From post

копировать удалить добавить публикацию в буфер
Запись сообщества
посмотреть историю данной записи
URL
DOI
BibTeX
EndNote
APA
Chicago
DIN 1505
Harvard
MSOffice XML

Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers

A. Antoniou, C. Kartsonaki, O. Sinilnikova, P. Soucy, L. McGuffog, S. Healey, A. Lee, P. Peterlongo, S. Manoukian, B. Peissel, D. Zaffaroni, E. Cattaneo, M. Barile, V. Pensotti, B. Pasini, R. Dolcetti, G. Giannini, A. Putignano, L. Varesco, P. Radice, P. Mai, M. Greene, I. Andrulis, G. Glendon, H. Ozcelik, M. Thomassen, A. Gerdes, T. Kruse, U. Birk Jensen, D. Crüger, M. Caligo, Y. Laitman, R. Milgrom, B. Kaufman, S. Paluch-Shimon, E. Friedman, N. Loman, K. Harbst, A. Lindblom, B. Arver, H. Ehrencrona, B. Melin, K. Nathanson, S. Domchek, T. Rebbeck, A. Jakubowska, J. Lubinski, J. Gronwald, T. Huzarski, T. Byrski, C. Cybulski, B. Gorski, A. Osorio, Ramón y Cajal, Teresa, F. Fostira, R. Andrés, J. Benitez, U. Hamann, F. Hogervorst, M. Rookus, M. Hooning, M. Nelen, van der Luijt, Rob B, van Os, Theo A M, van Asperen, Christi J, P. Devilee, Meijers-Heijboer, Hanne E J, Gómez Garcia, Encarna B, S. Peock, M. Cook, D. Frost, R. Platte, J. Leyland, D. Evans, F. Lalloo, R. Eeles, L. Izatt, J. Adlard, R. Davidson, D. Eccles, K. Ong, J. Cook, F. Douglas, J. Paterson, M. Kennedy, Z. Miedzybrodzka, A. Godwin, D. Stoppa-Lyonnet, B. Buecher, M. Belotti, C. Tirapo, S. Mazoyer, L. Barjhoux, C. Lasset, D. Leroux, L. Faivre, M. Bronner, F. Prieur, C. Nogues, E. Rouleau, P. Pujol, I. Coupier, M. Frénay, J. Hopper, M. Daly, M. Terry, E. John, S. Buys, Y. Yassin, A. Miron, D. Goldgar, C. Singer, M. Tea, G. Pfeiler, A. Dressler, Hansen, Thomas V O, L. Jønson, B. Ejlertsen, R. Barkardottir, T. Kirchhoff, K. Offit, M. Piedmonte, G. Rodriguez, L. Small, J. Boggess, S. Blank, J. Basil, M. Azodi, A. Toland, M. Montagna, S. Tognazzo, S. Agata, E. Imyanitov, R. Janavicius, C. Lazaro, I. Blanco, Pharoah, Paul D P, L. Sucheston, B. Karlan, C. Walsh, E. Olah, A. Bozsik, S. Teo, J. Seldon, M. Beattie, van Rensburg, Elizabeth J, M. Sluiter, O. Diez, R. Schmutzler, B. Wappenschmidt, C. Engel, A. Meindl, I. Ruehl, R. Varon-Mateeva, K. Kast, H. Deissler, D. Niederacher, N. Arnold, D. Gadzicki, I. Schönbuchner, T. Caldes, de la Hoya, Miguel, H. Nevanlinna, K. Aittomäki, M. Dumont, J. Chiquette, M. Tischkowitz, X. Chen, J. Beesley, A. Spurdle, S. Neuhausen, Y. Chun Ding, Z. Fredericksen, X. Wang, V. Pankratz, F. Couch, J. Simard, D. Easton, и G. Chenevix-Trench. Human molecular genetics, 20 (16): 3304–3321 (2011)

Please choose a person to relate this publication to

To differ between persons with the same name, the academic degree and the title of an important publication will be displayed.

Maria A Martin

Maria A Slowinska

Maria A Diefenbach

Petra Marialke-Kandaouroff

Manuel Mariadasa

Другие публикации лиц с тем же именем

Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer riskF. Couch, X. Wang, L. McGuffog, A. Lee, C. Olswold, K. Kuchenbaecker, P. Soucy, Z. Fredericksen, D. Barrowdale, J. Dennis и 252 other автор(ы). PLoS genetics, 9 (3): e1003212 (2013)Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2A. Mulligan, F. Couch, D. Barrowdale, S. Domchek, D. Eccles, H. Nevanlinna, S. Ramus, M. Robson, M. Sherman, A. Spurdle и 172 other автор(ы). Breast cancer research : BCR, 13 (6): R110 (2011)Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriersS. Ramus, A. Antoniou, K. Kuchenbaecker, P. Soucy, J. Beesley, X. Chen, L. McGuffog, O. Sinilnikova, S. Healey, D. Barrowdale и 176 other автор(ы). Human mutation, 33 (4): 690–702 (2012)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 carriersF. Couch, M. Gaudet, A. Antoniou, S. Ramus, K. Kuchenbaecker, P. Soucy, J. Beesley, X. Chen, X. Wang, T. Kirchhoff и 180 other автор(ы). Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 21 (4): 645–657 (2012)Common breast cancer-predisposition alleles are associated with breast cancer risk in BRCA1 and BRCA2 mutation carriersA. Antoniou, A. Spurdle, O. Sinilnikova, S. Healey, K. Pooley, R. Schmutzler, B. Versmold, C. Engel, A. Meindl, N. Arnold и 76 other автор(ы). American journal of human genetics, 82 (4): 937–948 (2008)Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriersD. Cox, J. Simard, D. Sinnett, Y. Hamdi, P. Soucy, M. Ouimet, L. Barjhoux, C. Verny-Pierre, L. McGuffog, S. Healey и 99 other автор(ы). Human molecular genetics, 20 (23): 4732–4747 (2011)Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriersA. Antoniou, C. Kartsonaki, O. Sinilnikova, P. Soucy, L. McGuffog, S. Healey, A. Lee, P. Peterlongo, S. Manoukian, B. Peissel и 169 other автор(ы). Human molecular genetics, 20 (16): 3304–3321 (2011)Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriersA. Antoniou, K. Kuchenbaecker, P. Soucy, J. Beesley, X. Chen, L. McGuffog, A. Lee, D. Barrowdale, S. Healey, O. Sinilnikova и 171 other автор(ы). Breast cancer research : BCR, 14 (1): R33 (2012)A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general populationA. Antoniou, X. Wang, Z. Fredericksen, L. McGuffog, R. Tarrell, O. Sinilnikova, S. Healey, J. Morrison, C. Kartsonaki, T. Lesnick и 168 other автор(ы). Nature genetics, 42 (10): 885–892 (2010)Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriersA. Antoniou, O. Sinilnikova, L. McGuffog, S. Healey, H. Nevanlinna, T. Heikkinen, J. Simard, A. Spurdle, J. Beesley, X. Chen и 127 other автор(ы). Human molecular genetics, 18 (22): 4442–4456 (2009)

Что такое BibSonomy?: С чего начать; Кнопки для браузера; Помощь
Разработчикам: Обзор; API-документация

Контакт и защита личных данных: о нас; Cookies; Сообщить о проблеме; BibSonomy Вики

Интеграция: PUMA; Расширение для TYPO3; Плагин для; Клиент Java REST; Поддерживаемые источники; далее

О BibSonomy: Команда; Блог; Список рассылки
Социальные сети: Наш Twitter