-
1دورية أكاديمية
المؤلفون: Zeng, C, Guo, X, Long, J, Kuchenbaecker, KB, Droit, A, Michailidou, K, Ghoussaini, M, Kar, S, Freeman, A, Hopper, JL, Milne, RL, Bolla, MK, Wang, Q, Dennis, J, Agata, S, Ahmed, S, Aittomäki, K, Andrulis, IL, Anton-Culver, H, Antonenkova, NN, Arason, A, Arndt, V, Arun, BK, Arver, B, Bacot, F, Barrowdale, D, Baynes, C, Beeghly-Fadiel, A, Benitez, J, Bermisheva, M, Blomqvist, C, Blot, WJ, Bogdanova, NV, Bojesen, SE, Bonanni, B, Borresen-Dale, A-L, Brand, JS, Brauch, H, Brennan, P, Brenner, H, Broeks, A, Brüning, T, Burwinkel, B, Buys, SS, Cai, Q, Caldes, T, Campbell, I, Carpenter, J, Chang-Claude, J, Choi, J-Y, Claes, KBM, Clarke, C, Cox, A, Cross, SS, Czene, K, Daly, MB, de la Hoya, M, De Leeneer, K, Devilee, P, Diez, O, Domchek, SM, Doody, M, Dorfling, CM, Dörk, T, Dos-Santos-Silva, I, Dumont, M, Dwek, M, Dworniczak, B, Egan, K, Eilber, U, Einbeigi, Z, Ejlertsen, B, Ellis, S, Frost, D, Lalloo, F, EMBRACE, Fasching, PA, Figueroa, J, Flyger, H, Friedlander, M, Friedman, E, Gambino, G, Gao, Y-T, Garber, J, García-Closas, M, Gehrig, A, Damiola, F, Lesueur, F, Mazoyer, S, Stoppa-Lyonnet, D, behalf of GEMO Study Collaborators, Giles, GG, Godwin, AK, Goldgar, DE, González-Neira, A, Greene, MH, Guénel, P, Haeberle, L, Haiman, CA, Hallberg, E, Hamann, U, Hansen, TVO, Hart, S, Hartikainen, JM, Hartman, M, Hassan, N, Healey, S, Hogervorst, FBL, Verhoef, S, HEBON, Hendricks, CB, Hillemanns, P, Hollestelle, A, Hulick, PJ, Hunter, DJ, Imyanitov, EN, Isaacs, C, Ito, H, Jakubowska, A, Janavicius, R, Jaworska-Bieniek, K, Jensen, UB, John, EM, Joly Beauparlant, C, Jones, M, Kabisch, M, Kang, D, Karlan, BY, Kauppila, S, Kerin, MJ, Khan, S, Khusnutdinova, E, Knight, JA, Konstantopoulou, I, Kraft, P, Kwong, A, Laitman, Y, Lambrechts, D, Lazaro, C, Le Marchand, L, Lee, CN, Lee, MH, Lester, J, Li, J, Liljegren, A, Lindblom, A, Lophatananon, A, Lubinski, J, Mai, PL, Mannermaa, A, Manoukian, S, Margolin, S, Marme, F, Matsuo, K, McGuffog, L, Meindl, A, Menegaux, F, Montagna, M, Muir, K, Mulligan, AM, Nathanson, KL, Neuhausen, SL, Nevanlinna, H, Newcomb, PA, Nord, S, Nussbaum, RL, Offit, K, Olah, E, Olopade, OI, Olswold, C, Osorio, A, Papi, L, Park-Simon, T-W, Paulsson-Karlsson, Y, Peeters, S, Peissel, B, Peterlongo, P, Peto, J, Pfeiler, G, Phelan, CM, Presneau, N, Radice, P, Rahman, N, Ramus, SJ, Rashid, MU, Rennert, G, Rhiem, K, Rudolph, A, Salani, R, Sangrajrang, S, Sawyer, EJ, Schmidt, MK, Schmutzler, RK, Schoemaker, MJ, Schürmann, P, Seynaeve, C, Shen, C-Y, Shrubsole, MJ, Shu, X-O, Sigurdson, A, Singer, CF, Slager, S, Soucy, P, Southey, M, Steinemann, D, Swerdlow, A, Szabo, CI, Tchatchou, S, Teixeira, MR, Teo, SH, Terry, MB, Tessier, DC, Teulé, A, Thomassen, M, Tihomirova, L, Tischkowitz, M, Toland, AE, Tung, N, Turnbull, C, van