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1. 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
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2. Full Text Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk
by Couch, Fergus J and Wang, Xianshu and McGuffog, Lesley and Lee, Anew and Olswold, Curtis and Kuchenbaecker, Karoline B and Soucy, Penny and Fredericksen, Zachary and Barrowdale, Daniel and Dennis, Joe and Gaudet, Mia M and Dicks, Ed and Kosel, Matthew and Healey, Sue and Sinilnikova, Olga M and Lee, Adam and Bacot, François and Vincent, Daniel and Hogervorst, Frans B. L and Peock, Susan and Stoppa-Lyonnet, Dominique and Jakubowska, Anna and Radice, Paolo and Schmutzler, Rita Katharina and Domchek, Susan M and Piedmonte, Marion and Singer, Christian F and Friedman, Eitan and Thomassen, Mads and Hansen, Thomas V. O and Neuhausen, Susan L and Szabo, Csilla I and Blanco, Ignacio and Greene, Mark H and Karlan, Beth Y and Garber, Judy and Phelan, Catherine M and Weitzel, Jeffrey N and Montagna, Marco and Olah, Edith and Anulis, Irene L and Godwin, Anew K and Yannoukakos, koulis and Goldgar, David E and Caldes, Trinidad and Nevanlinna, Heli and Osorio, Ana and Terry, Mary Beth and Daly, Mary B and van Rensburg, Elizabeth J and Hamann, Ute and Ramus, Susan J and Toland, Amanda Ewart and Caligo, Maria A and Olopade, Olufunmilayo I and Tung, Nadine and Claes, Kathleen and Beattie, Mary S and Southey, Melissa C and Imyanitov, Evgeny N and Tischkowitz, Marc and Janavicius, Ramunas and John, Esther M and Kwong, Ava and Diez, Orland and Balmaña, Judith and Barkardottir, Rosa B and Arun, Banu K and Rennert, Gad and teo, Soo-Hwang and Ganz, Patricia A and Campbell, Ian and van der Hout, Annemarie H and van Deurzen, Carolien H. M and Seynaeve, Caroline and Gómez Garcia, Encarna B and van Leeuwen, Flora E and Meijers-Heijboer, Hanne E. J and Gille, Johannes J. P and Ausems, Margreet G. E. M and Blok, Marinus J and Ligtenberg, Marjolijn J. L and Rookus, Matti A and Devilee, Peter and Verhoef, Senno and van Os, Theo A. M and Wijnen, Juul T and Frost, Debra and Ellis, Steve and Fineberg, Elena and Platte, Radka and Evans, D. Gareth and Izatt, Louise and Eeles, Rosalind A and Adlard, Julian and Eccles, Diana M and Cook, Jackie and Brewer, Carole and Douglas, Fiona and Hodgson, Shirley and ... and KConFab Investigators and Ontario Canc Genetics Network and EMBRACE and GEMO Study Collaborators and CIMBA and HEBON and BCFR and SWE-BRCA and Ontario Cancer Genetics Network and kConFab Investigators and on behalf of CIMBA and Linköpings universitet and Institutionen för klinisk och experimentell medicin and Onkologi and Hälsouniversitetet
PLoS genetics, ISSN 1553-7390, 2013, Volume 9, Issue 3, p. e1003212
BRCA1-associated breast and ovarian cancer risks can be modified by common genetic variants. To identify further cancer risk-modifying loci, we performed a... 
