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Cambridge Public Health

 

My main focus is the fine-scale mapping of the breast cancer susceptibility loci in order to identify the causal variant and the defective molecular mechanisms.

Publications from Elements

Journal articles

2016

  • Dunning, AM., Michailidou, K., Kuchenbaecker, KB., Thompson, D., French, JD., Beesley, J., Healey, CS., Kar, S., Pooley, KA., Lopez-Knowles, E., Dicks, E., Barrowdale, D., Sinnott-Armstrong, NA., Sallari, RC., Hillman, KM., Kaufmann, S., Sivakumaran, H., Moradi Marjaneh, M., Lee, JS., Hills, M., Jarosz, M., Drury, S., Canisius, S., Bolla, MK., Dennis, J., Wang, Q., Hopper, JL., Southey, MC., Broeks, A., Schmidt, MK., Lophatananon, A., Muir, K., Beckmann, MW., Fasching, PA., Dos-Santos-Silva, I., Peto, J., Sawyer, EJ., Tomlinson, I., Burwinkel, B., Marme, F., Guénel, P., Truong, T., Bojesen, SE., Flyger, H., González-Neira, A., Perez, JIA., Anton-Culver, H., Eunjung, L., Arndt, V., Brenner, H., Meindl, A., Schmutzler, RK., Brauch, H., Hamann, U., Aittomäki, K., Blomqvist, C., Ito, H., Matsuo, K., Bogdanova, N., Dörk, T., Lindblom, A., Margolin, S., Kosma, V-M., Mannermaa, A., Tseng, C-C., Wu, AH., Lambrechts, D., Wildiers, H., Chang-Claude, J., Rudolph, A., Peterlongo, P., Radice, P., Olson, JE., Giles, GG., Milne, RL., Haiman, CA., Henderson, BE., Goldberg, MS., Teo, SH., Yip, CH., Nord, S., Borresen-Dale, A-L., Kristensen, V., Long, J., Zheng, W., Pylkäs, K., Winqvist, R., Andrulis, IL., Knight, JA., Devilee, P., Seynaeve, C., Figueroa, J., Sherman, ME., Czene, K., Darabi, H., Hollestelle, A., van den Ouweland, AMW., Humphreys, K., Gao, Y-T., Shu, X-O., Cox, A., Cross, SS., Blot, W., Cai, Q., Ghoussaini, M., Perkins, BJ., Shah, M., Choi, J-Y., Kang, D., Lee, SC., Hartman, M., Kabisch, M., Torres, D., Jakubowska, A., Lubinski, J., Brennan, P., Sangrajrang, S., Ambrosone, CB., Toland, AE., Shen, C-Y., Wu, P-E., Orr, N., Swerdlow, A., McGuffog, L., Healey, S., Lee, A., Kapuscinski, M., John, EM., Terry, MB., Daly, MB., Goldgar, DE., Buys, SS., Janavicius, R., Tihomirova, L., Tung, N., Dorfling, CM., van Rensburg, EJ., Neuhausen, SL., Ejlertsen, B., Hansen, TVO., Osorio, A., Benitez, J., Rando, R., Weitzel, JN., Bonanni, B., Peissel, B., Manoukian, S., Papi, L., Ottini, L., Konstantopoulou, I., Apostolou, P., Garber, J., Rashid, MU., Frost, D., EMBRACE, , Izatt, L., Ellis, S., Godwin, AK., Arnold, N., Niederacher, D., Rhiem, K., Bogdanova-Markov, N., Sagne, C., Stoppa-Lyonnet, D., Damiola, F., GEMO Study Collaborators, , Sinilnikova, OM., Mazoyer, S., Isaacs, C., Claes, KBM., De Leeneer, K., de la Hoya, M., Caldes, T., Nevanlinna, H., Khan, S., Mensenkamp, AR., HEBON, , Hooning, MJ., Rookus, MA., Kwong, A., Olah, E., Diez, O., Brunet, J., Pujana, MA., Gronwald, J., Huzarski, T., Barkardottir, RB., Laframboise, R., Soucy, P., Montagna, M., Agata, S., Teixeira, MR., kConFab Investigators, , Park, SK., Lindor, N., Couch, FJ., Tischkowitz, M., Foretova, L., Vijai, J., Offit, K., Singer, CF., Rappaport, C., Phelan, CM., Greene, MH., Mai, PL., Rennert, G., Imyanitov, EN., Hulick, PJ., Phillips, K-A., Piedmonte, M., Mulligan, AM., Glendon, G., Bojesen, A., Thomassen, M., Caligo, MA., Yoon, S-Y., Friedman, E., Laitman, Y., Borg, A., von Wachenfeldt, A., Ehrencrona, H., Rantala, J., Olopade, OI., Ganz, PA., Nussbaum, RL., Gayther, SA., Nathanson, KL., Domchek, SM., Arun, BK., Mitchell, G., Karlan, BY., Lester, J., Maskarinec, G., Woolcott, C., Scott, C., Stone, J., Apicella, C., Tamimi, R., Luben, R., Khaw, K-T., Helland, Å., Haakensen, V., Dowsett, M., Pharoah, PDP., Simard, J., Hall, P., García-Closas, M., Vachon, C., Chenevix-Trench, G., Antoniou, AC., Easton, DF. and Edwards, SL., 2016. Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170. Nat Genet, v. 48
    Doi: http://doi.org/10.1038/ng.3521
  • 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., Grip, M., 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., Choudary Putti, T., Rudolph, A., Sangrajrang, S., Sawyer, EJ., Schmidt, MK., Schmutzler, RK., Shen, C-Y., Hou, M-F., Shrubsole, MJ., Southey, MC., Swerdlow, A., Hwang Teo, S., Thienpont, B., Toland, AE., Tollenaar, RAEM., Tomlinson, I., Truong, T., Tseng, C-C., Wen, W., Winqvist, R., Wu, AH., Har Yip, C., 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. and Long, J., 2016. Fine-scale mapping of 8q24 locus identifies multiple independent risk variants for breast cancer. International Journal of Cancer, v. 139
    Doi: http://doi.org/10.1002/ijc.30150
  • Couch, FJ., Kuchenbaecker, KB., Michailidou, K., Mendoza-Fandino, GA., Nord, S., Lilyquist, J., Olswold, C., Hallberg, E., Agata, S., Ahsan, H., Aittomäki, K., Ambrosone, C., Andrulis, IL., Anton-Culver, H., Arndt, V., Arun, BK., Arver, B., Barile, M., Barkardottir, RB., Barrowdale, D., Beckmann, L., Beckmann, MW., Benitez, J., Blank, SV., Blomqvist, C., Bogdanova, NV., Bojesen, SE., Bolla, MK., Bonanni, B., Brauch, H., Brenner, H., Burwinkel, B., Buys, SS., Caldes, T., Caligo, MA., Canzian, F., Carpenter, J., Chang-Claude, J., Chanock, SJ., Chung, WK., Claes, KBM., Cox, A., Cross, SS., Cunningham, JM., Czene, K., Daly, MB., Damiola, F., Darabi, H., de la Hoya, M., Devilee, P., Diez, O., Ding, YC., Dolcetti, R., Domchek, SM., Dorfling, CM., Dos-Santos-Silva, I., Dumont, M., Dunning, AM., Eccles, DM., Ehrencrona, H., Ekici, AB., Eliassen, H., Ellis, S., Fasching, PA., Figueroa, J., Flesch-Janys, D., Försti, A., Fostira, F., Foulkes, WD., Friebel, T., Friedman, E., Frost, D., Gabrielson, M., Gammon, MD., Ganz, PA., Gapstur, SM., Garber, J., Gaudet, MM., Gayther, SA., Gerdes, A-M., Ghoussaini, M., Giles, GG., Glendon, G., Godwin, AK., Goldberg, MS., Goldgar, DE., González-Neira, A., Greene, MH., Gronwald, J., Guénel, P., Gunter, M., Haeberle, L., Haiman, CA., Hamann, U., Hansen, TVO., Hart, S., Healey, S., Heikkinen, T., Henderson, BE., Herzog, J., Hogervorst, FBL., Hollestelle, A., Hooning, MJ., Hoover, RN., Hopper, JL., Humphreys, K., Hunter, DJ., Huzarski, T., Imyanitov, EN., Isaacs, C., Jakubowska, A., James, P., Janavicius, R., Jensen, UB., John, EM., Jones, M., Kabisch, M., Kar, S., Karlan, BY., Khan, S., Khaw, K-T., Kibriya, MG., Knight, JA., Ko, Y-D., Konstantopoulou, I., Kosma, V-M., Kristensen, V., Kwong, A., Laitman, Y., Lambrechts, D., Lazaro, C., Lee, E., Le Marchand, L., Lester, J., Lindblom, A., Lindor, N., Lindstrom, S., Liu, J., Long, J., Lubinski, J., Mai, PL., Makalic, E., Malone, KE., Mannermaa, A., Manoukian, S., Margolin, S., Marme, F., Martens, JWM., McGuffog, L., Meindl, A., Miller, A., Milne, RL., Miron, P., Montagna, M., Mazoyer, S., Mulligan, AM., Muranen, TA., Nathanson, KL., Neuhausen, SL., Nevanlinna, H., Nordestgaard, BG., Nussbaum, RL., Offit, K., Olah, E., Olopade, OI., Olson, JE., Osorio, A., Park, SK., Peeters, PH., Peissel, B., Peterlongo, P., Peto, J., Phelan, CM., Pilarski, R., Poppe, B., Pylkäs, K., Radice, P., Rahman, N., Rantala, J., Rappaport, C., Rennert, G., Richardson, A., Robson, M., Romieu, I., Rudolph, A., Rutgers, EJ., Sanchez, M-J., Santella, RM., Sawyer, EJ., Schmidt, DF., Schmidt, MK., Schmutzler, RK., Schumacher, F., Scott, R., Senter, L., Sharma, P., Simard, J., Singer, CF., Sinilnikova, OM., Soucy, P., Southey, M., Steinemann, D., Stenmark-Askmalm, M., Stoppa-Lyonnet, D., Swerdlow, A., Szabo, CI., Tamimi, R., Tapper, W., Teixeira, MR., Teo, S-H., Terry, MB., Thomassen, M., Thompson, D., Tihomirova, L., Toland, AE., Tollenaar, RAEM., Tomlinson, I., Truong, T., Tsimiklis, H., Teulé, A., Tumino, R., Tung, N., Turnbull, C., Ursin, G., van Deurzen, CHM., van Rensburg, EJ., Varon-Mateeva, R., Wang, Z., Wang-Gohrke, S., Weiderpass, E., Weitzel, JN., Whittemore, A., Wildiers, H., Winqvist, R., Yang, XR., Yannoukakos, D., Yao, S., Zamora, MP., Zheng, W., Hall, P., Kraft, P., Vachon, C., Slager, S., Chenevix-Trench, G., Pharoah, PDP., Monteiro, AAN., García-Closas, M., Easton, DF. and Antoniou, AC., 2016. Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer. Nature Communications, v. 7
    Doi: http://doi.org/10.1038/ncomms11375
  • 2015