den Ouweland, AMW, van Rensburg, EJ, Ven den Berg, D, Vijai, J, Wang-Gohrke, S, Weitzel, JN, Whittemore, AS, Winqvist, R, Wong, TY, Wu, AH, Yannoukakos, D, Yu, J-C, Pharoah, PDP, Hall, P, Chenevix-Trench, G, KConFab, AOCS Investigators, Dunning, AM, Simard, J, Couch, FJ, Antoniou, AC, Easton, DF, Zheng, W
المساهمون: Jones, Michael, Schoemaker, Minouk, Swerdlow, Anthony, Turnbull, Clare
مصطلحات موضوعية: EMBRACE, behalf of GEMO Study Collaborators, HEBON, KConFab, AOCS Investigators, Chromosomes, Human, Pair 12, Humans, Breast Neoplasms, Genetic Predisposition to Disease, BRCA1 Protein, Population Surveillance, Odds Ratio, Risk, Case-Control Studies, Chromosome Mapping, Computational Biology, Epigenesis, Genetic, Genotype, Haplotypes, Heterozygote, Mutation, Polymorphism, Single Nucleotide, Alleles, Quantitative Trait Loci, Databases, European Continental Ancestry Group
وصف الملف: Electronic; ?; application/pdf
العلاقة: Breast cancer research : BCR, 2016, 18 (1), pp. 64 - ?; https://repository.icr.ac.uk/handle/internal/492Test
الإتاحة: https://doi.org/10.1186/s13058-016-0718-0Test
https://repository.icr.ac.uk/handle/internal/492Test -
2دورية أكاديمية
المؤلفون: Zeng, C, Guo, X, Long, J, Kuchenbaecker, KB, Droit, A, Michailidou, K, Ghoussaini, M, Kar, S, Freeman, A, Hopper, JL, Milne, RL, Bolla, MK, Wang, Q, Dennis, J, Agata, S, Ahmed, S, Aittomäki, K, Andrulis, IL, Anton-Culver, H, Antonenkova, NN, Arason, A, Arndt, V, Arun, BK, Arver, B, Bacot, F, Barrowdale, D, Baynes, C, Beeghly-Fadiel, A, Benitez, J, Bermisheva, M, Blomqvist, C, Blot, WJ, Bogdanova, NV, Bojesen, SE, Bonanni, B, Borresen-Dale, A-L, Brand, JS, Brauch, H, Brennan, P, Brenner, H, Broeks, A, Brüning, T, Burwinkel, B, Buys, SS, Cai, Q, Caldes, T, Campbell, I, Carpenter, J, Chang-Claude, J, Choi, J-Y, Claes, KBM, Clarke, C, Cox, A, Cross, SS, Czene, K, Daly, MB, de la Hoya, M, De Leeneer, K, Devilee, P, Diez, O, Domchek, SM, Doody, M, Dorfling, CM, Dörk, T, Dos-Santos-Silva, I, Dumont, M, Dwek, M, Dworniczak, B, Egan, K, Eilber, U, Einbeigi, Z, Ejlertsen, B, Ellis, S, Frost, D, Lalloo, F, EMBRACE, ., Fasching, PA, Figueroa, J, Flyger, H, Friedlander, M, Friedman, E, Gambino, G, Gao, Y-T, Garber, J, García-Closas, M, Gehrig, A, Damiola, F, Lesueur, F, Mazoyer, S, Stoppa-Lyonnet, D, behalf of GEMO Study