Jerzy Bal

3.0k citations

113 papers · 1.1k indexed · h-index 19

Impact in

Sensory Systems top 5%
- Hearing, Cochlea, Tinnitus, Genetics
Neurology top 10%
- Parkinson's Disease Mechanisms and Treatments

Papers in ⓘ

Molecular Biology 41
- RNA modifications and cancer 6
Genetics 37
- Genetics and Neurodevelopmental Disorders 17

Co-authors: Katarzyna Wertheim‐Tysarowska (26 shared papers)Tadeusz Mazurczak (23 shared papers)Agnieszka Sobczyńska‐Tomaszewska (14 shared papers)Norman J. Pieniąžek (4 shared papers)Marta Jurek (11 shared papers)Dorota Hoffman‐Zacharska (13 shared papers)Ewa Obersztyn (15 shared papers)Magdalena Nawara (9 shared papers)
Journals: Pancreatology (5 papers)Journal of Pediatric Gastroenterology and Nutrition (4 papers)Human Mutation (3 papers)Journal of Cancer Research and Clinical Oncology (3 papers)Journal of Cystic Fibrosis (2 papers)
Partner nations: Poland United Kingdom Germany

In The Last Decade

Jerzy Bal

107 papers receiving 1.1k citations

Peers

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-authors

The 25 scholars most cited alongside Jerzy Bal, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Jerzy Bal Line = papers co-authored together Jerzy Bal links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 113 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Mutation A1555G in the 12S rRNA gene and its epidemiological importance in German, Hungarian, and Polish patients Human Mutation ·Susan Kupka, Tímea Tóth, Maciej Wróbel, Ulrike Zeißler, Witold Szyfter, Krzysztof Szyfter, Grażyna Mielnik–Niedzielska, Jerzy Bal, Hans-Peter Zenner, István Sziklai, Nikolaus Blin, Markus Pfister	2002	84
2	Novel A18T and pA29S substitutions in α-synuclein may be associated with sporadic Parkinson's disease Parkinsonism & Related Disorders ·Dorota Hoffman‐Zacharska, Dariusz Koziorowski, Owen A. Ross, Michał Milewski, Jarosław Poznański, Marta Jurek, Zbigniew K. Wszołek, Alexandra I. Soto‐Ortolaza, Jarosław Sławek, Piotr Janik, Zygmunt Jamrozik, Anna Potulska‐Chromik, Barbara Jasińska‐Myga, Grzegorz Opala, Anna Krygowska‐Wajs, K Czyźewski, Dennis W. Dickson, Jerzy Bal, Andrzej Friedman	2013	65
3	Analysis of CFTR, SPINK1, PRSS1 and AAT Mutations in Children With Acute or Chronic Pancreatitis Journal of Pediatric Gastroenterology and Nutrition ·Agnieszka Sobczyńska‐Tomaszewska, Daniel Bąk, Beata Oralewska, Grzegorz Oracz, A. Norek, Kamila Czerska, Tadeusz Mazurczak, M Teisseyre, Jerzy Socha, Marek Zagulski, Jerzy Bal	2006	51
4	The COL7A1 mutation database Human Mutation ·Katarzyna Wertheim‐Tysarowska, Agnieszka Sobczyńska‐Tomaszewska, Cezary Kowaléwski, Michał Skroński, Grzegorz Święćkowski, Anna Kutkowska‐Kaźmierczak, Katarzyna Woźniak, Jerzy Bal	2011	49
5	4-nitroquinoline-1-oxide: A good mutagen for Aspergillus nidulans Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis ·Jerzy Bal, Elżbieta M. Kajtaniak, Norman J. Pieniąžek	1977	40
6	Hypomyelinating leukodystrophies — a molecular insight into the white matter pathology Clinical Genetics ·Agnieszka Charzewska, Jolanta Wierzba, Ewa Iżycka‐Świeszewska, Monika Bekiesińska‐Figatowska, Marta Jurek, Aleksandra Gintowt, Anna Kłosowska, Jerzy Bal, Dorota Hoffman‐Zacharska	2016	40
7	Novel mutation of IL1RAPL1 gene in a nonspecific X‐linked mental retardation (MRX) family American Journal of Medical Genetics Part A ·Magdalena Nawara, Jakub Klapecki, Katarzyna Borg, Marta Jurek, Sarah Moreno, Jolanta Tryfon, Jerzy Bal, Jamel Chelly, Tadeusz Mazurczak	2008	38
8	Newborn screening for cystic fibrosis: Polish 4 years’ experience with CFTR sequencing strategy European Journal of Human Genetics ·(unknown), Agnieszka Sobczyńska‐Tomaszewska, Mariusz Ołtarzewski, Kamila Czerska, Katarzyna Wertheim‐Tysarowska, Dorota Sands, Jarosław Walkowiak, Jerzy Bal, Tadeusz Mazurczak	2012	36
9	Contribution of RIT1 mutations to the pathogenesis of Noonan syndrome: Four new cases and further evidence of heterogeneity American Journal of Medical Genetics Part A ·Monika Goś, Somayyeh Fahiminiya, Jarosław Poznański, Jakub Klapecki, Ewa Obersztyn, Małgorzata Piotrowicz, Jolanta Wierzba, Renata Posmyk, Jerzy Bal, Jacek Majewski	2014	34
10	The ARX mutations: A frequent cause of X‐linked mental retardation American Journal of Medical Genetics Part A ·Magdalena Nawara, Krzysztof Szczałuba, Karine Poirier, Krystyńa Chrzańowska, Jacek Pilch, Jerzy Bal, Jamel Chelly, Tadeusz Mazurczak	2006	29
11	Founder effect for a 26-bp deletion in the RFXANK gene in North African major histocompatibility complex class II-deficient patients belonging to complementation group B Immunogenetics ·Wojciech Wiszniewski, M.-C. Fondanèche, Nathalie Lambert, Krzysztof Masternak, Capucine Pïcard, Luigi D. Notarangelo, Klaus Schwarz, Jerzy Bal, Walter Reith, Carlos Alcaide, Geneviève de Saint Basile, Alain Fischer, Barbara Lisowska‐Grospierre	2000	29
12	An Aspergillus nidulans mutant lacking serine transacetylase: Evidence for two pathways of cysteine biosynthesis Molecular and General Genetics MGG ·Norman J. Pieniąžek, Jerzy Bal, Ewa Balbin, Piotr P. Stępień	1974	22
13	High Frequency of GJB2 Gene Mutations in Polish Patients with Prelingual Nonsyndromic Deafness Genetic Testing ·Wojciech Wiszniewski, L Sobieszczańska-Radoszewska, Ewa Nowakowska-Szyrwińska, Ewa Obersztyn, Jerzy Bal	2001	21
14	Discrimination between recurrent mutation and identity by descent: application to point mutations in exon 11 of the cystic fibrosis (CFTR) gene Human Genetics ·Jochen Reiss, D.N. Cooper, Jerzy Bal, Ryszard Słomski, GarryR. Cutting, Michael Krawczak	1991	21
15	Molecular characterization of Polish patients with classical galactosaemia Journal of Inherited Metabolic Disease ·C. Żdekanowski, Barbara Radomyska, Jerzy Bal	1999	21
16	Genetic and biochemical background of chronic granulomatous disease. PubMed ·Monika Jurkowska, Ewa Bernatowska, Jerzy Bal	2004	21
17	Low frequency of the PARK2 gene mutations in Polish patients with the early-onset form of Parkinson disease Parkinsonism & Related Disorders ·Dariusz Koziorowski, Dorota Hoffman‐Zacharska, Jarosław Sławek, Walentyna Szirkowiec, Piotr Janik, Jerzy Bal, Andrzej Friedman	2009	19
18	Incidence of mutations in the PARK2, PINK1, PARK7 genes in Polish early-onset Parkinson disease patients Neurologia i Neurochirurgia Polska ·Dariusz Koziorowski, Dorota Hoffman‐Zacharska, Jarosław Sławek, Zygmunt Jamrozik, Piotr Janik, Anna Potulska‐Chromik, Anna Roszmann, Renata Tataj, Jerzy Bal, Andrzej Friedman	2013	18
19	Chymotrypsinogen C Genetic Variants, Including c.180TT, Are Strongly Associated With Chronic Pancreatitis in Pediatric Patients Journal of Pediatric Gastroenterology and Nutrition ·Alicja Grabarczyk, Grzegorz Oracz, Katarzyna Wertheim‐Tysarowska, Aleksandra Kujko, Karolina Wejnarska, Elwira Kołodziejczyk, Jerzy Bal, Dorota Kozieł, Artur Kowalik, Stanisław Głuszek, Agnieszka Magdalena Rygiel	2017	18
20	A cystic fibrosis patient homozygous for the nonsense mutation R553X. Journal of Medical Genetics ·Jerzy Bal, Manfred Stuhrmann, M. Schloesser, J. Schmidtke, Jochen Reiss	1991	17

