Rafał Płoski

14.8k citations

396 papers · 6.6k indexed · h-index 38

Impact in

Genetics top 1%
- Diabetes and associated disorders
- Forensic and Genetic Research
Immunology top 2%
- Immune Cell Function and Interaction

Papers in

Genetics 119
- Genetics and Neurodevelopmental Disorders 27
- Genomics and Rare Diseases 21
- Diabetes and associated disorders 20
Molecular Biology 175
- Mitochondrial Function and Pathology 23
- RNA regulation and disease 21
- RNA modifications and cancer 20

Co-authors: Małgorzata Rydzanicz Øystein Førre Tomasz Bednarczuk Agnieszka Pollak Piotr Stawiński Erik Thorsby Wojciech Branicki Tarra L. McDowell
Journals: PLoS ONE (23 papers)Genes (16 papers)Clinical Genetics (15 papers)International Journal of Molecular Sciences (7 papers)European Journal of Medical Genetics (6 papers)
Partner nations: Poland United States Germany

In The Last Decade

Rafał Płoski

379 papers receiving 6.4k citations

Peers

Countries citing papers authored by Rafał Płoski

Since Specialization

Citations

This map shows the geographic impact of Rafał Płoski'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 Rafał Płoski with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Rafał Płoski more than expected).

Fields of papers citing papers by Rafał Płoski

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rafał Płoski. 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 Rafał Płoski. The network helps show where Rafał Płoski may publish in the future.

