Karin Segers
Impact in
- Genetics top 5%
- Genetic Syndromes and Imprinting
- Genetic and phenotypic traits in livestock
- Genetic Mapping and Diversity in Plants and Animals
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- Cancer-related molecular mechanisms research
Papers in
- Genetics 17
- Genetic Syndromes and Imprinting 6
- BRCA gene mutations in cancer 5
- Genomic variations and chromosomal abnormalities 4
- Genomics and Rare Diseases 4
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- Epigenetics and DNA Methylation 3
- Genomics and Chromatin Dynamics 3
- RNA modifications and cancer 3
- Co-authors
- Michel Georges (9 shared papers)Carole Charlier (9 shared papers)Noelle Cockett (6 shared papers)T. L. Shay (5 shared papers)Gàbor Gyapay (3 shared papers)Latifa Karim (2 shared papers)Vincent Bours (16 shared papers)Stéphane Berghmans (2 shared papers)
- Journals
- Genome Research (2 papers)BMC Cancer (2 papers)Mammalian Genome (2 papers)Journal of Personalized Medicine (1 paper)The Journal of Pediatrics (1 paper)
- Partner nations
- BelgiumUnited StatesFrance
In The Last Decade
Karin Segers
29 papers receiving 815 citations
Peers
Comparison fields: 5 of 70
- Genetics 516
- Cancer Research 109
- Molecular Biology 519
- Pediatrics, Perinatology and Child Health 129
- Genetics 59
Countries citing papers authored by Karin Segers
This map shows the geographic impact of Karin Segers'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 Karin Segers with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Karin Segers more than expected).
Fields of papers citing papers by Karin Segers
This network shows the impact of papers produced by Karin Segers. 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 Karin Segers. The network helps show where Karin Segers may publish in the future.
Co-authors
The 25 scholars most cited alongside Karin Segers, 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 29 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2001 | 170 | |
| 2 | 2001 | 137 | |
| 3 | 2001 | 108 | |
| 4 | 2003 | 86 | |
| 5 | 2004 | 45 | |
| 6 | 2017 | 31 | |
| 7 | 2011 | 28 | |
| 8 | 2016 | 26 | |
| 9 | 2008 | 24 | |
| 10 | 2008 | 23 | |
| 11 | 2001 | 20 | |
| 12 | 2018 | 20 | |
| 13 | 2015 | 19 | |
| 14 | 2015 | 19 | |
| 15 | 2000 | 15 | |
| 16 | 2001 | 14 | |
| 17 | 2010 | 13 | |
| 18 | 2008 | 12 | |
| 19 | 2020 | 8 | |
| 20 | 2018 | 6 |
About Karin Segers
Karin Segers is a scholar working on Genetics, Molecular Biology, Pathology and Forensic Medicine, Pediatrics, Perinatology and Child Health and Clinical Biochemistry, having authored 29 papers that have together received 843 indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (6 papers), BRCA gene mutations in cancer (5 papers), Genomic variations and chromosomal abnormalities (4 papers), Genomics and Rare Diseases (4 papers), Genetic factors in colorectal cancer (4 papers), Epigenetics and DNA Methylation (3 papers), Genomics and Chromatin Dynamics (3 papers) and RNA modifications and cancer (3 papers). The work is most often cited by research in Genetics (516 citations), Cancer Research (109 citations), Molecular Biology (519 citations), Pediatrics, Perinatology and Child Health (129 citations) and Genetics (59 citations). Karin Segers has collaborated with scholars based in Belgium, United States and France. Frequent co-authors include Michel Georges, Carole Charlier, Noelle Cockett, T. L. Shay, Gàbor Gyapay, Latifa Karim, Vincent Bours, Stéphane Berghmans, Olivier Jaillon and Jean Weissenbach. Their work appears in journals such as Genome Research, BMC Cancer, Mammalian Genome, Journal of Personalized Medicine and The Journal of Pediatrics.
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.