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1. Full Text Breast-Cancer Risk in Families with Mutations in PALB2
by Antoniou, Antonis C and Casadei, Silvia and Heikkinen, Tuomas and Barrowdale, Daniel and Pylkäs, Katri and Roberts, Jonathan and Lee, Andrew and Subramanian, Deepak and De Leeneer, Kim and Fostira, Florentia and Tomiak, Eva and Neuhausen, Susan L and Teo, Zhi L and Khan, Sofia and Aittomäki, Kristiina and Moilanen, Jukka S and Turnbull, Clare and Seal, Sheila and Mannermaa, Arto and Kallioniemi, Anne and Lindeman, Geoffrey J and Buys, Saundra S and Andrulis, Irene L and Radice, Paolo and Tondini, Carlo and Manoukian, Siranoush and Toland, Amanda E and Miron, Penelope and Weitzel, Jeffrey N and Domchek, Susan M and Poppe, Bruce and Claes, Kathleen B.M and Yannoukakos, Drakoulis and Concannon, Patrick and Bernstein, Jonine L and James, Paul A and Easton, Douglas F and Goldgar, David E and Hopper, John L and Rahman, Nazneen and Peterlongo, Paolo and Nevanlinna, Heli and King, Mary-Claire and Couch, Fergus J and Southey, Melissa C and Winqvist, Robert and Foulkes, William D and Tischkowitz, Marc
The New England journal of medicine, ISSN 0028-4793, 08/2014, Volume 371, Issue 6, pp. 497 - 506
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Gynecology. Andrology. Obstetrics | Mammary gland diseases | General aspects | Biological and medical sciences | Multiple tumors. Solid tumors. Tumors in childhood (general aspects) | Medical sciences | Tumors | Sequence Deletion | Genetic Predisposition to Disease | Humans | Middle Aged | Risk | Receptors, Estrogen - analysis | Receptors, Progesterone - analysis | Breast Neoplasms - genetics | Breast Neoplasms - congenital | Tumor Suppressor Proteins - genetics | Aged, 80 and over | Genes, BRCA2 | Germ-Line Mutation | Adult | Female | Heterozygote | Aged | Receptor, ErbB-2 - analysis | Nuclear Proteins - genetics | Fanconi Anemia Complementation Group N Protein | Development and progression | Breast cancer | Genetic aspects | Research | Gene mutations | BRCA2 protein | Women | Genes | Family medical history | Mutation | Gene deletion | Age | Risk factors | Genotypes | Index Medicus | Abridged Index Medicus
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2. Full Text Tamoxifen and Risk of Contralateral Breast Cancer for BRCA1 and BRCA2 Mutation Carriers
by Kelly-Anne Phillips and Roger L. Milne and Matti A. Rookus and Mary B. Daly and Antonis C. Antoniou and Susan Peock and Debra Frost and Douglas F. Easton and Steve Ellis and Michael L. Friedlander and Saundra S. Buys and Nadine Andrieu and Catherine Noguès and Dominique Stoppa-Lyonnet and Valérie Bonadona and Pascal Pujol and Sue Anne McLachlan and Esther M. John and Maartje J. Hooning and Caroline Seynaeve and Rob A.E.M. Tollenaar and David E. Goldgar and Mary Beth Terry and Trinidad Caldes and Prue C. Weideman and Irene L. Andrulis and Christian F. Singer and Kate Birch and Jacques Simard and Melissa C. Southey and Håkan L. Olsson and Anna Jakubowska and Edith Olah and Anne-Marie Gerdes and Lenka Foretova and John L. Hopper
Journal of clinical oncology, ISSN 0732-183X, 09/2013, Volume 31, Issue 25, pp. 3091 - 3099
Life Sciences & Biomedicine | Oncology | Science & Technology | Gynecology. Andrology. Obstetrics | Mammary gland diseases | Biological and medical sciences | Multiple tumors. Solid tumors. Tumors in childhood (general aspects) | Medical sciences | Tumors | Humans | Middle Aged | Risk Factors | Proportional Hazards Models | Breast Neoplasms - prevention & control | Breast Neoplasms - genetics | Estrogen Antagonists - therapeutic use | Tamoxifen - therapeutic use | Genes, BRCA2 | Adult | Female | Heterozygote | Aged | Genes, BRCA1 | Mutation | Index Medicus | ORIGINAL REPORTS | Bc7 | Clinical Medicine | Medical and Health Sciences | Klinisk medicin | Cancer and Oncology | Medicin och hälsovetenskap | Cancer och onkologi
