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Spurdle, Amanda B., Marquart, Louise, McGuffog, Lesley, Healey, Sue, Sinilnikova, Olga, Wan, Fei, Chen, Xiaoqing, Beesley, Jonathan, Singer, Christian F., Dressler, Anne-Catharine, Gschwantler-Kaulich, Daphne, Blum, Joanne L., Tung, Nadine, Weitzel, Jeff, Lynch, Henry, Garber, Judy, Easton, Douglas F., Peock, Susan, Cook, Margaret, Oliver, Clare T., Frost, Debra, Conroy, Don, Evans, D. Gareth, Lalloo, Fiona, Eeles, Ros, Izatt, Louise, Davidson, Rosemarie, Chu, Carol, Eccles, Diana, Selkirk, Christina G., Daly, Mary, Isaacs, Claudine, Stoppa-Lyonnet, Dominique, Sinilnikova, Olga M., Buecher, Bruno, Belotti, Muriel, Mazoyer, Sylvie, Barjhoux, Laure, Verny-Pierre, Carole, Lasset, Christine, Dreyfus, Helene, Pujol, Pascal, Collonge-Rame, Marie-Agnes, Rookus, Matti A., Verhoef, Senno, Kriege, Mieke, Hoogerbrugge, Nicoline, Ausems, Margreet G. E. M., van Os, Theo A., Wijnen, Juul, Devilee, Peter, Meijers-Heijboer, Hanne E. J., Blok, Marinus J., Heikkinen, Tuomas, Nevanlinna, Heli, Jakubowska, Anna, Lubinski, Jan, Huzarski, Tomasz, Byrski, Tomasz, Durocher, Francine, Couch, Fergus J., Lindor, Noralane M., Wang, Xianshu, Thomassen, Mads, Domchek, Susan, Nathanson, Kate, Caligo, M. A., Jernstrom, Helena, Liljegren, Annelie, Ehrencrona, Hans, Karlsson, Per, Ganz, Patricia A., Olopade, Olufunmilayo I., Tomlinson, Gail, Neuhausen, Susan, Antoniou, Antonis C., Chenevix-Trench, Georgia and Rebbeck, Timothy R. (2011) Common genetic variation at BARD1 is not associated with breast cancer risk in BRCA1 or BRCA2 mutation carriers. Cancer Epidemiology Biomarkers and Prevention, 20 5: 1032-1038. doi:10.1158/1055-9965.EPI-10-0909 72 2 2 Cited 4 times in Scopus4 0
Stevens, K.N., Wang, X., Fredericksen, Z., Pankratz, V.S., Greene, M.H., Andrulis, I.L., Thomassen, M., Caligo, M., Nathanson, K.L., Jakubowska, A., Osorio, A., Hamann, U., Godwin, A.K., Stoppa-Lyonnet, D., Southey, M., Buys, S.S., Singer, C.F., Hansen, T.V.O., Arason, A., Offit, K., Piedmonte, M., Montagna, M., Imyanitov, E., Tihomirova, L., Sucheston, L., Beattie, M., Neuhausen, S.L., Szabo, C.I., Simard, J., Spurdle, A.B., Healey, S., Chen, X., Rebbeck, T.R., Easton, D.F., Chenevix-Trench, G., Antoniou, A.C. and Couch, F.J. (2012) Evaluation of chromosome 6p22 as a breast cancer risk modifier locus in a follow-up study of BRCA2 mutation carriers. Breast Cancer Research and Treatment, 136 1: 295-302. doi:10.1007/s10549-012-2255-6 40   1 Cited 1 times in Scopus1 0
Osorio, A., Milne, R. L., Alonso, R., Pita, G., Peterlongo, P., Teule, A., Nathanson, K. L., Domchek, S. M., Rebbeck, T., Lasa, A., Konstantopoulou, I., Hogervorst, F. B., Verhoef, S., van Dooren, M. F., Jager, A., Ausems, M. G. E. M., Aalfs, C. M., van Asperen, C. J., Vreeswijk, M., Waisfisz, Q., Van Roozendaal, C. E., Ligtenberg, M. J., Easton, D. F., Peock, S., Cook, M., Oliver, C. T., Frost, D., Curzon, B., Evans, D. G., Lalloo, F., Eeles, R., Izatt, L., Davidson, R., Adlard, J., Eccles, D., Ong, K-R, Douglas, F., Downing, S., Brewer, C., Walker, L., Nevanlinna, H., Aittomaki, K., Couch, F. J., Fredericksen, Z., Lindor, N. M., Godwin, A., Isaacs, C., Caligo, M. A., Loman, N., Jernstrom, H., Barbany-Bustinza, G., Liljegren, A., Ehrencrona, H., Stenmark-Askmalm, M., Feliubadalo, L., Manoukian, S., Peissel, B., Zaffaroni, D., Bonanni, B., Fortuzzi, S., Johannsson, O. T., Chenevix-Trench, G., Chen, X-C, Beesley, J., Spurdle, A. B., Sinilnikova, O. M., Healey, S., McGuffog, L., Antoniou, A. C., Brunet, J., Radice, P. and Benitez, J. (2011) Evaluation of the XRCC1 gene as a phenotypic modifier in BRCA1/2 mutation carriers. Results from the consortium of investigators of modifiers of BRCA1/BRCA2. British Journal of Cancer, 104 8: 1356-1361. doi:10.1038/bjc.2011.91 87   3 Cited 3 times in Scopus3 0
Couch F.J., Wang X., McGuffog L., Lee A., Olswold C., Kuchenbaecker K.B., Soucy P., Fredericksen Z., Barrowdale D., Dennis J., Gaudet M.M., Dicks E., Kosel M., Healey S., Sinilnikova O.M., Lee A., Bacot F., Vincent D., Hogervorst F.B.L., Peock S., Stoppa-Lyonnet D., Jakubowska A., Radice P., Schmutzler R.K., Domchek S.M., Piedmonte M., Singer C.F., Friedman E., Thomassen M., Hansen T.V.O., Neuhausen S.L., Szabo C.I., Blanco I., Greene M.H., Karlan B.Y., Garber J., Phelan C.M., Weitzel J.N., Montagna M., Olah E., Andrulis I.L., Godwin A.K., Yannoukakos D., Goldgar D.E., Caldes T., Nevanlinna H., Osorio A., Terry M.B., Daly M.B., van Rensburg E.J., Hamann U., Ramus S.J., Ewart Toland A., Caligo M.A., Olopade O.I., Tung N., Claes K., Beattie M.S., Southey M.C., Imyanitov E.N., Tischkowitz M., Janavicius R., John E.M., Kwong A., Diez O., Balmana J., Barkardottir R.B., Arun B.K., Rennert G., Teo S.-H., Ganz P.A., Campbell I., van der Hout A.H., van Deurzen C.H.M., Seynaeve C., Gomez Garcia E.B., van Leeuwen F.E., Meijers-Heijboer H.E.J., Gille J.J.P., Ausems M.G.E.M., Blok M.J., Ligtenberg M.J.L., Rookus M.A., Devilee P., Verhoef S., van Os T.A.M., Wijnen J.T., Frost D., Ellis S., Fineberg E., Platte R., Evans D.G., Izatt L., Eeles R.A., Adlard J., Eccles D.M., Cook J., Brewer C., Douglas F., Hodgson S., Morrison P.J., Side L.E., Donaldson A., Houghton C., Rogers M.T., Dorkins H., Eason J., Gregory H., McCann E., Murray A., Calender A., Hardouin A., Berthet P., Delnatte C., Nogues C., Lasset C., Houdayer C., Leroux D., Rouleau E., Prieur F., Damiola F., Sobol H., Coupier I., Venat-Bouvet L., Castera L., Gauthier-Villars M., Leone M., Pujol P., Mazoyer S., Bignon Y.-J., Zlowocka-Perlowska E., Gronwald J., Lubinski J., Durda K., Jaworska K., Huzarski T., Spurdle A.B., Viel A., Peissel B., Bonanni B., Melloni G., Ottini L., Papi L., Varesco L., Tibiletti M.G., Peterlongo P., Volorio S., Manoukian S., Pensotti V., Arnold N., Engel C., Deissler H., Gadzicki D., Gehrig A., Kast K., Rhiem K., Meindl A., Niederacher D., Ditsch N., Plendl H., Preisler-Adams S., Engert S., Sutter C., Varon-Mateeva R., Wappenschmidt B., Weber B.H.F., Arver B., Stenmark-Askmalm M., Loman N., Rosenquist R., Einbeigi Z., Nathanson K.L., Rebbeck T.R., Blank S.V., Cohn D.E., Rodriguez G.C., Small L., Friedlander M., Bae-Jump V.L., Fink-Retter A., Rappaport C., Gschwantler-Kaulich D., Pfeiler G., Tea M.-K., Lindor N.M., Kaufman B., Shimon Paluch S., Laitman Y., Skytte A.-B., Gerdes A.-M., Pedersen I.S., Moeller S.T., Kruse T.A., Jensen U.B., Vijai J., Sarrel K., Robson M., Kauff N., Mulligan A.M., Glendon G., Ozcelik H., Ejlertsen B., Nielsen F.C., Jonson L., Andersen M.K., Ding Y.C., Steele L., Foretova L., Teule A., Lazaro C., Brunet J., Pujana M.A., Mai P.L., Loud J.T., Walsh C., Lester J., Orsulic S., Narod S.A., Herzog J., Sand S.R., Tognazzo S., Agata S., Vaszko T., Weaver J., Stavropoulou A.V., Buys S.S., Romero A., de la Hoya M., Aittomaki K., Muranen T.A., Duran M., Chung W.K., Lasa A., Dorfling C.M., Miron A., Benitez J., Senter L., Huo D., Chan