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1. Full Text Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
by Milne, Roger L and Kuchenbaecker, Karoline B and Michailidou, Kyriaki and Beesley, Jonathan and Kar, Siddhartha and Lindström, Sara and Hui, Shirley and Lemaçon, Auey and Soucy, Penny and Dennis, Joe and Jiang, Xia and Rostamianfar, Asha and Finucane, Hilary and Bolla, Manjeet K and McGuffog, Lesley and Wang, Qin and Aalfs, Cora M and Adams, Marcia and Adlard, Julian and Agata, Simona and Ahmed, Shahana and Ahsan, Habibul and Aittomäki, Kristiina and Al-Ejeh, Fares and Allen, Jamie and Ambrosone, Christine B and Amos, Christopher I and Anulis, Irene L and Anton-Culver, Hoda and Antonenkova, Natalia N and Arndt, Volker and Arnold, Norbert and Aronson, Kristan J and Auber, Bernd and Auer, Paul L and Ausems, Margreet G. E. M and Azzollini, Jacopo and Bacot, François and Balmaña, Judith and Barile, Monica and Barjhoux, Laure and Barkardottir, Rosa B and Barrdahl, Myrto and Barnes, Daniel and Barrowdale, Daniel and Baynes, Caroline and Beckmann, Matthias W and Benitez, Javier and Bermisheva, Marina and Bernstein, Leslie and Bignon, Yves-Jean and Blazer, Kathleen R and Blok, Marinus J and Blomqvist, Carl and Blot, William and Bobolis, Kristie and Boeckx, Bram and Bogdanova, Natalia V and Bojesen, Anders and Bojesen, Stig E and Bonanni, Bernardo and Børresen-Dale, Anne-Lise and Bozsik, Aniko and Bradbury, Angela R and Brand, Judith S and Brauch, Hiltrud and Brenner, Hermann and Bressac-de Paillerets, Brigitte and Brewer, Carole and Brinton, Louise and Broberg, Per and Brooks-Wilson, Angela and Brunet, Joan and Brüning, Thomas and Burwinkel, Barbara and Buys, Sauna S and Byun, Jinyoung and Cai, Qiuyin and Caldés, Trinidad and Caligo, Maria A and Campbell, Ian and Canzian, Federico and Caron, Olivier and Carracedo, Angel and Carter, Brian D and Castelao, J. Esteban and Castera, Laurent and Caux-Moncoutier, Virginie and Chan, Salina B and Chang-Claude, Jenny and Chanock, Stephen J and Chen, Xiaoqing and Cheng, Ting-Yuan David and Chiquette, Jocelyne and Christiansen, Hans and Claes, Kathleen B. M and Clarke, Christine L and Conner, Thomas and Conroy, Don M and Cook, Jackie and ... and ABCTB Investigators and HEBON and EMBRACE and GEMO Study Collaborators and kConFab AOCS Investigators and NBSC Collaborators and kConFab/AOCS Investigators
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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2. Full Text Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer
by Phelan, Catherine M and Kuchenbaecker, Karoline B and Tyrer, Jonathan P and Kar, Siddhartha P and Lawrenson, Kate and Winham, Stacey J and Dennis, Joe and Pirie, Ailith and Riggan, Marjorie J and Chornokur, Ganna and Earp, Madalene A and Lyra, Paulo C and Lee, Janet M and Coetzee, Simon and Beesley, Jonathan and McGuffog, Lesley and Soucy, Penny and Dicks, Ed and Lee, Anew and Barrowdale, Daniel and Lecarpentier, Julie and Leslie, Goska and Aalfs, Cora M and Aben, Katja K. H and Adams, Marcia and Adlard, Julian and Anulis, Irene L and Anton-Culver, Hoda and Antonenkova, Natalia and Aravantinos, Gerasimos and Arnold, Norbert and Arun, Banu K and Arver, Brita and Azzollini, Jacopo and Balmaña, Judith and Banerjee, Susana N and Barjhoux, Laure and Barkardottir, Rosa B and Bean, Yukie and Beckmann, Matthias W and Beeghly-Fadiel, Alicia and Benitez, Javier and Bermisheva, Marina and Bernardini, Marcus Q and Birrer, Michael J and Bjorge, Line and Black, Amanda and Blankstein, Kenneth and Blok, Marinus J and Bodelon, Clara and Bogdanova, Natalia and Bojesen, Anders and Bonanni, Bernardo and Borg, Åke and Bradbury, Angela R and Brenton, James D and Brewer, Carole and Brinton, Louise and Broberg, Per and Brooks-Wilson, Angela and Bruinsma, Fiona and Brunet, Joan and Buecher, Bruno and Butzow, Ralf and Buys, Sauna S and Caldes, Trinidad and Caligo, Maria A and Campbell, Ian and Cannioto, Rikki and Carney, Michael E and Cescon, Terence