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3. Risks of breast, ovarian, and contralateral breast cancer for BRCA1 and BRCA2 mutation carriers
by Kuchenbaecker, Karoline B and Hopper, John L and Barnes, Daniel R and Phillips, Kelly-Anne and Mooij, Thea M and Roos-Blom, Marie-José and Jervis, Sarah and Van Leeuwen, Flora E and Milne, Roger L and Andrieu, Nadine and Goldgar, David E and Terry, Mary Beth and Rookus, Matti A and Easton, Douglas F and Antoniou, Antonis C and BRCA1 BRCA2 Cohort Consortium and BRCA1 and BRCA2 Cohort Consortium
JAMA : the journal of the American Medical Association, ISSN 0098-7484, 06/2017, Volume 317, Issue 23, pp. 2402 - 2416
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Age Distribution | Prospective Studies | Age Factors | Risk Assessment | Humans | Middle Aged | Incidence | Neoplasms, Second Primary - epidemiology | Ovarian Neoplasms - epidemiology | Ovarian Neoplasms - genetics | Breast Neoplasms - genetics | Time Factors | Aged, 80 and over | Genes, BRCA2 | Adult | Family | Female | Aged | Genes, BRCA1 | Mutation | Neoplasms, Second Primary - genetics | Breast Neoplasms - epidemiology | BRCA2 protein | Ovarian carcinoma | BRCA1 protein | Health risks | Oncology | Population studies | Breast cancer | Estimates | Ovarian cancer | Carriers | Consortia | Design modifications | Risk assessment | Data collection | Genetics | Diagnosis | Genetic testing | Position (location) | Age | Cancer
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4. Full Text A Systematic Genetic Assessment of 1,433 Sequence Variants of Unknown Clinical Significance in the BRCA1 and BRCA2 Breast Cancer–Predisposition Genes
by Easton, Douglas F and Deffenbaugh, Amie M and Pruss, Dmitry and Frye, Cynthia and Wenstrup, Richard J and Allen-Brady, Kristina and Tavtigian, Sean V and Monteiro, Alvaro N.A and Iversen, Edwin S and Couch, Fergus J and Goldgar, David E
American journal of human genetics, ISSN 0002-9297, 2007, Volume 81, Issue 5, pp. 873 - 883
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | General aspects. Genetic counseling | Gynecology. Andrology. Obstetrics | Mammary gland diseases | Medical genetics | Biological and medical sciences | Molecular and cellular biology | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Tumors | Genetic Predisposition to Disease | Humans | Middle Aged | Male | Mutation - genetics | Sequence Analysis, DNA | BRCA1 Protein - genetics | Likelihood Functions | Breast Neoplasms - genetics | Adult | Female | Aged | Odds Ratio | BRCA2 Protein - genetics | Genetics | Breast cancer | Models | Mutation | Genes | Index Medicus
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5. Full Text Reproductive and Hormonal Factors, and Ovarian Cancer Risk for BRCA1 and BRCA2 Mutation Carriers: Results from the International BRCA1/2 Carrier Cohort Study
by Antonis C. Antoniou and Matti Rookus and Nadine Andrieu and Richard Brohet and Jenny Chang-Claude and Susan Peock and Margaret Cook and D. Gareth Evans and Rosalind Eeles and EMBRACE and Catherine Nogues and Laurence Faivre and Paul Gesta and GENEPSO and Flora E. van Leeuwen and Margreet G.E.M. Ausems and Ana Osorio and GEO-HEBON and Trinidad Caldes and Jacques Simard and Jan Lubinski and Anne-Marie Gerdes and Edith Olah and Christine Fürhauser and Hakan Olsson and Brita Arver and Paolo Radice and Douglas F. Easton and David E. Goldgar and GENEPSO and EMBRACE and GEO-HEBON
