Associations of common variants at 1p11.2 and 14q24.1 (RAD51L1) with breast cancer risk and heterogeneity by tumor subtype: findings from the Breast Cancer Association Consortium.
Associations of common variants at 1p11.2 and 14q24.1 (RAD51L1) with breast cancer risk and heterogeneity by tumor subtype: findings from the Breast Cancer Association Consortium. [electronic resource] - Human molecular genetics Dec 2011 - 4693-706 p. digital
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, N.I.H., Intramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.
1460-2083
10.1093/hmg/ddr368 doi
Alleles
Breast Neoplasms--classification
Case-Control Studies
Chromosomes, Human, Pair 1--genetics
Chromosomes, Human, Pair 14--genetics
Confidence Intervals
DNA-Binding Proteins--genetics
Female
Genetic Heterogeneity
Genetic Predisposition to Disease
Genome-Wide Association Study
Humans
Odds Ratio
Polymorphism, Single Nucleotide--genetics
Receptor, ErbB-2--metabolism
Receptors, Estrogen--metabolism
Receptors, Progesterone--metabolism
Risk Factors
Associations of common variants at 1p11.2 and 14q24.1 (RAD51L1) with breast cancer risk and heterogeneity by tumor subtype: findings from the Breast Cancer Association Consortium.
APA
Figueroa J. D., Garcia-Closas M., Humphreys M., Platte R., Hopper J. L., Southey M. C., Apicella C., Hammet F., Schmidt M. K., Broeks A., Tollenaar R. A. E. M., Van't Veer L. J., Fasching P. A., Beckmann M. W., Ekici A. B., Strick R., Peto J., dos Santos Silva I., Fletcher O., Johnson N., Sawyer E., Tomlinson I., Kerin M., Burwinkel B., Marme F., Schneeweiss A., Sohn C., Bojesen S., Flyger H., Nordestgaard B. G., Benítez J., Milne R. L., Ignacio Arias J., Zamora M. P., Brenner H., Müller H., Arndt V., Rahman N., Turnbull C., Seal S., Renwick A., Brauch H., Justenhoven C., Brüning T., Chang-Claude J., Hein R., Wang-Gohrke S., Dörk T., Schürmann P., Bremer M., Hillemanns P., Nevanlinna H., Heikkinen T., Aittomäki K., Blomqvist C., Bogdanova N., Antonenkova N., Rogov Y. I., Karstens J. H., Bermisheva M., Prokofieva D., Gantcev S. H., Khusnutdinova E., Lindblom A., Margolin S., Chenevix-Trench G., Beesley J., Chen X., Mannermaa A., Kosma V., Soini Y., Kataja V., Lambrechts D., Yesilyurt B. T., Chrisiaens M., Peeters S., Radice P., Peterlongo P., Manoukian S., Barile M., Couch F., Lee A. M., Diasio R., Wang X., Giles G. G., Severi G., Baglietto L., Maclean C., Offit K., Robson M., Joseph V., Gaudet M., John E. M., Winqvist R., Pylkäs K., Jukkola-Vuorinen A., Grip M., Andrulis I., Knight J. A., Mulligan A. M., O'Malley F. P., Brinton L. A., Sherman M. E., Lissowska J., Chanock S. J., Hooning M., Martens J. W. M., van den Ouweland A. M. W., Collée J. M., Hall P., Czene K., Cox A., Brock I. W., Reed M. W. R., Cross S. S., Pharoah P., Dunning A. M., Kang D., Yoo K., Noh D., Ahn S., Jakubowska A., Lubinski J., Jaworska K., Durda K., Sangrajrang S., Gaborieau V., Brennan P., McKay J., Shen C., Ding S., Hsu H., Yu J., Anton-Culver H., Ziogas A., Ashworth A., Swerdlow A., Jones M., Orr N., Trentham-Dietz A., Egan K., Newcomb P., Titus-Ernstoff L., Easton D. & Spurdle A. B. (20120222). Associations of common variants at 1p11.2 and 14q24.1 (RAD51L1) with breast cancer risk and heterogeneity by tumor subtype: findings from the Breast Cancer Association Consortium. : Human molecular genetics.