  • Lin, W-Y., Camp, NJ., Ghoussaini, M., Beesley, J., Michailidou, K., Hopper, JL., Apicella, C., Southey, MC., Stone, J., Schmidt, MK., Broeks, A., Van't Veer, LJ., Th Rutgers, EJ., Muir, K., Lophatananon, A., Stewart-Brown, S., Siriwanarangsan, P., Fasching, PA., Haeberle, L., Ekici, AB., Beckmann, MW., Peto, J., Dos-Santos-Silva, I., Fletcher, O., Johnson, N., Bolla, MK., Wang, Q., Dennis, J., Sawyer, EJ., Cheng, T., Tomlinson, I., Kerin, MJ., Miller, N., Marmé, F., Surowy, HM., Burwinkel, B., Guénel, P., Truong, T., Menegaux, F., Mulot, C., Bojesen, SE., Nordestgaard, BG., Nielsen, SF., Flyger, H., Benitez, J., Zamora, MP., Arias Perez, JI., Menéndez, P., González-Neira, A., Pita, G., Alonso, MR., Alvarez, N., Herrero, D., Anton-Culver, H., Brenner, H., Dieffenbach, AK., Arndt, V., Stegmaier, C., Meindl, A., Lichtner, P., Schmutzler, RK., Müller-Myhsok, B., Brauch, H., Brüning, T., Ko, Y-D., GENICA Network, , Tessier, DC., Vincent, D., Bacot, F., Nevanlinna, H., Aittomäki, K., Blomqvist, C., Khan, S., Matsuo, K., Ito, H., Iwata, H., Horio, A., Bogdanova, NV., Antonenkova, NN., Dörk, T., Lindblom, A., Margolin, S., Mannermaa, A., Kataja, V., Kosma, V-M., Hartikainen, JM., kConFab Investigators, , Australian Ovarian Cancer Study Group, , Wu, AH., Tseng, C-C., Van Den Berg, D., Stram, DO., Neven, P., Wauters, E., Wildiers, H., Lambrechts, D., Chang-Claude, J., Rudolph, A., Seibold, P., Flesch-Janys, D., Radice, P., Peterlongo, P., Manoukian, S., Bonanni, B., Couch, FJ., Wang, X., Vachon, C., Purrington, K., Giles, GG., Milne, RL., Mclean, C., Haiman, CA., Henderson, BE., Schumacher, F., Le Marchand, L., Simard, J., Goldberg, MS., Labrèche, F., Dumont, M., Teo, SH., Yip, CH., Hassan, N., Vithana, EN., Kristensen, V., Zheng, W., Deming-Halverson, S., Shrubsole, MJ., Long, J., Winqvist, R., Pylkäs, K., Jukkola-Vuorinen, A., Kauppila, S., Andrulis, IL., Knight, JA., Glendon, G., Tchatchou, S., Devilee, P., Tollenaar, RAEM., Seynaeve, C., Van Asperen, CJ., García-Closas, M., Figueroa, J., Lissowska, J., Brinton, L., Czene, K., Darabi, H., Eriksson, M., Brand, JS., Hooning, MJ., Hollestelle, A., Van Den Ouweland, AMW., Jager, A., Li, J., Liu, J., Humphreys, K., Shu, X-O., Lu, W., Gao, Y-T., Cai, H., Cross, SS., Reed, MWR., Blot, W., Signorello, LB., Cai, Q., Pharoah, PDP., Perkins, B., Shah, M., Blows, FM., Kang, D., Yoo, K-Y., Noh, D-Y., Hartman, M., Miao, H., Chia, KS., Putti, TC., Hamann, U., Luccarini, C., Baynes, C., Ahmed, S., Maranian, M., Healey, CS., Jakubowska, A., Lubinski, J., Jaworska-Bieniek, K., Durda, K., Sangrajrang, S., Gaborieau, V., Brennan, P., Mckay, J., Slager, S., Toland, AE., Yannoukakos, D., Shen, C-Y., Hsiung, C-N., Wu, P-E., Ding, S-L., Ashworth, A., Jones, M., Orr, N., Swerdlow, AJ., Tsimiklis, H., Makalic, E., Schmidt, DF., Bui, QM., Chanock, SJ., Hunter, DJ., Hein, R., Dahmen, N., Beckmann, L., Aaltonen, K., Muranen, TA., Heikkinen, T., Irwanto, A., Rahman, N., Turnbull, CA., Breast and Ovarian Cancer Susceptibility (BOCS) Study, , Waisfisz, Q., Meijers-Heijboer, HEJ., Adank, MA., Van Der Luijt, RB., Hall, P., Chenevix-Trench, G., Dunning, A., Easton, DF. and Cox, A., 2015. Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk. Hum Mol Genet, v. 24
    Doi: http://doi.org/10.1093/hmg/ddu431
  • Glubb, DM., Maranian, MJ., Michailidou, K., Pooley, KA., Meyer, KB., Kar, S., Carlebur, S., O'Reilly, M., Betts, JA., Hillman, KM., Kaufmann, S., Beesley, J., Canisius, S., Hopper, JL., Southey, MC., Tsimiklis, H., Apicella, C., Schmidt, MK., Broeks, A., Hogervorst, FB., van der Schoot, CE., Muir, K., Lophatananon, A., Stewart-Brown, S., Siriwanarangsan, P., Fasching, PA., Ruebner, M., Ekici, AB., Beckmann, MW., Peto, J., dos-Santos-Silva, I., Fletcher, O., Johnson, N., Pharoah, PDP., Bolla, MK., Wang, Q., Dennis, J., Sawyer, EJ., Tomlinson, I., Kerin, MJ., Miller, N., Burwinkel, B., Marme, F., Yang, R., Surowy, H., Guénel, P., Truong, T., Menegaux, F., Sanchez, M., Bojesen, SE., Nordestgaard, BG., Nielsen, SF., Flyger, H., González-Neira, A., Benitez, J., Zamora, MP., Arias Perez, JI., Anton-Culver, H., Neuhausen, SL., Brenner, H., Dieffenbach, AK., Arndt, V., Stegmaier, C., Meindl, A., Schmutzler, RK., Brauch, H., Ko, Y-D., Brüning, T., GENICA Network, , Nevanlinna, H., Muranen, TA., Aittomäki, K., Blomqvist, C., Matsuo, K., Ito, H., Iwata, H., Tanaka, H., Dörk, T., Bogdanova, NV., Helbig, S., Lindblom, A., Margolin, S., Mannermaa, A., Kataja, V., Kosma, V-M., Hartikainen, JM., kConFab Investigators, , Wu, AH., Tseng, C-C., Van Den Berg, D., Stram, DO., Lambrechts, D., Zhao, H., Weltens, C., van Limbergen, E., Chang-Claude, J., Flesch-Janys, D., Rudolph, A., Seibold, P., Radice, P., Peterlongo, P., Barile, M., Capra, F., Couch, FJ., Olson, JE., Hallberg, E., Vachon, C., Giles, GG., Milne, RL., McLean, C., Haiman, CA., Henderson, BE., Schumacher, F., Le Marchand, L., Simard, J., Goldberg, MS., Labrèche, F., Dumont, M., Teo, SH., Yip, CH., See, M-H., Cornes, B., Cheng, C-Y., Ikram, MK., Kristensen, V., Norwegian Breast Cancer Study, , Zheng, W., Halverson, SL., Shrubsole, M., Long, J., Winqvist, R., Pylkäs, K., Jukkola-Vuorinen, A., Kauppila, S., Andrulis, IL., Knight, JA., Glendon, G., Tchatchou, S., Devilee, P., Tollenaar, RAEM., Seynaeve, C., Van Asperen, CJ., García-Closas, M., Figueroa, J., Chanock, SJ., Lissowska, J., Czene, K., Klevebring, D., Darabi, H., Eriksson, M., Hooning, MJ., Hollestelle, A., Martens, JWM., Collée, JM., Hall, P., Li, J., Humphreys, K., Shu, X-O., Lu, W., Gao, Y-T., Cai, H., Cox, A., Cross, SS., Reed, MWR., Blot, W., Signorello, LB., Cai, Q., Shah, M., Ghoussaini, M., Kang, D., Choi, J-Y., Park, SK., Noh, D-Y., Hartman, M., Miao, H., Lim, WY., Tang, A., Hamann, U., Torres, D., Jakubowska, A., Lubinski, J., Jaworska, K., Durda, K., Sangrajrang, S., Gaborieau, V., Brennan, P., McKay, J., Olswold, C., Slager, S., Toland, AE., Yannoukakos, D., Shen, C-Y., Wu, P-E., Yu, J-C., Hou, M-F., Swerdlow, A., Ashworth, A., Orr, N., Jones, M., Pita, G., Alonso, MR., Álvarez, N., Herrero, D., Tessier, DC., Vincent, D., Bacot, F., Luccarini, C., Baynes, C., Ahmed, S., Healey, CS., Brown, MA., Ponder, BAJ., Chenevix-Trench, G., Thompson, DJ., Edwards, SL., Easton, DF., Dunning, AM. and French, JD., 2015. Fine-scale mapping of the 5q11.2 breast cancer locus reveals at least three independent risk variants regulating MAP3K1. Am J Hum Genet, v. 96
    Doi: http://doi.org/10.1016/j.ajhg.2014.11.009
  • Glubb, DM., Maranian, MJ., Michailidou, K., Pooley, KA., Meyer, KB., Kar, S., Carlebur, S., O'Reilly, M., Betts, JA., Hillman, KM., Kaufmann, S., Beesley, J., Canisius, S., Hopper, JL., Southey, MC., Tsimiklis, H., Apicella, C., Schmidt, MK., Broeks, A., Hogervorst, FB., Van Der Schoot, CE., Muir, K., Lophatananon, A., Stewart-Brown, S., Siriwanarangsan, P., Fasching, PA., Ruebner, M., Ekici, AB., Beckmann, MW., Peto, J., Dos-Santos-Silva, I., Fletcher, O., Johnson, N., Pharoah, PDP., Bolla, MK., Wang, Q., Dennis, J., Sawyer, EJ., Tomlinson, I., Kerin, MJ., Miller, N., Burwinkel, B., Marme, F., Yang, R., Surowy, H., Guénel, P., Truong, T., Menegaux, F., Sanchez, M., Bojesen, SE., Nordestgaard, BG., Nielsen, SF., Flyger, H., González-Neira, A., Benitez, J., Zamora, MP., Arias Perez, JI., Anton-Culver, H., Neuhausen, SL., Brenner, H., Dieffenbach, AK., Arndt, V., Stegmaier, C., Meindl, A., Schmutzler, RK., Brauch, H., Ko, YD., Brüning, T., Nevanlinna, H., Muranen, TA., Aittomäki, K., Blomqvist, C., Matsuo, K., Ito, H., Iwata, H., Tanaka, H., Dörk, T., Bogdanova, NV., Helbig, S., Lindblom, A., Margolin, S., Mannermaa, A., Kataja, V., Kosma, VM., Hartikainen, JM., Wu, AH., Tseng, CC., Van Den Berg, D., Stram, DO., Lambrechts, D., Zhao, H., Weltens, C., Van Limbergen, E., Chang-Claude, J., Flesch-Janys, D., Rudolph, A., Seibold, P., Radice, P., Peterlongo, P. and Barile, M., 2015. Fine-scale mapping of the 5q11.2 breast cancer locus reveals at least three independent risk variants regulating MAP3K1 American Journal of Human Genetics, v. 96
