Found: 29
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Breast cancer risk in BRCA1 and BRCA2 mutation carriers and polyglutamine repeat length in the AIB1 gene.
- Published in:
- International Journal of Cancer, 2005, v. 117, n. 2, p. 230, doi. 10.1002/ijc.21176
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- Article
Comparison of the Screening Practices of Unaffected Noncarriers under 40 and between 40 and 49 in BRCA1/2 Families.
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- Journal of Genetic Counseling, 2013, v. 22, n. 4, p. 469, doi. 10.1007/s10897-012-9569-8
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- Article
Cancer Risks Associated With Germline Mutations in MLH1, MSH2, and MSH6 Genes in Lynch Syndrome.
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- JAMA: Journal of the American Medical Association, 2011, v. 305, n. 22, p. 2304, doi. 10.1001/jama.2011.743
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- Article
Next-generation sequencing for the diagnosis of hereditary breast and ovarian cancer using genomic capture targeting multiple candidate genes.
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- European Journal of Human Genetics, 2014, v. 22, n. 11, p. 1305, doi. 10.1038/ejhg.2014.16
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- Article
Contribution of bioinformatics predictions and functional splicing assays to the interpretation of unclassified variants of the BRCA genes.
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- European Journal of Human Genetics, 2011, v. 19, n. 10, p. 1052, doi. 10.1038/ejhg.2011.100
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- Article
Cancer risk management strategies and perceptions of unaffected women 5 years after predictive genetic testing for BRCA1/2 mutations.
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- European Journal of Human Genetics, 2011, v. 19, n. 5, p. 500, doi. 10.1038/ejhg.2010.241
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- Article
Breast and ovarian cancer screening of non-carriers from BRCA1/2 mutation-positive families: 2-year follow-up of cohorts from France and Quebec.
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- European Journal of Human Genetics, 2011, v. 19, n. 5, p. 494, doi. 10.1038/ejhg.2010.227
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- Publication type:
- Article
Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3.
- Published in:
- Breast Cancer Research & Treatment, 2017, v. 161, n. 1, p. 117, doi. 10.1007/s10549-016-4018-2
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- Article
Mutation analysis of PALB2 gene in French breast cancer families.
- Published in:
- Breast Cancer Research & Treatment, 2015, v. 154, n. 3, p. 463, doi. 10.1007/s10549-015-3625-7
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- Article
Risk-reducing salpingo-oophorectomy, natural menopause, and breast cancer risk: an international prospective cohort of BRCA1 and BRCA2 mutation carriers.
- Published in:
- 2020
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- Publication type:
- journal article
Cost-effectiveness evaluation of pre-counseling telephone interviews before face-to-face genetic counseling in cancer genetics.
- Published in:
- Familial Cancer, 2018, v. 17, n. 3, p. 451, doi. 10.1007/s10689-017-0049-z
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- Publication type:
- Article
BRCA1 allele-specific expression in genetic predisposed breast/ovarian cancer.
- Published in:
- Familial Cancer, 2017, v. 16, n. 2, p. 167, doi. 10.1007/s10689-016-9940-2
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- Article
Uptake of a randomized breast cancer prevention trial comparing letrozole to placebo in BRCA1/ 2 mutations carriers: the LIBER trial.
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- Familial Cancer, 2012, v. 11, n. 1, p. 77, doi. 10.1007/s10689-011-9484-4
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- Publication type:
- Article
Associations of height, body mass index, and weight gain with breast cancer risk in carriers of a pathogenic variant in BRCA1 or BRCA2: the BRCA1 and BRCA2 Cohort Consortium.
- Published in:
- Breast Cancer Research, 2023, v. 25, n. 1, p. 1, doi. 10.1186/s13058-023-01673-w
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- Publication type:
- Article
Diagnostic chest X-rays and breast cancer risk among women with a hereditary predisposition to breast cancer unexplained by a BRCA1 or BRCA2 mutation.
- Published in:
- 2021
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- Publication type:
- journal article
EPAS1‐mutated paragangliomas associated with haemoglobin disorders.
- Published in:
- British Journal of Haematology, 2024, v. 204, n. 3, p. 1054, doi. 10.1111/bjh.19278
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- Article
How and when to refer patients for oncogenetic counseling in the era of PARP inhibitors.
- Published in:
- Therapeutic Advances in Medical Oncology, 2020, v. 12, p. 1, doi. 10.1177/1758835919897530
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- Article
Patients’ characteristics and rate of Internet use to obtain cancer information.
- Published in:
- Journal of Public Health, 2006, v. 28, n. 3, p. 235, doi. 10.1093/pubmed/fdl019
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- Article
A new mutation in the BRCA1 gene (g.5196-5201del6, 5195-5202ins12), a 6 bp deletion replaced by the duplication of a 12 bp adjacent upstream intronic sequence.
- Published in:
- Human Mutation, 2001, v. 17, n. 2, p. 154, doi. 10.1002/1098-1004(200102)17:2<154::AID-HUMU12>3.0.CO;2-O
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- Publication type:
- Article
Risk of second primary cancer following differentiated thyroid cancer.
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- European Journal of Nuclear Medicine & Molecular Imaging, 2004, v. 31, n. 5, p. 685, doi. 10.1007/s00259-003-1448-y
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- Publication type:
- Article
Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 women.
- Published in:
- 2016
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- Publication type:
- journal article
Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 women.
- Published in:
- Breast Cancer Research, 2016, v. 18, p. 1, doi. 10.1186/s13058-016-0768-3
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- Publication type:
- Article
Variation in breast cancer risk associated with factors related to pregnancies according to truncating mutation location, in the French National BRCA1 and BRCA2 mutations carrier cohort (GENEPSO).
- Published in:
- 2012
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- Publication type:
- journal article
The contribution of large genomic deletions at the CDKN2A locus to the burden of familial melanoma.
- Published in:
- 2008
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- Publication type:
- journal article
Two novel variants in the 3′UTR of the BRCA1 gene in familial breast and/or ovarian cancer.
- Published in:
- 2011
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- Publication type:
- Report
Novel germline MET pathogenic variants in French patients with papillary renal cell carcinomas type I.
- Published in:
- Human Mutation, 2022, v. 43, n. 3, p. 316, doi. 10.1002/humu.24313
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- Publication type:
- Article
Uptake of genetic counseling among adult children of BRCA1/2 mutation carriers in France.
- Published in:
- 2019
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- Publication type:
- journal article
Which factors predict proposal and uptake of psychological counselling after BRCA1/2 test result disclosure?
- Published in:
- Psycho-Oncology, 2014, v. 23, n. 4, p. 420, doi. 10.1002/pon.3435
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- Publication type:
- Article
Targeted Sequencing of the Mitochondrial Genome of Women at High Risk of Breast Cancer without Detectable Mutations in BRCA1/2.
- Published in:
- PLoS ONE, 2015, v. 10, n. 9, p. 1, doi. 10.1371/journal.pone.0136192
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- Article