Collaborators, ., Giles, GG, Godwin, AK, Goldgar, DE, González-Neira, A, Greene, MH, Guénel, P, Haeberle, L, Haiman, CA, Hallberg, E, Hamann, U, Hansen, TVO, Hart, S, Hartikainen, JM, Hartman, M, Hassan, N, Healey, S, Hogervorst, FBL, Verhoef, S, HEBON, ., Hendricks, CB, Hillemanns, P, Hollestelle, A, Hulick, PJ, Hunter, DJ, Imyanitov, EN, Isaacs, C, Ito, H, Jakubowska, A, Janavicius, R, Jaworska-Bieniek, K, Jensen, UB, John, EM, Joly Beauparlant, C, Jones, M, Kabisch, M, Kang, D, Karlan, BY, Kauppila, S, Kerin, MJ, Khan, S, Khusnutdinova, E, Knight, JA, Konstantopoulou, I, Kraft, P, Kwong, A, Laitman, Y, Lambrechts, D, Lazaro, C, Le Marchand, L, Lee, CN, Lee, MH, Lester, J, Li, J, Liljegren, A, Lindblom, A, Lophatananon, A, Lubinski, J, Mai, PL, Mannermaa, A, Manoukian, S, Margolin, S, Marme, F, Matsuo, K, McGuffog, L, Meindl, A, Menegaux, F, Montagna, M, Muir, K, Mulligan, AM, Nathanson, KL, Neuhausen, SL, Nevanlinna, H, Newcomb, PA, Nord, S, Nussbaum, RL, Offit, K, Olah, E, Olopade, OI, Olswold, C, Osorio, A, Papi, L, Park-Simon, T-W, Paulsson-Karlsson, Y, Peeters, S, Peissel, B, Peterlongo, P, Peto, J, Pfeiler, G, Phelan, CM, Presneau, N, Radice, P, Rahman, N, Ramus, SJ, Rashid, MU, Rennert, G, Rhiem, K, Rudolph, A, Salani, R, Sangrajrang, S, Sawyer, EJ, Schmidt, MK, Schmutzler, RK, Schoemaker, MJ, Schürmann, P, Seynaeve, C, Shen, C-Y, Shrubsole, MJ, Shu, X-O, Sigurdson, A, Singer, CF, Slager, S, Soucy, P, Southey, M, Steinemann, D, Swerdlow, A, Szabo, CI, Tchatchou, S, Teixeira, MR, Teo, SH, Terry, MB, Tessier, DC, Teulé, A, Thomassen, M, Tihomirova, L, Tischkowitz, M, Toland, AE, Tung, N, Turnbull, C, van den Ouweland, AMW, van Rensburg, EJ, Ven den Berg, D, Vijai, J, Wang-Gohrke, S, Weitzel, JN, Whittemore, AS, Winqvist, R, Wong, TY, Wu, AH, Yannoukakos, D, Yu, J-C, Pharoah, PDP, Hall, P, Chenevix-Trench, G, KConFab, ., AOCS Investigators, ., Dunning, AM, Simard, J, Couch, FJ, Antoniou, AC, Easton, DF, Zheng, W
المصدر: Breast Cancer Research , 18 , Article 64. (2016)
مصطلحات موضوعية: BRAC1 mutation carriers, Breast cancer, CCDC91, Fine-scale mapping, Genetic risk factor, PTHLH, Alleles, BRCA1 Protein, Breast Neoplasms, Case-Control Studies, Chromosome Mapping, Chromosomes, Human, Pair 12, Computational Biology, Databases, Genetic, Enhancer Elements, Epigenesis, European Continental Ancestry Group, Female, Genetic Predisposition to Disease, Genome-Wide Association Study, Genotype, Haplotypes, Heterozygote, Humans, Mutation, Odds Ratio, Polymorphism
وصف الملف: text
العلاقة: https://discovery.ucl.ac.uk/id/eprint/1574503/1/s13058-016-0718-0.pdfTest; https://discovery.ucl.ac.uk/id/eprint/1574503Test/