    Doi: http://doi.org/10.1016/j.ajhg.2014.11.009
  • Orr, N., Dudbridge, F., Dryden, N., Maguire, S., Novo, D., Perrakis, E., Johnson, N., Ghoussaini, M., Hopper, JL., Southey, MC., Apicella, C., Stone, J., Schmidt, MK., Broeks, A., Van't Veer, LJ., Hogervorst, FB., Fasching, PA., Haeberle, L., Ekici, AB., Beckmann, MW., Gibson, L., Aitken, Z., Warren, H., Sawyer, E., Tomlinson, I., Kerin, MJ., Miller, N., Burwinkel, B., Marme, F., Schneeweiss, A., Sohn, C., Guénel, P., Truong, T., Cordina-Duverger, E., Sanchez, M., Bojesen, SE., Nordestgaard, BG., Nielsen, SF., Flyger, H., Benitez, J., Zamora, MP., Arias Perez, JI., Menéndez, P., Anton-Culver, H., Neuhausen, SL., Brenner, H., Dieffenbach, AK., Arndt, V., Stegmaier, C., Hamann, U., Brauch, H., Justenhoven, C., Brüning, T., Ko, Y-D., Nevanlinna, H., Aittomäki, K., Blomqvist, C., Khan, S., Bogdanova, N., Dörk, T., Lindblom, A., Margolin, S., Mannermaa, A., Kataja, V., Kosma, V-M., Hartikainen, JM., 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, FJ., Olson, JE., Slettedahl, S., Vachon, C., Giles, GG., Milne, RL., McLean, C., Haiman, CA., Henderson, BE., Schumacher, F., Le Marchand, L., Simard, J., Goldberg, MS., Labrèche, F., Dumont, M., Kristensen, V., Alnæs, GG., Nord, S., Borresen-Dale, A-L., Zheng, W., Deming-Halverson, S., Shrubsole, M., Long, J., Winqvist, R., Pylkäs, K., Jukkola-Vuorinen, A., Grip, M., Andrulis, IL., Knight, JA., Glendon, G., Tchatchou, S., Devilee, P., Tollenaar, RAEM., Seynaeve, CM., Van Asperen, CJ., Garcia-Closas, M., Figueroa, J., Chanock, SJ., Lissowska, J., Czene, K., Darabi, H., Eriksson, M., Klevebring, D., Hooning, MJ., Hollestelle, A., van Deurzen, CHM., Kriege, M., Hall, P., Li, J., Liu, J., Humphreys, K., Cox, A., Cross, SS., Reed, MWR., Pharoah, PDP., Dunning, AM., Shah, M., Perkins, BJ., Jakubowska, A., Lubinski, J., Jaworska-Bieniek, K., Durda, K., Ashworth, A., Swerdlow, A., Jones, M., Schoemaker, MJ., Meindl, A., Schmutzler, RK., Olswold, C., Slager, S., Toland, AE., Yannoukakos, D., Muir, K., Lophatananon, A., Stewart-Brown, S., Siriwanarangsan, P., Matsuo, K., Ito, H., Iwata, H., Ishiguro, J., Wu, AH., Tseng, C-C., Van Den Berg, D., Stram, DO., Teo, SH., Yip, CH., Kang, P., Ikram, MK., Shu, X-O., Lu, W., Gao, Y-T., Cai, H., Kang, D., Choi, J-Y., Park, SK., Noh, D-Y., Hartman, M., Miao, H., Lim, WY., Lee, SC., Sangrajrang, S., Gaborieau, V., Brennan, P., Mckay, J., Wu, P-E., Hou, M-F., Yu, J-C., Shen, C-Y., Blot, W., Cai, Q., Signorello, LB., Luccarini, C., Bayes, C., Ahmed, S., Maranian, M., Healey, CS., González-Neira, A., Pita, G., Alonso, MR., Álvarez, N., Herrero, D., Tessier, DC., Vincent, D., Bacot, F., Hunter, DJ., Lindstrom, S., Dennis, J., Michailidou, K., Bolla, MK., Easton, DF., dos Santos Silva, I., Fletcher, O., Peto, J., GENICA Network, , kConFab Investigators, and Australian Ovarian Cancer Study Group, , 2015. Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2. Hum Mol Genet, v. 24
    Doi: http://doi.org/10.1093/hmg/ddv035
  • Darabi, H., McCue, K., Beesley, J., Michailidou, K., Nord, S., Kar, S., Humphreys, K., Thompson, D., Ghoussaini, M., Bolla, MK., Dennis, J., Wang, Q., Canisius, S., Scott, CG., Apicella, C., Hopper, JL., Southey, MC., Stone, J., Broeks, A., Schmidt, MK., Scott, RJ., Lophatananon, A., Muir, K., Beckmann, MW., Ekici, AB., Fasching, PA., Heusinger, K., Dos-Santos-Silva, I., Peto, J., Tomlinson, I., Sawyer, EJ., Burwinkel, B., Marme, F., Guénel, P., Truong, T., Bojesen, SE., Flyger, H., Benitez, J., González-Neira, A., Anton-Culver, H., Neuhausen, SL., Arndt, V., Brenner, H., Engel, C., Meindl, A., Schmutzler, RK., German Consortium of Hereditary Breast and Ovarian Cancer, , Arnold, N., Brauch, H., Hamann, U., Chang-Claude, J., Khan, S., Nevanlinna, H., Ito, H., Matsuo, K., Bogdanova, NV., Dörk, T., Lindblom, A., Margolin, S., kConFab/AOCS Investigators, , Kosma, V-M., Mannermaa, A., Tseng, C-C., Wu, AH., Floris, G., Lambrechts, D., Rudolph, A., Peterlongo, P., Radice, P., Couch, FJ., Vachon, C., Giles, GG., McLean, C., Milne, RL., Dugué, P-A., Haiman, CA., Maskarinec, G., Woolcott, C., Henderson, BE., Goldberg, MS., Simard, J., Teo, SH., Mariapun, S., Helland, Å., Haakensen, V., Zheng, W., Beeghly-Fadiel, A., Tamimi, R., Jukkola-Vuorinen, A., Winqvist, R., Andrulis, IL., Knight, JA., Devilee, P., Tollenaar, RAEM., Figueroa, J., García-Closas, M., Czene, K., Hooning, MJ., Tilanus-Linthorst, M., Li, J., Gao, Y-T., Shu, X-O., Cox, A., Cross, SS., Luben, R., Khaw, K-T., Choi, J-Y., Kang, D., Hartman, M., Lim, WY., Kabisch, M., Torres, D., Jakubowska, A., Lubinski, J., McKay, J., Sangrajrang, S., Toland, AE., Yannoukakos, D., Shen, C-Y., Yu, J-C., Ziogas, A., Schoemaker, MJ., Swerdlow, A., Borresen-Dale, A-L., Kristensen, V., French, JD., Edwards, SL., Dunning, AM., Easton, DF., Hall, P. and Chenevix-Trench, G., 2015. Polymorphisms in a Putative Enhancer at the 10q21.2 Breast Cancer Risk Locus Regulate NRBF2 Expression. Am J Hum Genet, v. 97
    Doi: http://doi.org/10.1016/j.ajhg.2015.05.002
  • Guo, X., Long, J., Zeng, C., Michailidou, K., Ghoussaini, M., Bolla, MK., Wang, Q., Milne, RL., Shu, X-O., Cai, Q., Beesley, J., Kar, SP., Andrulis, IL., Anton-Culver, H., Arndt, V., Beckmann, MW., Beeghly-Fadiel, A., Benitez, J., Blot, W., Bogdanova, N., 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., Dörk, T., Fasching, PA., Fletcher, O., Flyger, H., Fostira, F., Gaborieau, V., García-Closas, M., Giles, GG., Grip, M., Guénel, P., Haiman, CA., Hamann, U., Hartman, M., Hollestelle, A., Hopper, JL., Hsiung, C-N., Ito, H., Jakubowska, A., Johnson, N., Kabisch, M., Kang, D., Khan, S., Knight, JA., Kosma, V-M., Lambrechts, D., Le Marchand, L., Li, J., Lindblom, A., Lophatananon, A., Lubinski, J., Mannermaa, A., Manoukian, S., Margolin, S., Marme, F., Matsuo, K., McLean, CA., Meindl, A., Muir, K., Neuhausen, SL., Nevanlinna, H., Nord, S., Olson, JE., Orr, N., Peterlongo, P., Putti, TC., Rudolph, A., Sangrajrang, S., Sawyer, EJ., Schmidt, MK., Schmutzler, RK., Shen, C-Y., Shi, J., Shrubsole, MJ., Southey, MC., Swerdlow, A., Teo, SH., Thienpont, B., Toland, AE., Tollenaar, RAEM., Tomlinson, IPM., Truong, T., Tseng, C-C., van den Ouweland, A., Wen, W., Winqvist, R., Wu, A., Yip, CH., Zamora, MP., Zheng, Y., Hall, P., Pharoah, PDP., Simard, J., Chenevix-Trench, G., kConFab Investigators, , Dunning, AM., Easton, DF. and Zheng, W., 2015. Fine-scale mapping of the 4q24 locus identifies two independent loci associated with breast cancer risk. Cancer Epidemiol Biomarkers Prev, v. 24
    Doi: http://doi.org/10.1158/1055-9965.EPI-15-0363
  • 2014

