Stander Jansen
Impact in
- Genetics top 10%
- Blood disorders and treatments
- Genomics and Rare Diseases
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
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- DNA Repair Mechanisms
- Cell death mechanisms and regulation
Papers in
- Genetics 7
- Blood disorders and treatments 5
- Genomic variations and chromosomal abnormalities 2
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 1
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- Thyroid Cancer Diagnosis and Treatment 4
- Co-authors
- Charmaine Havenga (4 shared papers)Rachel A. Gibson (3 shared papers)Thomy J.L. de Ravel (3 shared papers)Hans Joenje (2 shared papers)Christopher George Mathew (3 shared papers)Neil V. Morgan (2 shared papers)L. P. Kuyt (1 shared paper)Alex J. Tipping (1 shared paper)
- Journals
- Nature Genetics (2 papers)Journal of Clinical Laboratory Analysis (1 paper)Blood (1 paper)Nuclear Medicine Communications (1 paper)Human Mutation (1 paper)
- Partner nations
- South AfricaUnited KingdomNetherlands
In The Last Decade
Stander Jansen
15 papers receiving 672 citations
Peers
Comparison fields: 5 of 41
- Genetics 336
- Molecular Biology 495
- Hematology 55
- Developmental Biology 4
- Endocrinology, Diabetes and Metabolism 12
Countries citing papers authored by Stander Jansen
This map shows the geographic impact of Stander 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 Stander Jansen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stander Jansen more than expected).
Fields of papers citing papers by Stander Jansen
This network shows the impact of papers produced by Stander 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 Stander Jansen. The network helps show where Stander Jansen may publish in the future.
Co-authors
The 25 scholars most cited alongside Stander 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 | 1996 | 248 | |
| 2 | 2000 | 185 | |
| 3 | 2001 | 97 | |
| 4 | 1995 | 77 | |
| 5 | 1996 | 38 | |
| 6 | 1994 | 13 | |
| 7 | 1998 | 11 | |
| 8 | 2001 | 9 | |
| 9 | Turner/Down mosaicism. A case report. | 1991 | 6 |
| 10 | 1992 | 6 | |
| 11 | 1994 | 5 | |
| 12 | Early thyroidectomy for medullary thyroid carcinoma in children and young adults with the multiple endocrine neoplasia type 2A (MEN 2A) syndrome. | 1991 | 3 |
| 13 | A 3-year cytogenetic survey of 9 661 patients in South Africa. | 1983 | 2 |
| 14 | Multiple endocrine neoplasia type 2A (MEN 2A) syndrome in a South African family. Biochemistry and molecular genetics. | 1991 | 2 |
| 15 | 2002 | 1 | |
| 16 | Evaluation of a family at risk for the multiple endocrine neoplasia type 2A (MEN 2A) syndrome. | 1991 | 0 |
About Stander Jansen
Stander Jansen is a scholar working on Genetics, Endocrinology, Diabetes and Metabolism, Molecular Biology, Radiology, Nuclear Medicine and Imaging and Nephrology, having authored 16 papers that have together received 703 indexed citations. Recurring topics across this work include DNA Repair Mechanisms (7 papers), Blood disorders and treatments (5 papers), Thyroid Cancer Diagnosis and Treatment (4 papers), Genomic variations and chromosomal abnormalities (2 papers), Neuroendocrine Tumor Research Advances (2 papers), Down syndrome and intellectual disability research (1 paper), Adrenal and Paraganglionic Tumors (1 paper) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (1 paper). The work is most often cited by research in Genetics (336 citations), Molecular Biology (495 citations), Hematology (55 citations), Developmental Biology (4 citations) and Endocrinology, Diabetes and Metabolism (12 citations). Stander Jansen has collaborated with scholars based in South Africa, United Kingdom and Netherlands. Frequent co-authors include Charmaine Havenga, Rachel A. Gibson, Thomy J.L. de Ravel, Hans Joenje, Christopher George Mathew, Neil V. Morgan, L. P. Kuyt, Alex J. Tipping, Éliane Gluckman and Deborah Ford. Their work appears in journals such as Nature Genetics, Journal of Clinical Laboratory Analysis, Blood, Nuclear Medicine Communications and Human Mutation.
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.