Karin Segers
Impact in
- Immunology top 10%
- interferon and immune responses
- Genetics top 10%
- Genetic Syndromes and Imprinting
- Genetic and phenotypic traits in livestock
Papers in
- Genetics 15
- BRCA gene mutations in cancer 5
- Genomics and Rare Diseases 4
- Genetic Syndromes and Imprinting 4
- Genomic variations and chromosomal abnormalities 3
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- Genomics and Chromatin Dynamics 3
- RNA modifications and cancer 3
- Co-authors
- Michel Georges (7 shared papers)Carole Charlier (7 shared papers)Noelle Cockett (5 shared papers)Tracy L. Shay (4 shared papers)Vincent Bours (16 shared papers)Gàbor Gyapay (2 shared papers)Latifa Karim (1 shared paper)Gary D. Snowder (2 shared papers)
- Journals
- Mammalian Genome (2 papers)BMC Cancer (2 papers)The Journal of Clinical Endocrinology & Metabolism (1 paper)Nature Genetics (1 paper)Clinica Chimica Acta (1 paper)
- Partner nations
- BelgiumUnited StatesFrance
In The Last Decade
Karin Segers
31 papers receiving 1.1k citations
Karin Segers's Hit Papers
Peers
Comparison fields: 5 of 81
- Immunology 321
- Genetics 337
- Rheumatology 142
- Molecular Biology 581
- Genetics 57
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 31 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Characterization of human disease phenotypes associated with mutations in TREX1 , RNASEH2A , RNASEH2B , RNASEH2C , SAMHD1 , ADAR , and IFIH1 Hit paper breakdown → | 2015 | 485 |
| 2 | 2001 | 137 | |
| 3 | 2003 | 83 | |
| 4 | 2004 | 50 | |
| 5 | 2017 | 33 | |
| 6 | 2018 | 32 | |
| 7 | 2011 | 29 | |
| 8 | 2008 | 27 | |
| 9 | 2016 | 27 | |
| 10 | 2008 | 26 | |
| 11 | 2015 | 21 | |
| 12 | 2015 | 21 | |
| 13 | 2018 | 20 | |
| 14 | 2001 | 19 | |
| 15 | 2018 | 15 | |
| 16 | 2010 | 14 | |
| 17 | 2008 | 13 | |
| 18 | 2000 | 13 | |
| 19 | 2001 | 12 | |
| 20 | 2020 | 9 |
About Karin Segers
Karin Segers is a scholar working on Genetics, Molecular Biology, Pathology and Forensic Medicine, Clinical Biochemistry and Immunology, having authored 31 papers that have together received 1.1k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (5 papers), Genomics and Rare Diseases (4 papers), Genetic factors in colorectal cancer (4 papers), Genetic Syndromes and Imprinting (4 papers), Genomic variations and chromosomal abnormalities (3 papers), Genomics and Chromatin Dynamics (3 papers), RNA modifications and cancer (3 papers) and Cancer Genomics and Diagnostics (2 papers). The work is most often cited by research in Immunology (321 citations), Genetics (337 citations), Rheumatology (142 citations), Molecular Biology (581 citations) and Genetics (57 citations). Karin Segers has collaborated with scholars based in Belgium, United States and France. Frequent co-authors include Michel Georges, Carole Charlier, Noelle Cockett, Tracy L. Shay, Vincent Bours, Gàbor Gyapay, Latifa Karim, Gary D. Snowder, Maria A. Smit and Claire Josse. Their work appears in journals such as Mammalian Genome, BMC Cancer, The Journal of Clinical Endocrinology & Metabolism, Nature Genetics and Clinica Chimica Acta.
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.