Jasmin Beygo
Impact in
- Genetics top 5%
- Genetic Syndromes and Imprinting
- Genomic variations and chromosomal abnormalities
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- Prenatal Screening and Diagnostics
Papers in
-
- Epigenetics and DNA Methylation 23
- Genetics 25
- Genetic Syndromes and Imprinting 23
- Craniofacial Disorders and Treatments 2
- Genomic variations and chromosomal abnormalities 2
- Co-authors
- Karin Buiting (21 shared papers)Bernhard Horsthemke (12 shared papers)Thomas Eggermann (8 shared papers)Deniz Kanber (6 shared papers)Gabriele Gillessen‐Kaesbach (6 shared papers)Reiner Siebert (6 shared papers)Matthias Begemann (4 shared papers)Dirk Prawitt (2 shared papers)
- Journals
- European Journal of Human Genetics (7 papers)Human Molecular Genetics (2 papers)Epigenetics (2 papers)PLoS ONE (2 papers)Scientific Reports (1 paper)
- Partner nations
- GermanyNetherlandsUnited Kingdom
In The Last Decade
Jasmin Beygo
31 papers receiving 685 citations
Peers
Comparison fields: 5 of 64
- Genetics 506
- Pediatrics, Perinatology and Child Health 313
- Molecular Biology 479
- Pathology and Forensic Medicine 91
- Reproductive Medicine 30
Countries citing papers authored by Jasmin Beygo
This map shows the geographic impact of Jasmin Beygo'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 Jasmin Beygo with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jasmin Beygo more than expected).
Fields of papers citing papers by Jasmin Beygo
This network shows the impact of papers produced by Jasmin Beygo. 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 Jasmin Beygo. The network helps show where Jasmin Beygo may publish in the future.
Co-authors
The 25 scholars most cited alongside Jasmin Beygo, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 32 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2016 | 70 | |
| 2 | 2012 | 64 | |
| 3 | 2009 | 50 | |
| 4 | 2014 | 49 | |
| 5 | 2014 | 48 | |
| 6 | 2019 | 38 | |
| 7 | 2014 | 36 | |
| 8 | 2018 | 32 | |
| 9 | 2017 | 31 | |
| 10 | 2013 | 25 | |
| 11 | 2013 | 22 | |
| 12 | 2018 | 21 | |
| 13 | 2014 | 20 | |
| 14 | 2020 | 19 | |
| 15 | 2020 | 19 | |
| 16 | 2017 | 18 | |
| 17 | 2016 | 18 | |
| 18 | 2017 | 18 | |
| 19 | 2011 | 16 | |
| 20 | 2018 | 13 |
About Jasmin Beygo
Jasmin Beygo is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Pathology and Forensic Medicine and Public Health, Environmental and Occupational Health, having authored 32 papers that have together received 690 indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (23 papers), Genetic Syndromes and Imprinting (23 papers), Prenatal Screening and Diagnostics (16 papers), Tumors and Oncological Cases (4 papers), Craniofacial Disorders and Treatments (2 papers), Gestational Trophoblastic Disease Studies (2 papers), Identity, Memory, and Therapy (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). The work is most often cited by research in Genetics (506 citations), Pediatrics, Perinatology and Child Health (313 citations), Molecular Biology (479 citations), Pathology and Forensic Medicine (91 citations) and Reproductive Medicine (30 citations). Jasmin Beygo has collaborated with scholars based in Germany, Netherlands and United Kingdom. Frequent co-authors include Karin Buiting, Bernhard Horsthemke, Thomas Eggermann, Deniz Kanber, Gabriele Gillessen‐Kaesbach, Reiner Siebert, Matthias Begemann, Dirk Prawitt, Elisabeth Petrasch‐Parwez and Jörg T. Epplen. Their work appears in journals such as European Journal of Human Genetics, Human Molecular Genetics, Epigenetics, PLoS ONE and Scientific Reports.
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.