Mariusz Berdyński

530 total citations
27 papers, 352 citations indexed

About

Mariusz Berdyński is a scholar working on Neurology, Genetics and Molecular Biology. According to data from OpenAlex, Mariusz Berdyński has authored 27 papers receiving a total of 352 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Neurology, 9 papers in Genetics and 7 papers in Molecular Biology. Recurrent topics in Mariusz Berdyński's work include Amyotrophic Lateral Sclerosis Research (12 papers), Neurogenetic and Muscular Disorders Research (8 papers) and Neurological diseases and metabolism (3 papers). Mariusz Berdyński is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (12 papers), Neurogenetic and Muscular Disorders Research (8 papers) and Neurological diseases and metabolism (3 papers). Mariusz Berdyński collaborates with scholars based in Poland, United States and Sweden. Mariusz Berdyński's co-authors include Cezary Żekanowski, Krzysztof Safranow, Magdalena Kuźma‐Kozakiewicz, Peter M. Andersen, Mitsuya Morita, Przemysław Miszta, Sławomir Filipek, Piotr Janik, Maria Barcikowska and Maria Jolanta Rędowicz and has published in prestigious journals such as PLoS ONE, Scientific Reports and Journal of Alzheimer s Disease.

In The Last Decade

Mariusz Berdyński

26 papers receiving 351 citations

Peers

Mariusz Berdyński
Amy W. Butler United Kingdom
Younghwi Kwon South Korea
Uriya Bekenstein Israel
Lavinia Palamiuc France
Ito Kawakami Japan
Tiziana Petrozziello Italy
Zygmunt Jamrozik Poland
Theo Hatzipetros United States
Christopher Eggett United Kingdom
Katherine D. LaClair United States
Amy W. Butler United Kingdom
Mariusz Berdyński
Citations per year, relative to Mariusz Berdyński Mariusz Berdyński (= 1×) peers Amy W. Butler

Countries citing papers authored by Mariusz Berdyński

Since Specialization
Citations

This map shows the geographic impact of Mariusz Berdyński's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Mariusz Berdyński with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mariusz Berdyński more than expected).

Fields of papers citing papers by Mariusz Berdyński

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mariusz Berdyński. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Mariusz Berdyński. The network helps show where Mariusz Berdyński may publish in the future.