  • Ghoussaini, M., Edwards, SL., Michailidou, K., Nord, S., Cowper-Sal Lari, R., Desai, K., Kar, S., Hillman, KM., Kaufmann, S., Glubb, DM., Beesley, J., Dennis, J., Bolla, MK., Wang, Q., Dicks, E., Guo, Q., Schmidt, MK., Shah, M., Luben, R., Brown, J., Czene, K., Darabi, H., Eriksson, M., Klevebring, D., Bojesen, SE., Nordestgaard, BG., Nielsen, SF., Flyger, H., Lambrechts, D., Thienpont, B., Neven, P., Wildiers, H., Broeks, A., Van't Veer, LJ., Th Rutgers, EJ., Couch, FJ., Olson, JE., Hallberg, E., Vachon, C., Chang-Claude, J., Rudolph, A., Seibold, P., Flesch-Janys, D., Peto, J., Dos-Santos-Silva, I., Gibson, L., Nevanlinna, H., Muranen, TA., Aittomäki, K., Blomqvist, C., Hall, P., Li, J., Liu, J., Humphreys, K., Kang, D., Choi, J-Y., Park, SK., Noh, D-Y., Matsuo, K., Ito, H., Iwata, H., Yatabe, Y., Guénel, P., Truong, T., Menegaux, F., Sanchez, M., Burwinkel, B., Marme, F., Schneeweiss, A., Sohn, C., Wu, AH., Tseng, C-C., Van Den Berg, D., Stram, DO., Benitez, J., Zamora, MP., Perez, JIA., Menéndez, P., Shu, X-O., Lu, W., Gao, Y-T., Cai, Q., Cox, A., Cross, SS., Reed, MWR., Andrulis, IL., Knight, JA., Glendon, G., Tchatchou, S., Sawyer, EJ., Tomlinson, I., Kerin, MJ., Miller, N., Haiman, CA., Henderson, BE., Schumacher, F., Le Marchand, L., Lindblom, A., Margolin, S., Teo, SH., Yip, CH., Lee, DSC., Wong, TY., Hooning, MJ., Martens, JWM., Collée, JM., van Deurzen, CHM., Hopper, JL., Southey, MC., Tsimiklis, H., Kapuscinski, MK., Shen, C-Y., Wu, P-E., Yu, J-C., Chen, S-T., Alnæs, GG., Borresen-Dale, A-L., Giles, GG., Milne, RL., McLean, C., Muir, K., Lophatananon, A., Stewart-Brown, S., Siriwanarangsan, P., Hartman, M., Miao, H., Buhari, SABS., Teo, YY., Fasching, PA., Haeberle, L., Ekici, AB., Beckmann, MW., Brenner, H., Dieffenbach, AK., Arndt, V., Stegmaier, C., Swerdlow, A., Ashworth, A., Orr, N., Schoemaker, MJ., García-Closas, M., Figueroa, J., Chanock, SJ., Lissowska, J., Simard, J., Goldberg, MS., Labrèche, F., Dumont, M., Winqvist, R., Pylkäs, K., Jukkola-Vuorinen, A., Brauch, H., Brüning, T., Koto, Y-D., Radice, P., Peterlongo, P., Bonanni, B., Volorio, S., Dörk, T., Bogdanova, NV., Helbig, S., Mannermaa, A., Kataja, V., Kosma, V-M., Hartikainen, JM., Devilee, P., Tollenaar, RAEM., Seynaeve, C., Van Asperen, CJ., Jakubowska, A., Lubinski, J., Jaworska-Bieniek, K., Durda, K., Slager, S., Toland, AE., Ambrosone, CB., Yannoukakos, D., Sangrajrang, S., Gaborieau, V., Brennan, P., McKay, J., Hamann, U., Torres, D., Zheng, W., Long, J., Anton-Culver, H., Neuhausen, SL., Luccarini, C., Baynes, C., Ahmed, S., Maranian, M., Healey, CS., González-Neira, A., Pita, G., Alonso, MR., Alvarez, N., Herrero, D., Tessier, DC., Vincent, D., Bacot, F., de Santiago, I., Carroll, J., Caldas, C., Brown, MA., Lupien, M., Kristensen, VN., Pharoah, PDP., Chenevix-Trench, G., French, JD., Easton, DF., Dunning, AM., Australian Ovarian Cancer Management Group, and Australian Ovarian Cancer Management Group, , 2014. Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation. Nature Communications, v. 5
    Doi: http://doi.org/10.1038/ncomms5999
  • 2013 (No publication date)

