Ewa Popowska

1.9k total citations
36 papers, 565 citations indexed

About

Ewa Popowska is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Ewa Popowska has authored 36 papers receiving a total of 565 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 8 papers in Genetics and 6 papers in Clinical Biochemistry. Recurrent topics in Ewa Popowska's work include Mitochondrial Function and Pathology (9 papers), Metabolism and Genetic Disorders (6 papers) and ATP Synthase and ATPases Research (6 papers). Ewa Popowska is often cited by papers focused on Mitochondrial Function and Pathology (9 papers), Metabolism and Genetic Disorders (6 papers) and ATP Synthase and ATPases Research (6 papers). Ewa Popowska collaborates with scholars based in Poland, Germany and Canada. Ewa Popowska's co-authors include Ewa Pronicka, Małgorzata Krajewska‐Walasek, Celina Janion, Dorota Piekutowska‐Abramczuk, Elżbieta Ciara, Dorota Jurkiewicz, Maciej Pronicki, Elżbieta Karczmarewicz, Jolanta Sykut‐Cegielska and Mikołaj Łabuda and has published in prestigious journals such as Nucleic Acids Research, Biochemical and Biophysical Research Communications and Acta Neuropathologica.

In The Last Decade

Ewa Popowska

35 papers receiving 555 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ewa Popowska Poland 15 346 125 83 80 68 36 565
Yuan-Yuan Ho Hong Kong 12 325 0.9× 275 2.2× 70 0.8× 83 1.0× 103 1.5× 18 785
Ben Pode‐Shakked Israel 15 330 1.0× 172 1.4× 85 1.0× 82 1.0× 38 0.6× 54 620
Shobha Ratnam United States 10 307 0.9× 231 1.8× 14 0.2× 66 0.8× 89 1.3× 23 623
Lucky K. Kelley United States 15 276 0.8× 41 0.3× 52 0.6× 63 0.8× 76 1.1× 19 806
Chiyoko N. Inoue Japan 12 292 0.8× 45 0.4× 55 0.7× 48 0.6× 33 0.5× 24 426
Godfrey T. Gillett United Kingdom 13 286 0.8× 138 1.1× 42 0.5× 50 0.6× 190 2.8× 20 677
François‐Guillaume Debray Belgium 14 305 0.9× 84 0.7× 211 2.5× 36 0.5× 84 1.2× 26 507
Jeffrey Hiken United States 14 525 1.5× 62 0.5× 21 0.3× 134 1.7× 115 1.7× 21 719
Giacomo Quilici Italy 12 448 1.3× 410 3.3× 58 0.7× 48 0.6× 46 0.7× 24 758
Yehani Wedatilake United Kingdom 10 329 1.0× 59 0.5× 187 2.3× 18 0.2× 41 0.6× 18 570

