Polymorphisms in a Putative Enhancer at the 10q21.2 Breast Cancer Risk Locus Regulate NRBF2 Expression.
Polymorphisms in a Putative Enhancer at the 10q21.2 Breast Cancer Risk Locus Regulate NRBF2 Expression. [electronic resource] - American journal of human genetics Jul 2015 - 22-34 p. digital
Publication Type: Journal Article
1537-6605
10.1016/j.ajhg.2015.05.002 doi
Age Factors
Asian People--genetics
Autophagy-Related Proteins
Body Mass Index
Breast Neoplasms--genetics
Chromosome Mapping
Chromosomes, Human, Pair 10--genetics
DNA-Binding Proteins--genetics
Enhancer Elements, Genetic--genetics
Female
Gene Expression Regulation--genetics
Genome-Wide Association Study
Genotype
Humans
Luciferases
Odds Ratio
Polymorphism, Single Nucleotide--genetics
Quantitative Trait Loci--genetics
Regression Analysis
Trans-Activators--genetics
Transcription Factors--genetics
White People--genetics
Polymorphisms in a Putative Enhancer at the 10q21.2 Breast Cancer Risk Locus Regulate NRBF2 Expression.
APA
Darabi H., McCue K., Beesley J., Michailidou K., Nord S., Kar S., Humphreys K., Thompson D., Ghoussaini M., Bolla M. K., Dennis J., Wang Q., Canisius S., Scott C. G., Apicella C., Hopper J. L., Southey M. C., Stone J., Broeks A., Schmidt M. K., Scott R. J., Lophatananon A., Muir K., Beckmann M. W., Ekici A. B., Fasching P. A., Heusinger K., Dos-Santos-Silva I., Peto J., Tomlinson I., Sawyer E. J., Burwinkel B., Marme F., Guénel P., Truong T., Bojesen S. E., Flyger H., Benitez J., González-Neira A., Anton-Culver H., Neuhausen S. L., Arndt V., Brenner H., Engel C., Meindl A., Schmutzler R. K., Arnold N., Brauch H., Hamann U., Chang-Claude J., Khan S., Nevanlinna H., Ito H., Matsuo K., Bogdanova N. V., Dörk T., Lindblom A., Margolin S., Kosma V., Mannermaa A., Tseng C., Wu A. H., Floris G., Lambrechts D., Rudolph A., Peterlongo P., Radice P., Couch F. J., Vachon C., Giles G. G., McLean C., Milne R. L., Dugué P., Haiman C. A., Maskarinec G., Woolcott C., Henderson B. E., Goldberg M. S., Simard J., Teo S. H., Mariapun S., Helland Å., Haakensen V., Zheng W., Beeghly-Fadiel A., Tamimi R., Jukkola-Vuorinen A., Winqvist R., Andrulis I. L., Knight J. A., Devilee P., Tollenaar R. A. E. M., Figueroa J., García-Closas M., Czene K., Hooning M. J., Tilanus-Linthorst M., Li J., Gao Y., Shu X., Cox A., Cross S. S., Luben R., Khaw K., Choi J., Kang D., Hartman M., Lim W. Y., Kabisch M., Torres D., Jakubowska A., Lubinski J., McKay J., Sangrajrang S., Toland A. E., Yannoukakos D., Shen C., Yu J., Ziogas A., Schoemaker M. J., Swerdlow A., Borresen-Dale A., Kristensen V., French J. D., Edwards S. L., Dunning A. M., Easton D. F., Hall P. & Chenevix-Trench G. (20150925). Polymorphisms in a Putative Enhancer at the 10q21.2 Breast Cancer Risk Locus Regulate NRBF2 Expression. : American journal of human genetics.
