Jerzy Bal

3.0k total citations
113 papers, 1.1k citations indexed

About

Jerzy Bal is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Jerzy Bal has authored 113 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Molecular Biology, 37 papers in Genetics and 18 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Jerzy Bal's work include Genetics and Neurodevelopmental Disorders (17 papers), Cystic Fibrosis Research Advances (15 papers) and Pancreatitis Pathology and Treatment (11 papers). Jerzy Bal is often cited by papers focused on Genetics and Neurodevelopmental Disorders (17 papers), Cystic Fibrosis Research Advances (15 papers) and Pancreatitis Pathology and Treatment (11 papers). Jerzy Bal collaborates with scholars based in Poland, United Kingdom and Germany. Jerzy Bal's co-authors include Katarzyna Wertheim‐Tysarowska, Tadeusz Mazurczak, Agnieszka Sobczyńska‐Tomaszewska, Norman J. Pieniąžek, Marta Jurek, Dorota Hoffman‐Zacharska, Ewa Obersztyn, Magdalena Nawara, Jarosław Poznański and Monika Jurkowska and has published in prestigious journals such as Neurology, FEBS Letters and International Journal of Molecular Sciences.

In The Last Decade

Jerzy Bal

107 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jerzy Bal Poland 19 486 244 134 115 112 113 1.1k
Michael J. Perry United Kingdom 12 256 0.5× 177 0.7× 149 1.1× 165 1.4× 75 0.7× 31 1.0k
Duan Ma China 19 643 1.3× 220 0.9× 78 0.6× 62 0.5× 87 0.8× 82 1.1k
Koko Urase Japan 19 776 1.6× 138 0.6× 81 0.6× 66 0.6× 169 1.5× 26 1.0k
Nobuyuki Shirasawa Japan 20 596 1.2× 141 0.6× 96 0.7× 66 0.6× 146 1.3× 55 1.2k
Hidefumi Tonoki Japan 18 751 1.5× 518 2.1× 84 0.6× 45 0.4× 110 1.0× 48 1.5k
Ayumi Kitano United States 18 842 1.7× 192 0.8× 71 0.5× 62 0.5× 173 1.5× 30 1.6k
Chaim Jalas United States 23 724 1.5× 375 1.5× 86 0.6× 32 0.3× 231 2.1× 60 1.7k
Shaoping Xie United Kingdom 17 874 1.8× 229 0.9× 73 0.5× 171 1.5× 38 0.3× 20 1.4k
Tamar Tenne Israel 11 618 1.3× 227 0.9× 87 0.6× 69 0.6× 63 0.6× 19 1.1k
Shanaz Pasha United Kingdom 14 515 1.1× 295 1.2× 48 0.4× 29 0.3× 141 1.3× 14 919

Countries citing papers authored by Jerzy Bal

Since Specialization
Citations

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

Fields of papers citing papers by Jerzy Bal

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jerzy Bal

This figure shows the co-authorship network connecting the top 25 collaborators of Jerzy Bal. A scholar is included among the top collaborators of Jerzy Bal 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 Jerzy Bal. Jerzy Bal 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.
Charzewska, Agnieszka, et al.. (2023). Genetic Risk Factors for Neurological Disorders in Children with Adverse Events Following Immunization: A Descriptive Study of a Polish Case Series. International Journal of Molecular Sciences. 24(2). 1117–1117. 2 indexed citations
2.
3.
Smyk, Marta, Magdalena Bartnik, Barbara Wiśniowiecka‐Kowalnik, et al.. (2022). Application of array comparative genomic hybridization (aCGH) for identification of chromosomal aberrations in the recurrent pregnancy loss. Journal of Assisted Reproduction and Genetics. 39(2). 357–367. 7 indexed citations
4.
Kutkowska‐Kaźmierczak, Anna, Paweł Gawliński, Wojciech Wiszniewski, et al.. (2020). The MED13L haploinsufficiency syndrome associated with de novo nonsense variant (p.Gln1981*). PubMed. 24(3). 32–36. 2 indexed citations
5.
Wertheim‐Tysarowska, Katarzyna, et al.. (2018). A novel de novo mutation p.Ala428Asp in KRT5 gene as a cause of localized epidermolysis bullosa simplex. Experimental Dermatology. 28(10). 1131–1134. 2 indexed citations
6.
Rygiel, Agnieszka Magdalena, et al.. (2017). Hearing impairment caused by mutations in two different genes responsible for nonsyndromic and syndromic hearing loss within a single family. Journal of Applied Genetics. 59(1). 67–72. 1 indexed citations
7.
Oracz, Grzegorz, Agnieszka Sobczyńska‐Tomaszewska, Maciej Dądalski, et al.. (2016). The clinical course of hereditary pancreatitis in children – A comprehensive analysis of 41 cases. Pancreatology. 16(4). 535–541. 13 indexed citations
8.
Gawliński, Paweł, Renata Posmyk, Tomasz Gambin, et al.. (2016). PEHO Syndrome May Represent Phenotypic Expansion at the Severe End of the Early-Onset Encephalopathies. Pediatric Neurology. 60. 83–87. 15 indexed citations
9.
Wertheim‐Tysarowska, Katarzyna, Monika Ołdak, Anna Kutkowska‐Kaźmierczak, et al.. (2015). Novel sporadic and recurrent mutations in KRT5 and KRT14 genes in Polish epidermolysis bullosa simplex patients: further insights into epidemiology and genotype–phenotype correlation. Journal of Applied Genetics. 57(2). 175–181. 16 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.
Wertheim‐Tysarowska, Katarzyna, Agnieszka Sobczyńska‐Tomaszewska, Cezary Kowaléwski, et al.. (2012). Novel and recurrent COL7A1 mutation in a Polish population. European Journal of Dermatology. 22(1). 23–28. 8 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.
Sobczyńska‐Tomaszewska, Agnieszka, Katarzyna Wertheim‐Tysarowska, Cezary Kowaléwski, et al.. (2009). Epidermolysis bullosa dystrophica. From clinics to genetics. 96(3). 227–233. 1 indexed citations
14.
Nawara, Magdalena, Krzysztof Szczałuba, Karine Poirier, et al.. (2006). The ARX mutations: A frequent cause of X‐linked mental retardation. American Journal of Medical Genetics Part A. 140A(7). 727–732. 29 indexed citations
15.
Jurkowska, Monika, Magdalena Kurenko-Deptuch, Jerzy Bal, & Dirk Roos. (2005). The search for a genetic defect in Polish patients with chronic granulomatous disease.. PubMed. 52(6). 441–6. 4 indexed citations
16.
Milewski, Michał, et al.. (2003). [Molecular pathogenesis of fragile X syndrome].. PubMed. 6(4). 295–308.
17.
Wiszniewski, Wojciech, et al.. (2001). High Frequency of GJB2 Gene Mutations in Polish Patients with Prelingual Nonsyndromic Deafness. Genetic Testing. 5(2). 147–148. 21 indexed citations
18.
Żekanowski, Cezary, et al.. (1999). Mutations in Exon 3 of the PAH Gene Causing Mild Hyperphenylalaninemia. Genetic Testing. 3(3). 297–299. 2 indexed citations
19.
Bal, Jerzy, Tadeusz Mazurczak, & Jochen Reiss. (1992). The frequency of mutations in exon 11 of the CF gene in Polish cystic fibrosis patients.. PubMed. 39(3). 245–9. 1 indexed citations
20.
Bal, Jerzy, et al.. (1977). 4-nitroquinoline-1-oxide: A good mutagen for Aspergillus nidulans. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 56(2). 153–156. 40 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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