-
1
المؤلفون: Andrew K. Godwin, Henry T. Lynch, Mary B. Daly, Levy Kopelovich, Lisa Vanderveer, James A. Crowell, Betsy Bove, Karthik Devarajan, Carolyn M. Slater, Alfred G. Knudson, Elena Caretti, Eric A. Ross, Suraj Peri, Kerry S. Campbell, Yan Zhou, Margie L. Clapper, Anthony T. Yeung, Emmanuelle Nicolas, Alfonso Bellacosa, Sharon Howard
المصدر: Cancer Prevention Research. 3:48-61
مصطلحات موضوعية: Heterozygote, Cancer Research, Tumor suppressor gene, Genes, BRCA2, Mutant, Genes, BRCA1, Gene Expression, Biology, medicine.disease_cause, Loss of heterozygosity, Mammaglobin, Breast cancer, Biomarkers, Tumor, medicine, Data Mining, Humans, Genetic Predisposition to Disease, Breast, RNA, Messenger, Oligonucleotide Array Sequence Analysis, Reverse Transcriptase Polymerase Chain Reaction, Gene Expression Profiling, Ovary, Cancer, Epithelial Cells, medicine.disease, Molecular biology, Oncology, Mutation, biology.protein, Cancer research, Female, Ovarian cancer, Carcinogenesis
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f1199866c0684479ca91aa9acb8c151
https://doi.org/10.1158/1940-6207.capr-09-0078 -
2
المؤلفون: Xiaowei Chen, JoEllen Weaver, Alexander Miron, Susan C. Weil, Andrew K. Godwin, Mary B. Daly, Lisa Vanderveer, Betsy Bove
المصدر: Human Molecular Genetics. 17:1336-1348
مصطلحات موضوعية: Adult, endocrine system diseases, Tumor suppressor gene, Lymphocyte, Breast Neoplasms, Allelic Imbalance, Biology, Polymerase Chain Reaction, Risk Assessment, White People, Frameshift mutation, Cohort Studies, Breast cancer, Genetics, medicine, Humans, Genetic Predisposition to Disease, RNA, Messenger, Allele, skin and connective tissue diseases, Molecular Biology, Genetics (clinical), BRCA2 Protein, BRCA1 Protein, Cancer, General Medicine, Middle Aged, Pennsylvania, Delaware, medicine.disease, medicine.anatomical_structure, Cancer research, Female, Breast disease, Apoptosis Regulatory Proteins
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ec495bd533749f9f1fc1cecb1c631c2
https://doi.org/10.1093/hmg/ddn022 -
3
المؤلفون: Tuyet-Trinh N. Truong, Betsy Bove, JoEllen Weaver, Mary B. Daly, Kimberly Cattie, Xiaowei Chen, Brock A. Armstrong, Andrew K. Godwin
المصدر: Human Mutation. 27:427-435
مصطلحات موضوعية: Antimetabolites, Antineoplastic, endocrine system diseases, Sequence analysis, RNA Splicing, DNA Mutational Analysis, Molecular Sequence Data, Nonsense-mediated decay, Biology, medicine.disease_cause, Cell Line, Germline mutation, Sequence Analysis, Protein, Mutant protein, Genetics, medicine, Humans, RNA, Messenger, skin and connective tissue diseases, Gene, Genetics (clinical), BRCA2 Protein, Mutation, Polymorphism, Genetic, Base Sequence, BRCA1 Protein, Intron, Molecular biology, Introns, RNA splicing, Female, Puromycin, RNA Splice Sites
-
4
المؤلفون: Hong Wu, Andrew K. Godwin, Andrey Frolov, Betsy Bove, Lisa Vanderveer, Amanda H. Prowse
المصدر: Genes, Chromosomes and Cancer. 35:232-241
مصطلحات موضوعية: Adult, Cancer Research, endocrine system diseases, DNA Mutational Analysis, Genes, BRCA1, Biology, Germline, Frameshift mutation, Loss of heterozygosity, Exon, Tumor Cells, Cultured, Genetics, Humans, skin and connective tissue diseases, Gene, Aged, Oligonucleotide Array Sequence Analysis, Gene Rearrangement, Ovarian Neoplasms, BRCA1 Protein, DNA, Neoplasm, Exons, Middle Aged, Molecular biology, genomic DNA, Female, DNA microarray, HeLa Cells
-
5
المؤلفون: Xiaoqi Yang, Yajue Huang, Irma H. Russo, Jose Russo, Yuli Wu, Abdel Zekri, Betsy Bove
المصدر: Molecular Carcinogenesis. 24:118-127
مصطلحات موضوعية: Cancer Research, Autosome, Loss of Heterozygosity, Chromosome, Microsatellite instability, Breast Neoplasms, Epithelial Cells, Locus (genetics), DNA, Neoplasm, DNA, Satellite, Biology, medicine.disease, Molecular biology, Chromosome 17 (human), Loss of heterozygosity, Cell Transformation, Neoplastic, medicine, Chromosomes, Human, Humans, Female, DNA mismatch repair, neoplasms, Molecular Biology, X chromosome