-
3دورية أكاديمية
المؤلفون: Darabi, H, Beesley, J, Droit, A, Kar, S, Nord, S, Moradi Marjaneh, M, Soucy, P, Michailidou, K, Ghoussaini, M, Fues Wahl, H, Bolla, MK, Wang, Q, Dennis, J, Alonso, MR, Andrulis, IL, Anton-Culver, H, Arndt, V, Beckmann, MW, Benitez, J, Bogdanova, NV, Bojesen, SE, Brauch, H, Brenner, H, Broeks, A, Brüning, T, Burwinkel, B, Chang-Claude, J, Choi, J-Y, Conroy, DM, Couch, FJ, Cox, A, Cross, SS, Czene, K, Devilee, P, Dörk, T, Easton, DF, Fasching, PA, Figueroa, J, Fletcher, O, Flyger, H, Galle, E, García-Closas, M, Giles, GG, Goldberg, MS, González-Neira, A, Guénel, P, Haiman, CA, Hallberg, E, Hamann, U, Hartman, M, Hollestelle, A, Hopper, JL, Ito, H, Jakubowska, A, Johnson, N, Kang, D, Khan, S, Kosma, V-M, Kriege, M, Kristensen, V, Lambrechts, D, Le Marchand, L, Lee, SC, Lindblom, A, Lophatananon, A, Lubinski, J, Mannermaa, A, Manoukian, S, Margolin, S, Matsuo, K, Mayes, R, McKay, J, Meindl, A, Milne, RL, Muir, K, Neuhausen, SL, Nevanlinna, H, Olswold, C, Orr, N, Peterlongo, P, Pita, G, Pylkäs, K, Rudolph, A, Sangrajrang, S, Sawyer, EJ, Schmidt, MK, Schmutzler, RK, Seynaeve, C, Shah, M, Shen, C-Y, Shu, X-O, Southey, MC, Stram, DO, Surowy, H, Swerdlow, A, Teo, SH, Tessier, DC, Tomlinson, I, Torres, D, Truong, T, Vachon, CM, Vincent, D, Winqvist, R, Wu, AH, Wu, P-E, Yip, CH, Zheng, W, Pharoah, PDP, Hall, P, Edwards, SL, Simard, J, French, JD, Chenevix-Trench, G, Dunning, AM
المساهمون: Fletcher, Olivia, Swerdlow, Anthony
مصطلحات موضوعية: Chromosomes, Human, Pair 17, Humans, Breast Neoplasms, Genetic Predisposition to Disease, Vesicular Transport Proteins, Chromosome Mapping, Genotype, Polymorphism, Single Nucleotide, Quantitative Trait Loci, European Continental Ancestry Group, Female, Genome-Wide Association Study
وصف الملف: Electronic; ?; application/pdf
العلاقة: Scientific reports, 2016, 6 pp. 32512 - ?; https://repository.icr.ac.uk/handle/internal/124Test
-
4دورية أكاديمية
المؤلفون: Zeng C., Guo X., Long J., Kuchenbaecker K. B., Droit A., Michailidou K., Ghoussaini M., Kar S., Freeman A., Hopper J. L., Milne R. L., Bolla M. K., Wang Q., Dennis J., Agata S., Ahmed S., Aittomaki K., Andrulis I. L., Anton-Culver H., Antonenkova N. N., Arason A., Arndt V., Arun B. K., Arver B., Bacot F., Barrowdale D., Baynes C., Beeghly-Fadiel A., Benitez J., Bermisheva M., Blomqvist C., Blot W. J., Bogdanova N. V., Bojesen S. E., Bonanni B., Borresen-Dale A. -L., Brand J. S., Brauch H., Brennan P., Brenner H., Broeks A., Bruning T., Burwinkel B., Buys S. S., Cai Q., Caldes