Ewa Pronicka

5.1k total citations
114 papers, 2.0k citations indexed

About

Ewa Pronicka is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Ewa Pronicka has authored 114 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 67 papers in Molecular Biology, 36 papers in Clinical Biochemistry and 20 papers in Genetics. Recurrent topics in Ewa Pronicka's work include Mitochondrial Function and Pathology (40 papers), Metabolism and Genetic Disorders (36 papers) and ATP Synthase and ATPases Research (21 papers). Ewa Pronicka is often cited by papers focused on Mitochondrial Function and Pathology (40 papers), Metabolism and Genetic Disorders (36 papers) and ATP Synthase and ATPases Research (21 papers). Ewa Pronicka collaborates with scholars based in Poland, Germany and Netherlands. Ewa Pronicka's co-authors include Maciej Pronicki, Jolanta Sykut‐Cegielska, Dorota Piekutowska‐Abramczuk, Ewa Popowska, Dariusz Rokicki, Rafał Płoski, Elżbieta Ciara, Małgorzata Krajewska‐Walasek, Agnieszka Karkucińska‐Więckowska and Elżbieta Karczmarewicz and has published in prestigious journals such as SHILAP Revista de lepidopterología, American Journal of Clinical Nutrition and Biochemical and Biophysical Research Communications.

In The Last Decade

Ewa Pronicka

110 papers receiving 1.9k 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 Pronicka Poland 26 1.2k 553 326 201 192 114 2.0k
Jolanta Sykut‐Cegielska Poland 24 998 0.9× 503 0.9× 336 1.0× 282 1.4× 53 0.3× 77 1.7k
Majid Alfadhel Saudi Arabia 28 1.4k 1.2× 625 1.1× 920 2.8× 232 1.2× 147 0.8× 157 2.5k
Callum Wilson New Zealand 21 956 0.8× 495 0.9× 241 0.7× 293 1.5× 79 0.4× 58 1.6k
Georg Christoph Korenke Germany 25 914 0.8× 404 0.7× 381 1.2× 410 2.0× 55 0.3× 57 1.7k
Xuefan Gu China 27 1.4k 1.2× 888 1.6× 540 1.7× 487 2.4× 358 1.9× 217 2.5k
Celia Pérez‐Cerdá Spain 30 1.8k 1.6× 1.3k 2.4× 325 1.0× 412 2.0× 120 0.6× 119 2.5k
José E. Abdenur United States 24 978 0.8× 818 1.5× 325 1.0× 446 2.2× 110 0.6× 63 1.8k
Enrico Zammarchi Italy 28 1.7k 1.5× 1.1k 1.9× 395 1.2× 626 3.1× 448 2.3× 101 3.2k
Stephanie Grünewald United Kingdom 28 1.4k 1.2× 558 1.0× 354 1.1× 516 2.6× 84 0.4× 85 2.1k
Silvia Tortorelli United States 30 1.0k 0.9× 1.1k 2.0× 310 1.0× 621 3.1× 97 0.5× 70 2.3k

