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Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer

S. Bojesen, K. Pooley, S. Johnatty, J. Beesley, K. Michailidou, J. Tyrer, S. Edwards, H. Pickett, H. Shen, C. Smart, K. Hillman, P. Mai, K. Lawrenson, M. Stutz, Y. Lu, R. Karevan, N. Woods, R. Johnston, J. French, X. Chen, M. Weischer, S. Nielsen, M. Maranian, M. Ghoussaini, S. Ahmed, C. Baynes, M. Bolla, Q. Wang, J. Dennis, L. McGuffog, D. Barrowdale, A. Lee, S. Healey, M. Lush, D. Tessier, D. Vincent, F. Bacot, I. Vergote, S. Lambrechts, E. Despierre, H. Risch, A. González-Neira, M. Rossing, G. Pita, J. Doherty, N. Alvarez, M. Larson, B. Fridley, N. Schoof, J. Chang-Claude, M. Cicek, J. Peto, K. Kalli, A. Broeks, S. Armasu, M. Schmidt, L. Braaf, B. Winterhoff, H. Nevanlinna, G. Konecny, D. Lambrechts, L. Rogmann, P. Guénel, A. Teoman, R. Milne, J. Garcia, A. Cox, V. Shridhar, B. Burwinkel, F. Marme, R. Hein, E. Sawyer, C. Haiman, S. Wang-Gohrke, I. Andrulis, K. Moysich, J. Hopper, K. Odunsi, A. Lindblom, G. Giles, H. Brenner, J. Simard, G. Lurie, P. Fasching, M. Carney, P. Radice, L. Wilkens, A. Swerdlow, M. Goodman, H. Brauch, M. Garcia-Closas, P. Hillemanns, R. Winqvist, M. Dürst, P. Devilee, I. Runnebaum, A. Jakubowska, J. Lubinski, A. Mannermaa, R. Butzow, N. Bogdanova, T. Dörk, L. Pelttari, W. Zheng, A. Leminen, H. Anton-Culver, C. Bunker, V. Kristensen, R. Ness, K. Muir, R. Edwards, A. Meindl, F. Heitz, K. Matsuo, A. Du Bois, A. Wu, P. Harter, S. Teo, I. Schwaab, X. Shu, W. Blot, S. Hosono, D. Kang, T. Nakanishi, M. Hartman, Y. Yatabe, U. Hamann, B. Karlan, S. Sangrajrang, S. Kjaer, V. Gaborieau, A. Jensen, D. Eccles, E. Høgdall, C. Shen, J. Brown, Y. Woo, M. Shah, Azmi, Mat Adenan Noor, R. Luben, S. Omar, K. Czene, R. Vierkant, B. Nordestgaard, H. Flyger, C. Vachon, J. Olson, X. Wang, D. Levine, A. Rudolph, R. Weber, D. Flesch-Janys, E. Iversen, S. Nickels, J. Schildkraut, Silva, Isabel Dos Santos, D. Cramer, L. Gibson, K. Terry, O. Fletcher, A. Vitonis, van der Schoot, C Ellen, E. Poole, Hogervorst, Frans B L, S. Tworoger, J. Liu, E. Bandera, J. Li, S. Olson, K. Humphreys, I. Orlow, C. Blomqvist, L. Rodriguez-Rodriguez, K. Aittomäki, H. Salvesen, T. Muranen, E. Wik, B. Brouwers, C. Krakstad, E. Wauters, M. Halle, H. Wildiers, L. Kiemeney, C. Mulot, K. Aben, P. Laurent-Puig, A. Altena, T. Truong, Massuger, Leon F A G, J. Benitez, T. Pejovic, Perez, Jose Ignacio Arias, M. Hoatlin, M. Zamora, L. Cook, S. Balasubramanian, L. Kelemen, A. Schneeweiss, N. Le, C. Sohn, A. Brooks-Wilson, I. Tomlinson, M. Kerin, N. Miller, C. Cybulski, B. Henderson, J. Menkiszak, F. Schumacher, N. Wentzensen, L. Le Marchand, H. Yang, A. Mulligan, G. Glendon, S. Engelholm, J. Knight, C. Høgdall, C. Apicella, M. Gore, H. Tsimiklis, H. Song, M. Southey, A. Jager, den