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Cited by 697

The DOI matches its Crossref record; 18 of the 18 references it cites were found in a registry or an index.

Hereditary Cancer Predisposition Syndromes

Garber, Judy E., Offit, Kenneth·2005·Journal of Clinical Oncology

Abstract

Cancer genetics is increasingly becoming integrated into the practice of modern medical oncology. The ability to distinguish a growing proportion of the 5% to 10% of all cancers that develop in individuals who have inherited a genetic mutation conferring heightened susceptibility to specific cancers may permit targeted efforts in cancer surveillance and prevention. While these individuals comprise a small proportion of the overall burden of cancer, strategies successful in reducing their remarkable cancer risks may be generalizable to the broader population. In this review, we highlight the most common hereditary cancer syndromes, most attributable to genes inherited in an autosomal dominant manner with incomplete penetrance, and a number of rare syndromes in which particular progress has been made. The prevalence, penetrance, tumor spectrum, and underlying genetic defects are discussed and summarized in a large table in which a more comprehensive enumeration of syndromes is provided.

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Metadata

Authors
Garber, J. E., & Offit, K.
Venue
Journal of Clinical Oncology
Published
2005-01-10
Volume
23
Issue
2
Pages
276-292
ISSN
  • 0732-183X (ISSN-L)
  • 1527-7755
OpenAlex
W2089155477
Cited by
697
References
18
FWCI
17.65
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Hereditary Cancer Predisposition Syndromes. https://app.cochat.ai/papers/10.1200/jco.2005.10.042
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Garber, J. E., & Offit, K. (2005). Hereditary Cancer Predisposition Syndromes. Journal of Clinical Oncology. https://doi.org/10.1200/jco.2005.10.042

Data sources

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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.