About Jerzy Bal

Jerzy Bal is a scholar working on Molecular Biology, Genetics, Pulmonary and Respiratory Medicine, Surgery and Cell Biology, having authored 113 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (17 papers), Cystic Fibrosis Research Advances (15 papers), Pancreatitis Pathology and Treatment (11 papers), Metabolism and Genetic Disorders (9 papers), Neonatal Respiratory Health Research (9 papers), Pancreatic and Hepatic Oncology Research (7 papers), Skin and Cellular Biology Research (7 papers) and RNA modifications and cancer (6 papers). The work is most often cited by research in Sensory Systems (85 citations), Neurology (82 citations), Clinical Biochemistry (60 citations), Genetics (244 citations) and Neurology (110 citations). Jerzy Bal has collaborated with scholars based in Poland, United Kingdom and Germany. Frequent co-authors include Katarzyna Wertheim‐Tysarowska, Tadeusz Mazurczak, Agnieszka Sobczyńska‐Tomaszewska, Norman J. Pieniąžek, Marta Jurek, Dorota Hoffman‐Zacharska, Ewa Obersztyn, Magdalena Nawara, Monika Jurkowska and Jarosław Poznański. Their work appears in journals such as Pancreatology, Journal of Pediatric Gastroenterology and Nutrition, Human Mutation, Journal of Cancer Research and Clinical Oncology and Journal of Cystic Fibrosis.

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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