Co-authors

The 25 scholars most cited alongside Rafał Płoski, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Rafał Płoski Line = papers co-authored together Rafał Płoski links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Acrodermatitis enteropathica – a diagnostic challenge: case report of late-onset, genetically proven disease with normal zinc serum levels Pediatria i Medycyna Rodzinna ·Monika Sztupecka-Rutkowska, Bożena Wojciechowska, Edyta Heropolitańska–Pliszka, Cezary Kowaléwski, Karolina Rutkowska, Anna Walczak, Rafał Płoski, Katarzyna Woźniak	2025	0
2	A Rare De Novo Mutation in the TRIM8 Gene in a 17-Year-Old Boy with Steroid-Resistant Nephrotic Syndrome: Case Report International Journal of Molecular Sciences ·Marta Badeńska, Małgorzata Pac, Andrzej Badeński, Karolina Rutkowska, Justyna Czubilińska-Łada, Rafał Płoski, Nadezda Bohynikova, Maria Szczepańska	2024	0
3	Genebe.net: Implementation and validation of an automatic ACMG variant pathogenicity criteria assignment Clinical Genetics ·Piotr Stawiński, Rafał Płoski	2024	12
4	Leukodystrophy with Macrocephaly, Refractory Epilepsy, and Severe Hyponatremia—The Neonatal Type of Alexander Disease Genes ·Justyna Paprocka, Magdalena Nowak, Magdalena Machnikowska-Sokołowska, Karolina Rutkowska, Rafał Płoski	2024	1
5	An Intronic Heterozygous SYNE2 Splice Site Mutation: A Rare Cause for Myalgia and hyperCKemia? SHILAP Revista de lepidopterología ·Theresa Paulus, Natalie Young, Emily Jessop, Carolin Berwanger, Christoph S. Clemen, Rolf Schröder, Rafał Płoski, Christian Hagel, Yorck Hellenbroich, Andréas Moser, Iakowos Karakesisoglou	2024	0
6	Neurodevelopmental disorder in a patient with HMBS and SCN3A variants—A possibly blended phenotype further delineating autosomal recessive HMBS related disease American Journal of Medical Genetics Part A ·Magdalena Kłaniewska, Małgorzata Rydzanicz, Joanna Bladowska, Borys ‐ Iwanicka A, Iwanicka ‐ Pronicka K, R Wasilewski, Edyta Odnoczko, Agnieszka Zubkiewicz‐Kucharska, Robert Śmigiel, Rafał Płoski	2024	0
7	2022TiP Stereotactic treatment with neoadjuvant radiotherapy and enfortumab vedotin: A phase I/II study for localized, cisplatin ineligible, muscle invasive bladder cancer (STAR-EV) Annals of Oncology ·Tian Zhang, Solomon L. Woldu, Qian Qin, Suzanne Cole, Waddah Arafat, C Jiang, Jing Wang, Kevin D. Courtney, A. DeVilbiss, Rafał Płoski, R. Hannan, Daniel X. Yang, A. Garant, Isamu Tachibana, Kris E. Gaston, Andrew Z. Wang, V. Margulis, Yair Lotan, Neil Desai	2024	1
8	Case Report: Expanded delineation of phenotype of TRPM3-related neurodevelopmental disorders Frontiers in Pediatrics ·Agnieszka Pawelak, Artur Polczyk, Ewelina Wolańska, Magdalena Kłaniewska, Mateusz Biela, Aleksander Basiak, Maria Franaszczyk, Małgorzata Rydzanicz, Rafał Płoski, Robert Śmigiel	2024	1
9	Epigenetic Findings in Twins with Esophageal Atresia Genes ·Michal Błoch, Piotr Gasperowicz, Sylwester Gerus, Katarzyna Rasiewicz, Arleta Lebioda, Paweł Skiba, Rafał Płoski, Dariusz Patkowski, Paweł Karpiński, Robert Śmigiel	2023	2
10	Clinical heterogeneity of polish patients with KAT6B–related disorder Molecular Genetics & Genomic Medicine ·Magdalena Kłaniewska, Bolanowska‐Tyszko Anna, Latos‐Bielenska Anna, Aleksandra Jezela‐Stanek, Krzysztof Szczałuba, Krajewska‐Walasek Malgorzata, Ciara Elzbieta, Magdalena Pelc, Dorota Jurkiewicz, Piotr Stawiński, Agnieszka Zubkiewicz‐Kucharska, Małgorzata Rydzanicz, Rafał Płoski, Robert Śmigiel	2023	1
11	Broadening the phenotypic spectrum of the presumably epilepsy-related SV2A gene variants Epilepsy Research ·Magdalena Badura‐Stronka, Łukasz Kuszel, Agnieszka Wencel-Warot, Kamila Cudnoch, Katarzyna Wicher, Karolina Rutkowska, Barbara Steinborn, Rafał Płoski	2023	4
12	The Impaired Wound Healing Process Is a Major Factor in Remodeling of the Corneal Epithelium in Adult and Adolescent Patients With Keratoconus Investigative Ophthalmology & Visual Science ·Katarzyna Jaśkiewicz, Magdalena Maleszka-Kurpiel, Eliza Matuszewska, Michał Kabza, Małgorzata Rydzanicz, Robert Malinowski, Rafał Płoski, Jan Matysiak, Marzena Gajęcka	2023	9