  • Antoniou, A., Bojesen, SE., Pooley, KA. and Chenevix-Trench, G., 2013 (No publication date). Multiple independent TERT variants associated with telomere length and risks of breast and ovarian cancer Nat Genet,
  • 2013

  • French, JD., Ghoussaini, M., Edwards, SL., Meyer, KB., Michailidou, K., Ahmed, S., Khan, S., Maranian, MJ., O'Reilly, M., Hillman, KM., Betts, JA., Carroll, T., Bailey, PJ., Dicks, E., Beesley, J., Tyrer, J., Maia, A-T., Beck, A., Knoblauch, NW., Chen, C., Kraft, P., Barnes, D., González-Neira, A., Alonso, MR., Herrero, D., Tessier, DC., Vincent, D., Bacot, F., Luccarini, C., Baynes, C., Conroy, D., Dennis, J., Bolla, MK., Wang, Q., Hopper, JL., Southey, MC., Schmidt, MK., Broeks, A., Verhoef, S., Cornelissen, S., Muir, K., Lophatananon, A., Stewart-Brown, S., Siriwanarangsan, P., Fasching, PA., Loehberg, CR., Ekici, AB., Beckmann, MW., Peto, J., dos Santos Silva, I., Johnson, N., Aitken, Z., Sawyer, EJ., Tomlinson, I., Kerin, MJ., Miller, N., Marme, F., Schneeweiss, A., Sohn, C., Burwinkel, B., Guénel, P., Truong, T., Laurent-Puig, P., Menegaux, F., Bojesen, SE., Nordestgaard, BG., Nielsen, SF., Flyger, H., Milne, RL., Zamora, MP., Arias Perez, JI., Benitez, J., Anton-Culver, H., Brenner, H., Müller, H., Arndt, V., Stegmaier, C., Meindl, A., Lichtner, P., Schmutzler, RK., Engel, C., Brauch, H., Hamann, U., Justenhoven, C., GENICA Network, , Aaltonen, K., Heikkilä, P., Aittomäki, K., Blomqvist, C., Matsuo, K., Ito, H., Iwata, H., Sueta, A., Bogdanova, NV., Antonenkova, NN., Dörk, T., Lindblom, A., Margolin, S., Mannermaa, A., Kataja, V., Kosma, V-M., Hartikainen, JM., kConFab Investigators, , Wu, AH., Tseng, C-C., Van Den Berg, D., Stram, DO., Lambrechts, D., Peeters, S., Smeets, A., Floris, G., Chang-Claude, J., Rudolph, A., Nickels, S., Flesch-Janys, D., Radice, P., Peterlongo, P., Bonanni, B., Sardella, D., Couch, FJ., Wang, X., Pankratz, VS., Lee, A., Giles, GG., Severi, G., Baglietto, L., Haiman, CA., Henderson, BE., Schumacher, F., Le Marchand, L., Simard, J., Goldberg, MS., Labrèche, F., Dumont, M., Teo, SH., Yip, CH., Ng, C-H., Vithana, EN., Kristensen, V., Zheng, W., Deming-Halverson, S., Shrubsole, M., Long, J., Winqvist, R., Pylkäs, K., Jukkola-Vuorinen, A., Grip, M., Andrulis, IL., Knight, JA., Glendon, G., Mulligan, AM., Devilee, P., Seynaeve, C., García-Closas, M., Figueroa, J., Chanock, SJ., Lissowska, J., Czene, K., Klevebring, D., Schoof, N., Hooning, MJ., Martens, JWM., Collée, JM., Tilanus-Linthorst, M., Hall, P., Li, J., Liu, J., Humphreys, K., Shu, X-O., Lu, W., Gao, Y-T., Cai, H., Cox, A., Balasubramanian, SP., Blot, W., Signorello, LB., Cai, Q., Pharoah, PDP., Healey, CS., Shah, M., Pooley, KA., Kang, D., Yoo, K-Y., Noh, D-Y., Hartman, M., Miao, H., Sng, J-H., Sim, X., Jakubowska, A., Lubinski, J., Jaworska-Bieniek, K., Durda, K., Sangrajrang, S., Gaborieau, V., McKay, J., Toland, AE., Ambrosone, CB., Yannoukakos, D., Godwin, AK., Shen, C-Y., Hsiung, C-N., Wu, P-E., Chen, S-T., Swerdlow, A., Ashworth, A., Orr, N., Schoemaker, MJ., Ponder, BAJ., Nevanlinna, H., Brown, MA., Chenevix-Trench, G., Easton, DF. and Dunning, AM., 2013. Functional variants at the 11q13 risk locus for breast cancer regulate cyclin D1 expression through long-range enhancers. Am J Hum Genet, v. 92
    Doi: http://doi.org/10.1016/j.ajhg.2013.01.002
  • Bonnefond, A., Raimondo, A., Stutzmann, F., Ghoussaini, M., Ramachandrappa, S., Bersten, DC., Durand, E., Vatin, V., Balkau, B., Lantieri, O., Raverdy, V., Pattou, F., Van Hul, W., Van Gaal, L., Peet, DJ., Weill, J., Miller, JL., Horber, F., Goldstone, AP., Driscoll, DJ., Bruning, JB., Meyre, D., Whitelaw, ML. and Froguel, P., 2013. Loss-of-function mutations in SIM1 contribute to obesity and Prader-Willi-like features. J Clin Invest, v. 123
    Doi: http://doi.org/10.1172/JCI68035
  • Ghoussaini, M., Pharoah, PDP. and Easton, DF., 2013. Inherited genetic susceptibility to breast cancer: the beginning of the end or the end of the beginning? Am J Pathol, v. 183
    Doi: http://doi.org/10.1016/j.ajpath.2013.07.003
  • Meyer, KB., O'Reilly, M., Michailidou, K., Carlebur, S., Edwards, SL., French, JD., Prathalingham, R., Dennis, J., Bolla, MK., Wang, Q., de Santiago, I., Hopper, JL., Tsimiklis, H., Apicella, C., Southey, MC., Schmidt, MK., Broeks, A., Van 't Veer, LJ., Hogervorst, FB., Muir, K., Lophatananon, A., Stewart-Brown, S., Siriwanarangsan, P., Fasching, PA., Lux, MP., Ekici, AB., Beckmann, MW., Peto, J., Dos Santos Silva, I., Fletcher, O., Johnson, N., Sawyer, EJ., Tomlinson, I., Kerin, MJ., Miller, N., Marme, F., Schneeweiss, A., Sohn, C., Burwinkel, B., Guénel, P., Truong, T., Laurent-Puig, P., Menegaux, F., Bojesen, SE., Nordestgaard, BG., Nielsen, SF., Flyger, H., Milne, RL., Zamora, MP., Arias, JI., Benitez, J., Neuhausen, S., Anton-Culver, H., Ziogas, A., Dur, CC., Brenner, H., Müller, H., Arndt, V., Stegmaier, C., Meindl, A., Schmutzler, RK., Engel, C., Ditsch, N., Brauch, H., Brüning, T., Ko, Y-D., GENICA Network, , Nevanlinna, H., Muranen, TA., Aittomäki, K., Blomqvist, C., Matsuo, K., Ito, H., Iwata, H., Yatabe, Y., Dörk, T., Helbig, S., Bogdanova, NV., Lindblom, A., Margolin, S., Mannermaa, A., Kataja, V., Kosma, V-M., Hartikainen, JM., Chenevix-Trench, G., kConFab Investigators, , Australian Ovarian Cancer Study Group, , Wu, AH., Tseng, C-C., Van Den Berg, D., Stram, DO., Lambrechts, D., Thienpont, B., Christiaens, M-R., Smeets, A., Chang-Claude, J., Rudolph, A., Seibold, P., Flesch-Janys, D., Radice, P., Peterlongo, P., Bonanni, B., Bernard, L., Couch, FJ., Olson, JE., Wang, X., Purrington, K., Giles, GG., Severi, G., Baglietto, L., McLean, C., Haiman, CA., Henderson, BE., Schumacher, F., Le Marchand, L., Simard, J., Goldberg, MS., Labrèche, F., Dumont, M., Teo, S-H., Yip, C-H., Phuah, S-Y., Kristensen, V., Grenaker Alnæs, G., Børresen-Dale, A-L., Zheng, W., Deming-Halverson, S., Shrubsole, M., Long, J., Winqvist, R., Pylkäs, K., Jukkola-Vuorinen, A., Kauppila, S., Andrulis, IL., Knight, JA., Glendon, G., Tchatchou, S., Devilee, P., Tollenaar, RAEM., Seynaeve, CM., García-Closas, M., Figueroa, J., Chanock, SJ., Lissowska, J., Czene, K., Darabi, H., Eriksson, K., Hooning, MJ., Martens, JWM., van den Ouweland, AMW., van Deurzen, CHM., Hall, P., Li, J., Liu, J., Humphreys, K., Shu, X-O., Lu, W., Gao, Y-T., Cai, H., Cox, A., Reed, MWR., Blot, W., Signorello, LB., Cai, Q., Pharoah, PDP., Ghoussaini, M., Harrington, P., Tyrer, J., Kang, D., Choi, J-Y., Park, SK., Noh, D-Y., Hartman, M., Hui, M., Lim, W-Y., Buhari, SA., Hamann, U., Försti, A., Rüdiger, T., Ulmer, H-U., Jakubowska, A., Lubinski, J., Jaworska, K., Durda, K., Sangrajrang, S., Gaborieau, V., Brennan, P., McKay, J., Vachon, C., Slager, S., Fostira, F., Pilarski, R., Shen, C-Y., Hsiung, C-N., Wu, P-E., Hou, M-F., Swerdlow, A., Ashworth, A., Orr, N., Schoemaker, MJ., Ponder, BAJ., Dunning, AM. and Easton, DF., 2013. Fine-scale mapping of the FGFR2 breast cancer risk locus: putative functional variants differentially bind FOXA1 and E2F1. Am J Hum Genet, v. 93
    Doi: http://doi.org/10.1016/j.ajhg.2013.10.026
