The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.
GERMLINE p53 MUTATIONS AND HERITABLE CANCER
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In the citing paper
“Germline TP53 mutations have been found in patients with Li–Fraumeni syndrome (LFS), an autosomal dominant cancer predisposition syndrome characterized by the early onset of a spectrum of childhood and adulthood cancers, including adrenocortical carcinomas, soft tissue sarcomas, osteosarcomas, brain tumors, and pre‐menopausal breast cancer [123, 124, 125].”
From The TP53 tumor suppressor gene: From molecular biology to clinical investigations (2025) · cites this paper as [125]
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Citations
Cites
Lane, D. P. (1992) · Nature · doi:10.1038/358015a0 · Cited by 5,138
Wild-type p53 activates transcription in vitro
Farmer, G., Bargonetti, J., Zhu, H., Friedman, P., Prywes, R., & Prives, C. (1992) · Nature · doi:10.1038/358083a0 · Cited by 579
Cited by
Understanding breast cancer risk - where do we stand in 2005?
Dumitrescu, R. G., & Cotarla, I. (2005) · Journal of Cellular and Molecular Medicine · doi:10.1111/j.1582-4934.2005.tb00350.x · Cited by 502
Genetic susceptibility to breast cancer
Mavaddat, N., Antoniou, A. C., Easton, D. F., & Garcia-Closas, M. (2010) · Molecular Oncology · doi:10.1016/j.molonc.2010.04.011 · Cited by 375
Effects of genetic background on tumorigenesis in p53‐deficient mice
Donehower, L. A., Harvey, M., Vogel, H., McArthur, M. J., Montgomery, C. A., Park, S. H., Thompson, T., Ford, R. J., & Bradley, A. (1995) · Molecular Carcinogenesis · doi:10.1002/mc.2940140105 · Cited by 252
The TP53 tumor suppressor gene: From molecular biology to clinical investigations
Baliakas, P., & Soussi, T. (2025) · Journal of Internal Medicine · doi:10.1111/joim.20106 · Cited by 50
Metadata
- Authors
- Malkin, D.
- Affiliations
- Division of Oncology, Department of Pediatrics, The Hospital for Sick Children, Toronto, Ontario, Canada
- Venue
- Annual Review of Genetics
- Publisher
- Annual Reviews
- Published
- 1994-12
- Volume
- 28
- Issue
- 1
- Pages
- 443-465
- ISSN
- 0066-4197
- 1545-2948
- Cited by
- 59
- References
- 2
- Language
- en
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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
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- This page
- CoChat. (2026). Citation check: GERMLINE p53 MUTATIONS AND HERITABLE CANCER. https://app.cochat.ai/papers/10.1146/annurev.ge.28.120194.002303
- The paper
- Malkin, D. (1994). GERMLINE p53 MUTATIONS AND HERITABLE CANCER. Annual Review of Genetics. https://doi.org/10.1146/annurev.ge.28.120194.002303
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.