T., Campbell I., Carpenter J., Chang-Claude J., Choi J. -Y., Claes K. B. M., Clarke C., Cox A., Cross S. S., Czene K., Daly M. B., de la Hoya M., De Leeneer K., Devilee P., Diez O., Domchek S. M., Doody M., Dorfling C. M., Dork T., dos-Santos-Silva I., Dumont M., Dwek M., Dworniczak B., Egan K., Eilber U., Einbeigi Z., Ejlertsen B., Ellis S., Frost D., Lalloo F., Fasching P. A., Figueroa J., Flyger H., Friedlander M., Friedman E., Gambino G., Gao Y. -T., Garber J., Garcia-Closas M., Gehrig A., Damiola F., Lesueur F., Mazoyer S., Stoppa-Lyonnet D., Giles G. G., Godwin A. K., Goldgar D. E., Gonzalez-Neira A., Greene M. H., Guenel P., Haeberle L., Haiman C. A., Hallberg E., Hamann U., Hansen T. V. O., Hart S., Hartikainen J. M., Hartman M., Hassan N., Healey S., Hogervorst F. B. L., Verhoef S., Hendricks C. B., Hillemanns P., Hollestelle A., Hulick P. J., Hunter D. J., Imyanitov E. N., Isaacs C., Ito H., Jakubowska A., Janavicius R., Jaworska-Bieniek K., Jensen U. B., John E. M., Joly Beauparlant C., Jones M., Kabisch M., Kang D., Karlan B. Y., Kauppila S., Kerin M. J., Khan S., Khusnutdinova E., Knight J. A., Konstantopoulou I., Kraft P., Kwong A., Laitman Y., Lambrechts D., Lazaro C., Le Marchand L., Lee C. N., Lee M. H., Lester J., Li J., Liljegren A., Lindblom A., Lophatananon A., Lubinski J., Mai P. L., Mannermaa A., Manoukian S., Margolin S., Marme F., Matsuo K., McGuffog L., Meindl A., Menegaux F., Montagna M., Muir K., Mulligan A. M., Nathanson K. L., Neuhausen S. L., Nevanlinna H., Newcomb P. A., Nord S., Nussbaum R. L., Offit K., Olah E., Olopade O. I., Olswold C., Osorio A., Papi L., Park-Simon T. -W., Paulsson-Karlsson Y., Peeters S., Peissel B., Peterlongo P., Peto J., Pfeiler G., Phelan C. M., Presneau N., Radice P., Rahman N., Ramus S. J., Rashid M. U., Rennert G., Rhiem K., Rudolph A., Salani R., Sangrajrang S., Sawyer E. J., Schmidt M. K., Schmutzler R. K., Schoemaker M. J., Schurmann P., Seynaeve C., Shen C. -Y., Shrubsole M. J., Shu X. -O., Sigurdson A., Singer C. F., Slager S., Soucy P., Southey M., Steinemann D., Swerdlow A., Szabo C. I., Tchatchou S., Teixeira M. R., Teo S. H., Terry M. B., Tessier D. C., Teule A., Thomassen M., Tihomirova L., Tischkowitz M., Toland A. E., Tung N., Turnbull C., van den Ouweland A. M. W., van Rensburg E. J., ven den Berg D., Vijai J., Wang-Gohrke S., Weitzel J. N., Whittemore A. S., Winqvist R., Wong T. Y., Wu A. H., Yannoukakos D., Yu J. -C., Pharoah P. D. P., Hall P., Chenevix-Trench G., Dunning A. M., Simard J., Couch F. J., Antoniou A. C., Easton D. F., Zheng W.
