The DOI matches its Crossref record.
MSH2 genomic deletions are a frequent cause of HNPCC
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Citations
Cited by
Umar, A., Boland, C. R., Terdiman, J. P., Syngal, S., Chapelle, A. D. L., Ruschoff, J., Fishel, R., Lindor, N. M., Burgart, L. J., Hamelin, R., et al. (2004) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/djh034 · Cited by 3,183
Self-citationSchouten, J. P. (2002) · Nucleic Acids Research · doi:10.1093/nar/gnf056 · Cited by 2,699
Microsatellite Instability in Colorectal Cancer
Boland, C. R., & Goel, A. (2010) · Gastroenterology · doi:10.1053/j.gastro.2009.12.064 · Cited by 2,456
Population-Based Molecular Detection of Hereditary Nonpolyposis Colorectal Cancer
Salovaara, R., Loukola, A., Kristo, P., Kääriäinen, H., Ahtola, H., Eskelinen, M., Härkönen, N., Julkunen, R., Kangas, E., Ojala, S., et al. (2000) · Journal of Clinical Oncology · doi:10.1200/jco.2000.18.11.2193 · Cited by 516
MLPA and MAPH: New techniques for detection of gene deletions
Sellner, L. N., & Taylor, G. R. (2004) · Human Mutation · doi:10.1002/humu.20035 · Cited by 291
Metadata
- Authors
- Wijnen, J., van der Klift, H., Vasen, H., Khan, P. M., Menko, F., Tops, C., Meijers Heijboer, H., Lindhout, D., Møller, P., & Fodde., R.
- Venue
- Nature Genetics
- Published
- 1998-12
- Volume
- 20
- Issue
- 4
- Pages
- 326-328
- ISSN
- 1061-4036 (ISSN-L)
- 1546-1718
- DOI
- 10.1038/3795
- OpenAlex
- W1534626339
- Cited by
- 230
- References
- 0
- FWCI
- 7.27
- Type
- journal article
- Language
- en
- Open access
- closed
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Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: MSH2 genomic deletions are a frequent cause of HNPCC. https://app.cochat.ai/papers/10.1038/3795
- The paper
- Wijnen, J., van der Klift, H., Vasen, H., Khan, P. M., Menko, F., Tops, C., Meijers Heijboer, H., Lindhout, D., Møller, P., & Fodde., R. (1998). MSH2 genomic deletions are a frequent cause of HNPCC. Nature Genetics. https://doi.org/10.1038/3795
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
