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TypeTitleAuthor(s)YearViews
Common variants at the 19p13.1 and ZNF365 loci are associated with ER subtypes of breast cancer and ovarian cancer risk in BRCA1 and BRCA2 mutation carriersCouch, FJ; Gaudet, MM; Antoniou, AC; Ramus, SJ; Kuchenbaecker, KB; Soucy, P; Beesley, J; Chen, X; Wang, X; Kirchhoff, T; McGuffog, L; Barrowdale, D; Lee, A; Healey, S; Sinilnikova, OM; Andrulis, IL; Ozcelik, H; Mulligan, AM; Thomassen, M; Gerdes, AM; Jensen, UB; Skytte, AB; Kruse, TA; Caligo, MA; Von Wachenfeldt, A; BarbanyBustinza, G; Loman, N; Soller, M; Ehrencrona, H; Karlsson, P; Nathanson, K; Rebbeck, TR; Domchek, SM; Jakubowska, A; Lubinski, J; Jaworska, K; Durda, K; Zołwocka, E; Huzarski, T; Byrski, T; Gronwald, J; Cybulski, C; Goŕski, B; Osorio, A; Durań, M; Tejada, MI; Benitez, J; Hamann, U; Hogervorst, FBL; Van Os, TA; Van Leeuwen, FE; MeijersHeijboer, HEJ; Wijnen, J; Blok, MJ; Kets, M; Hooning, MJ; Oldenburg, RA; Ausems, MGEM; Peock, S; Frost, D; Ellis, SD; Platte, R; Fineberg, E; Evans, DG; Jacobs, C; Eeles, RA; Adlard, J; Davidson, R; Eccles, DM; Cole, T; Cook, J; Paterson, J; Brewer, C; Douglas, F; Hodgson, SV; Morrison, PJ; Walker, L; Porteous, ME; Kennedy, MJ; Side, LE; Bove, B; Godwin, AK; StoppaLyonnet, D; FassyColcombet, M; Castera, L; Cornelis, F; Mazoyer, S; Leóne, M; BoutryKryza, N; Bressacde Paillerets, B; Caron, O; Pujol, P; Coupier, I; Delnatte, C; Akloul, L; Lynch, HT; Snyder, CL; Buys, SS; Daly, MB; Terry, M; Chung, WK; John, EM; Miron, A; Southey, MC; Hopper, JL; Goldgar, DE; Singer, CF; Rappaport, C; Tea, MKM; FinkRetter, A; Hansen, TVO; Nielsen, FC; Arason, A; Vijai, J; Shah, S; Sarrel, K; Robson, ME; Piedmonte, M; Phillips, K; Basil, J; Rubinstein, WS; Boggess, J; Wakeley, K; EwartToland, A; Montagna, M; Agata, S; Imyanitov, EN; Isaacs, C; Janavicius, R; Lazaro, C; Blanco, I; Feliubadalo, L; Brunet, J; Gayther, SA; Pharoah, PPD; Odunsi, KO; Karlan, BY; Walsh, CS; Olah, E; Teo, SH; Ganz, PA; Beattie, MS; Van Rensburg, EJ; Dorfling, CM; Diez, O; Kwong, A; Schmutzler, RK; Wappenschmidt, B; Engel, C; Meindl, A; Ditsch, N; Arnold, N; Heidemann, S; Niederacher, D; PreislerAdams, S; Gadzicki, D; VaronMateeva, R; Deissler, H; Gehrig, A; Sutter, C; Kast, K; Fiebig, B; Heinritz, W; Caldes, T; De La Hoya, M; Muranen, TA; Nevanlinna, H; Tischkowitz, MD; Spurdle, AB; Neuhausen, SL; Ding, YC; Lindor, NM; Fredericksen, Z; Pankratz, VS; Peterlongo, P; Manoukian, S; Peissel, B; Zaffaroni, D; Barile, M; Bernard, L; Viel, A; Giannini, G; Varesco, L; Radice, P; Greene, MH; Mai, PL; Easton, DF; ChenevixTrench, G; Offit, K; Simard, J2012100
 
Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriersRamus, SJ; Antoniou, AC; Kuchenbaecker, KB; Soucy, P; Beesley, J; Chen, X; McGuffog, L; Sinilnikova, OM; Sinilnikova, OM; Healey, S; Barrowdale, D; Pankratz, VS; Pharoah, PD; kConFab,; Lijegren, A; Schafer, D; de la Hoya, M; Duran, M; Ditsch, N; Ding, YC; Vijai, J; Pathak, H; Frost, D; Loustaiot, C; Platte, R; Southey, M; van Leeuwen, FE; Peterlongo, P; Rookus, M; Daly, M; Kwong, A; Huzarski, T; Kriege, M; Couch, FJ; Schmutzler, RK; Lindblom, A; Beattie, MS; Kast, K; Caligo, MA; Adlard, J; Engel, C; Peissel, B; Porteous, ME; Hodgson, S; Stoppa-Lyonnet, D; Benitez, J; Ejlertsen, B; Nevanlinna, H; Tornero, E; Radice, P; Toland, AE; Chung, W; Lasset, C; Peock, S; Cybuiski, C; Davidson, R; Hardouin, A; Papi, L; Margriet Callee, J; Gauthier-Villars, M; Caux-Moncoutier, V; Osorio, A; Isaacs, C; OCGN,; Navarro, M; Eccles, D; Godwin, AK; Lubinski, J; Byrski, T; HEBON,; Tea Maria, MK; Berth Terry, M; van Asperen, CJ; Hamann, U; Spurdle, AB; Kruse, TA; Kristoffersson, U; Montagna, M; Lazaro, C; Andrulis, IL; Aalfs, CM; Aittomaki, K; Offit, K; Tognazzo, S; Gayther, SA; Piedmonte, M; SWE-BRCA,; Morrison, PJ; Cole, T; Paterson, J; Stenmark-Askmalm, M; Olisson, H; Eeles, R; Durda, K; Domchek, SM; Evans, DG; Cook, J; Phillips, KA; Gehrig, A; Van Le, L; Jensen, UB; Wang, X; Wappenschmidt, B; Jacobs, C; Ozcelik, H; Ellis, SD; Berthet, P; Sutter, C; Heidemann, S; van Rensburg, EJ; Singer, CF; Gadzicki, D; Manoukian, S; Gross, J; Buys, S; Thomassen, M; Dolcetti, R; Dofling, CM; Neuhausen, SL; Johannsson, OT; Calender, A; Glendon, G; Plante, M; Ottini, L; Easton, DF; Mejiers-Hejboer, HE; Jakubowska, A; Fink-Retter, A; Mazoyer, S; Walker, L; Chenevix-Trench, G; Imyanitov, E; Zlowocka, E; Jaworska, K; Hoogerbrugge, N; van Roozendaal, KE; Lindor, N; de Pauw, A; Melin, B; Diez, O; Hansen, TV; Bernard, L; Bonanni, B; Leone, M; Robson, M; Brewer, C; Douglas, F; Teo, SH; Miron, A; Tejada, MI; Kirchhoff, T; Fredericksen, Z; Mai, PL; Preiser-Adams, S; Karfan, BY; Greene, MH; Meindl, A; Arnold, N; Vaszko, T; Zaffaroni, D; Bianco, I; Gaudet, MM; Deissler, H; Varon-Mateeva, R; Nathanson, KL; Fineberg, E; Faivre, L; Moysich, KB; Skytte, AB; Hoffman, JS; Toloczko-Grabarek, A; Uhrhammer, N; Ganz, PA; Gronwald, J; John, EM; Rebbeck, TR; Olah, E; Gerdes, AM; Bonadona, V; Kennedy, MJ; Caides, T; Bignon, YJ; GEMO,; Peock, S; Pfeiler, G; Goldgar, D; Lallco, F; van der Luijt, RB; EMBRACE,; Lee, A; Janavicius, R; Niederacher, D; Fiebig, B; Simard, J2012128
 
Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriersAntoniou, AC; Kuchenbaecker, KB; Soucy, P; Beesley, J; Chen, X; McGuffog, L; Lee, A; Barrowdale, D; Healey, S; Sinilnikova, OM; Caligo, MA; Chenevix-Trench, G; Teo, S-H; Ganz, PA; Ganz, PA; Loud, JT; Beattie, MS; Dorfling, CM; Peissel, B; van Resburg, EJ; Meindl, A; Offit, K; Neuhausen, SL; Simard, J; Caldes, T; Varon-Mateeva, R; EMBRACE,; Zaffaroni, D; Arver, B; Ding, YC; de la Hoya, M; Lalloo, F; Ligtenberg, MJ; Ozcelik, H; Wang, X; Bonanni, B; Fredericksen, Z; Douglas, F; Peock, S; Easton, DF; Bernard, L; Mulligan, AM; Dolcetti, R; Kriege, M; Bove, B; Jacobs, C; Rosenquist, R; Glendon, G; CIMBA,; Thomassen, M; Frost, D; Sobol, H; Brewer, C; Papi, L; Collee, JM; SWE-BRCA,; Karission, P; HEBON,; Eeles, R; John, EM; Stoppa-Lyonnet, D; Gerdes, A-M; Ellis, SD; Nathanson, K; Jensen, UB; Singer, CF; Domehek, S; Hodgson, S; Joseph, V; Frenay, M; EMBRACE,; Adlard, J; GEMO Collaborators Study,; kConFab Investigators,; Piedmonte, M; Rebbeck, T; Ausems, MGEM; Houdayer, C; Jabubowska, A; Southey, M; Lubinski, J; Morrison, PJ; Jaworska, K; Durda, K; Davidson, R; Zlowowcka-Perlowska, E; Platte, R; Oosterwijk, JC; Prieur, F; Osorio, A; Dutra-Clarke, A; Duran, M; Buecher, B; Andres, R; Benitez, J; Walker, L; Hamann, U; Cole, T; Mortemousque, I; Fineberg, E; Goldgar, D; Hogervorst, FB; van O, TA; Verhoef, S; Ferrer, SF; Meijers-Heijboer, HEJ; Wijnen, J; de Pauw, A; Gomez Garcia, EB; HEBON,; Rogers, MT; Fint-Retter, A; Cook, J; Gareth Evans, D; Harbst, K; Mazoyer, S; Kirk, J; Donaldson, A; Paterson, J; Ditsch, N; GEMO Study Collaborators,; Dorkins, H; Calender, A; Godwin, AK; Deissler, H; Diez, O; Tea, M-K; Leone, M; Buys, S; Bressac-de Paillerets, B; Nevanlinna, H; Arnold, N; Cohn, D; Daly, M; Kaulich, DG; Miron, A; Kwong, A; Pankratz, VS; Gehrig, A; Caron, O; Hansen, TVO; Hurtea, J; Nielsen, FC; Heidemann, S; Ottini, L; Muranen, TA; Terry, MB; Schmutzler, RK; Byron, J; Hopper, JL; Fiorica, J; Sutter, C; Skytte, A-B; Lindor, NM; Barkardottir, RB; Niederacher, D; Gaudet, M; Kirchhoff, T; Couch, FJ; Tolad, AE; Lesperance, B; SWE-BRCA,; Radice, P; Montagna, M; Kast, K; Oliani, C; Imyanitov, E; Lindblom, A; Isaacs, C; Wappenschmidt, B; Peterlongo, P; Tihomirova, L; Kruse, TA; Blanco, I; Spurdle, AB; Lazaro, C; Teule, A; Fiebig, B; Del Valle, J; Preister-Adams, S; Engel, C; Greene, MH; Gayther, SA; Loman, N; Odunsi, K; Manoukian, S; Gross, J; Karlan, BY; kConFab Investigators,; Olah, E; Schafer, D; Andrulis, IL; Gadzicki, D2012153
 
Altered expression and deletion of RMO1 in osteosarcomaEppert, K; Wunder, JS; Aneliunas, V; Tsui, LC; Scherer, SW; Andrulis, IL20051,151
 
Mutational analysis of BRCA1 and BRCA2 genes in Chinese ovarian cancer identifies 6 novel germline mutations.Khoo, US; Ngan, HY; Cheung, AN; Chan, KY; Lu, J; Chan, VW; Lau, S; Andrulis, IL; Ozcelik, H2000120
 
Somatic mutations in the BRCA1 gene in Chinese sporadic breast and ovarian cancerKhoo, US; Ozcelik, H; Cheung, ANY; Chow, LWC; Ngan, HYS; Done, SJ; Liang, ACT; Chan, VWY; Au, GKH; Ng, WF; Poon, CSP; Leung, YF; Loong, F; Ip, P; Chan, GSW; Andrulis, IL; Jing, L; Ho, FCS1999115
 
Short report: Somatic mutations in the BRCA1 gene in Chinese sporadic breast and ovarian cancerKhoo, US; Ozcelik, H; Cheung, ANY; Chow, LWC; Ngan, HYS; Done, SJ; Liang, ACT; Chan, VWY; Au, GKH; Ng, WF; Poon, CSP; Leung, YF; Loong, F; Ip, PPC; Chan, GSW; Andrulis, IL; Lu, J; Ho, FCS199996
 
MADR2 maps to 18q21 and encodes a TGFβ-regulated MAD-related protein that is functionally mutated in colorectal carcinomaEppert, K; Scherer, SW; Ozcelik, H; Pirone, R; Hoodless, P; Kim, H; Tsui, LC; Bapat, B; Gallinger, S; Andrulis, IL; Thomsen, GH; Wrana, JL; Attisano, L1996327
 
Detailed deletion mapping with a refined physical map of 7q31 localizes a putative tumor suppressor gene for breast cancer in the region of METLin, JC; Scherer, SW; Tougas, L; Traverso, G; Tsui, LC; Andrulis, IL; Jothy, S; Park, M1996247
 
Refined localization of the asparagine synthetase gene (ASNS) to chromosome 7, region q21.3, and characterization of the somatic cell hybrid line 4AF/106/K015Heng, HHQ; Shi, XM; Scherer, SW; Andrulis, IL; Tsui, LC1994239
 
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