Marta Jurek

557 total citations
24 papers, 345 citations indexed

About

Marta Jurek is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Marta Jurek has authored 24 papers receiving a total of 345 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 8 papers in Genetics and 6 papers in Neurology. Recurrent topics in Marta Jurek's work include RNA modifications and cancer (6 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Neurological disorders and treatments (4 papers). Marta Jurek is often cited by papers focused on RNA modifications and cancer (6 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Neurological disorders and treatments (4 papers). Marta Jurek collaborates with scholars based in Poland, United States and United Kingdom. Marta Jurek's co-authors include Michał Milewski, Jerzy Bal, Janusz Zimowski, I Hausmanowa-Pétrusewicz, Anna Kostera‐Pruszczyk, Maria Jędrzejowska, Janina Borkowska, Dorota Hoffman‐Zacharska, Andrzej Friedman and Tadeusz Mazurczak and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and International Journal of Molecular Sciences.

In The Last Decade

Marta Jurek

21 papers receiving 336 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marta Jurek Poland 9 193 118 83 80 67 24 345
Eric Villalón United States 12 274 1.4× 243 2.1× 69 0.8× 58 0.7× 33 0.5× 24 380
Tara Newcomb United States 10 263 1.4× 101 0.9× 63 0.8× 39 0.5× 116 1.7× 12 454
Marta Hereu Spain 8 185 1.0× 190 1.6× 117 1.4× 31 0.4× 19 0.3× 9 354
Xavier Lévêque France 11 151 0.8× 96 0.8× 45 0.5× 77 1.0× 24 0.4× 14 288
Maitane Ortiz‐Virumbrales United States 8 190 1.0× 52 0.4× 40 0.5× 41 0.5× 32 0.5× 9 309
Eric M. Roskelley United States 4 315 1.6× 282 2.4× 98 1.2× 95 1.2× 73 1.1× 4 482
Sohyun L. McElroy United States 8 299 1.5× 90 0.8× 160 1.9× 19 0.2× 49 0.7× 12 494
Carlos Cervera Spain 13 291 1.5× 143 1.2× 89 1.1× 66 0.8× 80 1.2× 20 465
Monica Bucchia Italy 9 229 1.2× 174 1.5× 113 1.4× 29 0.4× 15 0.2× 10 342
Samantha L. Sison United States 9 272 1.4× 85 0.7× 100 1.2× 19 0.2× 21 0.3× 10 412