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  • Warren, H., Dudbridge, F., Fletcher, O., Orr, N., Johnson, N., Hopper, JL., Apicella, C., Southey, MC., Mahmoodi, M., Schmidt, MK., Broeks, A., Cornelissen, S., Braaf, LM., Muir, KR., Lophatananon, A., Chaiwerawattana, A., Wiangnon, S., Fasching, PA., Beckmann, MW., Ekici, AB., Schulz-Wendtland, R., Sawyer, EJ., Tomlinson, I., Kerin, M., Burwinkel, B., Marme, F., Schneeweiss, A., Sohn, C., Guénel, P., Truong, T., Laurent-Puig, P., Mulot, C., Bojesen, SE., Nielsen, SF., Flyger, H., Nordestgaard, BG., Milne, RL., Benítez, J., Arias-Pérez, J-I., Zamora, MP., Anton-Culver, H., Ziogas, A., Bernstein, L., Dur, CC., Brenner, H., Müller, H., Arndt, V., Langheinz, A., Meindl, A., Golatta, M., Bartram, CR., Schmutzler, RK., Brauch, H., Justenhoven, C., Brüning, T., GENICA Network, , Chang-Claude, J., Wang-Gohrke, S., Eilber, U., Dörk, T., Schürmann, P., Bremer, M., Hillemanns, P., Nevanlinna, H., Muranen, TA., Aittomäki, K., Blomqvist, C., Bogdanova, N., Antonenkova, N., Rogov, Y., Bermisheva, M., Prokofyeva, D., Zinnatullina, G., Khusnutdinova, E., Lindblom, A., Margolin, S., Mannermaa, A., Kosma, V-M., Hartikainen, JM., Kataja, V., Chenevix-Trench, G., Beesley, J., Chen, X., kConFab Investigators, , Australian Ovarian Cancer Study Group, , Lambrechts, D., Smeets, A., Paridaens, R., Weltens, C., Flesch-Janys, D., Buck, K., Behrens, S., Peterlongo, P., Bernard, L., Manoukian, S., Radice, P., Couch, FJ., Vachon, C., Wang, X., Olson, J., Giles, G., Baglietto, L., McLean, CA., Severi, G., John, EM., Miron, A., Winqvist, R., Pylkäs, K., Jukkola-Vuorinen, A., Grip, M., Andrulis, IL., Knight, JA., Mulligan, AM., Weerasooriya, N., Devilee, P., Tollenaar, RAEM., Martens, JWM., Seynaeve, CM., Hooning, MJ., Hollestelle, A., Jager, A., Tilanus-Linthorst, MMA., Hall, P., Czene, K., Liu, J., Li, J., Cox, A., Cross, SS., Brock, IW., Reed, MWR., Pharoah, P., Blows, FM., Dunning, AM., Ghoussaini, M., Ashworth, A., Swerdlow, A., Jones, M., Schoemaker, M., Easton, DF., Humphreys, M., Wang, Q., Peto, J. and dos-Santos-Silva, I., 2012. 9q31.2-rs865686 as a susceptibility locus for estrogen receptor-positive breast cancer: evidence from the Breast Cancer Association Consortium. Cancer Epidemiol Biomarkers Prev, v. 21
    Doi: http://doi.org/10.1158/1055-9965.EPI-12-0526
  • Hein, R., Maranian, M., Hopper, JL., Kapuscinski, MK., Southey, MC., Park, DJ., Schmidt, MK., Broeks, A., Hogervorst, FBL., Bueno-de-Mesquita, HB., Muir, KR., Lophatananon, A., Rattanamongkongul, S., Puttawibul, P., Fasching, PA., Hein, A., Ekici, AB., Beckmann, MW., Fletcher, O., Johnson, N., dos Santos Silva, I., Peto, J., Sawyer, E., Tomlinson, I., Kerin, M., Miller, N., Marmee, F., Schneeweiss, A., Sohn, C., Burwinkel, B., Guénel, P., Cordina-Duverger, E., Menegaux, F., Truong, T., Bojesen, SE., Nordestgaard, BG., Flyger, H., Milne, RL., Perez, JIA., Zamora, MP., Benítez, J., Anton-Culver, H., Ziogas, A., Bernstein, L., Clarke, CA., Brenner, H., Müller, H., Arndt, V., Stegmaier, C., Rahman, N., Seal, S., Turnbull, C., Renwick, A., Meindl, A., Schott, S., Bartram, CR., Schmutzler, RK., Brauch, H., Hamann, U., Ko, Y-D., GENICA Network, , Wang-Gohrke, S., Dörk, T., Schürmann, P., Karstens, JH., Hillemanns, P., Nevanlinna, H., Heikkinen, T., Aittomäki, K., Blomqvist, C., Bogdanova, NV., Zalutsky, IV., Antonenkova, NN., Bermisheva, M., Prokovieva, D., Farahtdinova, A., Khusnutdinova, E., Lindblom, A., Margolin, S., Mannermaa, A., Kataja, V., Kosma, V-M., Hartikainen, J., Chen, X., Beesley, J., Kconfab Investigators, , AOCS Group, , Lambrechts, D., Zhao, H., Neven, P., Wildiers, H., Nickels, S., Flesch-Janys, D., Radice, P., Peterlongo, P., Manoukian, S., Barile, M., Couch, FJ., Olson, JE., Wang, X., Fredericksen, Z., Giles, GG., Baglietto, L., McLean, CA., Severi, G., Offit, K., Robson, M., Gaudet, MM., Vijai, J., Alnæs, GG., Kristensen, V., Børresen-Dale, A-L., John, EM., Miron, A., Winqvist, R., Pylkäs, K., Jukkola-Vuorinen, A., Grip, M., Andrulis, IL., Knight, JA., Glendon, G., Mulligan, AM., Figueroa, JD., García-Closas, M., Lissowska, J., Sherman, ME., Hooning, M., Martens, JWM., Seynaeve, C., Collée, M., Hall, P., Humpreys, K., Czene, K., Liu, J., Cox, A., Brock, IW., Cross, SS., Reed, MWR., Ahmed, S., Ghoussaini, M., Pharoah, PDP., Kang, D., Yoo, K-Y., Noh, D-Y., Jakubowska, A., Jaworska, K., Durda, K., Złowocka, E., Sangrajrang, S., Gaborieau, V., Brennan, P., McKay, J., Shen, C-Y., Yu, J-C., Hsu, H-M., Hou, M-F., Orr, N., Schoemaker, M., Ashworth, A., Swerdlow, A., Trentham-Dietz, A., Newcomb, PA., Titus, L., Egan, KM., Chenevix-Trench, G., Antoniou, AC., Humphreys, MK., Morrison, J., Chang-Claude, J., Easton, DF. and Dunning, AM., 2012. Comparison of 6q25 breast cancer hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC). PLoS One, v. 7
    Doi: http://doi.org/10.1371/journal.pone.0042380
  • Hein, R., Maranian, M., Hopper, JL., Kapuscinski, MK., Southey, MC., Park, DJ., Schmidt, MK., Broeks, A., Hogervorst, FB., Bueno-de-Mesquit, HB., Muir, KR., Lophatananon, A., Rattanamongkongul, S., Puttawibul, P., Fasching, PA., Hein, A., Ekici, AB., Beckmann, MW., Fletcher, O., Johnson, N., Dos Santos Silva, I., Peto, J., Sawyer, E., Tomlinson, I., Kerin, M., Miller, N., Marmee, F., Schneeweiss, A., Sohn, C., Burwinkel, B., Guénel, P., Cordina-Duverger, E., Menegaux, F., Truong, T., Bojesen, SE., Nordestgaard, BG., Flyger, H., Milne, RL., Perez, JI., Zamora, MP., Benítez, J., Anton-Culver, H., Ziogas, A., Bernstein, L., Clarke, CA., Brenner, H., Müller, H., Arndt, V., Stegmaier, C., Rahman, N., Seal, S., Turnbull, C., Renwick, A., Meindl, A., Schott, S., Bartram, CR., Schmutzler, RK., Brauch, H., Hamann, U., Ko, YD., GENICA Network, , Wang-Gohrke, S., Dörk, T., Schürmann, P., Karstens, JH., Hillemanns, P., Nevanlinna, H., Heikkinen, T., Aittomäki, K., Blomqvist, C., Bogdanova, NV., Zalutsky, IV., Antonenkova, NN., Bermisheva, M., Prokovieva, D., Farahtdinova, A., Khusnutdinova, E., Lindblom, A., Margolin, S., Mannermaa, A., Kataja, V., Kosma, VM., Hartikainen, J., Chen, X., Beesley, J., Investigators, K., CS Group, , Lambrechts, D., Zhao, H., Neven, P., Wildiers, H., Nickels, S., Flesch-Janys, D., Radice, P., Peterlongo, P., Manoukian, S., Barile, M., Couch, FJ., Olson, JE., Wang, X., Fredericksen, Z., Giles, GG., Baglietto, L., McLean, CA., Severi, G., Offit, K., Robson, M., Gaudet, MM., Vijai, J., Alnæs, GG., Kristensen, V., Børresen-Dale, AL., John, EM., Miron, A., Winqvist, R., Pylkäs, K., Jukkola-Vuorinen, A., Grip, M., Andrulis, IL., Knight, JA., Glendon, G., Mulligan, AM., Figueroa, JD., García-Closas, M., Lissowska, J., Sherman, ME., Hooning, M., Martens, JW., Seynaeve, C., Collée, M., Hall, P., Humpreys, K., Czene, K., Liu, J., Cox, A., Brock, IW., Cross, SS., Reed, MW., Ahmed, S., Ghoussaini, M., Pharoah, PD., Kang, D., Yoo, KY., Noh, DY., Jakubowska, A., Jaworska, K., Durda, K., Złowocka, E., Sangrajrang, S., Gaborieau, V., Brennan, P., McKay, J., Shen, CY., Yu, JC., Hsu, HM., Hou, MF., Orr, N., Schoemaker, M., Ashworth, A., Swerdlow, A., Trentham-Dietz, A., Newcomb, PA., Titus, L., Egan, KM., Chenevix-Trench, G., Antoniou, AC., Humphreys, MK., Morrison, J., Chang-Claude, J., Easton, DF. and Dunning, AM., 2012. Correction: Comparison of 6q25 Breast Cancer Hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC). PLoS One, v. 7
    Doi: http://doi.org/10.1371/annotation/e5de602c-0ffc-4e6f-a2ed-f79913c2e57c
  • 2011