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac7d6a141af2547ae11cfcf5cc30b788
https://doi.org/10.1002/(sici)1098-2744(199902)24:2<118::aid-mc6>3.0.co;2-l -
6
المؤلفون: Neal J. Meropol, Fang Zhu, Frank Zambito, Efrat Dotan, Kathy Q. Cai, Andrew K. Godwin, Steven J. Cohen, Erica A. Golemis, Betsy Bove, Igor Astsaturov
المصدر: British Journal of Cancer
مصطلحات موضوعية: Male, Cancer Research, Colorectal cancer, medicine.medical_treatment, Gene Dosage, Biology, Protein Serine-Threonine Kinases, medicine.disease_cause, Bioinformatics, aurora kinase A, Gene dosage, Disease-Free Survival, Proto-Oncogene Proteins p21(ras), 03 medical and health sciences, 0302 clinical medicine, Aurora Kinases, Proto-Oncogene Proteins, copy number, Antineoplastic Combined Chemotherapy Protocols, medicine, Humans, In patient, Neoplasm Metastasis, Molecular Diagnostics, 030304 developmental biology, 0303 health sciences, Mutation, Chemotherapy, KRAS mutation, Middle Aged, medicine.disease, Prognosis, digestive system diseases, 3. Good health, Aurora Kinase A Gene, Oncology, colon cancer, 030220 oncology & carcinogenesis, embryonic structures, Cancer research, ras Proteins, Female, Aurora Kinase A, biological phenomena, cell phenomena, and immunity, Colorectal Neoplasms, Kras mutation
-
7
المؤلفون: Antoniou, Antonis C., Kuchenbaecker, Karoline B., Penny, Soucy, Jonathan, Beesley, Xiaoqing, Chen, Lesley, Mcguffog, Andrew, Lee, Daniel, Barrowdale, Sue, Healey, Sinilnikova, Olga M., Caligo, Maria A., Niklas, Loman, Katja, Harbst, Annika, Lindblom, Brita, Arver, Richard, Rosenquist, Per, Karlsson, Kate, Nathanson, Susan, Domchek, Tim, Rebbeck, Anna, Jakubowska, Jan, Lubinski, Katarzyna, Jaworska, Katarzyna, Durda, Zlowocka Perlowska, E., Elzbieta Złowowcka Perłowska, Ana, Osorio, Mercedes, Duran, Raquel, Andres, Javier, Benitez, Ute, Hamann, Hogervorst, Frans B., Van, A., Van Os, Theo A., Senno, Verhoef, Meijers Heijboer, Hanne E. J., Juul, Wijnen, Gomez Garcia, Encarna B., Ligtenberg, Marjolijn J., Mieke, Kriege, Margriet Collee, J., Margreet Gem Ausems, Oosterwijk, Jan C., Susan, Peock, Debra, Frost, Ellis, Steve D., Radka, Platte, Elena, Fineberg, Gareth Evans, D., Fiona, Lalloo, Chris, Jacobs, Ros, Eeles, Julian, Adlard, Rosemarie, Davidson, Trevor, Cole, Jackie, Cook, Joan, Paterson, Fiona, Douglas, Carole, Brewer, Shirley, Hodgson, Morrison, Patrick J., Lisa, Walker, Rogers, Mark T., Alan, Donaldson, Huw, Dorkins, Godwin, Andrew K., Betsy, Bove, Dominique Stoppa Lyonnet, Claude, Houdayer, Bruno, Buecher, De Pauw, A., Antoine Pauw, D. E., Sylvie, Mazoyer, Alain, Calender, Melanie, Leone, Brigitte Bressac De Paillerets, Olivier, Caron, Hagay, Sobol, Marc, Frenay, Fabienne, Prieur, Sandra, Ferrer, Isabelle, Mortemousque, Saundra, Buys, Mary, Daly, Alexander, Miron, Terry, Mb, Terry, Mu, Mary, Terry, Hopper, John L., John, Em, Esther, John M., Melissa, Southey, David, Goldgar, Singer, Christian F., Anneliese Fink Retter, Muy Kheng Tea, Geschwantler Kaulich, D., Daphne, Kaulich, Hansen, Thomas V. O., Nielsen, Finn C., Barkardottir, Rosa B., Mia, Gaudet, Tomas, Kirchhoff, Joseph, V., Joseph, Vijai, Ana Dutra Clarke, Kenneth, Offit, Marion, Piedmonte, Judy, Kirk, David, Cohn, Jean, Hurteau, John, Byron, James, Fiorica, Toland, Amanda E., Marco, Montagna, Cristina, Oliani, Evgeny, Imyanitov, Claudine, Isaacs, Laima, Tihomirova, Ignacio, Blanco, Conxi, Lazaro, Alex, Teule, Del Valle, J., Gayther, Simon A., Kunle, Odunsi, Jenny, Gross, Karlan, Beth Y., Edith, Olah, Soo Hwang Teo, Ganz, Patricia A., Beattie, Mary S., Dorfling, Cecelia M., Jansen Van