Chicago
Darabi Hatef, McCue Karen, Beesley Jonathan, Michailidou Kyriaki, Nord Silje, Kar Siddhartha, Humphreys Keith, Thompson Deborah, Ghoussaini Maya, Bolla Manjeet K, Dennis Joe, Wang Qin, Canisius Sander, Scott Christopher G, Apicella Carmel, Hopper John L, Southey Melissa C, Stone Jennifer, Broeks Annegien, Schmidt Marjanka K, Scott Rodney J, Lophatananon Artitaya, Muir Kenneth, Beckmann Matthias W, Ekici Arif B, Fasching Peter A, Heusinger Katharina, Dos-Santos-Silva Isabel, Peto Julian, Tomlinson Ian, Sawyer Elinor J, Burwinkel Barbara, Marme Frederik, Guénel Pascal, Truong Thérèse, Bojesen Stig E, Flyger Henrik, Benitez Javier, González-Neira Anna, Anton-Culver Hoda, Neuhausen Susan L, Arndt Volker, Brenner Hermann, Engel Christoph, Meindl Alfons, Schmutzler Rita K, Arnold Norbert, Brauch Hiltrud, Hamann Ute, Chang-Claude Jenny, Khan Sofia, Nevanlinna Heli, Ito Hidemi, Matsuo Keitaro, Bogdanova Natalia V, Dörk Thilo, Lindblom Annika, Margolin Sara, Kosma Veli-Matti, Mannermaa Arto, Tseng Chiu-Chen, Wu Anna H, Floris Giuseppe, Lambrechts Diether, Rudolph Anja, Peterlongo Paolo, Radice Paolo, Couch Fergus J, Vachon Celine, Giles Graham G, McLean Catriona, Milne Roger L, Dugué Pierre-Antoine, Haiman Christopher A, Maskarinec Gertraud, Woolcott Christy, Henderson Brian E, Goldberg Mark S, Simard Jacques, Teo Soo H, Mariapun Shivaani, Helland Åslaug, Haakensen Vilde, Zheng Wei, Beeghly-Fadiel Alicia, Tamimi Rulla, Jukkola-Vuorinen Arja, Winqvist Robert, Andrulis Irene L, Knight Julia A, Devilee Peter, Tollenaar Robert A E M, Figueroa Jonine, García-Closas Montserrat, Czene Kamila, Hooning Maartje J, Tilanus-Linthorst Madeleine, Li Jingmei, Gao Yu-Tang, Shu Xiao-Ou, Cox Angela, Cross Simon S, Luben Robert, Khaw Kay-Tee, Choi Ji-Yeob, Kang Daehee, Hartman Mikael, Lim Wei Yen, Kabisch Maria, Torres Diana, Jakubowska Anna, Lubinski Jan, McKay James, Sangrajrang Suleeporn, Toland Amanda E, Yannoukakos Drakoulis, Shen Chen-Yang, Yu Jyh-Cherng, Ziogas Argyrios, Schoemaker Minouk J, Swerdlow Anthony, Borresen-Dale Anne-Lise, Kristensen Vessela, French Juliet D, Edwards Stacey L, Dunning Alison M, Easton Douglas F, Hall Per and Chenevix-Trench Georgia. 20150925. Polymorphisms in a Putative Enhancer at the 10q21.2 Breast Cancer Risk Locus Regulate NRBF2 Expression. : American journal of human genetics.
Harvard
Darabi H., McCue K., Beesley J., Michailidou K., Nord S., Kar S., Humphreys K., Thompson D., Ghoussaini M., Bolla M. K., Dennis J., Wang Q., Canisius S., Scott C. G., Apicella C., Hopper J. L., Southey M. C., Stone J., Broeks A., Schmidt M. K., Scott R. J., Lophatananon A., Muir K., Beckmann M. W., Ekici A. B., Fasching P. A., Heusinger K., Dos-Santos-Silva I., Peto J., Tomlinson I., Sawyer E. J., Burwinkel B., Marme F., Guénel P., Truong T., Bojesen S. E., Flyger H., Benitez J., González-Neira A., Anton-Culver H., Neuhausen S. L., Arndt V., Brenner H., Engel C., Meindl A., Schmutzler R. K., Arnold N., Brauch H., Hamann U., Chang-Claude J., Khan S., Nevanlinna H., Ito H., Matsuo K., Bogdanova N. V., Dörk T., Lindblom A., Margolin S., Kosma V., Mannermaa A., Tseng C., Wu A. H., Floris G., Lambrechts D., Rudolph A., Peterlongo P., Radice P., Couch F. J., Vachon C., Giles G. G., McLean C., Milne R. L., Dugué P., Haiman C. A., Maskarinec G., Woolcott C., Henderson B. E., Goldberg M. S., Simard J., Teo S. H., Mariapun S., Helland Å., Haakensen V., Zheng W., Beeghly-Fadiel A., Tamimi R., Jukkola-Vuorinen A., Winqvist R., Andrulis I. L., Knight J. A., Devilee P., Tollenaar R. A. E. M., Figueroa J., García-Closas M., Czene K., Hooning M. J., Tilanus-Linthorst M., Li J., Gao Y., Shu X., Cox A., Cross S. S., Luben R., Khaw K., Choi J., Kang D., Hartman M., Lim W. Y., Kabisch M., Torres D., Jakubowska A., Lubinski J., McKay J., Sangrajrang S., Toland A. E., Yannoukakos D., Shen C., Yu J., Ziogas A., Schoemaker M. J., Swerdlow A., Borresen-Dale A., Kristensen V., French J. D., Edwards S. L., Dunning A. M., Easton D. F., Hall P. and Chenevix-Trench G. (20150925). Polymorphisms in a Putative Enhancer at the 10q21.2 Breast Cancer Risk Locus Regulate NRBF2 Expression. : American journal of human genetics.