Cancer epidemiology, biomarkers & prevention, ISSN 1055-9965, 02/2009, Volume 18, Issue 2, pp. 601 - 610
parity | weighted Cox regression | oral contraceptive | tubal ligation | BRCA1/BRCA2 | Ovarian cancer | Oncology | Public, Environmental & Occupational Health | Life Sciences & Biomedicine | Science & Technology | Gynecology. Andrology. Obstetrics | Biological and medical sciences | Medical sciences | Tumors | Female genital diseases | Humans | Middle Aged | Risk Factors | Proportional Hazards Models | Sterilization, Tubal | Ovarian Neoplasms - genetics | Pregnancy | BRCA1 Protein - genetics | Contraceptives, Oral - administration & dosage | Adult | Female | Mutation | Parity | BRCA2 Protein - genetics | Cohort Studies | Index Medicus | Clinical Medicine | Medical and Health Sciences | Klinisk medicin | Cancer and Oncology | Medicin och hälsovetenskap | Cancer och onkologi
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6. Full Text Gene-Panel Sequencing and the Prediction of Breast-Cancer Risk
by Easton, Douglas F and Pharoah, Paul D.P and Antoniou, Antonis C and Tischkowitz, Marc and Tavtigian, Sean V and Nathanson, Katherine L and Devilee, Peter and Meindl, Alfons and Couch, Fergus J and Southey, Melissa and Goldgar, David E and Evans, D. Gareth R and Chenevix-Trench, Georgia and Rahman, Nazneen and Robson, Mark and Domchek, Susan M and Foulkes, William D
The New England journal of medicine, ISSN 0028-4793, 06/2015, Volume 372, Issue 23, pp. 2243 - 2257
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Genetic Predisposition to Disease | Guidelines as Topic | Genetic Testing - standards | United States | Humans | Risk | Genotyping Techniques | Centers for Disease Control and Prevention (U.S.) | Sequence Analysis, DNA | Genetic Variation | Breast Neoplasms - genetics | Genes, BRCA2 | Female | Heterozygote | Breast Neoplasms - diagnosis | Genes, BRCA1 | Care and treatment | Usage | BRCA mutations | Clinical trials | Breast cancer | Diagnosis | Research | Genetics | Health risk assessment | Genes | Index Medicus | Abridged Index Medicus
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7. Full Text A Population-Based Study of Genes Previously Implicated in Breast Cancer
by Hu, Chunling and Hart, Steven N and Gnanaolivu, Rohan and Huang, Hongyan and Lee, Kun Y and Na, Jie and Gao, Chi and Lilyquist, Jenna and Yadav, Siddhartha and Boddicker, Nicholas J and Samara, Raed and Klebba, Josh and Ambrosone, Christine B and Anton-Culver, Hoda and Auer, Paul and Bandera, Elisa V and Bernstein, Leslie and Bertrand, Kimberly A and Burnside, Elizabeth S and Carter, Brian D and Eliassen, Heather and Gapstur, Susan M and Gaudet, Mia and Haiman, Christopher and Hodge, James M and Hunter, David J and Jacobs, Eric J and John, Esther M and Kooperberg, Charles and Kurian, Allison W and Le Marchand, Loic and Lindstroem, Sara and Lindstrom, Tricia and Ma, Huiyan and Neuhausen, Susan and Newcomb, Polly A and O’Brien, Katie M and Olson, Janet E and Ong, Irene M and Pal, Tuya and Palmer, Julie R and Patel, Alpa V and Reid, Sonya and Rosenberg, Lynn and Sandler, Dale P and Scott, Christopher and Tamimi, Rulla and Taylor, Jack A and Trentham-Dietz, Amy and Vachon, Celine M and Weinberg, Clarice and Yao, Song and Ziogas, Argyrios and Weitzel, Jeffrey N and Goldgar, David E and Domchek, Susan M and Nathanson, Katherine L and Kraft, Peter and Polley, Eric C and Couch, Fergus J