CONSORTIUM | COMMON VARIANTS | POPULATION | INVESTIGATORS | MODIFIERS | SUBTYPES | SUSCEPTIBILITY ALLELES | GENETICS & HEREDITY | GENETIC-VARIANTS | SELECTION | ZNF365 | Genetic Predisposition to Disease | Genome-Wide Association Study | Prognosis | Humans | Middle Aged | Risk Factors | Ovarian Neoplasms - pathology | Genotype | Ovarian Neoplasms - genetics | BRCA1 Protein - genetics | Breast Neoplasms - genetics | Breast Neoplasms - pathology | Female | Heterozygote | Polymorphism, Single Nucleotide | Mutation | BRCA2 Protein - genetics | Gene mutations | Genomics | Physiological aspects | Breast cancer | Genetic aspects | Research | Risk factors | Ovarian cancer | Cancer | Càncer d'ovari | Càncer de mama | Malalties hereditàries | Genètica humana | Genetic diseases | Human genetics | Life Sciences | Medical and Health Sciences | Medicin och hälsovetenskap | Medical research
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3. 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 and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Institutionen för immunologi, genetik och patologi and Medicinsk genetik och genomik and Ortopedi and Uppsala universitet and Institutionen för kirurgiska vetenskaper
Nature genetics, ISSN 1061-4036, 2017, Volume 49, Issue 12, pp. 1767 - 1778
Most common breast cancer susceptibility variants have been identified through genome-wide association studies (GWAS) of predominantly estrogen receptor... 
FUNCTIONAL VARIANTS | COMMON VARIANTS | MODIFIERS | MUTATION CARRIERS | OVARIAN CANCERS | GENETICS & HEREDITY | SUSCEPTIBILITY LOCI | ENHANCER | CONFER SUSCEPTIBILITY | GENOME-WIDE ASSOCIATION | REVEALS | 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 | Breast | Hormone replacement therapy | Mutation | Gene mapping | Health risk assessment | Bioinformatics | Cancer | Medical and Health Sciences | Medicin och hälsovetenskap
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4. 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 and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Ortopedi and Uppsala universitet and Institutionen för kirurgiska vetenskaper
Nature genetics, ISSN 1061-4036, 2017, Volume 49, Issue 5, pp. 680 - 691
To identify common alleles associated with different histotypes of epithelial ovarian cancer (EOC), we pooled data from multiple genome-wide genotyping... 
BREAST-CANCER | COMMON VARIANTS | METAANALYSIS | CLEAR-CELL | ALGORITHM | GENETICS & HEREDITY | RISK | ASSOCIATION | CARCINOMA | ENDOMETRIOSIS | TELOMERE LENGTH | 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 | Life Sciences | Human health and pathology | Genetics | Medical and Health Sciences | Medicin och hälsovetenskap
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5. 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 and Prevention, ISSN 1055-9965, 08/2017, Volume 26, Issue 8, pp. 1233 - 1241
Background: This double-blind, placebo-controlled parallel group trial assessed whether oral supplementation with 1,000, 2,000, or 3,000 IU/day vitamin D3 over... 
Intervention | Vitamin D3 | Calcium | Health problems | Breasts | Dietary supplements | Health risks | Mammography | Breast cancer | Density | Randomization | Calcium (blood) | Vitamin D | Biomarkers | Breast | Bioindicators | Supplementation | Health risk assessment | Cancer
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6. Full Text Increased Use of BRCA Mutation Test in Unaffected Women Over the Period 2004-2014 in the US: Further Evidence of the "Angelina Jolie Effect"?
by Nabi, H and Dorval, M and Chiquette, J and Simard, J
AMERICAN JOURNAL OF PREVENTIVE MEDICINE, ISSN 0749-3797, 11/2017, Volume 53, Issue 5, pp. E195 - E196
MEDICINE, GENERAL & INTERNAL | PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH
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7. Full Text Usefulness of Canadian Public Health Insurance Administrative Databases to Assess Breast and Ovarian Cancer Screening Imaging Technologies for BRCA1/2 Mutation Carriers
by Larouche, Geneviève, MSc and Chiquette, Jocelyne, MD and Plante, Marie, MD and Pelletier, Sylvie, MPs and Simard, Jacques, PhD and Dorval, Michel, PhD
Canadian Association of Radiologists Journal, ISSN 0846-5371, 2016, Volume 67, Issue 4, pp. 308 - 312
Abstract Purpose In Canada, recommendations for clinical management of hereditary breast and ovarian cancer among individuals carrying a deleterious BRCA1 or... 
