학술논문

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학술논문
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'학술논문' 에서의 검색결과 56건 | 목록 20~30

  • 21 . Academic Journal
    No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer
    저자
    by Diether Lambrechts; Maren Weischer; Irene Konstantopoulou; Douglas F. Easton; Caroline Weltens, et al. 
    소스
    Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
    Consejería de Sanidad de la Comunidad de Madrid
    Digital.CSIC. Repositorio Institucional del CSIC
    Consejo Superior de Investigaciones Científicas (CSIC)
    instname
    Hollestelle, A, van der Baan, F H, Berchuck, A, Johnatty, S E, Aben, K K, Agnarsson, B A, Aittomäki, K, Alducci, E, Andrulis, I L, Anton-Culver, H, Antonenkova, N N, Antoniou, A C, Apicella, C, Arndt, V, Arnold, N, Arun, B K, Arver, B, Ashworth, A, Baglietto, L, Balleine, R, Bandera, E V, Barrowdale, D, Bean, Y T, Beckmann, L, Beckmann, M W, Benitez, J, Berger, A, Berger, R, Beuselinck, B, Bisogna, M, Bjorge, L, Blomqvist, C, Bogdanova, N V, Bojesen, A, Bojesen, S E, Bolla, M K, Bonanni, B, Brand, J S, Brauch, H, Brenner, H, Brinton, L, Brooks-Wilson, A, Bruinsma, F, Brunet, J, Brüning, T, Budzilowska, A, Bunker, C H, Burwinkel, B, Butzow, R, Pedersen, I S & Ovarian Cancer Association Consortium, Breast Cancer Association Consortium, and Consortium of Modifiers of BRCA1 and BRCA2 2016, ' No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer ', Gynecologic Oncology, vol. 141, no. 2, pp. 386-401 . https://doi.org/10.1016/j.ygyno.2015.04.034
    Gynecologic Oncology, 141, 2, pp. 386-401
    Ovarian Cancer Association Consortium, Breast Cancer Association Consortium, and Consortium of Modifiers of BRCA1 and BRCA2, Australian Ovarian Cancer Study Group, Breast Cancer Family Register, EMBRACE, GEMO Study Collaborators, GENICA Network, HEBON, kConFab Investigators & SWE-BRCA 2016, ' No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer ', Gynecologic Oncology, vol. 141, no. 2, pp. 386-401 . https://doi.org/10.1016/j.ygyno.2015.04.034
    Hollestelle, A, van der Baan, F H, Berchuck, A, Johnatty, S E, Aben, K K, Agnarsson, B A, Aittomäki, K, Alducci, E, Andrulis, I L, Anton-Culver, H, Antonenkova, N N, Antoniou, A C, Apicella, C, Arndt, V, Arnold, N, Arun, B K, Arver, B, Ashworth, A, Baglietto, L, Balleine, R, Bandera, E V, Barrowdale, D, Bean, Y T, Beckmann, L, Beckmann, M W, Benitez, J, Berger, A, Berger, R, Beuselinck, B, Bisogna, M, Bjorge, L, Blomqvist, C, Bogdanova, N V, Bojesen, A, Bojesen, S E, Bolla, M K, Bonanni, B, Brand, J S, Brauch, H, Brenner, H, Brinton, L, Brooks-Wilson, A, Bruinsma, F, Brunet, J, Brüning, T, Budzilowska, A, Bunker, C H, Burwinkel, B, Butzow, R, Jensen, U B & Ovarian Cancer Association Consortium, Breast Cancer Association Consortium, and Consortium of Modifiers of BRCA1 and BRCA2 2015, ' No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer ', Gynecologic Oncology . https://doi.org/10.1016/j.ygyno.2015.04.034
  • 27 . Academic Journal
    Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170
    저자
    by Caroline Seynaeve; Henrik Flyger; Manjeet K. Bolla; Cheng Har Yip; Gertraud Maskarinec, et al. 
    소스
    Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
    Consejería de Sanidad de la Comunidad de Madrid
    Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))
    Dipòsit Digital de la UB
    Universidad de Barcelona
    Recercat. Dipósit de la Recerca de Catalunya
    instname
    Nature Genetics, 48, 4, pp. 374-86
    Dunning, A M, Michailidou, K, Kuchenbaecker, K B, Thompson, D J, French, J D, Beesley, J, Healey, C S, Kar, S, Pooley, K A, Lopez-Knowles, E, Dicks, E, Barrowdale, D, Sinnott-Armstrong, N A, Sallari, R C, Hillman, K M, Kaufmann, S, Sivakumaran, H, Moradi Marjaneh, M, Lee, J S, Hills, M, Jarosz, M, Drury, S, Canisius, S, Bolla, M K, Dennis, J, Wang, Q, Hopper, J L, Southey, M C, Broeks, A, Schmidt, M K, Lophatananon, A, Muir, K, Beckmann, M W, Fasching, P A, Dos Santos Silva, I, Peto, J, Sawyer, E J, Tomlinson, I, Burwinkel, B, Marme, F, Guénel, P, Truong, T, Bojesen, S E, Flyger, H, González-Neira, A, Perez, J I A, Shen, C-Y, Hansen, T V O, Bojesen, A, Thomassen, M & EMBRACE 2016, ' Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170 ', Nature Genetics, vol. 48, no. 4, pp. 374-386 . https://doi.org/10.1038/ng.3521
    Dunning, A M, Michailidou, K, Kuchenbaecker, K B, Thompson, D, French, J D, Beesley, J, Healey, C S, Kar, S, Pooley, K A, Lopez-Knowles, E, Dicks, E, Barrowdale, D, Sinnott-Armstrong, N A, Sallari, R C, Hillman, K M, Kaufmann, S, Sivakumaran, H, Moradi Marjaneh, M, Lee, J S, Hills, M, Jarosz, M, Drury, S, Canisius, S, Bolla, M K, Dennis, J, Wang, Q, Hopper, J L, Southey, M C, Broeks, A, Schmidt, M K, Lophatananon, A, Muir, K, Beckmann, M W, Fasching, P A, Dos-Santos-Silva, I, Peto, J, Sawyer, E J, Tomlinson, I, Burwinkel, B, Marme, F, Guénel, P, Truong, T, Bojesen, S E, Flyger, H, González-Neira, A & Perez, J I A & Anton-Culver, H & Eunjung, L & Arndt, V & Figueroa, J 2016, ' Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170 ', Nature Genetics, vol. 48, no. 4, pp. 374-386 . https://doi.org/10.1038/ng.3521
  • 27 . Academic Journal
    Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer
    저자
    by Arndt Hartmann; Steve Ellis; Paolo Radice; Elizabeth M. Poole; Theo A. Mvan Os, et al. 
