Zsolt Bánfai
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- Forensic and Genetic Research 6
- Genetic diversity and population structure 3
- Genetics and Neurodevelopmental Disorders 2
- Race, Genetics, and Society 2
- Genomic variations and chromosomal abnormalities 1
- Genetic Syndromes and Imprinting 1
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- Romani and Gypsy Studies 3
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- Epigenetics and DNA Methylation 2
In The Last Decade
Zsolt Bánfai
13 papers receiving 89 citations
Peers
Comparison fields: 5 of 43
- Genetics 56
- General Health Professions 24
- Cancer Research 9
- Pharmacology 5
- Gastroenterology 3
Countries citing papers authored by Zsolt Bánfai
This map shows the geographic impact of Zsolt Bánfai'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 Zsolt Bánfai with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Zsolt Bánfai more than expected).
Fields of papers citing papers by Zsolt Bánfai
This network shows the impact of papers produced by Zsolt Bánfai. 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 Zsolt Bánfai. The network helps show where Zsolt Bánfai may publish in the future.
Co-authorship network
The 19 scholars most cited alongside Zsolt Bánfai, 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 | 2023 | 0 | |
| 2 | 2023 | 3 | |
| 3 | 2022 | 1 | |
| 4 | 2021 | 3 | |
| 5 | 2020 | 2 | |
| 6 | 2019 | 10 | |
| 7 | 2019 | 1 | |
| 8 | 2018 | 5 | |
| 9 | 2017 | 19 | |
| 10 | 2017 | 6 | |
| 11 | 2017 | 6 | |
| 12 | 2017 | 6 | |
| 13 | 2014 | 6 | |
| 14 | 2014 | 22 |
About Zsolt Bánfai
Zsolt Bánfai is a scholar working on Genetics, Genetics and Speech and Hearing, having authored 14 papers that have together received 90 indexed citations. Recurring topics across this work include Forensic and Genetic Research (6 papers), Genetic diversity and population structure (3 papers), Romani and Gypsy Studies (3 papers), Genetics and Neurodevelopmental Disorders (2 papers), Epigenetics and DNA Methylation (2 papers), Race, Genetics, and Society (2 papers), Genomic variations and chromosomal abnormalities (1 paper) and Genetic Syndromes and Imprinting (1 paper). The work is most often cited by research in Genetics (56 citations), General Health Professions (24 citations) and Cancer Research (9 citations). Zsolt Bánfai has collaborated with scholars based in Hungary, China and Germany. Frequent co-authors include Béla Melegh, Kinga Hadzsiev, Attila Miseta, Erzsébet Kövesdi, András Szabó, Lili Magyari, Katalin Sümegi, Patrícia Sarlós, Katalin Komlósi and Miklós Kásler. Their work appears in journals such as PLoS ONE, Scientific Reports and BMC Genomics.
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.