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EUROPEAN JOURNAL OF HUMAN GENETICS, ISSN 1018-4813, 12/2017, Volume 25, Issue 12, pp. 1345 - 1353
RAD51 paralogs (RAD51B, RAD51C, RAD51D, XRCC2, and XRCC3) have recently been involved in breast and ovarian cancer predisposition: RAD51B, RAD51C, and RAD51D... 
MISSENSE VARIANTS | 14Q24.1 RAD51L1 | GENE | MUTATION CARRIERS | FAMILIES | XRCC2 | BIOCHEMISTRY & MOLECULAR BIOLOGY | GENETICS & HEREDITY | CONFER SUSCEPTIBILITY | RISK | BRCA1 | GENOME-WIDE ASSOCIATION | Breast cancer | Deoxyribonucleic acid--DNA | Ovarian cancer | DNA sequencing | Sciences of the Universe
Journal Article
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
Journal Article
Journal of medical ethics, ISSN 0306-6800, 08/2019, p. medethics-2018-105212
Familial disclosure of genetic information is an important, long-standing ethical issue that still gives rise to much debate. In France, recent legislation has... 
Sociology | Humanities and Social Sciences
Journal Article
by Antoniou, Antonis C and Beesley, Jonathan and McGuffog, Lesley and Sinilnikova, Olga M and Healey, Sue and Neuhausen, Susan L and Ding, Yuan Chun and Rebbeck, Timothy R and Weitzel, Jeffrey N and Lynch, Henry T and Isaacs, Claudine and Ganz, Patricia A and Tomlinson, Gail and Olopade, Olufunmilayo I and Couch, Fergus J and Wang, Xianshu and Lindor, Noralane M and Pankratz, Vernon S and Radice, Paolo and Manoukian, Siranoush and Peissel, Bernard and Zaffaroni, Daniela and Barile, Monica and Viel, Alessana and Allavena, Anna and Dall'olio, Valentina and Peterlongo, Paolo and Szabo, Csilla I and Zikan, Michal and Claes, Kathleen and Poppe, Bruce and Foretova, Lenka and Mai, Phuong L and Greene, Mark H and Rennert, Gad and Lejbkowicz, Flavio and Glendon, Gord and Ozcelik, Hilmi and Anulis, Irene L and Thomassen, Mads and Gerdes, Anne-Marie and Sunde, Lone and Cruger, Dorthe and Birk Jensen, Uffe and Caligo, Maria and Friedman, Eitan and Kaufman, Bella and Laitman, Yael and Milgrom, Roni and Dubrovsky, Maya and Cohen, Shimrit and Borg, Ake and Jernström, Helena and Lindblom, Annika and Rantala, Johanna and Stenmark-Askmalm, Marie and Melin, Beatrice and Nathanson, Kate and Domchek, Susan and Jakubowska, Ania and Lubinski, Jan and Huzarski, Tomasz and Osorio, Ana and Lasa, Aiana and Durán, Mercedes and Tejada, Maria-Isabel and Godino, Javier and Benitez, Javier and Hamann, Ute and Kriege, Mieke and Hoogerbrugge, Nicoline and Luijt, Rob B. van der and Asperen, Christi J. van and Devilee, Peter and Meijers-Heijboer, E. J and Blok, Marinus J and Aalfs, Cora M and Hogervorst, Frans and Rookus, Matti and Cook, Margaret and Oliver, Clare and Frost, Debra and Conroy, Don and Evans, D. Gareth and Lalloo, Fiona and Pichert, Gabriella and Davidson, Rosemarie and Cole, Trevor and Cook, Jackie and Paterson, Joan and Hodgson, Shirley and Morrison, Patrick J and Porteous, Mary E and Walker, Lisa and Kennedy, M. John and Dorkins, Huw and Peock, Susan and Godwin, Anew K and Stoppa-Lyonnet, Dominique and Pauw, Antoine de and ... and Ontario Canc Genetics Network and EMBRACE and CIMBA and GEMO and HEBON and Breast Canc Family Registry and kConFab and SWE-BRCA and Ontario Cancer Genetics Network and Breast Cancer Family Registry and for kConFab and for EMBRACE and for HEBON and for SWE-BRCA and for GEMO and on behalf of CIMBA and for the Ontario Cancer Genetics Network and for the Breast Cancer Family Registry
Cancer research, ISSN 0008-5472, 2010, Volume 70, Issue 23, pp. 9742 - 9754
The known breast cancer susceptibility polymorphisms in FGFR2, TNRC9/TOX3, MAP3K1, LSP1, and 2q35 confer increased risks of breast cancer for BRCA1 or BRCA2... 
LOCI | VARIANTS | ONCOLOGY | ESTROGEN-RECEPTOR | GENOME-WIDE ASSOCIATION | Genetic Predisposition to Disease - genetics | Risk Assessment | Humans | Middle Aged | Risk Factors | Sodium-Bicarbonate Symporters - genetics | Vesicular Transport Proteins - genetics | Genotype | Receptors, Progesterone - genetics | BRCA1 Protein - genetics | Breast Neoplasms - genetics | Breast Neoplasms - pathology | Alleles | Survival Analysis | Aged, 80 and over | Adult | Female | Heterozygote | Aged | Polymorphism, Single Nucleotide | Mutation | BRCA2 Protein - genetics | genetic counseling | genome-wide association study | penetrance | common variant | BRCA1 | BRCA2 | genetic modifier | risk assessment | Medical and Health Sciences | Medicin och hälsovetenskap | single nucleotide polymorphism | major clinical study | attributable risk | Klinisk medicin | clinical evaluation | heterozygote | Breast Neoplasms | Single Nucleotide | follow up | 80 and over | Receptors | priority journal | female | human | tumor suppressor gene | Vesicular Transport Proteins | BRCA2 protein | Genetic Predisposition to Disease | cancer susceptibility | BRCA1 protein | gene mutation | probability | aged | breast cancer | article | gene frequency | genotype | Clinical Medicine | controlled study | cancer risk | Progesterone | Cancer and Oncology | adult | Sodium-Bicarbonate Symporters | Cancer och onkologi | Polymorphism
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 06/2013, Volume 92, Issue 6, pp. 974 - 980
Journal Article
Molecular and Cellular Biology, ISSN 0270-7306, 02/2006, Volume 26, Issue 3, pp. 789 - 809
Journal Article
Journal of Clinical Oncology, ISSN 0732-183X, 05/2017, Volume 35, Issue 15_suppl, pp. e13005 - e13005
Journal Article
International Journal of Environmental Research and Public Health, ISSN 1661-7827, 02/2018, Volume 15, Issue 2, p. 319
Journal Article
Familial Cancer, ISSN 1389-9600, 4/2018, Volume 17, Issue 2, pp. 281 - 285
Journal Article