المساهمون: Zeng, C., Guo, X., Long, J., Kuchenbaecker, K. B., Droit, A., Michailidou, K., Ghoussaini, M., Kar, S., Freeman, A., Hopper, J. L., Milne, R. L., Bolla, M. K., Wang, Q., Dennis, J., Agata, S., Ahmed, S., Aittomaki, K., Andrulis, I. L., Anton-Culver, H., Antonenkova, N. N., Arason, A., Arndt, V., Arun, B. K., Arver, B., Bacot, F., Barrowdale, D., Baynes, C., Beeghly-Fadiel, A., Benitez, J., Bermisheva, M., Blomqvist, C., Blot, W. J., Bogdanova, N. V., Bojesen, S. E., Bonanni, B., Borresen-Dale, A. -L., Brand, J. S., Brauch, H., Brennan, P., Brenner, H., Broeks, A., Bruning, T., Burwinkel, B., Buys, S. S., Cai, Q., Caldes, T., Campbell, I., Carpenter, J., Chang-Claude, J., Choi, J. -Y., Claes, K. B. M., Clarke, C., Cox, A., Cross, S. S., Czene, K., Daly, M. B., de la Hoya, M., De Leeneer, K., Devilee, P., Diez, O., Domchek, S. M., Doody, M., Dorfling, C. M., Dork, T., dos-Santos-Silva, I., Dumont, M., Dwek, M., Dworniczak, B., Egan, K., Eilber, U., Einbeigi, Z., Ejlertsen, B., Ellis, S., Frost, D., Lalloo, F., Fasching, P. A., Figueroa, J., Flyger, H., Friedlander, M., Friedman, E., Gambino, G., Gao, Y. -T., Garber, J., Garcia-Closas, M., Gehrig, A., Damiola, F., Lesueur, F., Mazoyer, S., Stoppa-Lyonnet, D., Giles, G. G., Godwin, A. K., Goldgar, D. E., Gonzalez-Neira, A., Greene, M. H., Guenel, P., Haeberle, L., Haiman, C. A., Hallberg, E., Hamann, U., Hansen, T. V. O.
مصطلحات موضوعية: BRAC1 mutation carrier, Breast cancer, CCDC91, Fine-scale mapping, Genetic risk factor, PTHLH, Allele, BRCA1 Protein, Breast Neoplasm, Case-Control Studie, Computational Biology, Databases, Genetic, Enhancer Elements, Epigenesis, European Continental Ancestry Group, Female, Genotype, Haplotype, Heterozygote, Human, Mutation, Odds Ratio, Polymorphism, Single Nucleotide, Population Surveillance, Promoter Regions, Quantitative Trait Loci, Risk, Chromosome Mapping
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/27459855; info:eu-repo/semantics/altIdentifier/wos/WOS:000380193900001; volume:18; issue:1; firstpage:64; journal:BREAST CANCER RESEARCH; http://hdl.handle.net/11568/1107038Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84979647977
-
5دورية أكاديمية
المؤلفون: Shi, J, Zhang, Y, Zheng, W, Michailidou, K, Ghoussaini, M, Bolla, MK, Wang, Q, Dennis, J, Lush, M, Milne, RL, Shu, X-O, Beesley, J, Kar, S, Andrulis, IL, Anton-Culver, H, Arndt, V, Beckmann, MW, Zhao, Z, Guo, X, Benitez, J, Beeghly-Fadiel, A, Blot, W, Bogdanova, NV, Bojesen, SE, Brauch, H, Brenner, H, Brinton, L, Broeks, A, Brüning, T, Burwinkel, B, Cai, H, Canisius, S, Chang-Claude, J, Choi, J-Y, Couch, FJ, Cox, A, Cross, SS, Czene, K, Darabi, H, Devilee, P, Droit, A, Dork, T, Fasching, PA, Fletcher, O, Flyger, H, Fostira, F, Gaborieau, V, García-Closas, M, Giles, GG, Mervi Grip, Guenel, P, Haiman, CA, Hamann, U, Hartman, M, Miao, H, Hollestelle, A, Hopper, JL, Hsiung, C-N, kConFab