Chicago
Figueroa Jonine D, Garcia-Closas Montserrat, Humphreys Manjeet, Platte Radka, Hopper John L, Southey Melissa C, Apicella Carmel, Hammet Fleur, Schmidt Marjanka K, Broeks Annegien, Tollenaar Rob A E M, Van't Veer Laura J, Fasching Peter A, Beckmann Matthias W, Ekici Arif B, Strick Reiner, Peto Julian, dos Santos Silva Isabel, Fletcher Olivia, Johnson Nichola, Sawyer Elinor, Tomlinson Ian, Kerin Michael, Burwinkel Barbara, Marme Federik, Schneeweiss Andreas, Sohn Christof, Bojesen Stig, Flyger Henrik, Nordestgaard Børge G, Benítez Javier, Milne Roger L, Ignacio Arias Jose, Zamora M Pilar, Brenner Hermann, Müller Heiko, Arndt Volker, Rahman Nazneen, Turnbull Clare, Seal Sheila, Renwick Anthony, Brauch Hiltrud, Justenhoven Christina, Brüning Thomas, Chang-Claude Jenny, Hein Rebecca, Wang-Gohrke Shan, Dörk Thilo, Schürmann Peter, Bremer Michael, Hillemanns Peter, Nevanlinna Heli, Heikkinen Tuomas, Aittomäki Kristiina, Blomqvist Carl, Bogdanova Natalia, Antonenkova Natalia, Rogov Yuri I, Karstens Johann Hinrich, Bermisheva Marina, Prokofieva Darya, Gantcev Shamil Hanafievich, Khusnutdinova Elza, Lindblom Annika, Margolin Sara, Chenevix-Trench Georgia, Beesley Jonathan, Chen Xiaoqing, Mannermaa Arto, Kosma Veli-Matti, Soini Ylermi, Kataja Vesa, Lambrechts Diether, Yesilyurt Betül T, Chrisiaens Marie-Rose, Peeters Stephanie, Radice Paolo, Peterlongo Paolo, Manoukian Siranoush, Barile Monica, Couch Fergus, Lee Adam M, Diasio Robert, Wang Xianshu, Giles Graham G, Severi Gianluca, Baglietto Laura, Maclean Catriona, Offit Ken, Robson Mark, Joseph Vijai, Gaudet Mia, John Esther M, Winqvist Robert, Pylkäs Katri, Jukkola-Vuorinen Arja, Grip Mervi, Andrulis Irene, Knight Julia A, Mulligan Anna Marie, O'Malley Frances P, Brinton Louise A, Sherman Mark E, Lissowska Jolanta, Chanock Stephen J, Hooning Maartje, Martens John W M, van den Ouweland Ans M W, Collée J Margriet, Hall Per, Czene Kamila, Cox Angela, Brock Ian W, Reed Malcolm W R, Cross Simon S, Pharoah Paul, Dunning Alison M, Kang Daehee, Yoo Keun-Young, Noh Dong-Young, Ahn Sei-Hyun, Jakubowska Anna, Lubinski Jan, Jaworska Katarzyna, Durda Katarzyna, Sangrajrang Suleeporn, Gaborieau Valerie, Brennan Paul, McKay James, Shen Chen-Yang, Ding Shian-ling, Hsu Huan-Ming, Yu Jyh-Cherng, Anton-Culver Hoda, Ziogas Argyrios, Ashworth Alan, Swerdlow Anthony, Jones Michael, Orr Nick, Trentham-Dietz Amy, Egan Kathleen, Newcomb Polly, Titus-Ernstoff Linda, Easton Doug and Spurdle Amanda B. 20120222. Associations of common variants at 1p11.2 and 14q24.1 (RAD51L1) with breast cancer risk and heterogeneity by tumor subtype: findings from the Breast Cancer Association Consortium. : Human molecular genetics.
Harvard
Figueroa J. D., Garcia-Closas M., Humphreys M., Platte R., Hopper J. L., Southey M. C., Apicella C., Hammet F., Schmidt M. K., Broeks A., Tollenaar R. A. E. M., Van't Veer L. J., Fasching P. A., Beckmann M. W., Ekici A. B., Strick R., Peto J., dos Santos Silva I., Fletcher O., Johnson N., Sawyer E., Tomlinson I., Kerin M., Burwinkel B., Marme F., Schneeweiss A., Sohn C., Bojesen S., Flyger H., Nordestgaard B. G., Benítez J., Milne R. L., Ignacio Arias J., Zamora M. P., Brenner H., Müller H., Arndt V., Rahman N., Turnbull C., Seal S., Renwick A., Brauch H., Justenhoven C., Brüning T., Chang-Claude J., Hein R., Wang-Gohrke S., Dörk T., Schürmann P., Bremer M., Hillemanns P., Nevanlinna H., Heikkinen T., Aittomäki K., Blomqvist C., Bogdanova N., Antonenkova N., Rogov Y. I., Karstens J. H., Bermisheva M., Prokofieva D., Gantcev S. H., Khusnutdinova E., Lindblom A., Margolin S., Chenevix-Trench G., Beesley J., Chen X., Mannermaa A., Kosma V., Soini Y., Kataja V., Lambrechts D., Yesilyurt B. T., Chrisiaens M., Peeters S., Radice P., Peterlongo P., Manoukian S., Barile M., Couch F., Lee A. M., Diasio R., Wang X., Giles G. G., Severi G., Baglietto L., Maclean C., Offit K., Robson M., Joseph V., Gaudet M., John E. M., Winqvist R., Pylkäs K., Jukkola-Vuorinen A., Grip M., Andrulis I., Knight J. A., Mulligan A. M., O'Malley F. P., Brinton L. A., Sherman M. E., Lissowska J., Chanock S. J., Hooning M., Martens J. W. M., van den Ouweland A. M. W., Collée J. M., Hall P., Czene K., Cox A., Brock I. W., Reed M. W. R., Cross S. S., Pharoah P., Dunning A. M., Kang D., Yoo K., Noh D., Ahn S., Jakubowska A., Lubinski J., Jaworska K., Durda K., Sangrajrang S., Gaborieau V., Brennan P., McKay J., Shen C., Ding S., Hsu H., Yu J., Anton-Culver H., Ziogas A., Ashworth A., Swerdlow A., Jones M., Orr N., Trentham-Dietz A., Egan K., Newcomb P., Titus-Ernstoff L., Easton D. and Spurdle A. B. (20120222). Associations of common variants at 1p11.2 and 14q24.1 (RAD51L1) with breast cancer risk and heterogeneity by tumor subtype: findings from the Breast Cancer Association Consortium. : Human molecular genetics.
