Edyta Niewiadomska

2.0k total citations
13 papers, 467 citations indexed

About

Edyta Niewiadomska is a scholar working on Molecular Biology, Hematology and Genetics. According to data from OpenAlex, Edyta Niewiadomska has authored 13 papers receiving a total of 467 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 4 papers in Hematology and 2 papers in Genetics. Recurrent topics in Edyta Niewiadomska's work include RNA modifications and cancer (8 papers), Cancer-related gene regulation (8 papers) and RNA and protein synthesis mechanisms (5 papers). Edyta Niewiadomska is often cited by papers focused on RNA modifications and cancer (8 papers), Cancer-related gene regulation (8 papers) and RNA and protein synthesis mechanisms (5 papers). Edyta Niewiadomska collaborates with scholars based in Poland, United States and France. Edyta Niewiadomska's co-authors include Colin A. Sieff, Hanna T. Gazda, Jeffrey M. Lipton, Adrianna Vlachos, Eva Atsidaftos, Peter E. Newburger, Pierre‐Emmanuel Gleizes, Michał Matysiak, Bertil Glader and Marie-Françoise O’Donohue and has published in prestigious journals such as Blood, The American Journal of Human Genetics and British Journal of Haematology.

In The Last Decade

Edyta Niewiadomska

10 papers receiving 464 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Edyta Niewiadomska Poland 7 399 81 69 42 38 13 467
Pekka Jaako Sweden 9 307 0.8× 51 0.6× 56 0.8× 49 1.2× 35 0.9× 16 389
Alessandra Rossi Italy 9 300 0.8× 75 0.9× 47 0.7× 38 0.9× 14 0.4× 14 362
Roxanne Ghazvinian United States 6 369 0.9× 49 0.6× 76 1.1× 47 1.1× 74 1.9× 7 457
Caila Ryan United States 9 385 1.0× 67 0.8× 39 0.6× 36 0.9× 30 0.8× 9 456
Nirmalee Abayasekara United States 5 268 0.7× 68 0.8× 42 0.6× 35 0.8× 54 1.4× 5 368
Yue-Zhong Wu United States 10 416 1.0× 59 0.7× 85 1.2× 45 1.1× 31 0.8× 10 487
Alix Rousseau France 5 199 0.5× 54 0.7× 56 0.8× 40 1.0× 21 0.6× 6 281
Renae Domaschenz Australia 8 223 0.6× 54 0.7× 49 0.7× 32 0.8× 26 0.7× 12 323
Caroline Kubaczka Germany 8 305 0.8× 59 0.7× 53 0.8× 85 2.0× 16 0.4× 17 411
Leana Doherty United States 6 247 0.6× 50 0.6× 41 0.6× 18 0.4× 22 0.6× 7 312

Countries citing papers authored by Edyta Niewiadomska

Since Specialization
Citations

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

Fields of papers citing papers by Edyta Niewiadomska

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Edyta Niewiadomska

This figure shows the co-authorship network connecting the top 25 collaborators of Edyta Niewiadomska. A scholar is included among the top collaborators of Edyta Niewiadomska 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 Edyta Niewiadomska. Edyta Niewiadomska is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

13 of 13 papers shown
1.
Niewiadomska, Edyta, et al.. (2018). Disseminated intravascular coagulation in acute leukemia – pathophysiology, clinical picture, diagnostics and treatment.
2.
3.
Landowski, Michael, Marie-Françoise O’Donohue, Christopher Buros, et al.. (2013). Novel deletion of RPL15 identified by array-comparative genomic hybridization in Diamond–Blackfan anemia. Human Genetics. 132(11). 1265–1274. 77 indexed citations
4.
Gazda, Hanna T., Milena Preti, Mee Rie Sheen, et al.. (2012). Frameshift mutation in p53 regulator RPL26 is associated with multiple physical abnormalities and a specific pre-ribosomal RNA processing defect in diamond-blackfan anemia. Human Mutation. 33(7). 1037–1044. 109 indexed citations
5.
Doherty, Leana, Mee Rie Sheen, Adrianna Vlachos, et al.. (2010). Ribosomal Protein Genes RPS10 and RPS26 Are Commonly Mutated in Diamond-Blackfan Anemia. The American Journal of Human Genetics. 86(4). 655–656. 5 indexed citations
6.
Klukowska, Anna, Edyta Niewiadomska, Ulrich Budde, Florian Oyen, & Reinhard Schneppenheim. (2010). Difficulties in Diagnosing Congenital Thrombotic Thrombocytopenic Purpura. Journal of Pediatric Hematology/Oncology. 32(2). 103–107. 7 indexed citations
7.
Doherty, Leana, Mee Rie Sheen, Adrianna Vlachos, et al.. (2010). Ribosomal Protein Genes RPS10 and RPS26 Are Commonly Mutated in Diamond-Blackfan Anemia. The American Journal of Human Genetics. 86(2). 222–228. 167 indexed citations
8.
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Matysiak, Michał, et al.. (2009). Napadowa zimna hemoglobinuria – niedoceniana przyczyna niedokrwistości hemolitycznej u dzieci. Pediatria Polska. 84(1). 46–52. 1 indexed citations
10.
Gazda, Hanna T., Mee Rie Sheen, Leana Doherty, et al.. (2009). Ribosomal Protein Genes S10 and S26 Are Commonly Mutated in Diamond-Blackfan Anemia.. Blood. 114(22). 175–175. 5 indexed citations
11.
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Gazda, Hanna T., Mee Rie Sheen, Natasha Darras, et al.. (2007). Mutations of the Genes for Ribosomal Proteins L5 and L11 Are a Common Cause of Diamond-Blackfan Anemia.. Blood. 110(11). 421–421. 7 indexed citations
13.
Gazda, Hanna T., Rong Zhong, Edyta Niewiadomska, et al.. (2004). RNA and protein evidence for haplo‐insufficiency in Diamond–Blackfan anaemia patients with RPS19 mutations. British Journal of Haematology. 127(1). 105–113. 82 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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