S Jansen
Impact in
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- Carcinogens and Genotoxicity Assessment
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- DNA Repair Mechanisms
- CRISPR and Genetic Engineering
- Porphyrin Metabolism and Disorders
Papers in
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- DNA Repair Mechanisms 3
- Genetics 5
- Genomic variations and chromosomal abnormalities 3
- BRCA gene mutations in cancer 2
- Co-authors
- Charmaine Havenga (4 shared papers)Thomy de Ravel (3 shared papers)Rachel A. Gibson (3 shared papers)Neil V. Morgan (2 shared papers)Hans Joenje (2 shared papers)Christopher G. Mathew (3 shared papers)L. P. Kuyt (1 shared paper)Éliane Gluckman (1 shared paper)
- Journals
- Nuclear Medicine Communications (1 paper)Proceedings of the National Academy of Sciences (1 paper)Nature Genetics (1 paper)Journal of Clinical Laboratory Analysis (1 paper)Journal of Medical Genetics (1 paper)
- Partner nations
- South AfricaUnited KingdomItaly
In The Last Decade
S Jansen
12 papers receiving 209 citations
Peers
Comparison fields: 5 of 46
- Cancer Research 40
- Molecular Biology 156
- Genetics 60
- Hematology 10
- Cell Biology 15
Countries citing papers authored by S Jansen
This map shows the geographic impact of S Jansen'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 S Jansen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites S Jansen more than expected).
Fields of papers citing papers by S Jansen
This network shows the impact of papers produced by S Jansen. 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 S Jansen. The network helps show where S Jansen may publish in the future.
Co-authors
The 25 scholars most cited alongside S Jansen, 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 | 2001 | 84 | |
| 2 | 1995 | 78 | |
| 3 | 1994 | 13 | |
| 4 | 1998 | 10 | |
| 5 | 2001 | 9 | |
| 6 | Turner/Down mosaicism. A case report. | 1991 | 6 |
| 7 | 1992 | 5 | |
| 8 | 1994 | 4 | |
| 9 | Early thyroidectomy for medullary thyroid carcinoma in children and young adults with the multiple endocrine neoplasia type 2A (MEN 2A) syndrome. | 1991 | 3 |
| 10 | A 3-year cytogenetic survey of 9 661 patients in South Africa. | 1983 | 2 |
| 11 | Multiple endocrine neoplasia type 2A (MEN 2A) syndrome in a South African family. Biochemistry and molecular genetics. | 1991 | 2 |
| 12 | 2002 | 1 | |
| 13 | Evaluation of a family at risk for the multiple endocrine neoplasia type 2A (MEN 2A) syndrome. | 1991 | 0 |
About S Jansen
S Jansen is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Epidemiology and Surgery, having authored 13 papers that have together received 217 indexed citations. Recurring topics across this work include DNA Repair Mechanisms (3 papers), Neuroendocrine Tumor Research Advances (3 papers), Genomic variations and chromosomal abnormalities (3 papers), BRCA gene mutations in cancer (2 papers), Chromosomal and Genetic Variations (2 papers), Neuroblastoma Research and Treatments (2 papers), Prenatal Screening and Diagnostics (2 papers) and Thyroid Cancer Diagnosis and Treatment (2 papers). The work is most often cited by research in Cancer Research (40 citations), Molecular Biology (156 citations), Genetics (60 citations), Hematology (10 citations) and Cell Biology (15 citations). S Jansen has collaborated with scholars based in South Africa, United Kingdom and Italy. Frequent co-authors include Charmaine Havenga, Thomy de Ravel, Rachel A. Gibson, Neil V. Morgan, Hans Joenje, Christopher G. Mathew, L. P. Kuyt, Éliane Gluckman, Irene Roberts and Deborah Ford. Their work appears in journals such as Nuclear Medicine Communications, Proceedings of the National Academy of Sciences, Nature Genetics, Journal of Clinical Laboratory Analysis and Journal of Medical Genetics.
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.