Found: 56
Select item for more details and to access through your institution.
Risk-reducing salpingo-oophorectomy in BRCA1 and BRCA2 mutation carriers.
- Published in:
- Archives of Gynecology & Obstetrics, 2011, v. 283, n. 3, p. 623, doi. 10.1007/s00404-010-1476-3
- By:
- Publication type:
- Article
Implementing mainstream genetic counseling within the area‐wide network of the German Consortium Hereditary Breast and Ovarian Cancer (GC‐HBOC): Satisfaction of primary care providers with the provided state‐of‐the‐art training by the Cologne Center
- Published in:
- Journal of Genetic Counseling, 2024, v. 33, n. 1, p. 206, doi. 10.1002/jgc4.1870
- By:
- Publication type:
- Article
Prevalence of pathogenic BRCA1/2 germline mutations among 802 women with unilateral triple-negative breast cancer without family cancer history.
- Published in:
- 2018
- By:
- Publication type:
- journal article
A tandem duplication of BRCA1 exons 1-19 through DHX8 exon 2 in four families with hereditary breast and ovarian cancer syndrome.
- Published in:
- Breast Cancer Research & Treatment, 2018, v. 172, n. 3, p. 561, doi. 10.1007/s10549-018-4957-x
- By:
- Publication type:
- Article
Substantial evidence for the clinical significance of missense variant BRCA1 c.5309G>T p.(Gly1770Val).
- Published in:
- Breast Cancer Research & Treatment, 2018, v. 172, n. 2, p. 497, doi. 10.1007/s10549-018-4903-y
- By:
- Publication type:
- Article
Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene.
- Published in:
- Nature Genetics, 2010, v. 42, n. 5, p. 410, doi. 10.1038/ng.569
- By:
- Publication type:
- Article
Analysis of 30 Putative BRCA1 Splicing Mutations in Hereditary Breast and Ovarian Cancer Families Identifies Exonic Splice Site Mutations That Escape In Silico Prediction.
- Published in:
- PLoS ONE, 2012, v. 7, n. 12, p. 1, doi. 10.1371/journal.pone.0050800
- By:
- Publication type:
- Article
Association of Prolactin and Its Receptor Gene Regions with Familial Breast Cancer.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2006, v. 91, n. 4, p. 1513, doi. 10.1210/jc.2005-1899
- By:
- Publication type:
- Article
Association of germline variation with the survival of women with BRCA1/2 pathogenic variants and breast cancer.
- Published in:
- NPJ Breast Cancer, 2020, v. 6, n. 1, p. N.PAG, doi. 10.1038/s41523-020-00185-6
- By:
- Publication type:
- Article
Association of a Common AKAP9 Variant With Breast Cancer Risk: A Collaborative Analysis.
- Published in:
- JNCI: Journal of the National Cancer Institute, 2008, v. 100, n. 6, p. 437, doi. 10.1093/jnci/djn037
- By:
- Publication type:
- Article
Re: Associate of a Common Variant of the CASP8 Gene With Reduced Risk of Breast Cancer.
- Published in:
- 2005
- By:
- Publication type:
- Letter
Performance of In Silico Prediction Tools for the Detection of Germline Copy Number Variations in Cancer Predisposition Genes in 4208 Female Index Patients with Familial Breast and Ovarian Cancer.
- Published in:
- Cancers, 2021, v. 13, n. 1, p. 118, doi. 10.3390/cancers13010118
- By:
- Publication type:
- Article
Klassifizierung von 'variants of unknown significance' (VUS) beim familiären Brust- und Eierstockkrebs.
- Published in:
- Medizinische Genetik, 2015, v. 27, n. 2, p. 211, doi. 10.1007/s11825-015-0049-z
- By:
- Publication type:
- Article
The KL-VS sequence variant of Klotho and cancer risk in BRCA1 and BRCA2 mutation carriers.
- Published in:
- Breast Cancer Research & Treatment, 2012, v. 132, n. 3, p. 1119, doi. 10.1007/s10549-011-1938-8
- By:
- Publication type:
- Article
A variant affecting miRNAs binding in the circadian gene Neuronal PAS domain protein 2 ( NPAS2) is not associated with breast cancer risk.
- Published in:
- Breast Cancer Research & Treatment, 2011, v. 127, n. 3, p. 769, doi. 10.1007/s10549-010-1157-8
- By:
- Publication type:
- Article
Genetic variants within miR-126 and miR-335 are not associated with breast cancer risk.
