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Nature genetics, ISSN 1061-4036, 2017, Volume 49, Issue 12, pp. 1767 - 1778
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | European Continental Ancestry Group - genetics | Genetic Predisposition to Disease - genetics | Receptors, Estrogen - metabolism | Humans | Risk Factors | Breast Neoplasms - metabolism | BRCA1 Protein - genetics | Breast Neoplasms - genetics | Female | Genetic Predisposition to Disease - ethnology | Heterozygote | Polymorphism, Single Nucleotide | Mutation | Genome-Wide Association Study - methods | Breast Neoplasms - ethnology | Breast cancer | Genetic aspects | Genetic variation | Health aspects | Risk factors | Disease | BRCA1 protein | Genes | Estrogens | Health risks | Estrogen receptors | Risk | Genomes | Carriers | Consortia | Cell cycle | Hormone replacement therapy | Gene mapping | Health risk assessment | Bioinformatics | Cancer | Index Medicus | Medicinsk genetik | Basic Medicine | Medical Genetics | Clinical Medicine | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper | Klinisk medicin | Cancer and Oncology | Cancer och onkologi
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Nature genetics, ISSN 1061-4036, 2017, Volume 49, Issue 5, pp. 680 - 691
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Neoplasms, Glandular and Epithelial - pathology | Genetic Predisposition to Disease - genetics | Genome-Wide Association Study | Meta-Analysis as Topic | Humans | Risk Factors | Genetic Loci - genetics | Ovarian Neoplasms - pathology | Genotype | Ovarian Neoplasms - genetics | BRCA1 Protein - genetics | Neoplasms, Glandular and Epithelial - genetics | Telomere-Binding Proteins - genetics | Alleles | Carcinoma, Ovarian Epithelial | Female | Polymorphism, Single Nucleotide | Mutation | BRCA2 Protein - genetics | Genetic susceptibility | Physiological aspects | Genetic aspects | Single nucleotide polymorphisms | Identification and classification | Health aspects | Risk factors | Ovarian cancer | Carriers | Medical research | Ovarian carcinoma | Genes | Gene regulation | Genomes | Breast cancer | Loci | Cancer | Index Medicus | Life Sciences | Human health and pathology | Genetics | Medicinsk genetik | Basic Medicine | Medical Genetics | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
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Mutational Spectrum in a Worldwide Study of 29,700 Families with BRCA1 or BRCA2 Mutations
Human mutation, ISSN 1059-7794, 2018, Volume 39, Issue 5, pp. 593 - 620
mutation | ethnicity | ovarian cancer | geography | breast cancer | BRCA1 | BRCA2 | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Geography | BRCA1 Protein - genetics | Internationality | Humans | Databases, Genetic | Family | Mutation - genetics | BRCA2 Protein - genetics | Genetic aspects | BRCA mutations | Genetic screening | Singers | Ovarian cancer | BRCA2 protein | Mutation | Genotyping | BRCA1 protein | Minority & ethnic groups | Index Medicus | Life Sciences | Genetics | Human genetics | Medicin och hälsovetenskap
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American journal of preventive medicine, ISSN 0749-3797, 11/2017, Volume 53, Issue 5, pp. e195 - e196
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European journal of human genetics : EJHG, ISSN 1018-4813, 02/2020, Volume 28, Issue 2, pp. 213 - 221
Biochemistry & Molecular Biology | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | Risk assessment | Hospice care | Biobanks | Palliative care | Heritability | Family medical history | Risk factors | Genetic screening | Deoxyribonucleic acid--DNA | Cancer | Genetic testing | Index Medicus
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Palliative medicine, ISSN 0269-2163, 7/2019, Volume 33, Issue 7, pp. 856 - 858
Health Care Sciences & Services | Medicine, General & Internal | Public, Environmental & Occupational Health | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Medical History Taking | Humans | Health Personnel - psychology | Palliative Care | Surveys and Questionnaires | Terminal Care | Neoplasms | Feasibility Studies | Medical personnel | Palliative care | End of life decisions | Family medical history | Cancer | Index Medicus
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Cancer epidemiology, biomarkers & prevention, ISSN 1055-9965, 08/2017, Volume 26, Issue 8, pp. 1233 - 1241
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Nature genetics, ISSN 1061-4036, 2020, Volume 52, Issue 1, pp. 56 - 73
Genetics | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Genetic Predisposition to Disease | Genome-Wide Association Study | Humans | Regulatory Sequences, Nucleic Acid | Risk Factors | Linkage Disequilibrium | Breast Neoplasms - genetics | Chromosome Mapping - methods | Bayes Theorem | Female | Biomarkers, Tumor - genetics | Polymorphism, Single Nucleotide | Quantitative Trait Loci | Epigenetic inheritance | Chromatin | Oncology, Experimental | Genes | Genomics | Breast cancer | Genomes | DNA binding proteins | Genetic transcription | Research | Risk factors | Quantitative genetics | Genetic research | Genetic aspects | Health aspects | Cancer | Transcription factors | Target recognition | Linkage disequilibrium | Association analysis | Risk | Mapping | Regulatory sequences | Consortia | Annotations | Deoxyribonucleic acid--DNA | Immune system | Knowledge representation | Health risks | Gene expression | Quantitative trait loci | Mutation | Gene mapping | Bayesian analysis | Binding sites | Apoptosis | Tumors | Index Medicus | Medicinsk genetik | Basic Medicine | Medical Genetics | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
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