Ouweland, Ans M Wvan, R. Brown, Martens, John W M, J. Flanagan, M. Kriege, J. Paul, S. Margolin, N. Siddiqui, G. Severi, A. Whittemore, L. Baglietto, V. McGuire, C. Stegmaier, W. Sieh, H. Müller, V. Arndt, F. Labrèche, Y. Gao, M. Goldberg, G. Yang, M. Dumont, J. McLaughlin, A. Hartmann, A. Ekici, M. Beckmann, C. Phelan, M. Lux, J. Permuth-Wey, B. Peissel, T. Sellers, F. Ficarazzi, M. Barile, A. Ziogas, A. Ashworth, A. Gentry-Maharaj, M. Jones, S. Ramus, N. Orr, U. Menon, C. Pearce, T. Brüning, M. Pike, Y. Ko, J. Lissowska, J. Figueroa, J. Kupryjanczyk, S. Chanock, A. Dansonka-Mieszkowska, A. Jukkola-Vuorinen, I. Rzepecka, K. Pylkäs, M. Bidzinski, S. Kauppila, A. Hollestelle, C. Seynaeve, Tollenaar, Rob A E M, K. Durda, K. Jaworska, J. Hartikainen, V. Kosma, V. Kataja, N. Antonenkova, J. Long, M. Shrubsole, S. Deming-Halverson, A. Lophatananon, P. Siriwanarangsan, S. Stewart-Brown, N. Ditsch, P. Lichtner, R. Schmutzler, H. Ito, H. Iwata, K. Tajima, C. Tseng, D. Stram, van den Berg, David, C. Yip, M. Ikram, Y. Teh, H. Cai, W. Lu, L. Signorello, Q. Cai, D. Noh, K. Yoo, H. Miao, P. Iau, Y. Teo, J. McKay, C. Shapiro, F. Ademuyiwa, G. Fountzilas, C. Hsiung, J. Yu, M. Hou, C. Healey, C. Luccarini, S. Peock, D. Stoppa-Lyonnet, P. Peterlongo, T. Rebbeck, M. Piedmonte, C. Singer, E. Friedman, M. Thomassen, K. Offit, Hansen, Thomas V O, S. Neuhausen, C. Szabo, I. Blanco, J. Garber, S. Narod, J. Weitzel, M. Montagna, E. Olah, A. Godwin, D. Yannoukakos, D. Goldgar, T. Caldes, E. Imyanitov, L. Tihomirova, B. Arun, I. Campbell, A. Mensenkamp, van Asperen, Christi J, van Roozendaal, Kees E P, H. Meijers-Heijboer, J. Collée, J. Oosterwijk, M. Hooning, M. Rookus, van der Luijt, Rob B, Os, Theo A Mvan, D. Evans, D. Frost, E. Fineberg, J. Barwell, L. Walker, M. Kennedy, R. Platte, R. Davidson, S. Ellis, T. Cole, B. Bressac-de Paillerets, B. Buecher, F. Damiola, L. Faivre, M. Frenay, O. Sinilnikova, O. Caron, S. Giraud, S. Mazoyer, V. Bonadona, V. Caux-Moncoutier, A. Toloczko-Grabarek, J. Gronwald, T. Byrski, A. Spurdle, B. Bonanni, D. Zaffaroni, G. Giannini, L. Bernard, R. Dolcetti, S. Manoukian, N. Arnold, C. Engel, H. Deissler, K. Rhiem, D. Niederacher, H. Plendl, C. Sutter, B. Wappenschmidt, A. Borg, B. Melin, J. Rantala, M. Soller, K. Nathanson, S. Domchek, G. Rodriguez, R. Salani, D. Kaulich, M. Tea, S. Paluch, Y. Laitman, A. Skytte, T. Kruse, U. Jensen, M. Robson, A. Gerdes, B. Ejlertsen, L. Foretova, S. Savage, J. Lester, P. Soucy, K. Kuchenbaecker, C. Olswold, J. Cunningham, S. Slager, V. Pankratz, E. Dicks, S. Lakhani, F. Couch, P. Hall, Monteiro, Alvaro N A, S. Gayther, Pharoah, Paul D P, R. Reddel, E. Goode, M. Greene, D. Easton, A. Berchuck, A. Antoniou, G. Chenevix-Trench, and A. Dunning. Nature genetics, 45 (4): 371-84, 384e1-2 (2013)

