Krystyna Szymańska
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- Genetics and Neurodevelopmental Disorders 11
- Genomics and Rare Diseases 5
- Genomic variations and chromosomal abnormalities 4
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- Metabolism and Genetic Disorders 3
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- RNA regulation and disease 5
- Ion Transport and Channel Regulation 3
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- Cellular transport and secretion 4
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- Amino Acid Enzymes and Metabolism 3
- Co-authors
- Krzysztof SzczałubaRobert ŚmigielRafał PłoskiJoanna KosińskaEwa ObersztynMałgorzata RydzaniczMonika Bekiesińska‐FigatowskaB Schmidt-Sidor
- Partner nations
- PolandUnited StatesNetherlands
In The Last Decade
Krystyna Szymańska
42 papers receiving 474 citations
Peers
Comparison fields: 5 of 77
- Genetics 177
- Psychiatry and Mental health 52
- Clinical Biochemistry 23
- Molecular Biology 218
- Neurology 23
Countries citing papers authored by Krystyna Szymańska
This map shows the geographic impact of Krystyna Szymańska'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 Krystyna Szymańska with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Krystyna Szymańska more than expected).
Fields of papers citing papers by Krystyna Szymańska
This network shows the impact of papers produced by Krystyna Szymańska. 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 Krystyna Szymańska. The network helps show where Krystyna Szymańska may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Krystyna Szymańska, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2025 | 0 | |
| 2 | 2022 | 0 | |
| 3 | 2021 | 49 | |
| 4 | 2021 | 9 | |
| 5 | 2021 | 3 | |
| 6 | 2020 | 1 | |
| 7 | 2018 | 12 | |
| 8 | 2017 | 1 | |
| 9 | 2017 | 21 | |
| 10 | 2017 | 8 | |
| 11 | 2016 | 7 | |
| 12 | 2016 | 22 | |
| 13 | 2016 | 41 | |
| 14 | 2014 | 10 | |
| 15 | 2014 | 1 | |
| 16 | 2014 | 3 | |
| 17 | 2012 | 16 | |
| 18 | 2010 | 71 | |
| 19 | Wrodzone zaburzenia metabolizmuamin biogennych i pteryn | 2007 | 1 |
| 20 | 1996 | 8 |
About Krystyna Szymańska
Krystyna Szymańska is a scholar working on Genetics, Clinical Biochemistry and Biochemistry, having authored 48 papers that have together received 485 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (11 papers), Genomics and Rare Diseases (5 papers), RNA regulation and disease (5 papers), Cellular transport and secretion (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Amino Acid Enzymes and Metabolism (3 papers), Metabolism and Genetic Disorders (3 papers) and Ion Transport and Channel Regulation (3 papers). The work is most often cited by research in Genetics (177 citations), Psychiatry and Mental health (52 citations) and Clinical Biochemistry (23 citations). Krystyna Szymańska has collaborated with scholars based in Poland, United States and Netherlands. Frequent co-authors include Krzysztof Szczałuba, Robert Śmigiel, Rafał Płoski, Joanna Kosińska, Ewa Obersztyn, Małgorzata Rydzanicz, Monika Bekiesińska‐Figatowska, B Schmidt-Sidor, Piotr Stawiński and Beata Nowakowska. Their work appears in journals such as Brain, Neurology and The American Journal of Human Genetics.
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.