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Cited by 175

The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.

BRCA1, BRCA2 and TP53 mutations in very early-onset breast cancer with associated risks to relatives

Lalloo, Fiona, Varley, Jennifer, Moran, Anthony, Ellis, David, O’Dair, Lindsay, Pharoah, Paul, Antoniou, Antonis, Hartley, Roger, Shenton, Andrew, Seal, Sheila, Bulman, Barbara, Howell, Anthony, Evans, D. Gareth R.·2006·European Journal of Cancer
DOI 10.1016/j.ejca.2005.11.032
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Citations

Cites

Research works printed but not linked: 24

  1. Ford, 1998, Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families, Am J Hum Genet, 62, 676, 10.1086/301749 · DOI · Paper page
  2. Li, 1982, Prospective study of a cancer family syndrome, JAMA, 247, 2692, 10.1001/jama.1982.03320440040031 · DOI · Paper page
  3. Gayther, 1998, The genetics of inherited breast cancer, J Mamm Gland Biol Neopasia, 3, 365, 10.1023/A:1018779830743 · DOI
  4. Varley, 1997, Germ-line mutations of TP53 in Li–Fraumeni families: an extended study of 39 families, Cancer Res, 14, 865
  5. Fitzgerald, 1996, Germ-line BRCA1 mutations in jewish and non-jewish women with early-onset breast cancer, N Engl J Med, 334, 143, 10.1056/NEJM199601183340302 · DOI · Paper page
  6. Peto, 1999, Prevalence of BRCA1 and BRCA2 gene mutations in patients with early onset breast cancer, J Natl Cancer Inst, 91, 943, 10.1093/jnci/91.11.943 · DOI · Paper page
  7. Loman, 2001, Family history of breast and ovarian cancers and BRCA1 and BRCA2 mutations in a population-based series of early onset breast cancer, J Natl Cancer Inst, 93, 1215, 10.1093/jnci/93.16.1215 · DOI
  8. Krainer, 1997, Differential contributions of BRCA1 and BRCA2 to early onset breast cancer, N Engl J Med, 336, 1416, 10.1056/NEJM199705153362003 · DOI · Paper page
  9. Sidransky, 1992, Inherited p53 gene mutations in breast cancer, Cancer Res, 52, 2984
  10. van Der Luijt, 1994, Rapid detection of translation-terminating mutations at the adenomatous polyposis coli (APC) gene by direct protein truncation test, Genomics, 20, 1u, 10.1006/geno.1994.1119 · DOI · Paper page
  11. Orita, 1989, Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms, Proc Natl Acad Sci USA, 86, 2766, 10.1073/pnas.86.8.2766 · DOI · Paper page
  12. Ellis, 2000, Low prevalence of germline BRCA1 mutations in early onset sporadic breast cancer, J Med Genet, 37, 792, 10.1136/jmg.37.10.792 · DOI
  13. Rowley, 1995, Ultrarapid mutation detection by muliplex, solidphase chemical cleavage, Genomics, 30, 574, 10.1006/geno.1995.1279 · doi:10.1006/geno.1995.1279
  14. Lange, 1988, Programs for Pedigree Analysis: MENDEL, FISHER, and dGENE, Genet Epidemiol, 5, 471, 10.1002/gepi.1370050611 · DOI · Paper page
  15. de Sanjose, 2003, Prevalence of BRCA1 and BRCA2 germline mutations in young breast cancer patients: a population-based study, Int J Cancer, 106, 588, 10.1002/ijc.11271 · DOI
  16. Easton, 1993, Breast cancer linkage consortium. Genetic linkage analysis in familial breast and ovarian cancer: results from 214 families, Am J Hum Genet, 52, 678
  17. Narod, 1995, An evaluation of genetic heterogeneity in 145 breast–ovarian cancer families, Am J Hum Genet, 56, 254
  18. Börresen, 1992, Screening for germline TP53 mutations in breast cancer patients, Cancer Res, 52, 3234
  19. Sedlacek, 1998, Two Li–Fraumeni syndrome families with novel germline p53 mutations: loss of the wild-type p53 allele in only 50% of tumours, Br J Cancer, 77, 1034, 10.1038/bjc.1998.172 · DOI
  20. Chompret, 2000, P53 germline mutations in childhood cancers and cancer risk for carrier individuals, Br J Cancer, 82, 1932
  21. Anglian Breast Cancer Study Group, 2000, Prevalence and penetrance of BRCA1 and BRCA2 in a population based series of breast cancer cases, Br J Cancer, 83, 1301, 10.1054/bjoc.2000.1407 · DOI · Paper page
  22. Hopper, 1999, Population based estimate of the average age-specific cumulative risk of breast cancer for a defined set of protein-truncating mutations in BRCA1 and BRCA2. Australian Breast Cancer Family Study, Cancer Epidemiol Biomarkers Prev, 8, 741
  23. Li, 1988, A cancer family syndrome in twenty-four kindreds, Cancer Res, 48, 5358
  24. Birch, 1994, Prevalence and diversity of constitutional mutations in the p53 gene among 21 Li–Fraumeni families, Cancer Res, 54, 1298

Cited by

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Metadata

Authors
Lalloo, F., Varley, J., Moran, A., Ellis, D., O’Dair, L., Pharoah, P., Antoniou, A., Hartley, R., Shenton, A., Seal, S., Bulman, B., Howell, A., & Evans, D. G. R.
Venue
European Journal of Cancer
Publisher
Elsevier BV
Published
2006-05
Volume
42
Issue
8
Pages
1143-1150
ISSN
0959-8049 (ISSN-L)
DOI
10.1016/j.ejca.2005.11.032
OpenAlex
W1999479708
Cited by
175
References
2
FWCI
4.77
Type
journal article
Language
en
Open access
closed
Licence
www.elsevier.com/tdm/userlicense/1.0/ (tdm)

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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.