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1. Full Text MRI versus mammography for breast cancer screening in women with familial risk (FaMRIsc): a multicentre, randomised, controlled trial
by Saadatmand, Sepideh, MD and Geuzinge, H Amarens, MSc and Rutgers, Emiel J T, Prof and Mann, Ritse M, MD and de Roy van Zuidewijn, Diderick B W, MD and Zonderland, Harmien M, MD and Tollenaar, Rob A E M, Prof and Lobbes, Marc B I, MD and Ausems, Margreet G E M, MD and van 't Riet, Martijne, MD and Hooning, Maartje J, MD and Mares-Engelberts, Ingeborg, MD and Luiten, Ernest J T, MD and Heijnsdijk, Eveline A M, PhD and Verhoef, Cees, Prof and Karssemeijer, Nico, PhD and Oosterwijk, Jan C, MD and Obdeijn, Inge-Marie, MD and de Koning, Harry J, Prof and Tilanus-Linthorst, Madeleine M A, MD and FaMRIsc study group and FaMRIsc Study Grp
The lancet oncology, ISSN 1470-2045, 2019, Volume 20, Issue 8, pp. 1136 - 1147
Hematology, Oncology, and Palliative Medicine | Life Sciences & Biomedicine | Oncology | Science & Technology | Breast cancer | Genetic aspects | Mammography | Diagnosis | Cancer | Index Medicus
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2. Full Text Improved overall survival after contralateral risk-reducing mastectomy in BRCA1/2 mutation carriers with a history of unilateral breast cancer: a prospective analysis
by Heemskerk-Gerritsen, Bernadette A. M and Rookus, Matti A and Aalfs, Cora M and Ausems, Margreet G. E. M and Collée, Johanna M and Jansen, Liesbeth and Kets, C. Marleen and Keymeulen, Kristien B. M. I and Koppert, Linetta B and Meijers-Heijboer, Hanne E. J and Mooij, Thea M and Tollenaar, Rob A. E. M and Vasen, Hans F. A and Hooning, Maartje J and Seynaeve, Caroline and HEBON
International journal of cancer, ISSN 0020-7136, 2015, Volume 136, Issue 3, pp. 668 - 677
no | contralateral risk‐reducing mastectomy | BRCA1/2 | breast cancer | prevention | survival | Prevention | Breast cancer | Contralateral risk-reducing mastectomy | Survival | Life Sciences & Biomedicine | Oncology | Science & Technology | Breast Neoplasms - surgery | Prospective Studies | Humans | Middle Aged | Breast Neoplasms - genetics | Aged, 80 and over | Genes, BRCA2 | Mastectomy | Adult | Breast Neoplasms - mortality | Female | Aged | Genes, BRCA1 | Mutation | Chemotherapy | Patient outcomes | Surgery | Genetic aspects | Cancer | Surveillance | Health risk assessment | Index Medicus
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3. Full Text Hereditary diffuse gastric cancer: updated clinical guidelines with an emphasis on germline CDH1 mutation carriers
by van der Post, Rachel S and Vogelaar, Ingrid P and Carneiro, Fátima and Guilford, Parry and Huntsman, David and Hoogerbrugge, Nicoline and Caldas, Carlos and Schreiber, Karen E Chelcun and Hardwick, Richard H and Ausems, Margreet G E M and Bardram, Linda and Benusiglio, Patrick R and Bisseling, Tanya M and Blair, Vanessa and Bleiker, Eveline and Boussioutas, Alex and Cats, Annemieke and Coit, Daniel and DeGregorio, Lynn and Figueiredo, Joana and Ford, James M and Heijkoop, Esther and Hermens, Rosella and Humar, Bostjan and Kaurah, Pardeep and Keller, Gisella and Lai, Jennifer and Ligtenberg, Marjolijn J L and O'Donovan, Maria and Oliveira, Carla and Pinheiro, Hugo and Ragunath, Krish and Rasenberg, Esther and Richardson, Susan and Roviello, Franco and Schackert, Hans and Seruca, Raquel and Taylor, Amy and ter Huurne, Anouk and Tischkowitz, Marc and Joe, Sheena Tjon A and van Dijck, Benjamin and van Grieken, Nicole C T and van Hillegersberg, Richard and van Sandick, Johanna W and Vehof, Rianne and van Krieken, J Han and Fitzgerald, Rebecca C
Journal of medical genetics, ISSN 0022-2593, 06/2015, Volume 52, Issue 6, pp. 361 - 374