MLA
Darabi Hatef, McCue Karen, Beesley Jonathan, Michailidou Kyriaki, Nord Silje, Kar Siddhartha, Humphreys Keith, Thompson Deborah, Ghoussaini Maya, Bolla Manjeet K, Dennis Joe, Wang Qin, Canisius Sander, Scott Christopher G, Apicella Carmel, Hopper John L, Southey Melissa C, Stone Jennifer, Broeks Annegien, Schmidt Marjanka K, Scott Rodney J, Lophatananon Artitaya, Muir Kenneth, Beckmann Matthias W, Ekici Arif B, Fasching Peter A, Heusinger Katharina, Dos-Santos-Silva Isabel, Peto Julian, Tomlinson Ian, Sawyer Elinor J, Burwinkel Barbara, Marme Frederik, Guénel Pascal, Truong Thérèse, Bojesen Stig E, Flyger Henrik, Benitez Javier, González-Neira Anna, Anton-Culver Hoda, Neuhausen Susan L, Arndt Volker, Brenner Hermann, Engel Christoph, Meindl Alfons, Schmutzler Rita K, Arnold Norbert, Brauch Hiltrud, Hamann Ute, Chang-Claude Jenny, Khan Sofia, Nevanlinna Heli, Ito Hidemi, Matsuo Keitaro, Bogdanova Natalia V, Dörk Thilo, Lindblom Annika, Margolin Sara, Kosma Veli-Matti, Mannermaa Arto, Tseng Chiu-Chen, Wu Anna H, Floris Giuseppe, Lambrechts Diether, Rudolph Anja, Peterlongo Paolo, Radice Paolo, Couch Fergus J, Vachon Celine, Giles Graham G, McLean Catriona, Milne Roger L, Dugué Pierre-Antoine, Haiman Christopher A, Maskarinec Gertraud, Woolcott Christy, Henderson Brian E, Goldberg Mark S, Simard Jacques, Teo Soo H, Mariapun Shivaani, Helland Åslaug, Haakensen Vilde, Zheng Wei, Beeghly-Fadiel Alicia, Tamimi Rulla, Jukkola-Vuorinen Arja, Winqvist Robert, Andrulis Irene L, Knight Julia A, Devilee Peter, Tollenaar Robert A E M, Figueroa Jonine, García-Closas Montserrat, Czene Kamila, Hooning Maartje J, Tilanus-Linthorst Madeleine, Li Jingmei, Gao Yu-Tang, Shu Xiao-Ou, Cox Angela, Cross Simon S, Luben Robert, Khaw Kay-Tee, Choi Ji-Yeob, Kang Daehee, Hartman Mikael, Lim Wei Yen, Kabisch Maria, Torres Diana, Jakubowska Anna, Lubinski Jan, McKay James, Sangrajrang Suleeporn, Toland Amanda E, Yannoukakos Drakoulis, Shen Chen-Yang, Yu Jyh-Cherng, Ziogas Argyrios, Schoemaker Minouk J, Swerdlow Anthony, Borresen-Dale Anne-Lise, Kristensen Vessela, French Juliet D, Edwards Stacey L, Dunning Alison M, Easton Douglas F, Hall Per and Chenevix-Trench Georgia. Polymorphisms in a Putative Enhancer at the 10q21.2 Breast Cancer Risk Locus Regulate NRBF2 Expression. : American journal of human genetics. 20150925.