- Published in:
- Breast Cancer Research & Treatment, 2011, v. 127, n. 2, p. 549, doi. 10.1007/s10549-010-1244-x
- By:
- Publication type:
- Article
A 24-color metaphase-based radiation assay discriminates heterozygous BRCA2 mutation carriers from controls by chromosomal radiosensitivity.
- Published in:
- Breast Cancer Research & Treatment, 2010, v. 135, n. 1, p. 167, doi. 10.1007/s10549-012-2119-0
- By:
- Publication type:
- Article
A genetic variant in the pre-miR-27a oncogene is associated with a reduced familial breast cancer risk.
- Published in:
- Breast Cancer Research & Treatment, 2010, v. 121, n. 3, p. 693, doi. 10.1007/s10549-009-0633-5
- By:
- Publication type:
- Article
Polymorphisms in BRCA2 resulting in aberrant codon-usage and their analysis on familial breast cancer risk.
- Published in:
- Breast Cancer Research & Treatment, 2010, v. 118, n. 2, p. 407, doi. 10.1007/s10549-009-0348-7
- By:
- Publication type:
- Article
Genetic variation in the major mitotic checkpoint genes does not affect familial breast cancer risk.
- Published in:
- Breast Cancer Research & Treatment, 2007, v. 106, n. 2, p. 205, doi. 10.1007/s10549-007-9496-9
- By:
- Publication type:
- Article
Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers.
- Published in:
- 2014
- By:
- Publication type:
- journal article
Refined histopathological predictors of BRCA1 and BRCA2 mutation status: a large-scale analysis of breast cancer characteristics from the BCAC, CIMBA, and ENIGMA consortia.
- Published in:
- 2014
- By:
- Publication type:
- journal article
RAD51C deletion screening identifies a recurrent gross deletion in breast cancer and ovarian cancer families.
- Published in:
- 2013
- By:
- Publication type:
- Letter
The association between breast cancer and S100P methylation in peripheral blood by multicenter case-control studies.
- Published in:
- Carcinogenesis, 2017, v. 38, n. 3, p. 312, doi. 10.1093/carcin/bgx004
- By:
- Publication type:
- Article
A variant affecting a putative miRNA target site in estrogen receptor (ESR) 1 is associated with breast cancer risk in premenopausal women.
- Published in:
- Carcinogenesis, 2009, v. 30, n. 1, p. 59, doi. 10.1093/carcin/bgn253
- By:
- Publication type:
- Article
SNPs in ultraconserved elements and familial breast cancer risk.
- Published in:
- Carcinogenesis, 2008, v. 29, n. 2, p. 351, doi. 10.1093/carcin/bgm290
- By:
- Publication type:
- Article
Copy number variant in the candidate tumor suppressor gene MTUS1 and familial breast cancer risk.
- Published in:
- Carcinogenesis, 2007, v. 28, n. 7, p. 1442, doi. 10.1093/carcin/bgm033
- By:
- Publication type:
- Article
Associations of genetic variants in the estrogen receptor coactivators PPARGC1A, PPARGC1B and EP300 with familial breast cancer.
- Published in:
- Carcinogenesis, 2006, v. 27, n. 11, p. 2201, doi. 10.1093/carcin/bgl067
- By:
- Publication type:
- Article
Association of the CASP10 V410I variant with reduced familial breast cancer risk and interaction with the CASP8 D302H variant.
- Published in:
- Carcinogenesis, 2006, v. 27, n. 3, p. 606, doi. 10.1093/carcin/bgi248
- By:
- Publication type:
- Article
Association of genetic variants in the Rho guanine nucleotide exchange factor AKAP13 with familial breast cancer.
- Published in:
- Carcinogenesis, 2006, v. 27, n. 3, p. 593, doi. 10.1093/carcin/bgi245
- By:
- Publication type:
- Article
Association of death receptor 4 haplotype 626C–683C with an increased breast cancer risk.
- Published in:
- Carcinogenesis, 2005, v. 26, n. 11, p. 1975, doi. 10.1093/carcin/bgi164
- By:
- Publication type:
- Article
The rare ERBB2 variant Ile654Val is associated with an increased familial breast cancer risk.
- Published in:
- Carcinogenesis, 2005, v. 26, n. 3, p. 643
- By:
- Publication type:
- Article
Variable number of tandem repeats polymorphism in the SMYD3 promoter region and the risk of familial breast cancer.
- Published in:
- International Journal of Cancer, 2006, v. 118, n. 11, p. 2917, doi. 10.1002/ijc.21696
- By:
- Publication type:
- Article
Association of the ARLTS1 Cys148Arg variant with familial breast cancer risk.