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Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers: implications for risk predictionA. Antoniou, J. Beesley, L. McGuffog, O. Sinilnikova, S. Healey, S. Neuhausen, Y. Ding, T. Rebbeck, J. Weitzel, H. Lynch and 168 other author(s). Cancer research, 70 (23): 9742–9754 (2010)Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European expertsVasen, Hans F A, I. Blanco, K. Aktan-Collan, J. Gopie, A. Alonso, S. Aretz, I. Bernstein, L. Bertario, J. Burn, G. Capella and 26 other author(s). Gut, 62 (6): 812–823 (2013)Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriersA. Antoniou, K. Kuchenbaecker, P. Soucy, J. Beesley, X. Chen, L. McGuffog, A. Lee, D. Barrowdale, S. Healey, O. Sinilnikova and 171 other author(s). Breast cancer research : BCR, 14 (1): R33 (2012)Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriersA. Antoniou, O. Sinilnikova, L. McGuffog, S. Healey, H. Nevanlinna, T. Heikkinen, J. Simard, A. Spurdle, J. Beesley, X. Chen and 127 other author(s). Human molecular genetics, 18 (22): 4442–4456 (2009)A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general populationA. Antoniou, X. Wang, Z. Fredericksen, L. McGuffog, R. Tarrell, O. Sinilnikova, S. Healey, J. Morrison, C. Kartsonaki, T. Lesnick and 168 other author(s). Nature genetics, 42 (10): 885–892 (2010)Key indicators for monitoring of audiovisual quality.M. Leszczuk, M. Hanusiak, I. Blanco, A. Dziech, J. Derkacz, E. Wyckens, and S. Borer. SIU, page 2301-2305. IEEE, (2014)Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriersD. Cox, J. Simard, D. Sinnett, Y. Hamdi, P. Soucy, M. Ouimet, L. Barjhoux, C. Verny-Pierre, L. McGuffog, S. Healey and 99 other author(s). Human molecular genetics, 20 (23): 4732–4747 (2011)Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriersA. Antoniou, C. Kartsonaki, O. Sinilnikova, P. Soucy, L. McGuffog, S. Healey, A. Lee, P. Peterlongo, S. Manoukian, B. Peissel and 169 other author(s). Human molecular genetics, 20 (16): 3304–3321 (2011)Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer riskF. Couch, X. Wang, L. McGuffog, A. Lee, C. Olswold, K. Kuchenbaecker, P. Soucy, Z. Fredericksen, D. Barrowdale, J. Dennis and 252 other author(s). PLoS genetics, 9 (3): e1003212 (2013)Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2A. Mulligan, F. Couch, D. Barrowdale, S. Domchek, D. Eccles, H. Nevanlinna, S. Ramus, M. Robson, M. Sherman, A. Spurdle and 172 other author(s). Breast cancer research : BCR, 13 (6): R110 (2011)

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Disambiguation of "Blanco, Ignacio"

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Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer

Please choose a person to relate this publication to

Ignacio Zubizarreta

Ignacio Cirac

Ignacio Rubio

Ignacio Avellino

Ignacio Sotelo

Other publications of authors with the same name

Disambiguation

BibSonomy

Disambiguation of "Blanco, Ignacio"

copydeleteadd this publication to your clipboardcommunity posthistory of this postURLDOIBibTeXEndNoteAPAChicagoDIN 1505HarvardMSOffice XML Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer

Please choose a person to relate this publication to

Ignacio Zubizarreta

Ignacio Cirac

Ignacio Rubio

Ignacio Avellino

Ignacio Sotelo

Other publications of authors with the same name

Disambiguation

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Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer