APA

Ramus S. J., Kartsonaki C., Gayther S. A., Pharoah P. D. P., Sinilnikova O. M., Beesley J., Chen X., McGuffog L., Healey S., Couch F. J., Wang X., Fredericksen Z., Peterlongo P., Manoukian S., Peissel B., Zaffaroni D., Roversi G., Barile M., Viel A., Allavena A., Ottini L., Papi L., Gismondi V., Capra F., Radice P., Greene M. H., Mai P. L., Andrulis I. L., Glendon G., Ozcelik H., Thomassen M., Gerdes A., Kruse T. A., Cruger D., Jensen U. B., Caligo M. A., Olsson H., Kristoffersson U., Lindblom A., Arver B., Karlsson P., Stenmark Askmalm M., Borg A., Neuhausen S. L., Ding Y. C., Nathanson K. L., Domchek S. M., Jakubowska A., Lubiński J., Huzarski T., Byrski T., Gronwald J., Górski B., Cybulski C., Dębniak T., Osorio A., Durán M., Tejada M., Benítez J., Hamann U., Rookus M. A., Verhoef S., Tilanus-Linthorst M. A., Vreeswijk M. P., Bodmer D., Ausems M. G. E. M., van Os T. A., Asperen C. J., Blok M. J., Meijers-Heijboer H. E. J., Peock S., Cook M., Oliver C., Frost D., Dunning A. M., Evans D. G., Eeles R., Pichert G., Cole T., Hodgson S., Brewer C., Morrison P. J., Porteous M., Kennedy M. J., Rogers M. T., Side L. E., Donaldson A., Gregory H., Godwin A., Stoppa-Lyonnet D., Moncoutier V., Castera L., Mazoyer S., Barjhoux L., Bonadona V., Leroux D., Faivre L., Lidereau R., Nogues C., Bignon Y., Prieur F., Collonge-Rame M., Venat-Bouvet L., Fert-Ferrer S., Miron A., Buys S. S., Hopper J. L., Daly M. B., John E. M., Terry M. B., Goldgar D., Hansen T. v. O., Jønson L., Ejlertsen B., Agnarsson B. A., Offit K., Kirchhoff T., Vijai J., Dutra-Clarke A. V. C., Przybylo J. A., Montagna M., Casella C., Imyanitov E. N., Janavicius R., Blanco I., Lázaro C., Moysich K. B., Karlan B. Y., Gross J., Beattie M. S., Schmutzler R., Wappenschmidt B., Meindl A., Ruehl I., Fiebig B., Sutter C., Arnold N., Deissler H., Varon-Mateeva R., Kast K., Niederacher D., Gadzicki D., Caldes T., de la Hoya M., Nevanlinna H., Aittomäki K., Simard J., Soucy P., Spurdle A. B., Holland H., Chenevix-Trench G., Easton D. F. & Antoniou A. C. (20110214). Genetic variation at 9p22.2 and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers. : Journal of the National Cancer Institute.

Chicago

Ramus Susan J, Kartsonaki Christiana, Gayther Simon A, Pharoah Paul D P, Sinilnikova Olga M, Beesley Jonathan, Chen Xiaoqing, McGuffog Lesley, Healey Sue, Couch Fergus J, Wang Xianshu, Fredericksen Zachary, Peterlongo Paolo, Manoukian Siranoush, Peissel Bernard, Zaffaroni Daniela, Roversi Gaia, Barile Monica, Viel Alessandra, Allavena Anna, Ottini Laura, Papi Laura, Gismondi Viviana, Capra Fabio, Radice Paolo, Greene Mark H, Mai Phuong L, Andrulis Irene L, Glendon Gord, Ozcelik Hilmi, Thomassen Mads, Gerdes Anne-Marie, Kruse Torben A, Cruger Dorthe, Jensen Uffe Birk, Caligo Maria Adelaide, Olsson Håkan, Kristoffersson Ulf, Lindblom Annika, Arver Brita, Karlsson Per, Stenmark Askmalm Marie, Borg Ake, Neuhausen Susan L, Ding Yuan Chun, Nathanson Katherine L, Domchek Susan M, Jakubowska Anna, Lubiński Jan, Huzarski Tomasz, Byrski Tomasz, Gronwald Jacek, Górski Bohdan, Cybulski Cezary, Dębniak Tadeusz, Osorio Ana, Durán Mercedes, Tejada Maria-Isabel, Benítez Javier, Hamann Ute, Rookus Matti A, Verhoef Senno, Tilanus-Linthorst Madeleine A, Vreeswijk Maaike P, Bodmer Danielle, Ausems Margreet G E M, van Os Theo A, Asperen Christi J, Blok Marinus J, Meijers-Heijboer Hanne E J, Peock Susan, Cook Margaret, Oliver Clare, Frost Debra, Dunning Alison M, Evans D Gareth, Eeles Ros, Pichert Gabriella, Cole Trevor, Hodgson Shirley, Brewer Carole, Morrison Patrick J, Porteous Mary, Kennedy M John, Rogers Mark T, Side Lucy E, Donaldson Alan, Gregory Helen, Godwin Andrew, Stoppa-Lyonnet Dominique, Moncoutier Virginie, Castera Laurent, Mazoyer Sylvie, Barjhoux Laure, Bonadona Valérie, Leroux Dominique, Faivre Laurence, Lidereau Rosette, Nogues Catherine, Bignon Yves-Jean, Prieur Fabienne, Collonge-Rame Marie-Agnès, Venat-Bouvet Laurence, Fert-Ferrer Sandra, Miron Alex, Buys Saundra S, Hopper John L, Daly Mary B, John Esther M, Terry Mary Beth, Goldgar David, Hansen Thomas v O, Jønson Lars, Ejlertsen Bent, Agnarsson Bjarni A, Offit Kenneth, Kirchhoff Tomas, Vijai Joseph, Dutra-Clarke Ana V C, Przybylo Jennifer A, Montagna Marco, Casella Cinzia, Imyanitov Evgeny N, Janavicius Ramunas, Blanco Ignacio, Lázaro Conxi, Moysich Kirsten B, Karlan Beth Y, Gross Jenny, Beattie Mary S, Schmutzler Rita, Wappenschmidt Barbara, Meindl Alfons, Ruehl Ina, Fiebig Britta, Sutter Christian, Arnold Norbert, Deissler Helmut, Varon-Mateeva Raymonda, Kast Karin, Niederacher Dieter, Gadzicki Dorothea, Caldes Trinidad, de la Hoya Miguel, Nevanlinna Heli, Aittomäki Kristiina, Simard Jacques, Soucy Penny, Spurdle Amanda B, Holland Helene, Chenevix-Trench Georgia, Easton Douglas F and Antoniou Antonis C. 20110214. Genetic variation at 9p22.2 and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers. : Journal of the National Cancer Institute.

Harvard

Ramus S. J., Kartsonaki C., Gayther S. A., Pharoah P. D. P., Sinilnikova O. M., Beesley J., Chen X., McGuffog L., Healey S., Couch F. J., Wang X., Fredericksen Z., Peterlongo P., Manoukian S., Peissel B., Zaffaroni D., Roversi G., Barile M., Viel A., Allavena A., Ottini L., Papi L., Gismondi V., Capra F., Radice P., Greene M. H., Mai P. L., Andrulis I. L., Glendon G., Ozcelik H., Thomassen M., Gerdes A., Kruse T. A., Cruger D., Jensen U. B., Caligo M. A., Olsson H., Kristoffersson U., Lindblom A., Arver B., Karlsson P., Stenmark Askmalm M., Borg A., Neuhausen S. L., Ding Y. C., Nathanson K. L., Domchek S. M., Jakubowska A., Lubiński J., Huzarski T., Byrski T., Gronwald J., Górski B., Cybulski C., Dębniak T., Osorio A., Durán M., Tejada M., Benítez J., Hamann U., Rookus M. A., Verhoef S., Tilanus-Linthorst M. A., Vreeswijk M. P., Bodmer D., Ausems M. G. E. M., van Os T. A., Asperen C. J., Blok M. J., Meijers-Heijboer H. E. J., Peock S., Cook M., Oliver C., Frost D., Dunning A. M., Evans D. G., Eeles R., Pichert G., Cole T., Hodgson S., Brewer C., Morrison P. J., Porteous M., Kennedy M. J., Rogers M. T., Side L. E., Donaldson A., Gregory H., Godwin A., Stoppa-Lyonnet D., Moncoutier V., Castera L., Mazoyer S., Barjhoux L., Bonadona V., Leroux D., Faivre L., Lidereau R., Nogues C., Bignon Y., Prieur F., Collonge-Rame M., Venat-Bouvet L., Fert-Ferrer S., Miron A., Buys S. S., Hopper J. L., Daly M. B., John E. M., Terry M. B., Goldgar D., Hansen T. v. O., Jønson L., Ejlertsen B., Agnarsson B. A., Offit K., Kirchhoff T., Vijai J., Dutra-Clarke A. V. C., Przybylo J. A., Montagna M., Casella C., Imyanitov E. N., Janavicius R., Blanco I., Lázaro C., Moysich K. B., Karlan B. Y., Gross J., Beattie M. S., Schmutzler R., Wappenschmidt B., Meindl A., Ruehl I., Fiebig B., Sutter C., Arnold N., Deissler H., Varon-Mateeva R., Kast K., Niederacher D., Gadzicki D., Caldes T., de la Hoya M., Nevanlinna H., Aittomäki K., Simard J., Soucy P., Spurdle A. B., Holland H., Chenevix-Trench G., Easton D. F. and Antoniou A. C. (20110214). Genetic variation at 9p22.2 and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers. : Journal of the National Cancer Institute.

MLA

Ramus Susan J, Kartsonaki Christiana, Gayther Simon A, Pharoah Paul D P, Sinilnikova Olga M, Beesley Jonathan, Chen Xiaoqing, McGuffog Lesley, Healey Sue, Couch Fergus J, Wang Xianshu, Fredericksen Zachary, Peterlongo Paolo, Manoukian Siranoush, Peissel Bernard, Zaffaroni Daniela, Roversi Gaia, Barile Monica, Viel Alessandra, Allavena Anna, Ottini Laura, Papi Laura, Gismondi Viviana, Capra Fabio, Radice Paolo, Greene Mark H, Mai Phuong L, Andrulis Irene L, Glendon Gord, Ozcelik Hilmi, Thomassen Mads, Gerdes Anne-Marie, Kruse Torben A, Cruger Dorthe, Jensen Uffe Birk, Caligo Maria Adelaide, Olsson Håkan, Kristoffersson Ulf, Lindblom Annika, Arver Brita, Karlsson Per, Stenmark Askmalm Marie, Borg Ake, Neuhausen Susan L, Ding Yuan Chun, Nathanson Katherine L, Domchek Susan M, Jakubowska Anna, Lubiński Jan, Huzarski Tomasz, Byrski Tomasz, Gronwald Jacek, Górski Bohdan, Cybulski Cezary, Dębniak Tadeusz, Osorio Ana, Durán Mercedes, Tejada Maria-Isabel, Benítez Javier, Hamann Ute, Rookus Matti A, Verhoef Senno, Tilanus-Linthorst Madeleine A, Vreeswijk Maaike P, Bodmer Danielle, Ausems Margreet G E M, van Os Theo A, Asperen Christi J, Blok Marinus J, Meijers-Heijboer Hanne E J, Peock Susan, Cook Margaret, Oliver Clare, Frost Debra, Dunning Alison M, Evans D Gareth, Eeles Ros, Pichert Gabriella, Cole Trevor, Hodgson Shirley, Brewer Carole, Morrison Patrick J, Porteous Mary, Kennedy M John, Rogers Mark T, Side Lucy E, Donaldson Alan, Gregory Helen, Godwin Andrew, Stoppa-Lyonnet Dominique, Moncoutier Virginie, Castera Laurent, Mazoyer Sylvie, Barjhoux Laure, Bonadona Valérie, Leroux Dominique, Faivre Laurence, Lidereau Rosette, Nogues Catherine, Bignon Yves-Jean, Prieur Fabienne, Collonge-Rame Marie-Agnès, Venat-Bouvet Laurence, Fert-Ferrer Sandra, Miron Alex, Buys Saundra S, Hopper John L, Daly Mary B, John Esther M, Terry Mary Beth, Goldgar David, Hansen Thomas v O, Jønson Lars, Ejlertsen Bent, Agnarsson Bjarni A, Offit Kenneth, Kirchhoff Tomas, Vijai Joseph, Dutra-Clarke Ana V C, Przybylo Jennifer A, Montagna Marco, Casella Cinzia, Imyanitov Evgeny N, Janavicius Ramunas, Blanco Ignacio, Lázaro Conxi, Moysich Kirsten B, Karlan Beth Y, Gross Jenny, Beattie Mary S, Schmutzler Rita, Wappenschmidt Barbara, Meindl Alfons, Ruehl Ina, Fiebig Britta, Sutter Christian, Arnold Norbert, Deissler Helmut, Varon-Mateeva Raymonda, Kast Karin, Niederacher Dieter, Gadzicki Dorothea, Caldes Trinidad, de la Hoya Miguel, Nevanlinna Heli, Aittomäki Kristiina, Simard Jacques, Soucy Penny, Spurdle Amanda B, Holland Helene, Chenevix-Trench Georgia, Easton Douglas F and Antoniou Antonis C. Genetic variation at 9p22.2 and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers. : Journal of the National Cancer Institute. 20110214.