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Colorectal Neoplasms - epidemiology | Stomach Neoplasms - genetics | Stomach Neoplasms - diagnosis | Early Detection of Cancer - methods | Colorectal Neoplasms - genetics | Humans | Genetic Counseling | Genetic Testing - methods | Colorectal Neoplasms - diagnosis | Pregnancy | Breast Neoplasms - genetics | DNA Mutational Analysis | Germ-Line Mutation | Female | Heterozygote | Stomach Neoplasms - epidemiology | Breast Neoplasms - diagnosis | Cadherins - genetics | Population Surveillance | Antigens, CD | Breast Neoplasms - epidemiology | Practice Guidelines as Topic | Practice guidelines (Medicine) | Genetic aspects | Diagnosis | Stomach cancer | Health aspects | Risk factors | Mutation (Biology) | Index Medicus | Clinical genetics | Diagnostics | Cancer: gastric | Cancer: breast | Review | 1506 | Stomach and duodenum
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4. Full Text TP53 germline mutation testing in 180 families suspected of Li–Fraumeni syndrome: mutation detection rate and relative frequency of cancers in different familial phenotypes
by Ruijs, Marielle W G and Verhoef, Senno and Rookus, Matti A and Pruntel, Roelof and van der Hout, Annemarie H and Hogervorst, Frans B L and Kluijt, I and Sijmons, Rolf H and Aalfs, Cora M and Wagner, Anja and Ausems, Margreet G E M and Hoogerbrugge, Nicoline and van Asperen, Christi J and Gomez Garcia, Encarna B and Meijers-Heijboer, Hanne and ten Kate, Leo P and Menko, Fred H and van 't Veer, Laura J
Journal of medical genetics, ISSN 0022-2593, 06/2010, Volume 47, Issue 6, pp. 421 - 428
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | General aspects. Genetic counseling | Medical genetics | Biological and medical sciences | Molecular and cellular biology | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Colonic Neoplasms - genetics | Pancreatic Neoplasms - diagnosis | Humans | Middle Aged | Colonic Neoplasms - diagnosis | Family Health | Male | Neoplasms - diagnosis | Li-Fraumeni Syndrome - diagnosis | Genetic Testing - methods | Tumor Suppressor Protein p53 - genetics | Young Adult | Li-Fraumeni Syndrome - genetics | Netherlands | Neoplasms - genetics | DNA Mutational Analysis | Germ-Line Mutation | Adult | Female | Genetic Predisposition to Disease | Gene Frequency | Risk Factors | Genotype | Pancreatic Neoplasms - genetics | Phenotype | Gene mutations | DNA | Analysis | Physiological aspects | Genetic aspects | Research | Risk factors | Li-Fraumeni syndrome | Liver cancer | Brain cancer | Pancreatic cancer | Colorectal cancer | Melanoma | Breast cancer | Mutation | Age | Deoxyribonucleic acid--DNA | Tumors | Index Medicus
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5. 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 and on behalf of GENEPSO, EMBRACE, and HEBON
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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6. Full Text Am I my Family's Keeper? : Disclosure Dilemmas in Next Generation Sequencing
by Wouters, Roel H P and Bijlsma, Rhodé M and Ausems, Margreet G E M and van Delden, Johannes J M and Voest, Emile E and Bredenoord, Annelien L
Human mutation, ISSN 1059-7794, 09/2016, Volume 37, Issue 12, pp. 1257–1262 - 1262
next-generation sequencing | unsolicited finding | moral accountability nudge | NGS | ethics | libertarian paternalism | Journal Article | next‐generation sequencing | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Humans | Moral Obligations | Incidental Findings | Disclosure - ethics | Family | Professional Role | High-Throughput Nucleotide Sequencing - ethics | Disease susceptibility | Psychiatric services | Genetic screening | Informed consent | Duty to warn | Genetic testing | Mutation | Patients | Index Medicus
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7. Full Text Survival after bilateral risk-reducing mastectomy in healthy BRCA1 and BRCA2 mutation carriers
by Heemskerk-Gerritsen, Bernadette A. M and Jager, Agnes and Koppert, Linetta B and Obdeijn, A. Inge-Marie and Collée, Margriet and Meijers-Heijboer, Hanne E. J and Jenner, Denise J and Oldenburg, Hester S. A and van Engelen, Klaartje and de Vries, Jakob and van Asperen, Christi J and Devilee, Peter and Blok, Marinus J and Kets, C. Marleen and Ausems, Margreet G. E. M and Seynaeve, Caroline and Rookus, Matti A and Hooning, Maartje J
