Dorota Jurkiewicz

556 total citations
34 papers, 340 citations indexed

About

Dorota Jurkiewicz is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Dorota Jurkiewicz has authored 34 papers receiving a total of 340 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 18 papers in Molecular Biology and 8 papers in Surgery. Recurrent topics in Dorota Jurkiewicz's work include Genetic Syndromes and Imprinting (8 papers), Pediatric Hepatobiliary Diseases and Treatments (7 papers) and Epigenetics and DNA Methylation (4 papers). Dorota Jurkiewicz is often cited by papers focused on Genetic Syndromes and Imprinting (8 papers), Pediatric Hepatobiliary Diseases and Treatments (7 papers) and Epigenetics and DNA Methylation (4 papers). Dorota Jurkiewicz collaborates with scholars based in Poland, United States and Germany. Dorota Jurkiewicz's co-authors include Małgorzata Krajewska‐Walasek, Elżbieta Ciara, Ewa Popowska, Krystyńa Chrzańowska, Dorota Piekutowska‐Abramczuk, Ewa Pronicka, Rafał Płoski, Joanna Pawłowska, Jennifer Gerfen and Nancy B. Spinner and has published in prestigious journals such as Human Mutation, Molecular Genetics and Metabolism and Journal of Inherited Metabolic Disease.

In The Last Decade

Dorota Jurkiewicz

32 papers receiving 326 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Dorota Jurkiewicz Poland 12 131 127 114 56 49 34 340
James B. Tee Canada 9 50 0.4× 270 2.1× 94 0.8× 56 1.0× 40 0.8× 13 368
Jessica Bonneau France 8 83 0.6× 88 0.7× 96 0.8× 21 0.4× 18 0.4× 10 314
Soledad Kleppe United States 8 54 0.4× 153 1.2× 82 0.7× 14 0.3× 15 0.3× 12 333
Daniel Taliun United States 9 26 0.2× 145 1.1× 220 1.9× 25 0.4× 30 0.6× 15 413
Pamela Ghosh India 9 61 0.5× 69 0.5× 54 0.5× 11 0.2× 13 0.3× 13 325
Namiki Ueda Japan 9 189 1.4× 191 1.5× 26 0.2× 16 0.3× 104 2.1× 18 403
Dina Ramadan Kuwait 12 47 0.4× 99 0.8× 71 0.6× 27 0.5× 12 0.2× 19 273
Xuan Tao China 9 41 0.3× 178 1.4× 28 0.2× 59 1.1× 29 0.6× 24 339
Daniel Fantus United States 6 53 0.4× 129 1.0× 29 0.3× 22 0.4× 39 0.8× 8 301
John A. Phillips United States 8 22 0.2× 144 1.1× 153 1.3× 45 0.8× 14 0.3× 9 324

Countries citing papers authored by Dorota Jurkiewicz

Since Specialization
Citations

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

Fields of papers citing papers by Dorota Jurkiewicz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dorota Jurkiewicz

This figure shows the co-authorship network connecting the top 25 collaborators of Dorota Jurkiewicz. A scholar is included among the top collaborators of Dorota Jurkiewicz 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 Dorota Jurkiewicz. Dorota Jurkiewicz 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.
Jezela‐Stanek, Aleksandra, Krzysztof Szczałuba, Dorota Jurkiewicz, et al.. (2023). Clinical heterogeneity of polish patients with KAT6B–related disorder. Molecular Genetics & Genomic Medicine. 11(12). e2265–e2265. 1 indexed citations
2.
Lipiński, Patryk, Elżbieta Ciara, Dorota Jurkiewicz, et al.. (2023). DCDC2-Related Ciliopathy: Report of Six Polish Patients, Novel DCDC2 Variant, and Literature Review of Reported Cases. Diagnostics. 13(11). 1917–1917. 1 indexed citations
3.
Świąder-Leśniak, Anna, et al.. (2023). The effects of 3-year growth hormone treatment and body composition in Polish patients with Silver-Russell syndrome. Endokrynologia Polska. 74(3). 285–293. 2 indexed citations
4.
Lipiński, Patryk, Maja Klaudel‐Dreszler, Elżbieta Ciara, et al.. (2021). Sterol 27-Hydroxylase Deficiency as a Cause of Neonatal Cholestasis: Report of 2 Cases and Review of the Literature. Frontiers in Pediatrics. 8. 616582–616582. 7 indexed citations
5.
Lipiński, Patryk, Dorota Jurkiewicz, Elżbieta Ciara, et al.. (2020). Neonatal cholestasis due to citrin deficiency: diagnostic pitfalls. Acta Biochimica Polonica. 67(2). 225–228. 4 indexed citations
6.
Jezela‐Stanek, Aleksandra, Elżbieta Ciara, Dorota Jurkiewicz, et al.. (2020). The phenotype‐driven computational analysis yields clinical diagnosis for patients with atypical manifestations of known intellectual disability syndromes. Molecular Genetics & Genomic Medicine. 8(9). e1263–e1263. 13 indexed citations
7.
Rojek, Aleksandra, et al.. (2020). X-linked hypophosphataemic rickets in children: clinical phenotype, therapeutic strategies, and molecular background. Endokrynologia Polska. 72(2). 108–119. 4 indexed citations
8.
Lipiński, Patryk, Elżbieta Ciara, Dorota Jurkiewicz, et al.. (2020). Targeted Next-Generation Sequencing in Diagnostic Approach to Monogenic Cholestatic Liver Disorders—Single-Center Experience. Frontiers in Pediatrics. 8. 414–414. 14 indexed citations
9.
Jurkiewicz, Dorota, Agata Skórka, Robert Śmigiel, et al.. (2016). A novel IGF2/H19 domain triplication in the 11p15.5 imprinting region causing either Beckwith–Wiedemann or Silver–Russell syndrome in a single family. American Journal of Medical Genetics Part A. 173(1). 72–78. 24 indexed citations
10.
Ciara, Elżbieta, Aleksandra Jezela‐Stanek, Dorota Jurkiewicz, et al.. (2016). Novel pathogenic variant in the HRAS gene with lethal outcome and a broad phenotypic spectrum among Polish patients with Costello syndrome. Clinical Dysmorphology. 26(2). 83–90. 1 indexed citations
11.
Jurkiewicz, Dorota & Małgorzata Krajewska‐Walasek. (2015). Rola piętnowanych genów w organizmie ludzkim na przykładzie regionu 11p15. Postepy Biologii Komorki. 42(1).
12.
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
13.
Gerfen, Jennifer, Brian Thiel, Dorota Jurkiewicz, et al.. (2010). Genomic alterations in biliary atresia suggest region of potential disease susceptibility in 2q37.3. American Journal of Medical Genetics Part A. 152A(4). 886–895. 52 indexed citations
14.
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
15.
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
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.
18.
Wolska, Krystyna I., et al.. (2000). Antibiotic Susceptibility of Escherichia coli dnaK and dnaJ Mutants. Microbial Drug Resistance. 6(2). 119–126. 16 indexed citations
19.
Wolska, Krystyna I., et al.. (2000). Biosynthesis and secretion of several enzymes in Escherichia coli dnaK and dnaJ mutants.. PubMed. 101(400). 157–68. 5 indexed citations
20.
Popowska, Ewa, Ewa Pronicka, Anna Sułek, et al.. (2000). X-linked hypophosphatemia in Polish patients. 1. Mutations in the PHEX gene.. PubMed. 41(4). 293–302. 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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