MLA
Figueroa Jonine D, Garcia-Closas Montserrat, Humphreys Manjeet, Platte Radka, Hopper John L, Southey Melissa C, Apicella Carmel, Hammet Fleur, Schmidt Marjanka K, Broeks Annegien, Tollenaar Rob A E M, Van't Veer Laura J, Fasching Peter A, Beckmann Matthias W, Ekici Arif B, Strick Reiner, Peto Julian, dos Santos Silva Isabel, Fletcher Olivia, Johnson Nichola, Sawyer Elinor, Tomlinson Ian, Kerin Michael, Burwinkel Barbara, Marme Federik, Schneeweiss Andreas, Sohn Christof, Bojesen Stig, Flyger Henrik, Nordestgaard Børge G, Benítez Javier, Milne Roger L, Ignacio Arias Jose, Zamora M Pilar, Brenner Hermann, Müller Heiko, Arndt Volker, Rahman Nazneen, Turnbull Clare, Seal Sheila, Renwick Anthony, Brauch Hiltrud, Justenhoven Christina, Brüning Thomas, Chang-Claude Jenny, Hein Rebecca, Wang-Gohrke Shan, Dörk Thilo, Schürmann Peter, Bremer Michael, Hillemanns Peter, Nevanlinna Heli, Heikkinen Tuomas, Aittomäki Kristiina, Blomqvist Carl, Bogdanova Natalia, Antonenkova Natalia, Rogov Yuri I, Karstens Johann Hinrich, Bermisheva Marina, Prokofieva Darya, Gantcev Shamil Hanafievich, Khusnutdinova Elza, Lindblom Annika, Margolin Sara, Chenevix-Trench Georgia, Beesley Jonathan, Chen Xiaoqing, Mannermaa Arto, Kosma Veli-Matti, Soini Ylermi, Kataja Vesa, Lambrechts Diether, Yesilyurt Betül T, Chrisiaens Marie-Rose, Peeters Stephanie, Radice Paolo, Peterlongo Paolo, Manoukian Siranoush, Barile Monica, Couch Fergus, Lee Adam M, Diasio Robert, Wang Xianshu, Giles Graham G, Severi Gianluca, Baglietto Laura, Maclean Catriona, Offit Ken, Robson Mark, Joseph Vijai, Gaudet Mia, John Esther M, Winqvist Robert, Pylkäs Katri, Jukkola-Vuorinen Arja, Grip Mervi, Andrulis Irene, Knight Julia A, Mulligan Anna Marie, O'Malley Frances P, Brinton Louise A, Sherman Mark E, Lissowska Jolanta, Chanock Stephen J, Hooning Maartje, Martens John W M, van den Ouweland Ans M W, Collée J Margriet, Hall Per, Czene Kamila, Cox Angela, Brock Ian W, Reed Malcolm W R, Cross Simon S, Pharoah Paul, Dunning Alison M, Kang Daehee, Yoo Keun-Young, Noh Dong-Young, Ahn Sei-Hyun, Jakubowska Anna, Lubinski Jan, Jaworska Katarzyna, Durda Katarzyna, Sangrajrang Suleeporn, Gaborieau Valerie, Brennan Paul, McKay James, Shen Chen-Yang, Ding Shian-ling, Hsu Huan-Ming, Yu Jyh-Cherng, Anton-Culver Hoda, Ziogas Argyrios, Ashworth Alan, Swerdlow Anthony, Jones Michael, Orr Nick, Trentham-Dietz Amy, Egan Kathleen, Newcomb Polly, Titus-Ernstoff Linda, Easton Doug and Spurdle Amanda B. Associations of common variants at 1p11.2 and 14q24.1 (RAD51L1) with breast cancer risk and heterogeneity by tumor subtype: findings from the Breast Cancer Association Consortium. : Human molecular genetics. 20120222.