Renata Posmyk

1.1k total citations
24 papers, 262 citations indexed

About

Renata Posmyk is a scholar working on Genetics, Molecular Biology and Oncology. According to data from OpenAlex, Renata Posmyk has authored 24 papers receiving a total of 262 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 7 papers in Molecular Biology and 5 papers in Oncology. Recurrent topics in Renata Posmyk's work include Genomic variations and chromosomal abnormalities (4 papers), Immunotherapy and Immune Responses (3 papers) and Cancer Genomics and Diagnostics (3 papers). Renata Posmyk is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Immunotherapy and Immune Responses (3 papers) and Cancer Genomics and Diagnostics (3 papers). Renata Posmyk collaborates with scholars based in Poland, Belgium and Netherlands. Renata Posmyk's co-authors include Monika Chorąży, Natalia Wawrusiewicz‐Kurylonek, Adam Krętowski, Halina Car, Jan Kochanowicz, Anna Zalewska, Mateusz Maciejczyk, R Leśniewicz, Alina Kułakowska and Jerzy Bal and has published in prestigious journals such as Nature Communications, Cancers and Cancer Biology & Therapy.

In The Last Decade

Renata Posmyk

24 papers receiving 247 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Renata Posmyk Poland 11 129 85 62 33 28 24 262
Sandra Deliard United States 10 200 1.6× 133 1.6× 45 0.7× 26 0.8× 46 1.6× 14 373
Ulf Schulze Germany 10 188 1.5× 52 0.6× 20 0.3× 39 1.2× 21 0.8× 13 340
Stefan Rentas United States 11 200 1.6× 73 0.9× 40 0.6× 23 0.7× 9 0.3× 17 332
Francesca Clementina Radio Italy 15 194 1.5× 149 1.8× 24 0.4× 14 0.4× 17 0.6× 40 421
Beate Vollenbröker Germany 10 171 1.3× 52 0.6× 27 0.4× 32 1.0× 35 1.3× 15 374
Rebecca S. Henkhaus United States 11 229 1.8× 90 1.1× 22 0.4× 62 1.9× 12 0.4× 16 375
Aarti D. Rohira United States 6 273 2.1× 63 0.7× 28 0.5× 35 1.1× 22 0.8× 7 355
John D. Ansell United Kingdom 9 283 2.2× 61 0.7× 33 0.5× 62 1.9× 30 1.1× 10 375
Yuyin Yi Canada 14 205 1.6× 27 0.3× 74 1.2× 29 0.9× 11 0.4× 24 393
Sophie Roy Canada 5 235 1.8× 31 0.4× 77 1.2× 47 1.4× 50 1.8× 7 383