The New England journal of medicine, ISSN 0028-4793, 02/2021, Volume 384, Issue 5, pp. 440 - 451
Genetic Predisposition to Disease - genetics | Humans | Middle Aged | Risk | Sequence Analysis, DNA | Case-Control Studies | Genetic Variation | Young Adult | Breast Neoplasms - genetics | Aged, 80 and over | Adult | Female | Aged | Mutation | Odds Ratio | BRCA2 protein | BRCA1 protein | Genes | Estrogen receptors | Population studies | Mammography | Breast cancer | Family medical history | Medical diagnosis | Minority & ethnic groups | Estimates | E-cadherin | Consortia | Disease prevention | Womens health | Risk assessment | Population | Hispanics | Age | Tumors | Index Medicus | Abridged Index Medicus
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8. Full Text Exposure to diagnostic radiation and risk of breast cancer among carriers of BRCA1/2 mutations: retrospective cohort study (GENE-RAD-RISK)
by Pijpe, Anouk and Andrieu, Nadine and Easton, Douglas F and Kesminiene, Ausrele and Cardis, Elisabeth and Noguès, Catherine and Gauthier-Villars, Marion and Lasset, Christine and Fricker, Jean-Pierre and Peock, Susan and Frost, Debra and Evans, D Gareth and Eeles, Rosalind A and Paterson, Joan and Manders, Peggy and van Asperen, Christi J and Ausems, Margreet G E M and Meijers-Heijboer, Hanne and Thierry-Chef, Isabelle and Hauptmann, Michael and Goldgar, David and Rookus, Matti A and van Leeuwen, Flora E and GENEPSO and HEBON and EMBRACE
BMJ : British Medical Journal, ISSN 0959-8138, 9/2012, Volume 345, Issue 7878, pp. 14 - 14
Radiography | RESEARCH | Cohort studies | Questionnaires | Health hazards | Breast cancer | Mammography | Genetic mutation | Radiation dosage | Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Breast - radiation effects | Age Factors | Mutation - radiation effects | Humans | Middle Aged | Risk Factors | Breast Neoplasms - etiology | Proportional Hazards Models | Mammography - adverse effects | Young Adult | Breast Neoplasms - genetics | Genes, BRCA2 | Adult | Female | Heterozygote | Retrospective Studies | Genes, BRCA1 | Dose-Response Relationship, Radiation | Radiation therapy | Mutation | Health risk assessment | Womens health | Index Medicus | Abridged Index Medicus
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9. Full Text Assignment of a Locus for Familial Melanoma, MLM, to Chromosome 9p13-p22
by Lisa A. Cannon-Albright and David E. Goldgar and Laurence J. Meyer and Cathryn M. Lewis and David E. Anderson and Jane W. Fountain and Monika E. Hegi and Roger W. Wiseman and Elizabeth M. Petty and Allen E. Bale and Olufunmilayo I. Olopade and Manuel O. Diaz and David J. Kwiatkowski and Michael W. Piepkorn and John J. Zone and Mark H. Skolnick
Science (American Association for the Advancement of Science), ISSN 0036-8075, 11/1992, Volume 258, Issue 5085, pp. 1148 - 1152
Lod score | Genetic inheritance | Gene frequency | Genes | Melanoma | Alleles | Medical genetics | Genetic loci | Reports | Chromosomes | Tumors | Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Dysplastic Nevus Syndrome - genetics | Humans | Middle Aged | Molecular Sequence Data | Male | Chromosomes, Human, Pair 9 | Genetic Markers | Lod Score | Utah | Melanoma - genetics | Pedigree | Base Sequence | Skin Neoplasms - genetics | Texas | Adolescent | Chromosome Aberrations | Aged, 80 and over | Adult | Female | Aged | Child | Genes, Tumor Suppressor | Human chromosome abnormalities | Usage | Genetic aspects | Linkage (Genetics) | Research | melanoma | man | linkage analysis | genes | chromosome 9 | Index Medicus
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