and Chan, Salina B and Chang-Claude, Jenny and Chanock, Stephen and Chen, Xiao Qing and Chiew, Yoke-Eng and Chiquette, Jocelyne and Chung, Wendy K and Claes, Kathleen B. M and Conner, Thomas and Cook, Linda S and Cook, Jackie and Cramer, Daniel W and Cunningham, Julie M and D'Aloisio, Aimee A and Daly, Mary B and Damiola, Francesca and Damirovna, Sakaeva Dina and Dansonka-Mieszkowska, Agnieszka and Dao, Fanny and Davidson, Rosemarie and Defazio, Anna and Delnatte, Capucine and Doheny, Kimberly F and Diez, Orland and Ding, Yuan Chun and Doherty, Jennifer Anne and Domchek, Susan M and Dorfling, Cecilia M and Dörk, Thilo and ... and KConFab Investigators and EMEMBRACE Study and GEMO Study Collaborators and OPAL Study Grp and AOCS Study Grp and HEBON Study and AOCS study group and EMBRACE Study and OPAL study group
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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3. Full Text Mutational Spectrum in a Worldwide Study of 29,700 Families with BRCA1 or BRCA2 Mutations
by Rebbeck, Timothy R and Friebel, Tara M and Friedman, Eitan and Hamann, Ute and Huo, Dezheng and Kwong, Ava and Olah, Edith and Olopade, Olufunmilayo I and Solano, Angela R and teo, Soo-Hwang and Thomassen, Mads and Weitzel, Jeffrey N and Chan, T. L and Couch, Fergus J and Goldgar, David E and Kruse, Torben A and Palmero, Edenir Inêz and Park, Sue Kyung and Torres, Diana and van Rensburg, Elizabeth J and McGuffog, Lesley and Parsons, Michael T and Leslie, Goska and Aalfs, Cora M and Abugattas, Julio and Adlard, Julian and Agata, Simona and Aittomäki, Kristiina and Anews, Lesley and Anulis, Irene L and Arason, Adalgeir and Arnold, Norbert and Arun, Banu K and Asseryanis, Ella and Auerbach, Leo and Azzollini, Jacopo and Balmaña, Judith and Barile, Monica and Barkardottir, Rosa B and Barrowdale, Daniel and Benitez, Javier and Berger, Aneas and Berger, Raanan and Blanco, Amie M and Blazer, Kathleen R and Blok, Marinus J and Bonadona, Valérie and Bonanni, Bernardo and Bradbury, Angela R and Brewer, Carole and Buecher, Bruno and Buys, Sauna S and Caldes, Trinidad and Caliebe, Almuth and Caligo, Maria A and Campbell, Ian and Caputo, Sanine and Chiquette, Jocelyne and Chung, Wendy K and Claes, Kathleen B. M and Collée, J. Margriet and Cook, Jackie and Davidson, Rosemarie and de la Hoya, Miguel and de Leeneer, Kim and de Pauw, Antoine and Delnatte, Capucine and Diez, Orland and Ding, Yuan Chun and Ditsch, Nina and Domchek, Susan M and Dorfling, Cecilia M and Velazquez, Carolina and Dworniczak, Bernd and Eason, Jacqueline and Easton, Douglas F and Eeles, Ros and Ehrencrona, Hans and Ejlertsen, Bent and Engel, Christoph and Engert, Stefanie and Evans, D. Gareth and Faivre, Laurence and Feliubadaló, Lidia and Ferrer, Sana Fert and Foretova, Lenka and Fowler, Jeffrey and Frost, Debra and Galvão, Henrique C. R and Ganz, Patricia A and Garber, Judy and Gauthier-Villars, Marion and Gehrig, Anea and Gerdes, Anne-Marie and Gesta, Paul and Giannini, Giuseppe and Giraud, Sophie and Glendon, Gord and Godwin, Anew K and Greene, Mark H and ... and KConFab Investigators and HEBON and EMBRACE and GEMO Study Collaborators
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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4. Full Text Increased Use of BRCA Mutation Test in Unaffected Women Over the Period 2004–2014 in the U.S.: Further Evidence of the “Angelina Jolie Effect”?
by Nabi, Hermann and Dorval, Michel and Chiquette, Jocelyne and Simard, Jacques
American journal of preventive medicine, ISSN 0749-3797, 11/2017, Volume 53, Issue 5, pp. e195 - e196
Medicine, General & Internal | Public, Environmental & Occupational Health | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Genes, BRCA2 | Female | Genes, BRCA1 | Mutation | Humans | Index Medicus
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5. Full Text What do cancer patients’ relatives think about addressing cancer family history and performing genetic testing in palliative care?
