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1. Full Text “It’s not if I get cancer, it’s when I get cancer”: BRCA-positive patients’ (un)certain health experiences regarding hereditary breast and ovarian cancer risk
by Dean, Marleah
Social science & medicine (1982), ISSN 0277-9536, 08/2016, Volume 163, pp. 21 - 27
BRCA | Genetic risk | Hereditary breast and ovarian cancer | Communication | Public, Environmental & Occupational Health | Social Sciences | Life Sciences & Biomedicine | Biomedical Social Sciences | Social Sciences, Biomedical | Science & Technology | Decision Making | Genetic Predisposition to Disease - psychology | Ovarian Neoplasms - psychology | Risk Assessment - methods | Uncertainty | Humans | Middle Aged | Ovarian Neoplasms - genetics | Breast Neoplasms - genetics | Breast Neoplasms - psychology | Texas | Genes, BRCA2 | Adult | Female | Genes, BRCA1 | Women - psychology | Risk Assessment - standards | Development and progression | Breast cancer | Genetic aspects | Health aspects | Risk factors | Ovarian cancer | Health | Certainty | Attitudes | Risk | Mothers | Patients | Trauma | Medicine | Womens health | Risk assessment | Genetics | Internet | Mass media | Genetic testing | Mutation | Females | Cancer | Index Medicus
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2. Full Text Hereditary breast and ovarian cancer: New genes in confined pathways
by Nielsen, Finn Cilius and Van Overeem Hansen, Thomas and Sørensen, Claus Storgaard
Nature reviews. Cancer, ISSN 1474-175X, 09/2016, Volume 16, Issue 9, pp. 599 - 612
Life Sciences & Biomedicine | Oncology | Science & Technology | Breast Neoplasms, Male - genetics | Cell Cycle - genetics | Genetic Predisposition to Disease | Genetic Testing | Recombinational DNA Repair - genetics | Estrogens | Genes, Neoplasm | Humans | Apoptosis - genetics | Male | Signal Transduction - genetics | Mutation, Missense | DNA Mismatch Repair - genetics | Genetic Counseling | Neoplasms, Hormone-Dependent - genetics | Ovarian Neoplasms - genetics | Breast Neoplasms - genetics | RNA Splicing - genetics | Female | Neoplastic Syndromes, Hereditary - genetics | DNA Damage | Progesterone | Genes, cdc | Care and treatment | BRCA mutations | Breast cancer | Genetic aspects | Diagnosis | Health risk assessment | Health aspects | Identification and classification | Methods | Ovarian cancer | Index Medicus
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3. Full Text Germline BRCA mutation evaluation in a prospective triple-negative breast cancer registry: implications for hereditary breast and/or ovarian cancer syndrome testing
by Sharma, Priyanka and Klemp, Jennifer R and Kimler, Bruce F and Mahnken, Jonathan D and Geier, Larry J and Khan, Qamar J and Elia, Manana and Connor, Carol S and McGinness, Marilee K and Mammen, Joshua M. W and Wagner, Jamie L and Ward, Claire and Ranallo, Lori and Knight, Catherine J and Stecklein, Shane R and Jensen, Roy A and Fabian, Carol J and Godwin, Andrew K
Breast cancer research and treatment, ISSN 0167-6806, 6/2014, Volume 145, Issue 3, pp. 707 - 714
NCCN guidelines | Oncology | Germline BRCA mutation | Genetic testing guidelines | Medicine & Public Health | Triple-negative breast cancer | Life Sciences & Biomedicine | Science & Technology | Hereditary Breast and Ovarian Cancer Syndrome - genetics | Genetic Predisposition to Disease | Genetic Testing | Prospective Studies | Hereditary Breast and Ovarian Cancer Syndrome - diagnosis | Ovarian Neoplasms - diagnosis | Humans | Middle Aged | Ovarian Neoplasms - genetics | BRCA1 Protein - genetics | Breast Neoplasms - genetics | Triple Negative Breast Neoplasms - genetics | Triple Negative Breast Neoplasms - diagnosis | Aged, 80 and over | Adult | Female | Registries | Aged | Breast Neoplasms - diagnosis | Mutation | BRCA2 Protein - genetics | Medical tests | Breast cancer | Genetic screening | Ovarian cancer | Index Medicus
