The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
Determining Carrier Probabilities for Breast Cancer–Susceptibility Genes BRCA1 and BRCA2
Open accessOverview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Gail, M. H., Brinton, L. A., Byar, D. P., Corle, D. K., Green, S. B., Schairer, C., & Mulvihill, J. J. (1989) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/81.24.1879 · Cited by 3,334
Research works printed but not linked: 25
- Andersen, 1996, Genetic heterogeneity in breast cancer susceptibility, Acta Oncol, 35, 407, 10.3109/02841869609109913 · DOI
- Berry, 1997, Assessing the probability of carrying a breast cancer gene BRCA1 based on family history, J Natl Cancer Inst, 89, 9, 10.1093/jnci/89.3.227 · DOI · Paper page
- Claus, 1991, Genetic analysis of breast cancer in the Cancer and Steroid Hormone Study, Am J Hum Genet, 48, 232
- Claus, 1994, Autosomal dominant inheritance of early-onset breast cancer: implications for risk prediction, Cancer, 73, 643, 10.1002/1097-0142(19940201)73:3<643::AID-CNCR2820730323>3.0.CO;2-5 · DOI · Paper page
- Couch, 1997, BRCA1 mutations in women attending clinics that evaluate the risk of breast cancer, N Engl J Med, 336, 1409, 10.1056/NEJM199705153362002 · DOI · Paper page
- Easton, 1995, Breast and ovarian cancer incidence in BRCA1-mutation carriers, Am J Hum Genet, 56, 265
- Easton, 1997, Cancer risks in two large breast cancer families linked to BRCA2 on chromosome 13q12-13, Am J Hum Genet, 61, 120, 10.1086/513891 · DOI · Paper page
- Ford, 1995, The genetics of breast and ovarian cancer, Br J Cancer, 72, 805, 10.1038/bjc.1995.417 · DOI · Paper page
- Futreal, 1994, BRCA1 mutations in primary breast and ovarian carcinomas, Science, 226, 120, 10.1126/science.7939630 · DOI · Paper page
- Håkansson, 1997, Moderate frequency of BRCA1 and BRCA2 germ-line mutations in Scandinavian familial breast cancer, Am J Hum Genet, 60, 1068
- Hoskins, 1995, Assessment and counseling for women with a family history of breast cancer: a guide for clinicians, JAMA, 273, 577, 10.1001/jama.1995.03520310075033 · DOI · Paper page
- Houwing-Duistermaat, 1997, A family history score for breast cancer, Genet Epidemiol, 14, 530
- Leal, 1994, A likelihood approach to calculating risk support interval, Am J Hum Genet, 54, 913
- Miki, 1994, A strong candidate for the breast and ovarian cancer susceptibility: gene BRCA1, Science, 266, 66, 10.1126/science.7545954 · DOI · Paper page
- Moolgavkar, 1979, Effect of age on incidence of breast cancer in females, J Natl Cancer Inst, 62, 493, 10.1093/jnci/62.3.493 · DOI
- Murphy, 1969, The application of Bayesian methods in genetic counseling, Hum Hered, 19, 126, 10.1159/000152210 · doi:10.1159/000152210
- Oddoux, 1996, The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1%, Nat Genet, 14, 188, 10.1038/ng1096-188 · DOI · Paper page
- Roa, 1996, Ashkenazi Jewish population frequencies for common mutations in BRCA1 and BRCA2, Nat Genet, 14, 185, 10.1038/ng1096-185 · DOI · Paper page
- Shattuck-Eidens, 1995, A collaborative survey of 80 mutations in the BRCA1 breast and ovarian cancer susceptibility gene: implications for presymptomatic testing and screening, JAMA, 273, 535, 10.1001/jama.1995.03520310033026 · DOI · Paper page
- Struewing, 1997, The risk of cancer associated with specific mutations of BRCA1 and BRCA2 among Ashkenazi Jews, N Engl J Med, 336, 1401, 10.1056/NEJM199705153362001 · DOI · Paper page
- Szabo, 1997, Population genetics of BRCA1 and BRCA2, Am J Hum Genet, 60, 1013
- Thompson, 1991, Evaluation of likelihood ratios for complex genetic models, IMA J Math Appl Med Biol, 8, 149, 10.1093/imammb/8.3.149 · DOI
- Vehmanen, 1997, A low proportion of BRCA2 mutations in Finnish breast cancer families, Am J Hum Genet, 60, 1050
- Wooster, 1995, Identification of the breast cancer susceptibility gene BRCA2, Nature, 378, 789, 10.1038/378789a0 · DOI · Paper page
- Yancik, 1993, Ovarian cancer: age contrasts in incidence, histology, disease stage at diagnosis, and mortality, Cancer, 71, 517
Cited by
American Cancer Society Guidelines for Breast Screening with MRI as an Adjunct to Mammography
Saslow, D., Boetes, C., Burke, W., Harms, S., Leach, M. O., Lehman, C. D., Morris, E., Pisano, E., Schnall, M., Sener, S., et al. (2007) · CA: A Cancer Journal for Clinicians · doi:10.3322/canjclin.57.2.75 · Cited by 2,637
Meta-Analysis of BRCA1 and BRCA2 Penetrance
Chen, S., & Parmigiani, G. (2007) · Journal of Clinical Oncology · doi:10.1200/jco.2006.09.1066 · Cited by 1,802
Self-citationA breast cancer prediction model incorporating familial and personal risk factors
Tyrer, J., Duffy, S. W., & Cuzick, J. (2004) · Statistics in Medicine · doi:10.1002/sim.1668 · Cited by 1,345
Key steps for effective breast cancer prevention
Britt, K. L., Cuzick, J., & Phillips, K.-A. (2020) · Nature Reviews Cancer · doi:10.1038/s41568-020-0266-x · Cited by 992
American Cancer Society Guidelines for Breast Cancer Screening: Update 2003
Smith, R. A., Saslow, D., Andrews Sawyer, K., Burke, W., Costanza, M. E., Evans, W. P., Foster, R. S., Hendrick, E., Eyre, H. J., & Sener, S. (2003) · CA: A Cancer Journal for Clinicians · doi:10.3322/canjclin.53.3.141 · Cited by 770
Metadata
- Authors
- Parmigiani, G., Berry, D. A., & Aguilar, O.
- Venue
- The American Journal of Human Genetics
- Publisher
- Elsevier BV
- Published
- 1998-01
- Volume
- 62
- Issue
- 1
- Pages
- 145-158
- ISSN
- 0002-9297 (ISSN-L)
- OpenAlex
- W2005351661
- Cited by
- 753
- References
- 1
- FWCI
- 11.19
- Type
- journal article
- Language
- en
- Open access
- bronze
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (vor, 5678 d)
About these checks
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.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: Determining Carrier Probabilities for Breast Cancer–Susceptibility Genes BRCA1 and BRCA2. https://app.cochat.ai/papers/10.1086/301670
- The paper
- Parmigiani, G., Berry, D. A., & Aguilar, O. (1998). Determining Carrier Probabilities for Breast Cancer–Susceptibility Genes BRCA1 and BRCA2. The American Journal of Human Genetics. https://doi.org/10.1086/301670
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.