Investigators, Ito, H, Jakubowska, A, Johnson, N, Torres, D, Kabisch, M, Kang, D, Khan, S, Knight, JA, Kosma, V-M, Lambrechts, D, Li, J, Lindblom, A, Lophatananon, A, Lubinski, J, Mannermaa, A, Manoukian, S, Le Marchand, L, Margolin, S, Marme, F, Matsuo, K, McLean, C, Meindl, A, Muir, K, Neuhausen, SL, Nevanlinna, H, Nord, S, Børresen-Dale, A-L, Olson, JE, Orr, N, van den Ouweland, AMW, Peterlongo, P, Putti, TC, Rudolph, A, Sangrajrang, S, Sawyer, EJ, Schmidt, MK, Schmutzler, RK, Shen, C-Y, Hou, M-F, Shrubsole, MJ, Southey, MC, Swerdlow, A, Teo, SH, Thienpont, B, Toland, AE, Tollenaar, RAEM, Tomlinson, I, Truong, T, Tseng, C-C, Wen, W, Winqvist, R, Wu, AH, Yip, CH, Zamora, PM, Zheng, Y, Floris, G, Cheng, C-Y, Hooning, MJ, Martens, JWM, Seynaeve, C, Kristensen, VN, Hall, P, Pharoah, PDP, Simard, J, Chenevix-Trench, G, Dunning, AM, Antoniou, AC, Easton, DF, Cai, Q, Long, J
المساهمون: Fletcher, Olivia, Swerdlow, Anthony
مصطلحات موضوعية: Mervi Grip, kConFab Investigators, Chromosomes, Human, Pair 8, Humans, Breast Neoplasms, Odds Ratio, Risk, Case-Control Studies, Chromosome Mapping, Genotype, Haplotypes, Linkage Disequilibrium, Polymorphism, Single Nucleotide, Alleles, Quantitative Trait Loci, European Continental Ancestry Group, Female, Genetic Variation, Genome-Wide Association Study
وصف الملف: Print-Electronic; 1317; application/pdf
العلاقة: International journal of cancer, 2016, 139 (6), pp. 1303 - 1317; https://repository.icr.ac.uk/handle/internal/159Test
-
6
المؤلفون: Orr, N., Dudbridge, F., Dryden, N., Maguire, S., Novo, D., Perrakis, E., Johnson, N., Ghoussaini, M., Hopper, J.L., Southey, M.C., Apicella, C., Stone, J., Schmidt, M.K., Broeks, A., Van't Veer, L.J., Hogervorst, F.B., Fasching, P.A., Haeberle, L., Ekici, A.B., Beckmann, M.W., Gibson, L., Aitken, Z., Warren, H., Sawyer, E., Tomlinson, I., Kerin, M.J., Miller, N., Burwinkel, B., Marme, F., Schneeweiss, A., Sohn, C., Guenel, P., Truong, T., Cordina-Duverger, E., Sanchez, M., Bojesen, S.E., Nordestgaard, B.G., Nielsen, S.F., Flyger, H., Benitez, J., Zamora, M.P., Perez, J.I.A., Menendez, P., Anton-Culver, H., Neuhausen, S.L., Brenner, H., Dieffenbach, A.K., Arndt, V., Stegmaier, C., Hamann, U., Brauch, H., Justenhoven, C., Bruning, T., Ko, Y.D., Nevanlinna, H., Aittomaki, K., Blomqvist, C., Khan, S., Bogdanova, N., Dork, T., Lindblom, A., Margolin, S., Mannermaa, A., Kataja, V., Kosma, V.M., Hartikainen, J.M., Chenevix-Trench, G., Beesley, J., Lambrechts, D., Moisse, M., Floris, G., Beuselinck, B., Chang-Claude, J., Rudolph, A., Seibold, P., Flesch-Janys, D., Radice, P., Peterlongo, P., Peissel, B., Pensotti, V., Couch, F.J., Olson, J.E., Slettedahl, S., Vachon, C., Giles, G.G., Milne, R.L., McLean, C., Haiman, C.A., Henderson, B.E., Schumacher, F., Marchand, L. le, Simard, J., Goldberg, M.S., Labreche, F., Dumont, M., Kristensen, V., Alnaes, G.G., Nord, S., Borresen-Dale, A.L., Zheng