Rensburg, E., Elizabeth Van Rensburg, Orland, Diez, Ava, Kwong, Schmutzler, Rita K., Barbara, Wappenschmidt, Christoph, Engel, Alfons, Meindl, Nina, Ditsch, Norbert, Arnold, Simone, Heidemann, Dieter, Niederacher, Sabine Preisler Adams, Dorothea, Gadzicki, Raymonda Varon Mateeva, Helmut, Deissler, Andrea, Gehrig, Christian, Sutter, Karin, Kast, Britta, Fiebig, Dieter, Schafer, Trinidad, Caldes, Miguel De La Hoya, Heli, Nevanlinna, Muranen, Taru A., Bernard, Lesperance, Spurdle, Amanda B., Neuhausen, Susan L., Ding, Yuan C., Xianshu, Wang, Zachary, Fredericksen, Pankratz, Vernon S., Lindor, Noralane M., Paolo, Peterlongo, Siranoush, Manoukian, Bernard, Peissel, Daniela, Zaffaroni, Bernardo, Bonanni, Loris, Bernard, Riccardo, Dolcetti, Laura, Papi, Ottini, Laura, Paolo, Radice, Greene, Mark H., Loud, Jennifer T., Andrulis, Irene L., Hilmi, Ozcelik, Anna, Mulligan, Gord, Glendon, Mads, Thomassen, Anne Marie Gerdes, Jensen, Uffe B., Anne Bine Skytte, Kruse, Torben A., Georgia Chenevix Trench, Couch, Fergus J., Jacques, Simard, Easton, Douglas F., Swedish Breast, Cancer Study S. B., Facility, Research H., Study, E., Collaborators, Study G., Investigators, K., Swe Brca Cimba, Embrace, Hebon, Study Gemo Collaborators, Kconfab, Investigators
المساهمون: BMC, Ed., Collaborative Oncological Gene-environment Study - COGS - - EC:FP7:HEALTH2009-05-01 - 2014-01-31 - 223175 - VALID, Centre for Cancer Genetic Epidemiology, University of Cambridge [UK] (CAM), Cancer Genomics Laboratory, Centre Hospitalier Universitaire de Québec, Genetics and Population Health Division, Queensland Institute of Medical Research, Unité Mixte de Génétique Constitutionnelle des Cancers Fréquents, Centre Léon Bérard [Lyon]-Hospices Civils de Lyon (HCL), Centre de Recherche en Cancérologie de Lyon (UNICANCER/CRCL), Centre Léon Bérard [Lyon]-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Section of Genetic Oncology, University of Pisa - Università di Pisa, Department of Oncology, Lund University Hospital, Department of Clinical Genetics, Karolinska University Hospital [Stockholm], Department of Genetics and Pathology, Uppsala University-Rudbeck Laboratory, Sahlgrenska University Hospital [Gothenburg], Abramson Cancer Center, University of Pennsylvania-Perelman School of Medicine, University of Pennsylvania, International Hereditary Cancer Centre-Pomeranian Medical University [Szczecin] (PUM), Postgraduate School of Molecular Medicine, Warsaw Medical University, Human Genetics Group, Spanish National Cancer Research Centre, Biomedical Research Centre Network for Rare Diseases, CIBER de Enfermedades Raras (CIBERER), Institute of Biology and Molecular Genetics, Universidad de Valladolid [Valladolid] (UVa), Medical Oncology Division, Hospital Clínico de Zaragoza, Molecular Genetics of Breast Cancer, German Cancer Research Center - Deutsches Krebsforschungszentrum [Heidelberg] (DKFZ), Family Cancer Clinic, Netherlands Cancer Institute, Academic Medical Center - Academisch Medisch Centrum [Amsterdam] (AMC), University of Amsterdam [Amsterdam] (UvA)-University of Amsterdam [Amsterdam] (UvA), VU Medical Center, Department of Clinical Genetics and GROM, School for Oncology and Developmental Biology, Department of Human Genetics, Radboud University [Nijmegen], Erasmus University Medical Center [Rotterdam] (Erasmus MC)-Family Cancer Clinic, Department of Clinical Molecular Genetics, University Medical Center [Utrecht], Department of Genetics, VU University Medical Center [Amsterdam], Genetic Medicine, Manchester Academic Health Sciences Centre-Central Manchester University Hospitals, Clinical Genetics, Guy's and St. Thomas' NHS Foundation Trust, Oncogenetics Team, The Institute of Cancer Research-Royal Marsden NHS Foundation Trust, Yorkshire Regional Genetics Service, Ferguson-Smith