Breast cancer research and treatment, ISSN 0167-6806, 10/2019, Volume 177, Issue 3, pp. 723 - 733
Prevention | BRCA1/2 | Medicine & Public Health | Surveillance | Oncology | Bilateral risk-reducing mastectomy | Survival | Life Sciences & Biomedicine | Science & Technology | Breast Neoplasms - surgery | Prognosis | Risk Reduction Behavior | Humans | Mortality | Netherlands - epidemiology | Breast Neoplasms - etiology | Breast Neoplasms - prevention & control | BRCA1 Protein - genetics | Public Health Surveillance | Germ-Line Mutation | Prophylactic Mastectomy - methods | Breast Neoplasms - mortality | Female | Heterozygote | Mutation | BRCA2 Protein - genetics | Gene mutations | Surgery | Genetic aspects | Health aspects | Cancer | Index Medicus
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8. Full Text Association of Type and Location of BRCA1 and BRCA2 Mutations With Risk of Breast and Ovarian Cancer
by Rebbeck, Timothy R and Mitra, Nandita and Wan, Fei and Sinilnikova, Olga M and Healey, Sue and McGuffog, Lesley and Mazoyer, Sylvie and Chenevix-Trench, Georgia and Easton, Douglas F and Antoniou, Antonis C and Nathanson, Katherine L and Laitman, Yael and Kushnir, Anya and Paluch-Shimon, Shani and Berger, Raanan and Zidan, Jamal and Friedman, Eitan and Ehrencrona, Hans and Stenmark-Askmalm, Marie and Einbeigi, Zakaria and Loman, Niklas and Harbst, Katja and Rantala, Johanna and Melin, Beatrice and Huo, Dezheng and Olopade, Olufunmilayo I and Seldon, Joyce and Ganz, Patricia A and Nussbaum, Robert L and Chan, Salina B and Odunsi, Kunle and Gayther, Simon A and Domchek, Susan M and Arun, Banu K and Lu, Karen H and Mitchell, Gillian and Karlan, Beth Y and Walsh, Christine and Lester, Jenny and Godwin, Andrew K and Pathak, Harsh and Ross, Eric and Daly, Mary B and Whittemore, Alice S and John, Esther M and Miron, Alexander and Terry, Mary Beth and Chung, Wendy K and Goldgar, David E and Buys, Saundra S and Janavicius, Ramunas and Tihomirova, Laima and Tung, Nadine and Dorfling, Cecilia M and van Rensburg, Elizabeth J and Steele, Linda and Neuhausen, Susan L and Ding, Yuan Chun and Ejlertsen, Bent and Gerdes, Anne-Marie and Hansen, Thomas v. O and Ramón y Cajal, Teresa and Osorio, Ana and Benitez, Javier and Godino, Javier and Tejada, Maria-Isabel and Duran, Mercedes and Weitzel, Jeffrey N and Bobolis, Kristie A and Sand, Sharon R and Fontaine, Annette and Savarese, Antonella and Pasini, Barbara and Peissel, Bernard and Bonanni, Bernardo and Zaffaroni, Daniela and Vignolo-Lutati, Francesca and Scuvera, Giulietta and Giannini, Giuseppe and Bernard, Loris and Genuardi, Maurizio and Radice, Paolo and Dolcetti, Riccardo and Manoukian, Siranoush and Pensotti, Valeria and Gismondi, Viviana and Yannoukakos, Drakoulis and Fostira, Florentia and Garber, Judy and Torres, Diana and Rashid, Muhammad Usman and Hamann, Ute and Peock, Susan and Frost, Debra and Platte, Radka and Evans, D. Gareth and Eeles, Rosalind and Davidson, Rosemarie and Eccles, Diana and Cole, Trevor and ... and CIMBA Consortium
JAMA : the journal of the American Medical Association, ISSN 0098-7484, 04/2015, Volume 313, Issue 13, pp. 1347 - 1361
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Genetic Predisposition to Disease | Humans | Middle Aged | Risk Factors | Nucleotides | Ovarian Neoplasms - genetics | Breast Neoplasms - genetics | Age of Onset | Genes, BRCA2 | Adult | Female | Heterozygote | Genes, BRCA1 | Mutation | Women | Usage | BRCA mutations | Breast cancer | Health aspects | Risk factors | Ovarian cancer | Disease prevention | Womens health | Index Medicus | Abridged Index Medicus | Medicinsk genetik | Basic Medicine | Medical Genetics | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
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