, W., Deming-Halverson, S., Shrubsole, M., Long, J.R., Winqvist, R., Pylkas, K., Jukkola-Vuorinen, A., Grip, M., Andrulis, I.L., Knight, J.A., Glendon, G., Tchatchou, S., Devilee, P., Tollenaar, R.A.E.M., Seynaeve, C.M., Asperen, C.J. van, Garcia-Closas, M., Figueroa, J., Chanock, S.J., Lissowska, J., Czene, K., Darabi, H., Eriksson, M., Klevebring, D., Hooning, M.J., Hollestelle, A., Deurzen, C.H.M. van, Kriege, M., Hall, P., Li, J.M., Liu, J.J., Humphreys, K., Cox, A., Cross, S.S., Reed, M.W.R., Pharoah, P.D.P., Dunning, A.M., Shah, M., Perkins, B.J., Jakubowska, A., Lubinski, J., Jaworska-Bieniek, K., Durda, K., Ashworth, A., Swerdlow, A., Jones, M., Schoemaker, M.J., Meindl, A., Schmutzler, R.K., Olswold, C., Slager, S., Toland, A.E., Yannoukakos, D., Muir, K., Lophatananon, A., Stewart-Brown, S., Siriwanarangsan, P., Matsuo, K., Ito, H., Iwata, H., Ishiguro, J., Wu, A.H., Tseng, C.C., Berg, D. van den, Stram, D.O., Teo, S.H., Yip, C.H., Kang, P., Ikram, M.K., Shu, X.O., Lu, W., Gao, Y.T., Cai, H., Kang, D., Choi, J.Y., Park, S.K., Noh, D.Y., Hartman, M., Miao, H., Lim, W.Y., Lee, S.C., Sangrajrang, S., Gaborieau, V., Brennan, P., McKay, J., Wu, P.E., Hou, M.F., Yu, J.C., Shen, C.Y., Blot, W., Cai, Q.Y., Signorello, L.B., Luccarini, C., Bayes, C., Ahmed, S., Maranian, M., Healey, C.S., Gonzalez-Neira, A., Pita, G., Alonso, M.R., Alvarez, N., Herrero, D., Tessier, D.C., Vincent, D., Bacot, F., Hunter, D.J., Lindstrom, S., Dennis, J., Michailidou, K., Bolla, M.K., Easton, D.F., Silva, I.D., Fletcher, O., Peto, J., GENICA Network, kConFab Investigators, Australian Ovarian Canc Study Grp
المساهمون: Obstetrics & Gynecology, Medical Oncology, Pathology, Ophthalmology, Cardiothoracic Surgery, Clinical Genetics
المصدر: Human Molecular Genetics, 24(10), 2966-2984
Human Molecular Genetics, 24(10), 2966-2984. Oxford University Press
Human Molecular Genetics
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madridمصطلحات موضوعية: Asian Continental Ancestry Group, Adult, Hepatocyte Nuclear Factor 3-alpha, Risk, binding, European Continental Ancestry Group, Kruppel-Like Transcription Factors, estrogen-receptor-alpha, Breast Neoplasms, GATA3 Transcription Factor, Polymorphism, Single Nucleotide, White People, Kruppel-Like Factor 4, Asian People, SDG 3 - Good Health and Well-being, Medizinische Fakultät, common variants, expression, Humans, Genetic Predisposition to Disease, ddc:610, Genetic Association Studies, Aged, Association Studies Articles, Estrogen Receptor alpha, Chromosome Mapping, foxa1, Middle Aged, confer susceptibility, analyses reveal, Enhancer Elements, Genetic, risk locus, Genetic Loci, functional variants, genome-wide association, Female, Chromosomes, Human, Pair 9
وصف الملف: application/pdf; Print-Electronic
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::9ef2d9573ed30cc6e0eabf90899d16e8Test
http://hdl.handle.net/10379/13361Test