Countries citing papers authored by Ewa Popowska

Since Specialization
Citations

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

Fields of papers citing papers by Ewa Popowska

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ewa Popowska

This figure shows the co-authorship network connecting the top 25 collaborators of Ewa Popowska. A scholar is included among the top collaborators of Ewa Popowska 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 Ewa Popowska. Ewa Popowska 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.
Jamroz, Ewa, Justyna Paprocka, Maria Sokół, Ewa Popowska, & Elżbieta Ciara. (2013). Magnetic resonance spectroscopy and molecular studies in ornithine transcarbamylase deficiency novel mutation c.802A>G in exon 8 (p.Met268Val). Neurologia i Neurochirurgia Polska. 47(3). 283–289. 2 indexed citations
2.
Piekutowska‐Abramczuk, Dorota, Martin Magner, Ewa Popowska, et al.. (2009). SURF1 missense mutations promote a mild Leigh phenotype. Clinical Genetics. 76(2). 195–204. 29 indexed citations
3.
Ciara, Elżbieta, Dorota Piekutowska‐Abramczuk, Ewa Popowska, et al.. (2009). Heterozygous germ-line mutations in the NBN gene predispose to medulloblastoma in pediatric patients. Acta Neuropathologica. 119(3). 325–334. 21 indexed citations
4.
Piekutowska‐Abramczuk, Dorota, Ewa Popowska, Maciej Pronicki, et al.. (2008). High prevalence of SURF1 c.845_846delCT mutation in Polish Leigh patients. European Journal of Paediatric Neurology. 13(2). 146–153. 17 indexed citations
5.
Jurecka, Agnieszka, Ewa Popowska, Anna Tylki‐Szymańska, et al.. (2008). Hypoxanthine‐guanine phosphoribosylotransferase deficiency—The spectrum of Polish mutations. Journal of Inherited Metabolic Disease. 31(S2). 447–451. 8 indexed citations
6.
Pronicki, Maciej, Ewa Matyja, Dorota Piekutowska‐Abramczuk, et al.. (2007). Light and electron microscopy characteristics of the muscle of patients with SURF1 gene mutations associated with Leigh disease. Journal of Clinical Pathology. 61(4). 460–466. 23 indexed citations
7.
Jezela‐Stanek, Aleksandra, Elżbieta Ciara, E Małunowicz, et al.. (2007). Mild Smith-Lemli-Opitz syndrome: Further delineation of 5 Polish cases and review of the literature. European Journal of Medical Genetics. 51(2). 124–140. 14 indexed citations
8.
Ciara, Elżbieta, Ewa Popowska, Dorota Piekutowska‐Abramczuk, et al.. (2006). SLOS carrier frequency in Poland as determined by screening for Trp151X and Val326Leu DHCR7 mutations. European Journal of Medical Genetics. 49(6). 499–504. 22 indexed citations
9.
Jurkiewicz, Dorota, Ewa Popowska, Christiane Gläser, I. Hansmann, & Małgorzata Krajewska‐Walasek. (2005). Twelve novelJAG1gene mutations in polish Alagille syndrome patients. Human Mutation. 25(3). 321–321. 14 indexed citations
10.
11.
Pronicka, Ewa, et al.. (2003). Anthropometric characteristics of X‐linked hypophosphatemia. American Journal of Medical Genetics Part A. 126A(2). 141–149. 10 indexed citations
12.
13.
Karczmarewicz, Elżbieta, Maciej Pronicki, Dorota Piekutowska‐Abramczuk, et al.. (2001). Abnormal Calcium Homeostasis in Fibroblasts from Patients with Leigh Disease. Biochemical and Biophysical Research Communications. 283(3). 687–693. 14 indexed citations
14.
Popowska, Ewa, Elżbieta Ciara, Dariusz Rokicki, & Ewa Pronicka. (1999). Ornithine transcarbamylase gene mutations and genotype-phenotype correlation in Polish patients with hyperammonemia type 2. Journal of Applied Genetics. 40(1). 43–52. 1 indexed citations
15.
Popowska, Ewa, Anna Sułek, Jolanta Kubalska, et al.. (1998). Different mutations in Polish patients with HPRT deficiency - the Lesch-Nyhan and Kelley-Seegmiller syndromes. Journal of Applied Genetics. 39(1). 103–111. 3 indexed citations
16.
Popowska, Ewa, et al.. (1998). A case of Prader – Willi syndrome arising as a result of familial unbalanced translocation t(11;15)(q25;q13). Clinical Genetics. 54(1). 60–64. 5 indexed citations
17.
Bunge, Susanna, Cordula Steglich, Marie-Louise Bondeson, et al.. (1998). Homologous nonallelic recombinations between the iduronate-sulfatase gene and pseudogene cause various intragenic deletions and inversions in patients with mucopolysaccharidosis type II. European Journal of Human Genetics. 6(5). 492–500. 26 indexed citations
18.
Krajewska‐Walasek, Małgorzata, et al.. (1997). A clinical, cytogenetic and molecular study in Prader-Willi patients. Journal of Applied Genetics. 38(2).
19.
Popowska, Ewa, Anna Tylki‐Szymańska, Susanna Bunge, et al.. (1995). Mutations of the iduronate-2-sulfatase gene in 12 Polish. Patients with mucopolysaccharidosis type II (Hunter syndrome). Human Mutation. 5(1). 97–100. 30 indexed citations
20.
Popowska, Ewa & Celina Janion. (1977). The N4-hydroxycytidine reduction system in toluenized cells of Salmonella typhimurium.. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 24(3). 197–205. 5 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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