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Cited by 381

The DOI matches its Crossref record; 115 of the 115 references it cites were found in a registry or an index.

Susceptibility Pathways in Fanconi's Anemia and Breast Cancer

Open access
D'Andrea, Alan D.·2010·New England Journal of Medicine

Abstract

Fanconi's anemia is a rare disorder that arises from defective repair of damaged DNA. Of the 13 Fanconi's anemia genes, 3 are breast-cancer–susceptibility genes. One is identical to BRCA2. Cells from patients with the D1 subtype of Fanconi's anemia and their family members carry biallelic mutations in BRCA2, and heterozygote members of kindreds with the D1 subtype have an increased risk of breast and ovarian cancer. Studies of a rare disorder can thus illuminate a common disorder.

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Metadata

Authors
D'Andrea, A. D.
Venue
New England Journal of Medicine
Published
2010-05-20
Volume
362
Issue
20
Pages
1909-1919
ISSN
  • 0028-4793 (ISSN-L)
  • 1533-4406
OpenAlex
W2052215590
Cited by
381
References
115
FWCI
23.14
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Susceptibility Pathways in Fanconi's Anemia and Breast Cancer. https://app.cochat.ai/papers/10.1056/nejmra0809889
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D'Andrea, A. D. (2010). Susceptibility Pathways in Fanconi's Anemia and Breast Cancer. New England Journal of Medicine. https://doi.org/10.1056/nejmra0809889

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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.