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Clinical Genetics, ISSN 0009-9163, 03/2011, Volume 79, Issue 3, pp. 207 - 218
Previous studies on the counsellees' perception of DNA test results did not clarify whether counsellees were asked about their recollections or... 
genetic counselling | DISTRESS | SUSCEPTIBILITY | heuristic | RANDOMIZED-TRIAL | OVARIAN-CANCER | TERM PSYCHOLOGICAL IMPACT | oncology | perception | BRCA1/2 | WOMEN | psychology | interpretation | MUTATION | GENETICS & HEREDITY | FAMILIAL BREAST-CANCER | risk perception | HISTORY
Journal Article
Journal of the National Cancer Institute, ISSN 0027-8874, 2015, Volume 107, Issue 5, p. 1
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
Revue Internationale des Sciences Administratives, ISSN 0303-965X, 2018, Volume 84, Issue 2, pp. 419 - 435
Depuis le début des années 1990, le discours sur la « bonne gouvernance » gagne en importance. La question de savoir ce que signifie et ce que suppose la... 
Journal Article
Jnci-Journal of the national cancer institute, ISSN 0027-8874, 05/2015, Volume 107, Issue 5
Background: Previous studies have reported a breast cancer (BC) risk reduction of approximately 50% after risk-reducing salpingo-oophorectomy (RRSO) in BRCA1/2... 
Journal Article
Journal of the National Cancer Institute, ISSN 0027-8874, 05/2015, Volume 107, Issue 5
Background: Previous studies have reported a breast cancer (BC) risk reduction of approximately 50% after risk-reducing salpingo-oophorectomy (RRSO) in BRCA1/2... 
Journal Article
British Journal of Cancer, ISSN 0007-0920, 08/2005, Volume 93, Issue 3, pp. 287 - 292
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 09/2005, Volume 42, Issue 9, pp. 711 - 719
Journal Article
by Broeks, A and Schmidt, M.K and Sherman, M.E and Couch, F.J and Hopper, J.L and Dite, G.S and Apicella, C and Smith, L.D and Hammet, F and Southey, M.C and Veer, L.J. van 't and Groot, R. de and Smit, V.T and Fasching, P.A and Beckmann, M.W and Jud, S and Ekici, A.B and Hartmann, A and Hein, A and Schulz-Wendtland, R and Burwinkel, B and Marme, F and Schneeweiss, A and Sinn, H.P and Sohn, C and Tchatchou, S and Bojesen, S.E and Nordestgaard, B.G and Flyger, H and Orsted, D.D and Kaur-Knudsen, D and Milne, R.L and Perez, J.I and Zamora, P and Roiguez, P.M and Benitez, J and Brauch, H and Justenhoven, C and Ko, Y.D and Hamann, U and Fischer, H.P and Bruning, T and Pesch, B and Chang-Claude, J and Wang-Gohrke, S and Bremer, M and Karstens, J.H and Hillemanns, P and Dork, T and Nevanlinna, H.A and Heikkinen, T and Heikkila, P and Blomqvist, C and Aittomaki, K and Aaltonen, K and Lindblom, A and Margolin, S and Mannermaa, A and Kosma, V.M and Kauppinen, J.M and Kataja, V and Auvinen, P and Eskelinen, M and Soini, Y and Chenevix-Trench, G and Spurdle, A.B and Beesley, J and Chen, X and Holland, H and Lambrechts, D and Claes, B and Vandorpe, T and Neven, P and Wildiers, H and Flesch-Janys, D and Hein, R and Loning, T and Kosel, M and Fredericksen, Z.S and Wang, X and Giles, G.G and Baglietto, L and Severi, G and McLean, C and Haiman, C.A and Henderson, B.E and Marchand, L. le and Kolonel, L.N and Alnaes, G.G and Kristensen, V and Borresen-Dale, A.L and Hunter, D.J and Hankinson, S.E and Anulis, I.L and Mulligan, A.M and O'Malley, F.P and Devilee, P and Huijts, P.E and Tollenaar, R.A.E.M and Asperen, C.J. van and KConFab and Genica Network and AOCS and kConFab and The Genica Network
Human Molecular Genetics, ISSN 0964-6906, 2011, Volume 20, Issue 16, pp. 3289 - 3303
Journal Article
Journal of medical genetics, ISSN 0022-2593, 2010, Volume 47, Issue 6, pp. 421 - 428
Journal Article
Journal Article