  • Meyer, KB., Maia, A-T., O'Reilly, M., Ghoussaini, M., Prathalingam, R., Porter-Gill, P., Ambs, S., Prokunina-Olsson, L., Carroll, J. and Ponder, BAJ., 2011. A functional variant at a prostate cancer predisposition locus at 8q24 is associated with PVT1 expression. PLoS Genet, v. 7
    Doi: http://doi.org/10.1371/journal.pgen.1002165
  • 2010

  • Antoniou, AC., Wang, X., Fredericksen, ZS., McGuffog, L., Tarrell, R., Sinilnikova, OM., Healey, S., Morrison, J., Kartsonaki, C., Lesnick, T., Ghoussaini, M., Barrowdale, D., EMBRACE, , Peock, S., Cook, M., Oliver, C., Frost, D., Eccles, D., Evans, DG., Eeles, R., Izatt, L., Chu, C., Douglas, F., Paterson, J., Stoppa-Lyonnet, D., Houdayer, C., Mazoyer, S., Giraud, S., Lasset, C., Remenieras, A., Caron, O., Hardouin, A., Berthet, P., GEMO Study Collaborators, , Hogervorst, FBL., Rookus, MA., Jager, A., van den Ouweland, A., Hoogerbrugge, N., van der Luijt, RB., Meijers-Heijboer, H., Gómez García, EB., HEBON, , Devilee, P., Vreeswijk, MPG., Lubinski, J., Jakubowska, A., Gronwald, J., Huzarski, T., Byrski, T., Górski, B., Cybulski, C., Spurdle, AB., Holland, H., kConFab, , Goldgar, DE., John, EM., Hopper, JL., Southey, M., Buys, SS., Daly, MB., Terry, M-B., Schmutzler, RK., Wappenschmidt, B., Engel, C., Meindl, A., Preisler-Adams, S., Arnold, N., Niederacher, D., Sutter, C., Domchek, SM., Nathanson, KL., Rebbeck, T., Blum, JL., Piedmonte, M., Rodriguez, GC., Wakeley, K., Boggess, JF., Basil, J., Blank, SV., Friedman, E., Kaufman, B., Laitman, Y., Milgrom, R., Andrulis, IL., Glendon, G., Ozcelik, H., Kirchhoff, T., Vijai, J., Gaudet, MM., Altshuler, D., Guiducci, C., SWE-BRCA, , Loman, N., Harbst, K., Rantala, J., Ehrencrona, H., Gerdes, A-M., Thomassen, M., Sunde, L., Peterlongo, P., Manoukian, S., Bonanni, B., Viel, A., Radice, P., Caldes, T., de la Hoya, M., Singer, CF., Fink-Retter, A., Greene, MH., Mai, PL., Loud, JT., Guidugli, L., Lindor, NM., Hansen, TVO., Nielsen, FC., Blanco, I., Lazaro, C., Garber, J., Ramus, SJ., Gayther, SA., Phelan, C., Narod, S., Szabo, CI., MOD SQUAD, , Benitez, J., Osorio, A., Nevanlinna, H., Heikkinen, T., Caligo, MA., Beattie, MS., Hamann, U., Godwin, AK., Montagna, M., Casella, C., Neuhausen, SL., Karlan, BY., Tung, N., Toland, AE., Weitzel, J., Olopade, O., Simard, J., Soucy, P., Rubinstein, WS., Arason, A., Rennert, G., Martin, NG., Montgomery, GW., Chang-Claude, J., Flesch-Janys, D., Brauch, H., GENICA, , Severi, G., Baglietto, L., Cox, A., Cross, SS., Miron, P., Gerty, SM., Tapper, W., Yannoukakos, D., Fountzilas, G., Fasching, PA., Beckmann, MW., Dos Santos Silva, I., Peto, J., Lambrechts, D., Paridaens, R., Rüdiger, T., Försti, A., Winqvist, R., Pylkäs, K., Diasio, RB., Lee, AM., Eckel-Passow, J., Vachon, C., Blows, F., Driver, K., Dunning, A., Pharoah, PPD., Offit, K., Pankratz, VS., Hakonarson, H., Chenevix-Trench, G., Easton, DF. and Couch, FJ., 2010. 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 population. Nat Genet, v. 42
    Doi: http://doi.org/10.1038/ng.669
  • Ghoussaini, M., Stutzmann, F., Couturier, C., Vatin, V., Durand, E., Lecoeur, C., Degraeve, F., Heude, B., Tauber, M., Hercberg, S., Levy-Marchal, C., Tounian, P., Weill, J., Traurig, M., Bogardus, C., Baier, LJ., Michaud, JL., Froguel, P. and Meyre, D., 2010. Analysis of the SIM1 contribution to polygenic obesity in the French population. Obesity (Silver Spring), v. 18
    Doi: http://doi.org/10.1038/oby.2009.468
  • Turnbull, C., Ahmed, S., Morrison, J., Pernet, D., Renwick, A., Maranian, M., Seal, S., Ghoussaini, M., Hines, S., Healey, CS., Hughes, D., Warren-Perry, M., Tapper, W., Eccles, D., Evans, DG., Breast Cancer Susceptibility Collaboration (UK), , Hooning, M., Schutte, M., van den Ouweland, A., Houlston, R., Ross, G., Langford, C., Pharoah, PDP., Stratton, MR., Dunning, AM., Rahman, N. and Easton, DF., 2010. Genome-wide association study identifies five new breast cancer susceptibility loci. Nat Genet, v. 42
    Doi: http://doi.org/10.1038/ng.586
  • 2009