Radiology | Hereditary breast and ovarian cancer syndrome | Breast neoplasms/prevention and control | Genes BRCA1 | National Health Programs | Ovarian neoplasms/prevention and control | Genes BRCA2 | RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING | Ultrasonography, Mammary - statistics & numerical data | Humans | Quebec | British Columbia | Ovarian Neoplasms - diagnostic imaging | Ovarian Neoplasms - genetics | Breast Neoplasms - genetics | Magnetic Resonance Imaging - statistics & numerical data | Genes, BRCA2 | Female | Administrative Claims, Healthcare | Breast Neoplasms - diagnostic imaging | Genes, BRCA1 | Mammography - statistics & numerical data | Ontario | Early Detection of Cancer - statistics & numerical data | Insurance, Health | Databases, Factual | Breast cancer | Medical imaging | Mutation | Genes | Data bases | Ovarian cancer
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8. 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
MEDICINE, GENERAL & INTERNAL | PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH | ONCOLOGY | GENETICS | HEALTH CARE SCIENCES & SERVICES | Medical personnel | Palliative care | Genetic family histories | End of life decisions | Family medical history | Cancer
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9. 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, TL and Couch, Fergus J and Goldgar, David E and Kruse, Torben A and Palmero, Edenir Inêz and Park, Sue Kyung and Torres, Diana and 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 Andrews, Lesley and Andrulis, 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, Andreas 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, Saundra S and Caldes, Trinidad and Caliebe, Almuth and Caligo, Maria A and Campbell, Ian and Caputo, Sandrine M and Chiquette, Jocelyne and Chung, Wendy K and Claes, Kathleen B.M and Collée, J. Margriet and Cook, Jackie and Davidson, Rosemarie and la Hoya, Miguel and Leeneer, Kim and 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, Sandra 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, Andrea and Gerdes, Anne‐Marie and Gesta, Paul and Giannini, Giuseppe and Giraud, Sophie and Glendon, Gord and Godwin, Andrew K and Greene, Mark H and ... and KConFab Investigators and HEBON and EMBRACE and GEMO Study Collaborators
Human Mutation, ISSN 1059-7794, 05/2018, Volume 39, Issue 5, pp. 593 - 620
The prevalence and spectrum of germline mutations in BRCA1 and BRCA2 have been reported in single populations, with the majority of reports focused on White in... 
mutation | ethnicity | ovarian cancer | geography | breast cancer | BRCA1 | BRCA2 | GENE-MUTATIONS | HEREDITARY BREAST | 185DELAG MUTATION | FOUNDER MUTATIONS | RECURRENT BRCA1 | HAPLOTYPE ANALYSIS | PHENOTYPE ANALYSIS | HIGH-RISK | GENETICS & HEREDITY | BREAST-CANCER PATIENTS | GERMLINE MUTATIONS | Genetic aspects | BRCA mutations | Genetic screening | Singers | Ovarian cancer | BRCA2 protein | Mutation | Genotyping | BRCA1 protein | Minority & ethnic groups | Geography | Basic Medicine | Medical and Health Sciences | Medicin och hälsovetenskap | Breast cancer | Medicinsk genetik | Medical Genetics | Ethnicity | Medicinska och farmaceutiska grundvetenskaper
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10. Full Text Clinical follow-up and breast and ovarian cancer screening of true BRCA1/2 noncarriers: A qualitative investigation
by Pelletier, Sylvie and Wong, Nora and El Haffaf, Zaki and Foulkes, William D and Chiquette, Jocelyne and Hamet, Pavel and Simard, Jacques and Dorval, Michel
Genetics in Medicine, ISSN 1098-3600, 06/2016, Volume 18, Issue 6, pp. 627 - 634
Purpose: Most women from BRCA1/2 mutation positive families who did not inherit the familial mutation have breast and ovarian cancer risks similar to those of... 
