S Jansen

854 citations
14 papers · 216 · h-index 6

Impact in

    • Carcinogens and Genotoxicity Assessment
    • BRCA gene mutations in cancer
    • Genomic variations and chromosomal abnormalities

Papers in

    • DNA Repair Mechanisms 3
    • Genomic variations and chromosomal abnormalities 3
    • BRCA gene mutations in cancer 2

S Jansen

12 papers receiving 209 citations

Peers

S Jansen
Comparison fields: 5 of 47
  • Cancer Research 44
  • Genetics 65
  • Molecular Biology 159
  • Hematology 11
  • Cell Biology 16
Replace M. Murer‐Orlando with:
M. Murer‐Orlando United Kingdom
Laurence Meyer United States
Chi‐Fan Yang Taiwan
Dai‐Ying Wu United States
William F. Richter United States
Kayla Smith United States
Sarah G. Swygert United States
Amanda E. Conway United States
Christine Scamps France
Daniel S. Gerke United States
S Jansen relative to M. Murer‐Orlando United Kingdom M. Murer‐Orlando's profile →
Citations per field
00.5×
M. Murer‐Orlando · 1×
Citations per year

Countries citing papers authored by S Jansen

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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.

Border = papers with S Jansen Line = papers co-authored together S Jansen links everyone, so they are left out of the graph.

All Works

14 of 14 papers shown
#Work
1 200183
2 199578
3 199413
4 199810
5 20019
6
Turner/Down mosaicism. A case report.
19916
7 19925
8 19944
9
Early thyroidectomy for medullary thyroid carcinoma in children and young adults with the multiple endocrine neoplasia type 2A (MEN 2A) syndrome.
19913
10
A 3-year cytogenetic survey of 9 661 patients in South Africa.
19832
11
Multiple endocrine neoplasia type 2A (MEN 2A) syndrome in a South African family. Biochemistry and molecular genetics.
19912
12 20021
13 20250
14
Evaluation of a family at risk for the multiple endocrine neoplasia type 2A (MEN 2A) syndrome.
19910

About S Jansen

S Jansen is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Epidemiology and Surgery, having authored 14 papers that have together received 216 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), Radiation Dose and Imaging (2 papers), Neuroblastoma Research and Treatments (2 papers), Prenatal Screening and Diagnostics (2 papers), Thyroid Cancer Diagnosis and Treatment (2 papers) and BRCA gene mutations in cancer (2 papers). The work is most often cited by research in Cancer Research (44 citations), Genetics (65 citations), Molecular Biology (159 citations), Hematology (11 citations) and Cell Biology (16 citations). S Jansen has collaborated with scholars based in South Africa, United Kingdom and Netherlands. Frequent co-authors include Charmaine Havenga, Thomy de Ravel, Rachel A. Gibson, Christopher G. Mathew, Hans Joenje, Neil V. Morgan, L. P. Kuyt, Éliane Gluckman, Anna Savoia and Deborah Ford. Their work appears in journals such as Nature Genetics, Proceedings of the National Academy of Sciences, Journal of Medical Genetics, Nuclear Medicine Communications and Journal of Clinical Laboratory Analysis.

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.

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