  • Ghoussaini, M. and Pharoah, PDP., 2009. Polygenic susceptibility to breast cancer: current state-of-the-art. Future Oncol, v. 5
    Doi: http://doi.org/10.2217/fon.09.29
  • Stutzmann, F., Ghoussaini, M., Couturier, C., Vatin, V., Corset, L., Lecoeur, C., Balkau, B., Horber, F., Weill, J., Michaud, J., Meyre, D. and Froguel, P., 2009. Mutations of the hypothalamic transcription factor SIM1 are responsible for severe monogenic obesity of children DIABETES METAB, v. 35
  • Traurig, M., Mack, J., Hanson, RL., Ghoussaini, M., Meyre, D., Knowler, WC., Kobes, S., Froguel, P., Bogardus, C. and Baier, LJ., 2009. Common variation in SIM1 is reproducibly associated with BMI in Pima Indians. Diabetes, v. 58
    Doi: http://doi.org/10.2337/db09-0028
  • Ahmed, S., Thomas, G., Ghoussaini, M., Healey, CS., Humphreys, MK., Platte, R., Morrison, J., Maranian, M., Pooley, KA., Luben, R., Eccles, D., Evans, DG., Fletcher, O., Johnson, N., dos Santos Silva, I., Peto, J., Stratton, MR., Rahman, N., Jacobs, K., Prentice, R., Anderson, GL., Rajkovic, A., Curb, JD., Ziegler, RG., Berg, CD., Buys, SS., McCarty, CA., Feigelson, HS., Calle, EE., Thun, MJ., Diver, WR., Bojesen, S., Nordestgaard, BG., Flyger, H., Dörk, T., Schürmann, P., Hillemanns, P., Karstens, JH., Bogdanova, NV., Antonenkova, NN., Zalutsky, IV., Bermisheva, M., Fedorova, S., Khusnutdinova, E., SEARCH, , Kang, D., Yoo, K-Y., Noh, DY., Ahn, S-H., Devilee, P., van Asperen, CJ., Tollenaar, RAEM., Seynaeve, C., Garcia-Closas, M., Lissowska, J., Brinton, L., Peplonska, B., Nevanlinna, H., Heikkinen, T., Aittomäki, K., Blomqvist, C., Hopper, JL., Southey, MC., Smith, L., Spurdle, AB., Schmidt, MK., Broeks, A., van Hien, RR., Cornelissen, S., Milne, RL., Ribas, G., González-Neira, A., Benitez, J., Schmutzler, RK., Burwinkel, B., Bartram, CR., Meindl, A., Brauch, H., Justenhoven, C., Hamann, U., GENICA Consortium, , Chang-Claude, J., Hein, R., Wang-Gohrke, S., Lindblom, A., Margolin, S., Mannermaa, A., Kosma, V-M., Kataja, V., Olson, JE., Wang, X., Fredericksen, Z., Giles, GG., Severi, G., Baglietto, L., English, DR., Hankinson, SE., Cox, DG., Kraft, P., Vatten, LJ., Hveem, K., Kumle, M., Sigurdson, A., Doody, M., Bhatti, P., Alexander, BH., Hooning, MJ., van den Ouweland, AMW., Oldenburg, RA., Schutte, M., Hall, P., Czene, K., Liu, J., Li, Y., Cox, A., Elliott, G., Brock, I., Reed, MWR., Shen, C-Y., Yu, J-C., Hsu, G-C., Chen, S-T., Anton-Culver, H., Ziogas, A., Andrulis, IL., Knight, JA., kConFab, , Australian Ovarian Cancer Study Group, , Beesley, J., Goode, EL., Couch, F., Chenevix-Trench, G., Hoover, RN., Ponder, BAJ., Hunter, DJ., Pharoah, PDP., Dunning, AM., Chanock, SJ. and Easton, DF., 2009. Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2. Nat Genet, v. 41
    Doi: http://doi.org/10.1038/ng.354
  • 2008

  • Badii, R., Bener, A., Zirie, M., Al-Rikabi, A., Simsek, M., Al-Hamaq, AOAA., Ghoussaini, M., Froguel, P. and Wareham, NJ., 2008. Lack of association between the Pro12Ala polymorphism of the PPAR-gamma 2 gene and type 2 diabetes mellitus in the Qatari consanguineous population. Acta Diabetol, v. 45
    Doi: http://doi.org/10.1007/s00592-007-0013-8
  • Driver, KE., Song, H., Lesueur, F., Ahmed, S., Barbosa-Morais, NL., Tyrer, J., Ponder, BA., Easton, DF., Pharoah, PD. and Dunning, AM., 2008. Association of single-nucleotide polymorphisms in the Cell Cycle genes with breast cancer in the British population Carcinogenesis,
  • Ghoussaini, M., Song, H., Koessler, T., Al Olama, AA., Kote-Jarai, Z., Driver, KE., Pooley, KA., Ramus, SJ., Kjaer, SK., Hogdall, E., DiCioccio, RA., Whittemore, AS., Gayther, SA., Giles, GG., Guy, M., Edwards, SM., Morrison, J., Donovan, JL., Hamdy, FC., Dearnaley, DP., Ardern-Jones, AT., Hall, AL., O'Brien, LT., Gehr-Swain, BN., Wilkinson, RA., Brown, PM., Hopper, JL., Neal, DE., Pharoah, PDP., Ponder, BAJ., Eeles, RA., Easton, DF., Dunning, AM., UK Genetic Prostate Cancer Study Collaborators/British Association of Urological Surgeons' Section of Oncology, and UK ProtecT Study Collaborators, , 2008. Multiple loci with different cancer specificities within the 8q24 gene desert. J Natl Cancer Inst, v. 100
    Doi: http://doi.org/10.1093/jnci/djn190
  • 2007

  • Ghoussaini, M., Vatin, V., Lecoeur, C., Abkevich, V., Younus, A., Samson, C., Wachter, C., Heude, B., Tauber, M., Tounian, P., Hercberg, S., Weill, J., Levy-Marchal, C., Le Stunff, C., Bougnères, P., Froguel, P. and Meyre, D., 2007. Genetic study of the melanin-concentrating hormone receptor 2 in childhood and adulthood severe obesity. J Clin Endocrinol Metab, v. 92
    Doi: http://doi.org/10.1210/jc.2006-2316
  • 2005

  • Meyre, D., Bouatia-Naji, N., Tounian, A., Samson, C., Lecoeur, C., Vatin, V., Ghoussaini, M., Wachter, C., Hercberg, S., Charpentier, G., Patsch, W., Pattou, F., Charles, M-A., Tounian, P., Clément, K., Jouret, B., Weill, J., Maddux, BA., Goldfine, ID., Walley, A., Boutin, P., Dina, C. and Froguel, P., 2005. Variants of ENPP1 are associated with childhood and adult obesity and increase the risk of glucose intolerance and type 2 diabetes. Nat Genet, v. 37
    Doi: http://doi.org/10.1038/ng1604
  • Ghoussaini, M., Meyre, D., Lobbens, S., Charpentier, G., Clément, K., Charles, M-A., Tauber, M., Weill, J. and Froguel, P., 2005. Implication of the Pro12Ala polymorphism of the PPAR-gamma 2 gene in type 2 diabetes and obesity in the French population. BMC Med Genet, v. 6
    Doi: http://doi.org/10.1186/1471-2350-6-11
  • Conference proceedings

    2011

  • Ghoussaini, M., Ahmed, S., Michailidou, K., Gregory, K., Dicks, E., Driver, K., Pharoah, PD., Easton, DF. and Dunning, AM., 2011. Fine-Scale mapping of the 11q13 breast cancer susceptibility locus JOURNAL OF MEDICAL GENETICS, v. 48
  • 2010

  • Ghoussaini, M. and BCAC, , 2010. Fine-Scale mapping of breast cancer loci From tag SNP to causal variant JOURNAL OF MEDICAL GENETICS, v. 47
  • 2009

  • Stutzmann, F., Ghoussaini, M., Couturier, C., Marchand, M., Vatin, V., Corset, L., Lecoeur, C., Balkau, B., Horber, F., Driscoll, DJ., Goldstone, AP., Weill, J., Michaud, JL., Meyre, D. and Froguel, P., 2009. Loss-of-function mutations in SIM1 cause a specific form of Prader-Willi-like syndrome DIABETOLOGIA, v. 52