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4. Full Text Identifying sequence variants contributing to hereditary breast and ovarian cancer in BRCA1 and BRCA2 negative breast and ovarian cancer patients
by Jarhelle, Elisabeth and Stensland, Hilde Monica Frostad Riise and Hansen, Geir Asmund Myge and Skarsfjord, Siri and Jonsrud, Christoffer and Ingebrigtsen, Monica and Stromsvik, Nina and Van Ghelue, Marijke
Scientific reports, ISSN 2045-2322, 12/2019, Volume 9, Issue 1, pp. 19986 - 12
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Hereditary Breast and Ovarian Cancer Syndrome - genetics | Genetic Predisposition to Disease | Genetic Association Studies | Hereditary Breast and Ovarian Cancer Syndrome - diagnosis | Humans | Middle Aged | Genotype | Biomarkers, Tumor | BRCA1 Protein - genetics | Pedigree | Alleles | Aged, 80 and over | Germ-Line Mutation | Adult | Female | Aged | Polymorphism, Single Nucleotide | BRCA2 Protein - genetics | Amino Acid Substitution | BRCA2 protein | Next-generation sequencing | BRCA1 protein | p53 Protein | Breast | Breast cancer | Genetic diversity | Health risk assessment | Risk factors | Ovarian cancer | Index Medicus | Medisinske Fag: 700 | VDP | Medical disciplines: 700
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5. Full Text Time to incorporate germline multigene panel testing into breast and ovarian cancer patient care
by Graffeo, Rossella and Livraghi, Luca and Pagani, Olivia and Goldhirsch, Aron and Partridge, Ann H and Garber, Judy E
Breast cancer research and treatment, ISSN 0167-6806, 12/2016, Volume 160, Issue 3, pp. 393 - 410
BRCA | Breast and ovarian cancer | Medicine & Public Health | Surveillance | Multiple-gene panel testing | Oncology | Cancer genetic counseling | Genetic counselors | Life Sciences & Biomedicine | Science & Technology | Breast Neoplasms, Male - genetics | Hereditary Breast and Ovarian Cancer Syndrome - diagnosis | Humans | Male | Biomarkers, Tumor | Genetic Testing - methods | Breast Neoplasms - therapy | Ovarian Neoplasms - genetics | Hereditary Breast and Ovarian Cancer Syndrome - therapy | Genes, BRCA2 | Germ-Line Mutation | Female | Genes, BRCA1 | Stomach Neoplasms - genetics | Breast Neoplasms, Male - diagnosis | Hereditary Breast and Ovarian Cancer Syndrome - genetics | Genetic Predisposition to Disease | Stomach Neoplasms - diagnosis | Ovarian Neoplasms - prevention & control | Fanconi Anemia Complementation Group N Protein - genetics | Ovarian Neoplasms - diagnosis | Stomach Neoplasms - therapy | Penetrance | Breast Neoplasms - prevention & control | Breast Neoplasms - genetics | Breast Neoplasms, Male - therapy | Stomach Neoplasms - prevention & control | Ovarian Neoplasms - therapy | Breast Neoplasms - diagnosis | Disease Management | Mutation | Medical research | Care and treatment | Breast cancer | Disease susceptibility | Patients | Genetic screening | Ovarian cancer | Cancer patients | Risk assessment | Medicine, Experimental | Genetic aspects | Tumor proteins | Cancer | Index Medicus
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6. Hereditary breast and ovarian cancer susceptibility genes (Review)
by Kobayashi, Hiroshi and Ohno, Sumire and Sasaki, Yoshikazu and Matsuura, Miyuki
Oncology reports, ISSN 1021-335X, 09/2013, Volume 30, Issue 3, pp. 1019 - 1029
DNA repairs | BRCA | Hereditary breast and ovarian cancer | Pathogenesis | Life Sciences & Biomedicine | Oncology | Science & Technology | Ovarian Neoplasms - genetics | Female | Genetic Predisposition to Disease | Breast Neoplasms - genetics | Neoplasm Proteins - genetics | Humans
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