoS ONE15 citations Open access
Semantic Scholar
Mouse polyQ database: a new online resource for research using mouse models of neurodegenerative diseases
Wojciech J. Szlachcic, P. Switonski, M. Kurkowiak, Kalina Wiatr +1 more
2015Molecular Brain9 citations Open access
Semantic Scholar
Differential RNA editing landscapes in host cell versus the SARS-CoV-2 genome
M. Kurkowiak, S. Fletcher, Alison Daniels, P. Mozolewski +5 more
2023iScience8 citations Open access
Semantic Scholar
High maternal-fetal HLA eplet compatibility is associated with severe manifestation of preeclampsia
Katarzyna Stefańska, M. Kurkowiak, K. Piekarska, Elżbieta Chruściel +12 more
2023Frontiers in Immunology8 citations Open access
Semantic Scholar
What Inhibits Natural Killers’ Performance in Tumour
Ines Papak, Elżbieta Chruściel, K. Dziubek, M. Kurkowiak +4 more
2022International Journal of Molecular Sciences7 citations Open access
Semantic Scholar
The effects of p53 gene inactivation on mutant proteome expression in a human melanoma cell model.
J. Faktor, G. Grasso, Filip Zavadil Kokáš, M. Kurkowiak +9 more
2020Biochimica et Biophysica Acta - General Subjects6 citations Open access
Semantic Scholar
Genomic landscape of human erythroleukemia K562 cell line, as determined by next-generation sequencing and cytogenetics
M. Kurkowiak, M. Pępek, M. Machnicki, I. Solarska +5 more
20175 citations
Semantic Scholar
First familial cases of type 2 congenital erythrocytosis (ECYT2) with a Chuvash pathogenic variant in VHL gene in Poland: example of the clinical utility of next-generation sequencing in diagnostics of orphan diseases
M. Pępek, W. Bal, M. Radwańska, M. Machnicki +7 more
20202 citations Open access
Semantic Scholar
An integrated DNA and RNA variant detector identifies a highly conserved three base exon in the MAP4K5 kinase locus
M. Kurkowiak, G. Grasso, J. Faktor, Lisa Scheiblecker +8 more
2021RNA Biology1 citations Open access
Semantic Scholar
Gene discovery for motile cilia disorders: mutation spectrum in primary ciliary dyskinesia and discovery of mutations in CCDC151
A. Onoufriadis, R. Hjeij, C. Watson, CE Slagle +29 more
2015Cilia0 citations Open access
Semantic Scholar

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