Centre for Clinical Genetics, Yorkhill Hospitals, West Midlands Regional Genetics Service, Birmingham Women's and Children's NHS Foundation Trust, Sheffield Clinical Genetics Service, Sheffield Children's NHS Foundation Trust, Addenbrookes Hospital, Institute of Human Genetics, Newcastle Upon Tyne Hospitals NHS Foundation Trust, Royal Devon & Exeter Hospital, Medical Genetics Unit, University College of London [London] (UCL), Northern Ireland Regional Genetics Centre, Belfast Health and Social Care Trust, Department of Medical Genetics, Queen's University [Belfast] (QUB), Oxford Regional Genetics Service, Churchill Hospital Oxford Centre for Haematology, All Wales Medical Genetics Services, Singleton Hospital, Clinical Genetics Department, St Michael's Hospital, North West Thames Regional Genetics Service, Kennedy-Galton Centre, Department of Pathology and Laboratory Medicine, University of Kansas Medical Center [Kansas City, KS, USA], Clinical Molecular Genetics Laboratory, Fox Chase Cancer Center, Service de Génétique Oncologique, Institut Curie [Paris], Unité de génétique et biologie des cancers (U830), Université Paris Descartes - Paris 5 (UPD5)-Institut Curie [Paris]-Institut National de la Santé et de la Recherche Médicale (INSERM), Service de génétique, Institut Gustave Roussy (IGR), Variabilité Génétique et Maladies Humaines, Institut Universitaire d'Hématologie (IUH), Université Paris Diderot - Paris 7 (UPD7)-Université Paris Diderot - Paris 7 (UPD7)-Institut National de la Santé et de la Recherche Médicale (INSERM), Consultation de génétique, Hôpital Sainte-Marguerite [CHU - APHM] (Hôpitaux Sud ), Service d'Oncologie Génétique, de Prévention et Dépistage, Centre de Lutte contre le Cancer Antoine Lacassagne [Nice] (UNICANCER/CAL), UNICANCER-Université Côte d'Azur (UCA), Service de Génétique Clinique Chromosomique et Moléculaire, CHU Saint-Etienne, Laboratoire de Génétique Chromosomique, CH Chambéry, Service de génétique [Tours], Centre Hospitalier Régional Universitaire de Tours (CHRU Tours)-Hôpital Bretonneau, Department of Internal Medicine, Huntsman Cancer Institute, Division of Population Science, Department of Cancer Biology, Dana-Farber Cancer Institute [Boston], Department of Surgery, Harvard Medical School [Boston] (HMS), Department of Epidemiology, Columbia University [New York], Centre for Molecular , Environmental, Genetic and Analytic (MEGA) Epidemiology, University of Melbourne-Centre for Molecular, Melbourne School of Population Health, Cancer Prevention Institute of California, entre for Molecular, Environmental, Genetic and Analytic (MEGA) Epidemiology, University of Melbourne, Department of Dermatology, University of Utah School of Medicine [Salt Lake City], Dept of OB/GYN and Comprehensive Cancer Center, Medizinische Universität Wien = Medical University of Vienna, Center for Genomic Medicine, Copenhagen University Hospital-Rigshospitalet [Copenhagen], Copenhagen University Hospital, Department of Pathology, University of Iceland [Reykjavik]-Landspitali - University Hospital, Epidemiology Research Program, American Cancer Society, Department of Environmental Medicine, New York University School of Medicine, NYU System (NYU)-NYU System (NYU)-NYU Cancer Institute, Clinical Genetics Service, Memorial Sloane Kettering Cancer Center [New York], Statistical and Data Center, Roswell Park Cancer Institute [Buffalo], Australia New Zealand (ANZGOG), Westmead Hospital [Sydney], Ohio State University [Columbus] (OSU), Evanston CCOP - NorthShore University Health System, University of Chicago, Southern Pines Women's Health Center, University of North Carolina [Chapel Hill] (UNC), University of North Carolina System (UNC)-University of North Carolina System (UNC), Sarasota Memorial Healthcare, Tufts