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
-
- Epigenetics and DNA Methylation
- RNA modifications and cancer
- Muscle Physiology and Disorders
Papers in
- Genetics 20
- BRCA gene mutations in cancer 7
- Genetic Syndromes and Imprinting 6
- Genomics and Rare Diseases 4
- Genomic variations and chromosomal abnormalities 4
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- Genomics and Chromatin Dynamics 5
- Epigenetics and DNA Methylation 3
- Co-authors
- Carole Charlier (9 shared papers)Michel Georges (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 (4 shared papers)
- Journals
- BMC Cancer (2 papers)Genome Research (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
28 papers receiving 806 citations
Peers
Comparison fields: 5 of 72
- Genetics 533
- Molecular Biology 565
- Cancer Research 122
- Pediatrics, Perinatology and Child Health 149
- Genetics 74
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 | 169 | |
| 2 | 2001 | 137 | |
| 3 | 2001 | 108 | |
| 4 | 2003 | 86 | |
| 5 | 2004 | 45 | |
| 6 | 2017 | 29 | |
| 7 | 2011 | 28 | |
| 8 | 2016 | 25 | |
| 9 | 2008 | 24 | |
| 10 | 2008 | 22 | |
| 11 | 2001 | 20 | |
| 12 | 2015 | 19 | |
| 13 | 2015 | 19 | |
| 14 | 2018 | 18 | |
| 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, Clinical Biochemistry and Pediatrics, Perinatology and Child Health, having authored 29 papers that have together received 835 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (7 papers), Genetic factors in colorectal cancer (6 papers), Genetic Syndromes and Imprinting (6 papers), Genomics and Chromatin Dynamics (5 papers), Metabolism and Genetic Disorders (4 papers), Genomics and Rare Diseases (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Epigenetics and DNA Methylation (3 papers). The work is most often cited by research in Genetics (533 citations), Molecular Biology (565 citations), Cancer Research (122 citations), Pediatrics, Perinatology and Child Health (149 citations) and Genetics (74 citations). Karin Segers has collaborated with scholars based in Belgium, United States and France. Frequent co-authors include Carole Charlier, Michel Georges, Noelle Cockett, T. L. Shay, Gàbor Gyapay, Latifa Karim, Vincent Bours, Stéphane Berghmans, Jean Weissenbach and Olivier Jaillon. Their work appears in journals such as BMC Cancer, Genome Research, 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.