S.B., Sokolenko A.P., Chiquette J., Tihomirova L., Friebel T.M., Agnarsson B.A., Lu K.H., Lejbkowicz F., James P.A., Hall P., Dunning A.M., Tessier D., Cunningham J., Slager S.L., Wang C., Hart S., Stevens K., Simard J., Pastinen T., Pankratz V.S., Offit K., Easton D.F., Chenevix-Trench G., Antoniou A.C., Thorne H., Niedermayr E., Borg A., Olsson H., Jernstrom H., Henriksson K., Harbst K., Soller M., Loman N., Kristoffersson U., Ofverholm A., Nordling M., Karlsson P., Einbeigi Z., von Wachenfeldt A., Liljegren A., Lindblom A., Arver B., Bustinza G.B., Rantala J., Melin B., Ardnor C.E., Emanuelsson M., Ehrencrona H., Pigg M.H., Rosenquist R., Stenmark-Askmalm M., Liedgren S., Rookus M.A., Hogervorst F.B.L., Verhoef S., van Leeuwen F.E., Schmidt M.K., de Lange J., Collee J.M., van den Ouweland A.M.W., Hooning M.J., Seynaeve C., van Asperen C.J., Wijnen J.T., Tollenaar R.A., Devilee P., van Cronenburg T.C.T.E.F., Kets C.M., Mensenkamp A.R., Ausems M.G.E.M., van der Luijt R.B., Aalfs C.M., van Os T.A.M., Gille J.J.P., Waisfisz Q., Meijers-Heijboer H.E.J., Gomez-Garcia E.B., Blok M.J., Oosterwijk J.C., van der Hout H., Mourits M.J., de Bock G.H., Peock S., Frost D., Ellis S., Fineberg E., Platte R., Miedzybrodzka Z., Gregory H., Morrison P., Jeffers L., Cole T., Ong K.-R., Hoffman J., Donaldson A., James M., Tischkowitz M., Paterson J., Taylor A., Murray A., Rogers M.T., McCann E., Kennedy M.J., Barton D., Porteous M., Drummond S., Brewer C., Kivuva E., Searle A., Goodman S., Hill K., Davidson R., Murday V., Bradshaw N., Snadden L., Longmuir M., Watt C., Gibson S., Haque E., Tobias E., Duncan A., Izatt L., Jacobs C., Langman C., Dorkins H., Brady A., Melville A., Randhawa K., Barwell J., Adlard J., Serra-Feliu G., Ellis I., Houghton C., Evans D.G., Lalloo F., Taylor J., Side L., Male A., Berlin C., Eason J., Collier R., Douglas F., Claber O., Jobson I., Walker L., McLeod D., Halliday D., Durell S., Stayner B., Eeles R.A., Shanley S., Rahman N., Houlston R., Stormorken A., Bancroft E., Page E., Ardern-Jones A., Kohut K., Wiggins J., Castro E., Killick E., Martin S., Rea G., Kulkarni A., Cook J., Quarrell O., Bardsley C., Hodgson S., Goff S., Brice G., Winchester L., Eddy C., Tripathi V., Attard V., Lehmann A., Eccles D., Lucassen A., Crawford G., McBride D., Smalley S., Sinilnikova O., Mazoyer S., Damiola F., Barjhoux L., Verny-Pierre C., Giraud S., Leone M., Stoppa-Lyonnet D., Gauthier-Villars M., Buecher B., Houdayer C., Moncoutier V., Belotti M., Tirapo C., de Pauw A., Bressac-de-Paillerets B., Caron O., Bignon Y.-J., Uhrhammer N., Lasset C., Bonadona V., Handallou S., Hardouin A., Berthet P., Sobol H., Bourdon V., Noguchi T., Remenieras A., Eisinger F., Coupier I., Pujol P., Peyrat J.-P., Fournier J., Revillion F., Vennin P., Adenis C., Rouleau E., Lidereau R., Demange L., Nogues C., Muller D., Fricker J.-P., Barouk-Simonet E., Bonnet F., Bubien V., Sevenet N., Longy M., Toulas C., Guimbaud R., Gladieff L., Feillel V., Leroux D., Dreyfus H., Rebischung C., Peysselon M., Coron F., Faivre L., Prieur F., Lebrun M., Kientz C., Ferrer S.F., Frenay M., Venat-Bouvet L., Delnatte C., Mortemousque I., Coulet F., Colas C., Soubrier F., Sokolowska J., Bronner M., Lynch H.T., Snyder C.L., Angelakos M., Maskiell J. and Dite G. (2013) Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk. PLoS Genetics, 9 3: e1003212-1-e1003212-21. doi:10.1371/journal.pgen.1003212 27   28 Cited 32 times in Scopus32 118