13	Expanding the phenotype of DNAJC30 ‐ associated Leigh syndrome Clinical Genetics ·Marta Zawadzka, Magdalena Krygier, Małgorzata Pawłowicz, Matheus Vernet Machado Bressan Wilke, Karolina Rutkowska, Naïg Guéguen, Valérie Desquiret‐Dumas, Eric W. Klee, Lisa A. Schimmenti, Jarosław Sławek, Vincent Procaccio, Rafał Płoski, Maria Mazurkiewicz‐Bełdzińska	2022	6
14	Celiac Disease in Conjunction with Hereditary Fructose Intolerance as a Rare Cause of Liver Steatosis with Mild Hypertransaminasemia—A Case Report Pediatric Reports ·Anna Bobrus‐Chociej, Agnieszka Pollak, Natalia Kopiczko, Marta Flisiak‐Jackiewicz, Rafał Płoski, Dariusz Lebensztejn	2021	3
15	Searching for improvements in predicting human eye colour from DNA International Journal of Legal Medicine ·Magdalena Kukla‐Bartoszek, Paweł Teisseyre, Ewelina Pośpiech, Joanna Karłowska-Pik, Piotr Zieliński, Anna Woźniak, Michał Boroń, Michał Dąbrowski, Magdalena Zubańska, Agata Jarosz, Rafał Płoski, Tomasz Grzybowski, Magdalena Spólnicka, Jan Mielniczuk, Wojciech Branicki	2021	9
16	Variable degree of mosaicism for tetrasomy 18p in phenotypically discordant monozygotic twins—Diagnostic implications Molecular Genetics & Genomic Medicine ·Małgorzata Rydzanicz, Paweł Olszewski, Darek Kedra, Hanna Davies, Natalia Filipowicz, Bożena Bruhn‐Olszewska, Marco Cavalli, Krzysztof Szczałuba, Marlena Młynek, Marcin M. Machnicki, Piotr Stawiński, Grażyna Kostrzewa, Paweł Krajewski, Dariusz Śladowski, Krystyńa Chrzańowska, Jan P. Dumanski, Rafał Płoski	2020	5
17	Intracardiac tumor as a rare manifestation of genetic syndromes—presentation of a family with Gorlin syndrome and a literature review Journal of Applied Genetics ·Krzysztof Szczałuba, Ewa Makuła, Anna Piórecka-Makuła, Justyna Sicińska, Małgorzata Rydzanicz, Piotr Gasperowicz, Rafał Płoski, Bożena Werner	2020	2
18	Syndromic chorioretinal coloboma associated with heterozygous de novo RARA mutation affecting an amino acid critical for retinoic acid interaction Clinical Genetics ·Anna Jakubiuk‐Tomaszuk, Victor Murcia Pienkowski, Szymon Ziętkiewicz, Małgorzata Rydzanicz, Joanna Kosińska, Piotr Stawiński, Michał Szumiński, Rafał Płoski	2019	7
19	Novel de novo mutation affecting two adjacent aminoacids in the EED gene in a patient with Weaver syndrome Journal of Human Genetics ·Robert Śmigiel, Anna Biernacka, Mateusz Biela, Victor Murcia Pienkowski, Elżbieta Szmida, Piotr Gasperowicz, Joanna Kosińska, Grażyna Kostrzewa, Agnieszka Koppolu, Anna Walczak, Dominik Wawrzuta, Małgorzata Rydzanicz, Maria Sąsiadek, Rafał Płoski	2018	15
20	Evidence for troponin C (TNNC1) as a gene for autosomal recessive restrictive cardiomyopathy with fatal outcome in infancy American Journal of Medical Genetics Part A ·Rafał Płoski, Małgorzata Rydzanicz, Tomasz M. Książczyk, Maria Franaszczyk, Agnieszka Pollak, Joanna Kosińska, Ewa Michalak, Piotr Stawiński, Lidia Ziółkowska, Zofia T. Bilińska, Bożena Werner	2016	42

About Rafał Płoski

Rafał Płoski is a scholar working on Genetics, Molecular Biology, Clinical Biochemistry, Immunology and Cardiology and Cardiovascular Medicine, having authored 396 papers that have together received 6.6k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (27 papers), Mitochondrial Function and Pathology (23 papers), Cardiomyopathy and Myosin Studies (23 papers), RNA regulation and disease (21 papers), Genomics and Rare Diseases (21 papers), RNA modifications and cancer (20 papers), Diabetes and associated disorders (20 papers) and Metabolism and Genetic Disorders (17 papers). The work is most often cited by research in Genetics (1.6k citations), Immunology (1.0k citations), Molecular Biology (2.8k citations), Clinical Biochemistry (267 citations) and Gastroenterology (213 citations). Rafał Płoski has collaborated with scholars based in Poland, United States and Germany. Frequent co-authors include Małgorzata Rydzanicz, Øystein Førre, Tomasz Bednarczuk, Agnieszka Pollak, Piotr Stawiński, Erik Thorsby, Wojciech Branicki, Tarra L. McDowell, Julian Symons and Grażyna Kostrzewa. Their work appears in journals such as PLoS ONE, Genes, Clinical Genetics, International Journal of Molecular Sciences and European Journal of Medical Genetics.

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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