Medical Center, Department of Molecular Virology, Immunology and Medical Genetics [Colombus], Ohio State University [Columbus] (OSU)-College of Medicine and Public Health [Colombus], Immunology and Molecular Oncology Unit, Istituto Oncologico Veneto IOV - IRCCS, U.O.C. di Oncologia, Laboratory of Molecular Oncology, N.N. Petrov Institute of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University [Washington] (GU), Latvian Biomedical Research and Study Centre [Rīga], Genetic Counselling Unit, IDIBELL-Catalan Institute of Oncology, Molecular Diagnostic Unit, Department of Preventive Medicine, University of Southern California (USC)-Keck School of Medicine [Los Angeles], University of Southern California (USC), Department of Gynecologic Oncology, Women's Cancer Program, Samuel Oschin Comprehensive Cancer Institute, Department of Molecular Genetics, National Institute of Oncology, Cancer Research Initiatives Foundation, Sime Darby Medical Centre-Malaysia and University Malaya Cancer Research Institute-University Malaya Medical Centre, Jonsson Comprehensive Cancer Center at UCLA, Jonsson Comprehensive Cancer Center, UCSF Cancer Risk Program, University of California (UC), Departments of Medicine, Epidemiology, and Biostatistics, UCSF, Cancer Genetics Laboratory, University of Pretoria [South Africa], Oncogenetics Laboratory, Vall d'Hebron Institute of Oncology (VHIO), The Hong Kong Hereditary Breast Cancer Family Registry, The University of Hong Kong (HKU), Department of Gynaecology and Obstetrics, University Hospital of Cologne [Cologne]-Centre of Familial Breast and Ovarian Cancer-Centre for Integrated Oncology (CIO), Institute for Medical Informatics, Statistics and Epidemiology [Leipzig] (IMISE), Universität Leipzig [Leipzig], Technische Universität Munchen - Université Technique de Munich [Munich, Allemagne] (TUM), Ludwig-Maximilians-Universität München (LMU), University Hospital of Schleswig-Holstein-Christian-Albrechts-Universität zu Kiel (CAU), University Hospital Düsseldorf-Heinrich Heine Universität Düsseldorf = Heinrich Heine University [Düsseldorf], Westfälische Wilhelms-Universität Münster = University of Münster (WWU), Institute of Cell and Molecular Pathology, Hannover Medical School [Hannover] (MHH), Charité - UniversitätsMedizin = Charité - University Hospital [Berlin], Universitätsklinikum Ulm - University Hospital of Ulm, Julius-Maximilians-Universität Würzburg (JMU)-Centre of Familial Breast and Ovarian Cancer, Heidelberg University Hospital [Heidelberg], University Hospital Carl Gustav Carus, Universität Regensburg (UR), University Hospital Frankfurt a.M., Molecular Oncology Laboratory, Hospital Clínico San Carlos, Department of Obstetrics and Gynecology, Helsinki University Central Hospital, Hemato-oncology service, Hôpital du Sacré-Coeur de Montréal, Department of Population Sciences, Beckman Research Institute of City of Hope, Department of Laboratory Medicine and Pathology, Mayo Clinic, Unit of Molecular Bases of Genetic Risk and Genetic Testing, Fondazione IRCCS Istituto Nazionale Tumouri (INT)-Fondazione Istituto FIRC di Oncologia Molecolare, Unit of Medical Genetics, Fondazione IRCCS Istituto Nazionale Tumouri (INT), Division of Cancer Prevention and Genetics, Department of Experimental Oncology, Istituto Europeo di Oncologia-Consortium for Genomics Technology (Cogentech), Cancer Bioimmunotherapy Unit, IRCCS-Centro di Riferimento Oncologico, Università degli Studi di Firenze = University of Florence (UniFI), Department of Molecular Medicine, Università degli Studi di Roma 'La Sapienza' = Sapienza University [Rome] (UNIROMA), Clinical Genetics Branch, National Cancer Institute [Bethesda] (NCI-NIH), National Institutes of Health [Bethesda] (NIH)-National Institutes of Health [Bethesda] (NIH), Departments of Molecular Genetics and Laboratory Medicine and Pathobiology, University of Toronto-Cancer Care Ontario, Samuel Lunenfeld Research Institute, Mount Sinai Hospital [Toronto, Canada] (MSH), Department of Laboratory Medicine and Pathobiology, University of Toronto, Department of Laboratory Medicine, St Michael's Hospital-Keenan Research Centre of the Li Ka Shing Knowledge Institute [Toronto], Ontario Cancer Genetics Network, Cancer Care Ontario, Odense University Hospital, Department of Clinical Genetics [Copenhagen], Rigshospitalet [Copenhagen], Copenhagen University Hospital-Copenhagen University Hospital, Skejby Hospital, Department of Laboratory Medicine and Pathology and Health Sciences Research, This work was supported by Cancer Research UK grants C12292/A11174 and C1287/A10118. The research leading to these results has received funding from the European Community's Seventh Framework Programme under grant agreement n° 223175 (HEALTH-F2-2009-223175), from the Canadian Institutes of Health Research for the 'CIHR Team in Familial Risks of Breast Cancer' program and by the Canadian Breast Cancer Research Alliance-grant #019511. This research was also supported by NIH grant CA128978, an NCI Specialized Program of Research Excellence (SPORE) in Breast Cancer (CA116201), a U.S. Department of Defence Ovarian Cancer Idea award (W81XWH-10-1-0341) and grants from the Breast Cancer Research Foundation and the Komen Foundation for the Cure. ACA is a CR-UK Senior Cancer Research Fellow, DFE is CR-UK Principal Research Fellow, GCT is a NHMRC Senior Principal Research Fellow, J.S. is Chairholder of the Canada Research Chair in Oncogenetics, on behalf of CIMBA, SWE-BRCA, HEBON, EMBRACE, GEMO Study Collaborators and kConFab Investigators, European Project: 223175,EC:FP7:HEALTH,FP7-HEALTH-2007-B,COGS(2009), Pediatric Surgery, Neurology, Medical Oncology, Centre Hospitalier Universitaire de Saint-Etienne [CHU Saint-Etienne] (CHU ST-E), Roswell Park Cancer Institute [Buffalo] (RPCI), Universität Leipzig, Université de Lyon-Université de Lyon-Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM), University of Pennsylvania [Philadelphia]-Perelman School of Medicine, University of Pennsylvania [Philadelphia], Pomeranian Medical University-International Hereditary Cancer Centre, Radboud university [Nijmegen], University of Kansas Medical Center [Lawrence], Institut Curie [Paris]-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Paris Descartes - Paris 5 (UPD5), Georgetown University, University of California, Westfälische Wilhelms-Universität Münster (WWU), Julius-Maximilians-Universität Würzburg [Wurtzbourg, Allemagne] (JMU)-Centre of Familial Breast and Ovarian Cancer, Università degli Studi di Firenze = University of Florence [Firenze] (UNIFI), Università degli Studi di Roma 'La Sapienza' = Sapienza University [Rome], RS: GROW - School for Oncology and Reproduction, Genetica & Celbiologie, Hôpital Bretonneau-Centre Hospitalier Régional Universitaire de Tours (CHRU Tours), Human Genetics, CCA -Cancer Center Amsterdam, ARD - Amsterdam Reproduction and Development, Human genetics, CCA - Oncogenesis
المصدر: Breast Cancer Research; 14(1) (2012)
Breast cancer research, 14(1):33. BioMed Central Ltd.
Breast Cancer Research
Breast Cancer Research, 2012, 14 (1), pp.R33. ⟨10.1186/bcr3121⟩
Breast Cancer Research : BCR
Antoniou, Antonis C; Kuchenbaecker, Karoline B; Soucy, Penny; Beesley, Jonathan; Chen, Xiaoqing; McGuffog, Lesley; et al.(2012). Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers. Breast Cancer Research, 14(1), R33. doi: http://dx.doi.org/10.1186/bcr3121. Retrieved from: http://www.escholarship.org/uc/item/9n99d8tb
Breast Cancer Research, 14(1)
Breast Cancer Research, 14(1). BioMed Central Ltd.