Countries citing papers authored by Ewa Pronicka

Since Specialization
Citations

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

Fields of papers citing papers by Ewa Pronicka

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ewa Pronicka

This figure shows the co-authorship network connecting the top 25 collaborators of Ewa Pronicka. A scholar is included among the top collaborators of Ewa Pronicka 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 Pronicka. Ewa Pronicka 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.
Ciara, Elżbieta, Dariusz Rokicki, Paulina Halat, et al.. (2016). Difficulties in recognition of pyruvate dehydrogenase complex deficiency on the basis of clinical and biochemical features. The role of next-generation sequencing. Molecular Genetics and Metabolism Reports. 7. 70–76. 14 indexed citations
2.
Pronicka, Ewa, Dorota Piekutowska‐Abramczuk, Elżbieta Ciara, et al.. (2016). New perspective in diagnostics of mitochondrial disorders: two years’ experience with whole-exome sequencing at a national paediatric centre. Journal of Translational Medicine. 14(1). 174–174. 159 indexed citations
3.
Piekutowska‐Abramczuk, Dorota, Agnieszka Karkucińska‐Więckowska, Elżbieta Jurkiewicz, et al.. (2013). “Drop attacks” as first clinical symptoms in a child carrying MTTK m.8344A>G mutation. Folia Neuropathologica. 4(4). 347–354. 8 indexed citations
4.
Jędrzejowska, Maria, Agnieszka Madej‐Pilarczyk, Anna Fidziańska, et al.. (2013). Severe phenotypes of SMARD1 associated with novel mutations of the IGHMBP2 gene and nuclear degeneration of muscle and Schwann cells. European Journal of Paediatric Neurology. 18(2). 183–192. 21 indexed citations
5.
Pecina, Petr, et al.. (2012). Adaptation of respiratory chain biogenesis to cytochrome c oxidase deficiency caused by SURF1 gene mutations. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1822(7). 1114–1124. 26 indexed citations
6.
Lebiedzińska, Magdalena, Agnieszka Karkucińska‐Więckowska, Carlotta Giorgi, et al.. (2010). Oxidative stress-dependent p66Shc phosphorylation in skin fibroblasts of children with mitochondrial disorders. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1797(6-7). 952–960. 71 indexed citations
7.
Pronicka, Ewa, Joanna Taybert, Maciej Pronicki, et al.. (2010). Post mortem identification of deoxyguanosine kinase (DGUOK) gene mutations combined with impaired glucose homeostasis and iron overload features in four infants with severe progressive liver failure. Journal of Applied Genetics. 52(1). 61–66. 36 indexed citations
8.
Zeman, J, Hana Hansíková, Markéta Tesařová, et al.. (2008). CYTOCHROME C OXIDASE DEFICIENCY IN CHILDHOOD. Archives of Disease in Childhood. 93. 2 indexed citations
9.
Pronicka, Ewa, Dorota Piekutowska‐Abramczuk, & Maciej Pronicki. (2008). Choroby mitochondrialne u dzieci – podłoże biochemiczne i molekularne, ze szczególnym uwzględnieniem zespołu Leigha. Postępy Biochemii. 54(2). 2 indexed citations
10.
Kubalska, Jolanta, Magdalena Chmara, Janusz Limon, et al.. (2008). Clinical course of homozygous familial hypercholesterolemia during childhood: report on 4 unrelated patients with homozygous or compound heterozygous mutations in theLDLR gene. Journal of Applied Genetics. 49(1). 109–113. 5 indexed citations
11.
12.
Schollen, Els, Liesbeth Keldermans, François Foulquier, et al.. (2007). Characterization of two unusual truncating PMM2 mutations in two CDG-Ia patients. Molecular Genetics and Metabolism. 90(4). 408–413. 34 indexed citations
13.
Baumann, Ulrich, et al.. (2005). Lektin-reaktives Alpha-Fetoprotein bei Patienten mit Tyrosinämie Typ I. Klinische Pädiatrie. 217(3). 142–146. 6 indexed citations
14.
Pronicka, Ewa, et al.. (2005). Genetic background of HSH in three Polish families and a patient with an X;9 translocation. European Journal of Human Genetics. 14(1). 55–62. 11 indexed citations
15.
Linnebank, Michael, Miroslav Janošı́k, Viktor Kožich, et al.. (2004). The cystathionine ?-synthase (CBS) mutation c.1224-2A>C in Central Europe: Vitamin B6 nonresponsiveness and a common ancestral haplotype. Human Mutation. 24(4). 352–353. 13 indexed citations
16.
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
17.
Wolf, Barry, Kevin P. Jensen, Mübeccel Demirkol, et al.. (2002). Seventeen novel mutations that cause profound biotinidase deficiency. Molecular Genetics and Metabolism. 77(1-2). 108–111. 31 indexed citations
18.
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
19.
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
20.
Jaeken, Jaak, Michel Pirard, Maciej Adamowicz, Ewa Pronicka, & Emile Van Schaftingen. (1996). Inhibition of Phosphomannose Isomerase by Fructose 1-Phosphate: An Explanation for Defective N-Glycosylation in Hereditary Fructose Intolerance. Pediatric Research. 40(5). 764–766. 52 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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