BRCA1/2 genes | cancer screening | qualitative research | noncarriers | patient'physician interaction | MANAGEMENT | GENETICS & HEREDITY | HEREDITARY BREAST | MUTATION-NEGATIVE WOMEN | RISK | POSITIVE FAMILIES | patient-physician interaction | FAMILY-SPECIFIC BRCA1 | Ovarian Neoplasms - psychology | Follow-Up Studies | Early Detection of Cancer | Ovarian Neoplasms - diagnosis | Humans | Middle Aged | Risk Factors | Hospital-Physician Relations | Ovarian Neoplasms - epidemiology | Ovarian Neoplasms - genetics | BRCA1 Protein - genetics | Canada | Breast Neoplasms - genetics | Breast Neoplasms - psychology | Adolescent | Adult | Female | Heterozygote | Aged | Breast Neoplasms - diagnosis | Mutation | BRCA2 Protein - genetics | Breast Neoplasms - epidemiology
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11. Full Text Do women change their breast cancer mammogram screening behaviour after BRCA1/2 testing?
by Larouche, Geneviève and Chiquette, Jocelyne and Pelletier, Sylvie and Simard, Jacques and Dorval, Michel
Familial Cancer, ISSN 1389-9600, 1/2017, Volume 16, Issue 1, pp. 35 - 40
Little is known about the change in mammograms use by women after BRCA1/2 genetic testing. We compared the rate of bilateral mammograms after and prior to... 
Human Genetics | Biomedicine, general | Biomedicine | Cancer Research | Breast cancer genetic testing | Mammography | Epidemiology | Genes BRCA 2 | Genes BRCA 1 | Breast cancer screening | ONCOLOGY | GENETICS & HEREDITY | Genetic Predisposition to Disease | Genetic Testing | Humans | Middle Aged | Quebec | Health Knowledge, Attitudes, Practice | Mammography - psychology | BRCA1 Protein - genetics | Magnetic Resonance Imaging | Breast Neoplasms - genetics | Aged, 80 and over | Adult | Female | Heterozygote | Aged | Breast Neoplasms - diagnostic imaging | Mutation | Mammography - statistics & numerical data | BRCA2 Protein - genetics | Women | Analysis | Medical tests | Breast cancer | Diagnosis | Genetic screening | Cancer | Index Medicus
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12. Full Text A response to “Personalised medicine and population health: breast and ovarian cancer”
by Antoniou, Antonis and Anton-Culver, Hoda and Borowsky, Alexander and Broeders, Mireille and Brooks, Jennifer and Chiarelli, Anna and Chiquette, Jocelyne and Cuzick, Jack and Delaloge, Suzette and Devilee, Peter and Dorval, Michael and Easton, Douglas and Eisen, Andrea and Eklund, Martin and Eloy, Laurence and Esserman, Laura and Garcia-Closas, Montserrat and Goldgar, David and Hall, Per and Knoppers, Bartha Maria and Kraft, Peter and La Croix, Andrea and Madalensky, Lisa and Mavaddat, Nasim and Mittman, Nicole and Nabi, Hermann and Olopade, Olufunmilayo and Pashayan, Nora and Schmidt, Marjanka and Shieh, Yiwey and Simard, Jacques and Stover-Fiscallini, Allison and Tice, Jeffrey A and van’t Veer, Laura and Wenger, Neil and Wolfson, Michael and Yau, Christina and Ziv, Elad
Human Genetics, ISSN 0340-6717, 3/2019, Volume 138, Issue 3, pp. 287 - 289
Based on Dr. Narod’s assessment of the premise of personalized medicine in his review “Personalised medicine and population health: breast and ovarian cancer”,... 
Human Genetics | Gene Function | Molecular Medicine | Biomedicine | Metabolic Diseases | Disease prevention | Breast cancer | Precision medicine | Medical screening | Ovarian cancer
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13. Full Text Development of a Tool to Guide Parents Carrying a BRCA1/2 Mutation Share Genetic Results with Underage Children
by Santerre-Theil, Ariane and Bouchard, Karine and St-Pierre, Dominique and Drolet, Anne-Marie and Chiquette, Jocelyne and Dorval, Michel and Ctr ROSE and Centre ROSE and on behalf of Centre ROSE
Journal of Cancer Education, ISSN 0885-8195, 6/2018, Volume 33, Issue 3, pp. 569 - 575
Although most parents carrying a BRCA1/2 genetic mutation share their test result with their underage children, they report needing support to decide if, when,... 
Family communication | BRCA1/2 | Biomedicine | Parents | Hereditary breast and ovarian cancer syndrome | Educational material | Decision aid | Cancer genetic testing | Cancer Research<