Countries citing papers authored by Renata Posmyk

Since Specialization
Citations

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

Fields of papers citing papers by Renata Posmyk

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Renata Posmyk

This figure shows the co-authorship network connecting the top 25 collaborators of Renata Posmyk. A scholar is included among the top collaborators of Renata Posmyk 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 Renata Posmyk. Renata Posmyk 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.
Chorąży, Monika, Natalia Wawrusiewicz‐Kurylonek, Edyta Adamska-Patruno, et al.. (2021). Variants of Novel Immunomodulatory Fc Receptor Like 5 Gene Are Associated With Multiple Sclerosis Susceptibility in the Polish Population. Frontiers in Neurology. 12. 631134–631134. 4 indexed citations
2.
Chorąży, Monika, Natalia Wawrusiewicz‐Kurylonek, Edyta Adamska-Patruno, et al.. (2020). Some Common SNPs of the T‐Cell Homeostasis‐Related Genes Are Associated with Multiple Sclerosis, but Not with the Clinical Manifestations of the Disease, in the Polish Population. Journal of Immunology Research. 2020(1). 8838014–8838014. 3 indexed citations
3.
Wawrusiewicz‐Kurylonek, Natalia, Adam Krętowski, & Renata Posmyk. (2020). Frequency of thrombophilia associated genes variants: population-based study. BMC Medical Genetics. 21(1). 198–198. 5 indexed citations
4.
Walczak‐Sztulpa, Joanna, Renata Posmyk, Ewelina Bukowska‐Olech, et al.. (2020). Compound heterozygous IFT140 variants in two Polish families with Sensenbrenner syndrome and early onset end-stage renal disease. Orphanet Journal of Rare Diseases. 15(1). 36–36. 12 indexed citations
5.
Wawrusiewicz‐Kurylonek, Natalia, Joanna Gościk, Monika Chorąży, et al.. (2019). The interferon-induced helicase C domain-containing protein 1 gene variant (rs1990760) as an autoimmune-based pathology susceptibility factor. Immunobiology. 225(1). 151864–151864. 10 indexed citations
6.
Chorąży, Monika, Natalia Wawrusiewicz‐Kurylonek, Renata Posmyk, et al.. (2019). Analysis of chosen SNVs in GPC5, CD58 and IRF8 genes in multiple sclerosis patients. Advances in Medical Sciences. 64(2). 230–234. 10 indexed citations
7.
Filatova, Alina, Jörg Schaper, Maja Hempel, et al.. (2019). Mutations in SMARCB1 and in other Coffin–Siris syndrome genes lead to various brain midline defects. Nature Communications. 10(1). 2966–2966. 22 indexed citations
8.
Chorąży, Monika, Natalia Wawrusiewicz‐Kurylonek, Joanna Gościk, et al.. (2018). Association between polymorphisms of a folate – homocysteine – methionine – SAM metabolising enzyme gene and multiple sclerosis in a Polish population. Neurologia i Neurochirurgia Polska. 53(3). 194–198. 6 indexed citations
9.
Wawrusiewicz‐Kurylonek, Natalia, Monika Chorąży, Renata Posmyk, et al.. (2018). The FOXP3 rs3761547 Gene Polymorphism in Multiple Sclerosis as a Male-Specific Risk Factor. NeuroMolecular Medicine. 20(4). 537–543. 22 indexed citations
10.
Jóźwik, Maciej, Maciej Jóźwik, Renata Posmyk, et al.. (2018). Breast cancer in an 18-year-old female: A fatal case report and literature review. Cancer Biology & Therapy. 19(7). 543–548. 4 indexed citations
11.
Gawliński, Paweł, Renata Posmyk, Tomasz Gambin, et al.. (2016). PEHO Syndrome May Represent Phenotypic Expansion at the Severe End of the Early-Onset Encephalopathies. Pediatric Neurology. 60. 83–87. 15 indexed citations
12.
Knapp, Paweł, Adrian Chabowski, Renata Posmyk, & J Górski. (2016). Expression of the energy substrate transporters in uterine fibroids. Prostaglandins & Other Lipid Mediators. 123. 9–15. 6 indexed citations
13.
Ciara, Elżbieta, Dorota Jurkiewicz, Dorota Gieruszczak‐Białek, et al.. (2014). Is diagnosing cardio-facio-cutaneous (CFC) syndrome still a challenge? Delineation of the phenotype in 15 Polish patients with proven mutations, including novel mutations in the BRAF gene. European Journal of Medical Genetics. 58(1). 14–20. 10 indexed citations
14.
Posmyk, Renata, R Leśniewicz, Monika Chorąży, et al.. (2014). The smallest de novo deletion of 20q11.21–q11.23 in a girl with feeding problems, retinal dysplasia, and skeletal abnormalities. American Journal of Medical Genetics Part A. 164(4). 1056–1061. 19 indexed citations
15.
Śmigiel, Robert, et al.. (2014). Heterogenność kliniczna i genetyczna dyzostoz twarzowych. Pediatria Polska. 90(1). 1–12. 1 indexed citations
16.
Chorąży, Monika, et al.. (2011). The natural history of Möbius syndrome in a 32-year-old man. Neurologia i Neurochirurgia Polska. 45(1). 74–79. 1 indexed citations
17.
Iwanowski, Piotr, Barbara Panasiuk, Griet Van Buggenhout, et al.. (2011). Wolf–Hirschhorn syndrome due to pure and translocation forms of monosomy 4p16.1 → pter. American Journal of Medical Genetics Part A. 155(8). 1833–1847. 4 indexed citations
18.
Posmyk, Renata, R Leśniewicz, Monika Chorąży, & Sławomir Wołczyński. (2011). New case of Primrose syndrome with mild intellectual disability. American Journal of Medical Genetics Part A. 155(11). 2838–2840. 9 indexed citations
19.
Leśniewicz, R, et al.. (2010). Prenatal evaluation of a fetus with trisomy 18 and additional balanced de novo Rob(13;14).. Folia Histochemica et Cytobiologica. 47(5). S137–40. 5 indexed citations
20.
Kabzińska, Dagmara, Anna Kostera‐Pruszczyk, Barbara Ryniewicz, et al.. (2010). L239F founder mutation in GDAP1 is associated with a mild Charcot–Marie–Tooth type 4C4 (CMT4C4) phenotype. Neurogenetics. 11(3). 357–366. 14 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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