Breast Cancer Research; Vol 14
Antoniou, A, Kuchenbaecker, K, Soucy, P, Beesley, J, Chen, X, McGuffog, L, Lee, A, Barrowdale, D, Healey, S, Sinilnikova, O, Caligo, M, Loman, N, Harbst, K, Lindblom, A, Arver, B, Rosenquist, R, Karlsson, P, Nathanson, K, Domchek, S, Rebbeck, T, Jakubowska, A, Lubinski, J, Jaworska, K, Durda, K, Złowowcka-Perłowska, E, Osorio, A, Durán, M, Andrés, R, Benítez, J, Hamann, U, Hogervorst, F, van Os, T, Verhoef, S, Meijers-Heijboer, H, Wijnen, J, Gómez Garcia, E, Ligtenberg, M, Kriege, M, Collée, J M, Ausems, M, Oosterwijk, J, Peock, S, Frost, D, Ellis, S, Platte, R, Fineberg, E, Thomassen, M, Gerdes, A-M, Skytte, A-B, Kruse, T A & CIMBA, SWE-BRCA 2012, ' Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers ', Breast Cancer Research (Online Edition), vol. 14, no. 1, pp. R33 . https://doi.org/10.1186/bcr3121
Breast Cancer Research, BioMed Central, 2012, 14 (1), pp.R33. ⟨10.1186/bcr3121⟩
Breast Cancer Research, 14(1):R33. BioMed Central Ltd
Antoniou, A C, Kuchenbaecker, K B, Soucy, P, Beesley, J, Chen, X Q, McGuffog, L, Lee, A, Barrowdale, D, Healey, S, Sinilnikova, O M, Caligo, M A, Loman, N, Harbst, K, Lindblom, A, Arver, B, Rosenquist, R, Karlsson, P, Nathanson, K, Domchek, S, Rebbeck, T, Jakubowska, A, Lubinski, J, Jaworska, K, Durda, K, Zlowowcka-Perlowska, E, Osorio, A, Duran, M, Andres, R, Benitez, J, Hamann, U, Hogervorst, FB, Os, T A, Verhoef, S, Meijers-Heijboer, E J, van Wijnen, J, Garcia, E B G, Ligtenberg, M J, Kriege, M, Collee, M, Ausems, M G E M, Oosterwijk, J C, Peock, S, Frost, D, Ellis, S D, Platte, R, Fineberg, E, Evans, D G, Lalloo, F, Jacobs, C, Eeles, R, Adlard, J, Davidson, R, Cole, T, Cook, J, Paterson, J, Douglas, F, Brewer, C, Hodgson, S, Morrison, P J, Walker, L, Rogers, M T, Donaldson, A, Dorkins, H, Godwin, A K, Bove, B, Stoppa-Lyonnet, D, Houdayer, C, Buecher, B, de Pauw, A, Mazoyer, S, Calender, A, Leone, M, Bressac-de Paillerets, B, Caron, O, Sobol, H, Frenay, M, Prieur, F, Ferrer, S F, Mortemousque, I, Buys, S, Daly, M, Miron, A, Terry, M B, Hopper, J L, John, E M, Southey, M, Goldgar, D, Singer, C F, Fink-Retter, A, Tea, M K, Kaulich, D G, Hansen, T V O, Nielsen, F C, Barkardottir, R B, Gaudet, M, Kirchhoff, T, Joseph, V, Dutra-Clarke, A & Offit, K 2012, ' Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers ', Breast Cancer Research, vol. 14, no. 1, R33 . https://doi.org/10.1186/bcr3121
Antoniou, AC; Kuchenbaecker, KB; Soucy, P; Beesley, J; Chen, X; McGuffog, L; et al.(2012). Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers. BREAST CANCER RESEARCH, 14(1). doi: 10.1186/bcr3121. UCLA: Retrieved from: http://www.escholarship.org/uc/item/4pr3h3nc
Breast cancer research, 14(1). BioMed Central
Breast Cancer Research, 14(1):R33. BioMed Central
Antoniou, A C, Kuchenbaecker, K B, Soucy, P, Beesley, J, Chen, X, McGuffog, L, Lee, A R, Barrowdale, D, Healey, S, Sinilnikova, O M, Caligo, M A, Loman, N, Harbst, K, Lindblom, A, Arver, B, Rosenquist, R, Karlsson, P W, Nathanson, K, Domchek, S, Rebbeck, T, Jakubowska, A, Lubinski, J, Jaworska, K, Durda, K, Złowowcka-Perłowska, E, Osorio, A, Durán, M, Andrés, R, Benítez, J, Hamann, U, Hogervorst, F B, van Os, T A, Verhoef, S, Meijers-Heijboer, H E J, Wijnen, J, Gómez Garcia, E B, Ligtenberg, M J, Kriege, M, Collée, J M, Ausems, M G E M, Oosterwijk, J C, Peock, S, Frost, D, Ellis, S D, Platte, R, Fineberg, E, Evans, D G, Lalloo, F, Jacobs, C, Jensen, U B, Skytte, A-B S & CIMBA, SWE-BRCA 2012, ' Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers ', Breast Cancer Research (Online Edition), vol. 14, no. 1, pp. R33 . https://doi.org/10.1186/bcr3121مصطلحات موضوعية: Oncology, Medicin och hälsovetenskap, Estrogen receptor, Genome-wide association study, HORMONE-RELATED PROTEIN, Chromosomes, Human, Pair 9 - genetics, Medical and Health Sciences, 0302 