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Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

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    Peterlongo P; Chang-Claude J; Moysich KB; Rudolph A; Schmutzler RK; Simard J; Soucy P; Eeles RA; Easton DF; Hamann U; Wilkening S; Chen B; Rookus MA; Schmidt MK; van der Baan FH; Spurdle AB; Walker LC; Lose F; Maia AT; Montagna M; Matricardi L; Lubinski J; Jakubowska A; Gómez Garcia EB; Olopade OI; Nussbaum RL; Nathanson KL; Domchek SM; Rebbeck TR; Arun BK; Karlan BY; Orsulic S; Lester J; Chung WK; Miron A; Southey MC; Goldgar DE; Buys SS; Janavicius R; Dorfling CM; van Rensburg EJ; Ding YC; Neuhausen SL; Hansen TV; Gerdes AM; Ejlertsen B; Jønson L; Osorio A; Martínez-Bouzas C; Benitez J; Conway EE; Blazer KR; Weitzel JN; Manoukian S; Peissel B; Zaffaroni D; Scuvera G; Barile M; Ficarazzi F; Mariette F; Fortuzzi S; Viel A; Giannini G; Papi L; Martayan A; Tibiletti MG; Radice P; Vratimos A; Fostira F; Garber JE; Donaldson A; Brewer C; Foo C; Evans DG; Frost D; Eccles D; Brady A; Cook J; Tischkowitz M; Adlard J; Barwell J; Walker L; Izatt L; Side LE; Kennedy MJ; Rogers MT; Porteous ME; Morrison PJ; Platte R; Davidson R; Hodgson SV; Ellis S; Cole T; ; Godwin AK; Claes K; Van Maerken T; Meindl A; Gehrig A; Sutter C; Engel C; Niederacher D; Steinemann D; Plendl H; Kast K; Rhiem K; Ditsch N; Arnold N; Varon-Mateeva R; Wappenschmidt B; Wang-Gohrke S; Bressac-de Paillerets B; Buecher B; Delnatte C; Houdayer C; Stoppa-Lyonnet D; Damiola F; Coupier I; Barjhoux L; Venat-Bouvet L; Golmard L; Boutry-Kryza N; Sinilnikova OM; Caron O; Pujol P; Mazoyer S; Belotti M; ; Piedmonte M; Friedlander ML; Rodriguez GC; Copeland LJ; de la Hoya M; Segura PP; Nevanlinna H; Aittomäki K; van Os TA; Meijers-Heijboer HE; van der Hout AH; Vreeswijk MP; Hoogerbrugge N; Ausems MG; van Doorn HC; Collée JM; ; Olah E; Diez O; Blanco I; Lazaro C; Brunet J; Feliubadalo L; Cybulski C; Gronwald J; Durda K; Jaworska-Bieniek K; Sukiennicki G; Arason A; Chiquette J; Teixeira MR; Olswold C; Couch FJ; Lindor NM; Wang X; Szabo CI; Offit K; Corines M; Jacobs L; Robson ME; Zhang L; Joseph V; Berger A; Singer CF; Rappaport C; Kaulich DG; Pfeiler G; Tea MK; Phelan CM; Greene MH; Mai PL; Rennert G; Mulligan AM; Glendon G; Tchatchou S; Andrulis IL; Toland AE; Bojesen A; Pedersen IS; Thomassen M; Jensen UB; Laitman Y; Rantala J; von Wachenfeldt A; Ehrencrona H; Askmalm MS; Borg Å; Kuchenbaecker KB; McGuffog L; Barrowdale D; Healey S; Lee A; Pharoah PD; Chenevix-Trench G; ; Antoniou AC; Friedman E
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  • 14. Evidence for SMAD3 as a modifier of breast cancer risk in BRCA2 mutation carriers.
    Walker LC; Fredericksen ZS; Wang X; Tarrell R; Pankratz VS; Lindor NM; Beesley J; Healey S; Chen X; ; Stoppa-Lyonnet D; Tirapo C; Giraud S; Mazoyer S; Muller D; Fricker JP; Delnatte C; ; Schmutzler RK; Wappenschmidt B; Engel C; Schönbuchner I; Deissler H; Meindl A; Hogervorst FB; Verheus M; Hooning MJ; van den Ouweland AM; Nelen MR; Ausems MG; Aalfs CM; van Asperen CJ; Devilee P; Gerrits MM; Waisfisz Q; ; Szabo CI; ; Easton DF; Peock S; Cook M; Oliver CT; Frost D; Harrington P; Evans DG; Lalloo F; Eeles R; Izatt L; Chu C; Davidson R; Eccles D; Ong KR; Cook J; ; Rebbeck T; Nathanson KL; Domchek SM; Singer CF; Gschwantler-Kaulich D; Dressler AC; Pfeiler G; Godwin AK; Heikkinen T; Nevanlinna H; Agnarsson BA; Caligo MA; Olsson H; Kristoffersson U; Liljegren A; Arver B; Karlsson P; Melin B; ; Sinilnikova OM; McGuffog L; Antoniou AC; Chenevix-Trench G; Spurdle AB; Couch FJ
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  • 15. Evaluation of chromosome 6p22 as a breast cancer risk modifier locus in a follow-up study of BRCA2 mutation carriers.
    Stevens KN; Wang X; Fredericksen Z; Pankratz VS; Greene MH; Andrulis IL; Thomassen M; Caligo M; ; Nathanson KL; Jakubowska A; Osorio A; Hamann U; Godwin AK; Stoppa-Lyonnet D; Southey M; Buys SS; Singer CF; Hansen TV; Arason A; Offit K; Piedmonte M; Montagna M; Imyanitov E; Tihomirova L; Sucheston L; Beattie M; ; ; Neuhausen SL; ; Szabo CI; ; Simard J; Spurdle AB; Healey S; Chen X; Rebbeck TR; Easton DF; Chenevix-Trench G; Antoniou AC; Couch FJ
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  • 16. Association of PHB 1630 C>T and MTHFR 677 C>T polymorphisms with breast and ovarian cancer risk in BRCA1/2 mutation carriers: results from a multicenter study.
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  • 17. Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers.
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  • 18. A single-nucleotide polymorphism in the RAD51 gene modifies breast cancer risk in BRCA2 carriers, but not in BRCA1 carriers or noncarriers.
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  • 19. Skewed X chromosome inactivation and breast and ovarian cancer status: evidence for X-linked modifiers of BRCA1.
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  • 20. Breast cancer risk in BRCA1 and BRCA2 mutation carriers and polyglutamine repeat length in the AIB1 gene.
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