Co-authorship network of co-authors of Mariusz Berdyński

This figure shows the co-authorship network connecting the top 25 collaborators of Mariusz Berdyński. A scholar is included among the top collaborators of Mariusz Berdyński based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Mariusz Berdyński. Mariusz Berdyński is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Berdyński, Mariusz, Krzysztof Safranow, Peter M. Andersen, & Cezary Żekanowski. (2025). Phenotypic Characterization of ALS‐Causing SOD1 Mutations Affecting Polypeptide Length. Human Mutation. 2025(1). 9792233–9792233.
2.
Gawęda-Walerych, Katarzyna, Emilia J. Sitek, Małgorzata Borczyk, et al.. (2021). Two Rare Variants in PLAU and BACE1 Genes—Do They Contribute to Semantic Dementia Clinical Phenotype?. Genes. 12(11). 1806–1806. 3 indexed citations
3.
Pepłońska, Beata, Kinga Humińska‐Lisowska, Jakub Grzegorz Adamczyk, et al.. (2021). Common Myelin Regulatory Factor Gene Variants Predisposing to Excellence in Sports. Genes. 12(2). 262–262. 3 indexed citations
4.
Gawęda-Walerych, Katarzyna, Dawid Walerych, Mariusz Berdyński, Emanuele Buratti, & Cezary Żekanowski. (2021). Parkin Levels Decrease in Fibroblasts With Progranulin (PGRN) Pathogenic Variants and in a Cellular Model of PGRN Deficiency. Frontiers in Molecular Neuroscience. 14. 676478–676478. 13 indexed citations
5.
Berdyński, Mariusz, et al.. (2021). Common ALDH3A1 Gene Variant Associated with Keratoconus Risk in the Polish Population. Journal of Clinical Medicine. 11(1). 8–8. 4 indexed citations
6.
Kuźma‐Kozakiewicz, Magdalena, Peter M. Andersen, Elahe Elahi, et al.. (2020). Putative founder effect in the Polish, Iranian and United States populations for the L144S SOD1 mutation associated with slowly uniform phenotype of amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 22(1-2). 80–85. 7 indexed citations
7.
Pepłońska, Beata, Mariusz Berdyński, Anna Barczak, et al.. (2018). TREM2 variants in neurodegenerative disorders in the Polish population. Homozygosity and compound heterozygosity in FTD patients. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 19(5-6). 407–412. 10 indexed citations
8.
Markopoulou, Katerina, Bruce A. Chase, Piotr Robowski, et al.. (2016). Assessment of Olfactory Function in MAPT-Associated Neurodegenerative Disease Reveals Odor-Identification Irreproducibility as a Non-Disease-Specific, General Characteristic of Olfactory Dysfunction. PLoS ONE. 11(11). e0165112–e0165112. 11 indexed citations
9.
Berdyński, Mariusz, et al.. (2015). Sporadic inclusion body myositis: clinical, pathological, and genetic analysis of eight Polish patients. Folia Neuropathologica. 4(4). 355–366. 8 indexed citations
10.
Janik, Piotr, Mariusz Berdyński, Krzysztof Safranow, & Cezary Żekanowski. (2014). The BTBD9 gene polymorphisms in Polish patients with Gilles de la Tourette syndrome. Acta Neurobiologiae Experimentalis. 74(2). 218–226. 8 indexed citations
11.
Wierzba‐Bobrowicz, Teresa, Eliza Lewandowska, Jacek Zaremba, et al.. (2014). Frontotemporal lobar degeneration with MAPT mutation in an Italian-Polish family. A. Folia Neuropathologica. 4(4). 457–466. 3 indexed citations
12.
Fichna, Jakub, Anna Potulska‐Chromik, Przemysław Miszta, et al.. (2014). Two Desmin Gene Mutations Associated with Myofibrillar Myopathies in Polish Families. PLoS ONE. 9(12). e115470–e115470. 13 indexed citations
13.
Berdyński, Mariusz, et al.. (2013). A novel mutation in the DNM2 gene impairs dynamin 2 localization in skeletal muscle of a patient with late onset centronuclear myopathy. Neuromuscular Disorders. 23(3). 219–228. 21 indexed citations
14.
LaPointe, Nichole E., Mariusz Berdyński, Elmer Guzman, et al.. (2013). A Novel MAPT Mutation, G55R, in a Frontotemporal Dementia Patient Leads to Altered Tau Function. PLoS ONE. 8(9). e76409–e76409. 18 indexed citations
15.
Jamrozik, Zygmunt, Mariusz Berdyński, Cezary Żekanowski, et al.. (2013). Analysis of PITX3 gene in patients with multisystem atrophy, progressive supranuclear palsy and corticobasal degeneration.. PubMed. 43(2). 151–3. 1 indexed citations
16.
Sitek, Emilia J., Anna Barczak, Barbara Jasińska‐Myga, et al.. (2012). Agraphia in patients with frontotemporal dementia and parkinsonism linked to chromosome 17 with P301LMAPTmutation: dysexecutive, aphasic, apraxic or spatial phenomenon?. Neurocase. 20(1). 69–86. 12 indexed citations
17.
Berdyński, Mariusz, et al.. (2012). Proteinopatie TDP-43 – od zwyrodnienia czołowo-skroniowego do wtrętowego zapalenia mięśni. Neurologia i Neurochirurgia Polska. 46(4). 384–391. 1 indexed citations
18.
Sitek, Emilia J., Anna Barczak, Małgorzata Chodakowska-Żebrowska, et al.. (2011). The role of neuropsychological assessment in the detection of early symptoms in frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17). Acta Neuropsychologica. 9(2). 209–226. 1 indexed citations
19.
Berdyński, Mariusz, Magdalena Kuźma‐Kozakiewicz, Claudia Ricci, et al.. (2011). Recurrent G41S mutation in Cu/Zn superoxide dismutase gene (SOD1) causing familial amyotrophic lateral sclerosis in a large Polish family. Amyotrophic Lateral Sclerosis. 13(1). 132–136. 5 indexed citations
20.
Maruszak, Aleksandra, Krzysztof Safranow, Katarzyna Jakubowska, et al.. (2009). PIN1 gene variants in Alzheimer's disease. BMC Medical Genetics. 10(1). 115–115. 20 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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