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Showing results 6 to 11 of 11 < previous

	Title	Author(s)	Issue Date	Views
	Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations Journal:Human Mutation	Rebbeck, TR Friebel, TM Friedman, E Hamann, U Huo, D Kwong, A Olah, E Olopade, OI Solano, AR Teo, SH Thomassen, M Weitzel, JN Chan, TL Couch, FJ Goldgar, DE Kruse, TA Palmero, EI Park, SK Torres, D van Rensburg, EJ McGuffog, L Parsons, MT Leslie, G Aalfs, CM Abugattas, J Adlard, J Agata, S Aittomäki, K Andrews, L Andrulis, IL Arason, A Arnold, N Arun, BK Asseryanis, E Auerbach, L Azzollini, J Balmaña, J Barile, M Barkardottir, RB Barrowdale, D Benitez, J Berger, A Berger, R Blanco, AM Blazer, KR Blok, MJ Bonadona, V Bonanni, B Bradbury, AR Brewer, C Buecher, B Buys, SS Caldes, T Caliebe, A Caligo, MA Campbell, I Caputo, SM Chiquette, J Chung, WK Claes, KBM Collée, JM Cook, J Davidson, R de la Hoya, M De Leeneer, K de Pauw, A Delnatte, C Diez, O Ding, YC Ditsch, N Domchek, SM Dorfling, CM Velazquez, C Dworniczak, B Eason, J Easton, DF Eeles, R Ehrencrona, H Ejlertsen, B Engel, C Engert, S Evans, DG Faivre, L Feliubadaló, L Ferrer, SF Foretova, L Fowler, J Frost, D Galvão, HCR Ganz, PA Garber, J Gauthier-Villars, M Gehrig, A Gerdes, AM Gesta, P Giannini, G Giraud, S Glendon, G Godwin, AK Greene, MH Gronwald, J Gutierrez-Barrera, A Hahnen, E Hauke, J Henderson, A Hentschel, J Hogervorst, FBL Honisch, E Imyanitov, EN Isaacs, C Izatt, L Izquierdo, A Jakubowska, A James, P Janavicius, R Jensen, UB John, EM Vijai, J Kaczmarek, K Karlan, BY Kast, K Investigators, K Kim, SW Konstantopoulou, I Korach, J Laitman, Y Lasa, A Lasset, C Lázaro, C Lee, A Lee, MH Lester, J Lesueur, F Liljegren, A Lindor, NM Longy, M Loud, JT Lu, KH Lubinski, J Machackova, E Manoukian, S Mari, V Martínez-Bouzas, C Matrai, Z Mebirouk, N Meijers-Heijboer, HEJ Meindl, A Mensenkamp, AR Mickys, U Miller, A Montagna, M Moysich, KB Mulligan, AM Musinsky, J Neuhausen, SL Nevanlinna, H Ngeow, J Nguyen, HP Niederacher, D Nielsen, HR Nielsen, FC Nussbaum, RL Offit, K Öfverholm, A Ong, KR Osorio, A Papi, L Papp, J Pasini, B Pedersen, IS Peixoto, A Peruga, N Peterlongo, P Pohl, E Pradhan, N Prajzendanc, K Prieur, F Pujol, P Radice, P Ramus, SJ Rantala, J Rashid, MU Rhiem, K Robson, M Rodriguez, GC Rogers, MT Rudaitis, V Schmidt, AY Schmutzler, RK Senter, L Shah, PD Sharma, P Side, LE Simard, J Singer, DF Skytte, AB Slavin, TP Snape, K Sobol, H Southey, M Steele, L Steinemann, D Sukiennicki, G Sutter, G Szabo, CI Tan, YY Teixeira, MR Terry, MB Teu, A Thomas, A Thull, DL Tischkowitz, M Tognazzo, S Toland, AE Topka, S Trainer, AH Tung, N van Asperen, CJ van der Hout, AH van der Kolk, LE van der Luijt, RB VanHeetvelde, M Varesco, L Varon-Mateeva, R Vega, A Villarreal-Garza, C von Wachenfeldt, A Walker, L Wang-Gohrke, S Wappenschmidt, B Weber, BHF Yannoukakos, D Yoon, SY Zanzottera, C Zidan, J Zorn, KK Hutten Selkirk, CG Hulick, PJ Chenevix-Trench, G Spurdle, AB Antoniou, AC Nathanson, KL	2018
	Risks of breast and ovarian cancer for women harboring pathogenic missense variants in BRCA1 and BRCA2 compared with those harboring protein truncating variants Journal:Genetics In Medicine	Li, H Engel, C de la Hoya, M Peterlongo, P Yannoukakos, D Livraghi, L Radice, P Thomassen, M Hansen, TVO Gerdes, AM Nielsen, HR Caputo, SM Zambelli, A Borg, A Solano, A Thomas, A Parsons, MT Antoniou, AC Leslie, G Yang, X Chenevix-Trench, G Caldes, T Kwong, A Pedersen, IS Lautrup, CK John, EM Terry, MB Hopper, JL Southey, MC Andrulis, IL Tischkowitz, M Janavicius, R Boonen, SE Kroeldrup, L Varesco, L Hamann, U Vega, A Palmero, EI Garber, J Montagna, M Van Asperen, CJ Foretova, L Greene, MH Selkirk, T Moller, P Toland, AE Domchek, SM James, PA Thorne, H Eccles, DM Nielsen, SM Manoukian, S Pasini, B Caligo, MA Lazaro, C Kirk, J Wappenschmidt, B Spurdle, AB Couch, FJ Schmutzler, R Goldgar, DE	2022	14
	The Ten Year Experience of A Regional Specialist Gynaecology Cancer Genetics Clinic with Lynch Syndrome Proceeding/Conference:The European Society of Gynaecological Oncology International Meeting, ESGO 2017	Crawford, R Newcombe, B Bolton, H Ngu, SF Freeman, S Addley, H Jimenez-Linan, M Armstrong, R Tischkowitz, M	2017	66
	Universal BRCA1/BRCA2 testing for ovarian cancer patients is welcomed, but with care: how women and staff contextualize experiences of expanded access Journal:Journal of Genetic Counseling	Shipman, HE Flynn, S MacDonald-Smith, CF Brenton, J Crawford, R Tischkowitz, M Hulbert-Williams, N	2017	18
	“We can talk about it. We can joke about it, you know, which is nice”: Tensions surrounding (in)directness in talk about death and dying involving women with ovarian cancer Proceeding/Conference:International Pragmatics Association Conference	Shipman, HE Zayts, OA Tischkowitz, M	2017
	'Well, we can talk about it. We can joke about it, which is nice': Indirectness in talk about end-of-life involving women with ovarian cancer Proceeding/Conference:JCECC Conference on Collaboration in Creating Compassionate Holistic End- of-Life Care for the Future	Shipman, HE Zayts, OA Tischkowitz, M	2017	17

Showing results 6 to 11 of 11 < previous