- Published in:
- International Journal of Cancer, 2006, v. 118, n. 10, p. 2505, doi. 10.1002/ijc.21687
- By:
- Publication type:
- Article
c-MYC Asn11Ser is associated with increased risk for familial breast cancer.
- Published in:
- International Journal of Cancer, 2005, v. 117, n. 4, p. 638, doi. 10.1002/ijc.21225
- By:
- Publication type:
- Article
Limited relevance of the CHEK2 gene in hereditary breast cancer.
- Published in:
- International Journal of Cancer, 2004, v. 110, n. 3, p. 320, doi. 10.1002/ijc.20073
- By:
- Publication type:
- Article
Biallelic germline BRCA1 mutations in a patient with early onset breast cancer, mild Fanconi anemia‐like phenotype, and no chromosome fragility.
- Published in:
- Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 9, p. N.PAG, doi. 10.1002/mgg3.863
- By:
- Publication type:
- Article
Combined genetic and splicing analysis of BRCA1 c.[594-2A>C; 641A>G] highlights the relevance of naturally occurring in-frame transcripts for developing disease gene variant classification algorithms.
- Published in:
- Human Molecular Genetics, 2016, v. 25, n. 11, p. 2256, doi. 10.1093/hmg/ddw094
- By:
- Publication type:
- Article
Breast cancer risk in BRCA1/2 mutation carriers and noncarriers under prospective intensified surveillance.
- Published in:
- International Journal of Cancer, 2020, v. 146, n. 4, p. 999, doi. 10.1002/ijc.32396
- By:
- Publication type:
- Article
The GPRC5A frameshift variant c.183del is not associated with increased breast cancer risk in BRCA1 mutation carriers.
- Published in:
- International Journal of Cancer, 2019, v. 144, n. 7, p. 1761, doi. 10.1002/ijc.32016
- By:
- Publication type:
- Article
DNA methylation array analyses identified breast cancer-associated HYAL2 methylation in peripheral blood.
- Published in:
- International Journal of Cancer, 2015, v. 136, n. 8, p. 1845, doi. 10.1002/ijc.29205
- By:
- Publication type:
- Article
Association of death receptor 4 variant (683A>C) with ovarian cancer risk in BRCA1 mutation carriers.
- Published in:
- International Journal of Cancer, 2012, v. 130, n. 6, p. 1314, doi. 10.1002/ijc.26134
- By:
- Publication type:
- Article
Low-risk variants FGFR2, TNRC9 and LSP1 in German familial breast cancer patients.
- Published in:
- International Journal of Cancer, 2010, v. 126, n. 12, p. 2858, doi. 10.1002/ijc.24986
- By:
- Publication type:
- Article
Pathological features of breast and ovarian cancers in RAD51C germline mutation carriers.
- Published in:
- 2014
- By:
- Publication type:
- Letter
Novel diagnostic tool for prediction of variant spliceogenicity derived from a set of 395 combined in silico/in vitro studies: an international collaborative effort.
- Published in:
- Nucleic Acids Research, 2020, v. 48, n. 3, p. 1600, doi. 10.1093/nar/gkz1212
- By:
- Publication type:
- Article
Polygenic risk scores indicate extreme ages at onset of breast cancer in female BRCA1/2 pathogenic variant carriers.
- Published in:
- 2022
- By:
- Publication type:
- journal article
Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification.
- Published in:
- Human Mutation, 2019, v. 40, n. 9, p. 1557, doi. 10.1002/humu.23818
- By:
- Publication type:
- Article
The <italic>BRCA2</italic> c.68‐7T > A variant is not pathogenic: A model for clinical calibration of spliceogenicity.
- Published in:
- Human Mutation, 2018, v. 39, n. 5, p. 729, doi. 10.1002/humu.23411
- By:
- Publication type:
- Article
ENIGMA-Evidence-based network for the interpretation of germline mutant alleles: An international initiative to evaluate risk and clinical significance associated with sequence variation in BRCA1 and BRCA2 genes.
- Published in:
- Human Mutation, 2012, v. 33, n. 1, p. 2, doi. 10.1002/humu.21628
- By:
- Publication type:
- Article
Germline mutations in the PALB2 gene are population specific and occur with low frequencies in familial breast cancer.
- Published in:
- Human Mutation, 2011, v. 32, n. 6, p. E2176, doi. 10.1002/humu.21478
- By:
- Publication type:
- Article