by Cléophat, Jude E and Marin, Ana and Pelletier, Sylvie and Joly, Yann and Gagnon, Pierre and Déry, Alberte and Chiquette, Jocelyne and Gagnon, Bruno and Roy, Louis and Bitzas, Vasiliki and Nabi, Hermann and Dorval, Michel
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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6. Full Text Addressing cancer family history at the end of life: How frequent, relevant, and feasible is it? A survey of palliative care providers
by Cleophat, Jude E and Pelletier, Sylvie and Joly, Yann and Gagnon, Pierre and Déry, Alberte and Marin, Ana and Chiquette, Jocelyne and Gagnon, Bruno and Roy, Louis and Bitzas, Vasiliki and Nabi, Hermann and Dorval, Michel
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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7. Full Text A randomized double-blind placebo-controlled trial of the effect of Vitamin D3 supplementation on breast density in premenopausal women
by Brisson, Jacques and Bérubé, Sylvie and Diorio, Caroline and Mâsse, Benoît and Lemieux, Julie and Duchesne, Thierry and Delvin, Edgar and Vieth, Reinhold and Yaffe, Martin J and Chiquette, Jocelyne
Cancer epidemiology, biomarkers & prevention, ISSN 1055-9965, 08/2017, Volume 26, Issue 8, pp. 1233 - 1241
Intervention | Vitamin D3 | Calcium | Health problems | Breasts | Dietary supplements | Health risks | Mammography | Breast cancer | Density | Randomization | Calcium (blood) | Vitamin D | Biomarkers | Supplementation | Health risk assessment | Cancer | Index Medicus
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8. Full Text Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes
by Fachal, Laura and Aschard, Hugues and Beesley, Jonathan and Barnes, Daniel R and Allen, Jamie and Kar, Siddhartha and Dennis, Joe and Michailidou, Kyriaki and Turman, Constance and Soucy, Penny and Lemaçon, Audrey and Lush, Michael and Tyrer, Jonathan P and Ghoussaini, Maya and Marjaneh, Mahdi Moradi and Jiang, Xia and Agata, Simona and Aittomäki, Kristiina and Alonso, M. Rosario and Andrulis, Irene L and Anton-Culver, Hoda and Antonenkova, Natalia N and Arason, Adalgeir and Arndt, Volker and Aronson, Kristan J and Arun, Banu K and Auer, Paul L and Azzollini, Jacopo and Balmaña, Judith and Barkardottir, Rosa B and Beeghly-Fadiel, Alicia and Benitez, Javier and Bialkowska, Katarzyna and Blanco, Amie M and Blomqvist, Carl and Blot, William and Bogdanova, Natalia V and Bolla, Manjeet K and Bonanni, Bernardo and Borg, Ake and Bosse, Kristin and Brauch, Hiltrud and Brenner, Hermann and Briceno, Ignacio and Brooks-Wilson, Angela and Brüning, Thomas and Burwinkel, Barbara and Buys, Saundra S and Cai, Qiuyin and Caldés, Trinidad and Caligo, Maria A and Camp, Nicola J and Campbell, Ian and Canzian, Federico and Carter, Brian D and Castelao, Jose E and Chiquette, Jocelyne and Christiansen, Hans and Chung, Wendy K and Claes, Kathleen B. M and Clarke, Christine L and Mari, Véronique and Berthet, Pascaline and Castera, Laurent and Vaur, Dominique and Lallaoui, Hakima and Bignon, Yves-Jean and Uhrhammer, Nancy and Bonadona, Valérie and Lasset, Christine and Révillion, Françoise and Muller, Daniele and Gomes, Denise Molina and Ingster, Olivier and Coupier, Isabelle and Pujol, Pascal and Collonge-Rame, Marie-Agnès and Bera, Odile and Rose, Mickaelle and Baurand, Amandine and Bertolone, Geoffrey and Faivre, Laurence and Dreyfus, Hélène and Leroux, Dominique and Venat-Bouvet, Laurence and Delnatte, Capucine and Chiesa, Jean and Gilbert-Dussardier, Brigitte and Gesta, Paul and Prieur, Fabienne Prieur and Bronner, Myriam and Sokolowska, Johanna and Coulet, Florence and Boutry-Kryza, Nadia and Calender, Alain and Giraud, Sophie and Leone, Mélanie and Fert-Ferrer, Sandra and Stoppa-Lyonnet, Dominique and Jiao, Yue and ... and KConFab Investigators and ABCTB Investigators and HEBON Investigators and GEMO Study Collaborators and EMBRACE Collaborators
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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