Countries citing papers authored by Marta Jurek

Since Specialization
Citations

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

Fields of papers citing papers by Marta Jurek

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marta Jurek

This figure shows the co-authorship network connecting the top 25 collaborators of Marta Jurek. A scholar is included among the top collaborators of Marta Jurek 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 Marta Jurek. Marta Jurek 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.
Witkowski, Grzegorz, Bartłomiej Szulczyk, Marta Jurek, et al.. (2024). Functional Characteristics of the Nav1.1 p.Arg1596Cys Mutation Associated with Varying Severity of Epilepsy Phenotypes. International Journal of Molecular Sciences. 25(3). 1745–1745. 1 indexed citations
2.
Jurek, Marta, Ewa Obersztyn, Monika Bekiesińska‐Figatowska, et al.. (2023). Congenital coenzyme Q5-linked pathology: causal genetic association, core phenotype, and molecular mechanism. Journal of Applied Genetics. 64(3). 507–514. 2 indexed citations
3.
Bartoszewski, Sławomir, Roma Durak, Marta Jurek, et al.. (2022). A Zebrafish/Drosophila Dual System Model for Investigating Human Microcephaly. Cells. 11(17). 2727–2727. 1 indexed citations
4.
Kutkowska‐Kaźmierczak, Anna, Ewelina Bukowska‐Olech, Marta Jurek, et al.. (2022). De Novo ACTG1 Variant Expands the Phenotype and Genotype of Partial Deafness and Baraitser–Winter Syndrome. International Journal of Molecular Sciences. 23(2). 692–692. 4 indexed citations
5.
Sobstyl, Michał, et al.. (2021). Bilateral Pallidal Stimulation in a Family With Myoclonus Dystonia Syndrome Due to a Mutation in the Sarcoglycan Gene. Neuromodulation Technology at the Neural Interface. 25(6). 918–924.
6.
Ross, Owen A., Andrzej Friedman, Dorota Hoffman‐Zacharska, et al.. (2021). Genetics of Parkinson’s disease in the Polish population. Neurologia i Neurochirurgia Polska. 55(3). 241–252. 15 indexed citations
7.
Jurek, Marta, et al.. (2020). Speech Understanding by Children Diagnosed with Delayed Verbal Development in the Context of Family Functioning. SHILAP Revista de lepidopterología. 9(1(17)). 173–198.
8.
Jurek, Marta, Ewa Obersztyn, & Michał Milewski. (2020). The mutation responsible for torsion dystonia type 1 shows the ability to stimulate intracellular aggregation of mutant huntingtin. PubMed. 22(1). 33–38. 1 indexed citations
9.
Charzewska, Agnieszka, Jolanta Wierzba, Ewa Iżycka‐Świeszewska, et al.. (2016). Hypomyelinating leukodystrophies — a molecular insight into the white matter pathology. Clinical Genetics. 90(4). 293–304. 40 indexed citations
10.
Jurek, Marta, et al.. (2014). Intrafamilial variability of the primary dystonia DYT6 phenotype caused by p.Cys5Trp mutation in THAP1 gene. Neurologia i Neurochirurgia Polska. 48(4). 254–257. 1 indexed citations
11.
Hoffman‐Zacharska, Dorota, Dariusz Koziorowski, Owen A. Ross, et al.. (2013). Novel A18T and pA29S substitutions in α-synuclein may be associated with sporadic Parkinson's disease. Parkinsonism & Related Disorders. 19(11). 1057–1060. 65 indexed citations
12.
Hoffman‐Zacharska, Dorota, Tomasz Kmieć, Jarosław Poznański, Marta Jurek, & Jerzy Bal. (2012). Mutations in the PLP1 gene residue p. Gly198 as the molecular basis of Pelizeaus–Merzbacher phenotype. Brain and Development. 35(9). 877–880. 1 indexed citations
13.
Milewski, Michał, et al.. (2012). Nuclear Import and Export Signals of Human Cohesins SA1/STAG1 and SA2/STAG2 Expressed in Saccharomyces cerevisiae. PLoS ONE. 7(6). e38740–e38740. 7 indexed citations
14.
Sobczyńska‐Tomaszewska, Agnieszka, et al.. (2011). Novel de Novo Large Deletion in Cystic Fibrosis Transmembrane Conductance Regulator Gene Results in a Severe Cystic Fibrosis Phenotype. The Journal of Pediatrics. 159(2). 343–346.e1. 4 indexed citations
15.
Jędrzejowska, Maria, Michał Milewski, Janusz Zimowski, et al.. (2010). Incidence of Spinal Muscular Atrophy in Poland – More Frequent than Predicted?. Neuroepidemiology. 34(3). 152–157. 44 indexed citations
16.
Szczałuba, Krzysztof, Marta Jurek, Elżbieta Szczepanik, et al.. (2009). A Family With Paroxysmal Nonkinesigenic Dyskinesia: Genetic and Treatment Issues. Pediatric Neurology. 41(2). 135–138. 14 indexed citations
17.
Nawara, Magdalena, Marta Jurek, Jerzy Bal, & Tadeusz Mazurczak. (2009). [Gene mapping in 14 families with X-linked nonspecific mental retardation].. PubMed. 13(2). 94–113. 1 indexed citations
18.
Jędrzejowska, Maria, Janina Borkowska, Janusz Zimowski, et al.. (2008). Unaffected patients with a homozygous absence of the SMN1 gene. European Journal of Human Genetics. 16(8). 930–934. 42 indexed citations
19.
Nawara, Magdalena, Jakub Klapecki, Katarzyna Borg, et al.. (2008). Novel mutation of IL1RAPL1 gene in a nonspecific X‐linked mental retardation (MRX) family. American Journal of Medical Genetics Part A. 146A(24). 3167–3172. 38 indexed citations
20.
Szczałuba, Krzysztof, Marta Jurek, Michał Milewski, et al.. (2007). Clinical characteristics of carriers of a GAG deletion in the DYT1 gene amongst Polish patients with primary dystonia. European Journal of Neurology. 14(6). 659–662. 6 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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