clinical medicine, 610 Medical sciences Medicine, CDKN2A, Risk Factors, Genotype, INVESTIGATORS, Chromosomes, Human, Pair 12 - genetics, skin and connective tissue diseases, MAMMOGRAPHIC DENSITY, Medicine(all), 0303 health sciences, BRCA1 Protein, Middle Aged, BRCA2 Protein, 3. Good health, DNA-Binding Proteins, Hereditary Breast and Ovarian Cancer Syndrome - genetics, 030220 oncology & carcinogenesis, Hereditary Breast and Ovarian Cancer Syndrome, TUMOR SUBTYPES, Female, Chromosomes, Human, Pair 9, Research Article, Adult, Breast cancer, BRCA1, BRCA2, medicine.medical_specialty, Heterozygote, SUSCEPTIBILITY LOCI, Single-nucleotide polymorphism, [SDV.CAN]Life Sciences [q-bio]/Cancer, Biology, Polymorphism, Single Nucleotide, OVARIAN-CANCER, 03 medical and health sciences, [SDV.CAN] Life Sciences [q-bio]/Cancer, SDG 3 - Good Health and Well-being, Internal medicine, medicine, Humans, ddc:610, GENOME-WIDE ASSOCIATION, ddc:611, Genetic Association Studies, 030304 developmental biology, Aged, Gynecology, Chromosomes, Human, Pair 12, CONSORTIUM, BRCA1 Protein - genetics, ALLELES, medicine.disease, BRCA2 Protein - genetics, Cancer and Oncology, GENETIC MODIFIERS, Ovarian cancer, Transcription Factors
وصف الملف: application/pdf
-
8
المؤلفون: Cynthia Bergman, Andrew K. Godwin, Betsy Bove, Mitchell I. Edelson, Norman G. Rosenblum, Suzanne M. Miller, Steven D. Douglas, Donald E. Campbell, Carolyn Y. Fang, Dana H. Bovbjerg
المصدر: Annals of behavioral medicine : a publication of the Society of Behavioral Medicine. 35(1)
مصطلحات موضوعية: Adult, Cross-sectional study, T-Lymphocytes, Cervical intraepithelial neoplasia, Severity of Illness Index, Article, 03 medical and health sciences, 0302 clinical medicine, Immunity, Reference Values, Uterine Cervical Dysplasia, Severity of illness, medicine, Humans, 030212 general & internal medicine, Psychology(all), General Psychology, Human papillomavirus 16, business.industry, Papillomavirus Infections, HPV infection, Case-control study, virus diseases, Middle Aged, medicine.disease, female genital diseases and pregnancy complications, 3. Good health, Psychiatry and Mental health, Cross-Sectional Studies, Dysplasia, 030220 oncology & carcinogenesis, Case-Control Studies, Immunology, Female, business, Stress, Psychological
-
9
المؤلفون: John Malick, Mary B. Daly, Betsy Bove, Josephine Wagner Costalas, James Babb, Andrew K. Godwin, Mark Itzen
المصدر: American journal of medical genetics. Part C, Seminars in medical genetics. (1)
مصطلحات موضوعية: Proband, Adult, congenital, hereditary, and neonatal diseases and abnormalities, endocrine system diseases, Adolescent, Genetic counseling, Genes, BRCA2, Genes, BRCA1, Breast Neoplasms, Disclosure, Risk Assessment, Cancer risk assessment, Medicine, Humans, Family, Genetic Testing, Risk factor, skin and connective tissue diseases, Genetics (clinical), Genetic testing, Aged, Genetics, Family Health, Ovarian Neoplasms, medicine.diagnostic_test, business.industry, Communication, Data Collection, Middle Aged, Test (assessment), Distress, Female, business, Risk assessment, Stress, Psychological, Clinical psychology
-
10
المؤلفون: Andrew K. Godwin, Betsy Bove, Joellen Dangel, Mark Itzen, Mary B. Daly, Lisa Vanderveer, Josephine Wagner-Costalas
المصدر: Human Mutation. 14:545-545
مصطلحات موضوعية: Adult, African american, Molecular Sequence Data, Genes, BRCA1, Black People, Biology, medicine.disease, Polymerase Chain Reaction, Germline, Breast cancer, Genetics, medicine, Cancer research, Humans, Female, Frameshift Mutation, Novel mutation, Genetics (clinical), Brca1 gene, Chromosomes, Human, Pair 17, Sequence Deletion, Early onset
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a092a1194070d808ba7031efccd95903
https://doi.org/10.1002/(sici)1098-1004(199912)14:6<545::aid-humu19>3.0.co;2-g