    소스
    Articles publicats en revistes (Patologia i Terapèutica Experimental)
    Dipòsit Digital de la UB
    instname
    Universidad de Barcelona
    Nature Genetics; Vol 45
    Nature Genetics
    Bojesen, S E, Pooley, K A, Johnatty, S E, Beesley, J, Michailidou, K, Tyrer, J P, Edwards, S L, Pickett, H A, Shen, H C, Smart, C E, Hillman, K M, Mai, P L, Lawrenson, K, Stutz, M D, Lu, Y, Karevan, R, Woods, N, Johnstonw, R L, French, J D, Chen, X Q, Weischer, M, Nielsen, S F, Maranian, M J, Ghoussaini, M, Ahmed, S, Baynes, C, Bolla, M K, Wang, Q, Dennis, J, McGuffog, L, Barrowdale, D, Lee, A, Healey, S, Lush, M, Tessier, D C, Vincent, D, Bacot, F, Vergote, I, Lambrechts, S, Despierre, E, Risch, H A, Gonzaalez-Neira, A, Rossing, M A, Pita, G, Doherty, J A, Alvarez, N, Larson, M C, Fridley, B L, Schoof, N, Chang-Claude, J, Cicek, M S, Peto, J, Kalli, K R, Broeks, A, Armasu, S M, Schmidt, M K, Braaf, L M, Winterhoff, B, Nevanlinna, H, Konecny, G E, Lambrechts, D, Rogmann, L, Guenel, P, Teoman, A, Milne, R L, Garcia, J J, Cox, A, Shridhar, V, Burwinkel, B, Marme, F, Hein, R, Sawyer, E J, Haiman, C A, Wang-Gohrke, S, Andrulis, I L, Moysich, K B, Hopper, J L, Odunsi, K, Lindblom, A, Giles, G G, Brenner, H, Simard, J, Lurie, G, Fasching, P A, Carney, M E, Radice, P, Wilkens, L R, Swerdlow, A, Goodman, M T, Brauch, H, Garcia-Closas, M, Hillemanns, P, Winqvist, R, Durst, M, Devilee, P, Runnebaum, I, Jakubowska, A, Lubinski, J, Mannermaa, A, Meijers-Heijboer, E J, Chenevix-Trench, G & Dunning, A M 2013, ' Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer ', Nature Genetics, vol. 45, no. 4, pp. 371-384 . https://doi.org/10.1038/ng.2566
    Nature Genetics, 45, 4, pp. 371-84
    Bojesen, S E, Pooley, K A, Johnatty, S E, Beesley, J, Michailidou, K, Tyrer, J P, Edwards, S L, Pickett, H A, Shen, H C, Smart, C E, Hillman, K M, Mai, P L, Lawrenson, K, Stutz, M D, Lu, Y, Karevan, R, Woods, N, Johnston, R L, French, J D, Chen, X, Weischer, M, Nielsen, S F, Maranian, M J, Ghoussaini, M, Ahmed, S, Baynes, C, Bolla, M K, Wang, Q, Dennis, J, McGuffog, L, Barrowdale, D, Lee, A R, Healey, S, Lush, M, Tessier, D C, Vincent, D, Bacot, F, Vergote, I, Lambrechts, S, Despierre, E, Risch, H A, González-Neira, A, Rossing, M A, Pita, G, Doherty, J A, Alvarez, N, Thomassen, M, Skytte, A B, Kruse, T A, Gerdes, A-M & Australian Cancer Study 2013, ' Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer ', Nature Genetics, vol. 45, no. 4, pp. 371-384 . https://doi.org/10.1038/ng.2566
    Bojesen, S E, Pooley, K A, Johnatty, S E, Beesley, J, Michailidou, K, Tyrer, J P, Edwards, S L, Pickett, H A, Shen, H C, Smart, C E, Hillman, K M, Mai, P L, Lawrenson, K, Stutz, M D, Lu, Y, Karevan, R, Woods, N, Johnston, R L, French, J D, Chen, X, Weischer, M, Nielsen, S F, Maranian, M J, Ghoussaini, M, Ahmed, S, Baynes, C, Bolla, M K, Wang, Q, Dennis, J, McGuffog, L, Barrowdale, D, Lee, A, Healey, S, Lush, M, Tessier, D C, Vincent, D, Bacot, F, Vergote, I, Lambrechts, S, Despierre, E, Risch, H A, González-Neira, A, Rossing, M A, Pita, G, Doherty, J A, Álvarez, N, Larson, M C, Fridley, B L, Schoof, N, Chang-Claude, J, Cicek, M S, Peto, J, Kalli, K R, Broeks, A, Armasu, S M, Schmidt, M K, Braaf, L M, Winterhoff, B, Nevanlinna, H, Konecny, G E, Lambrechts, D, Rogmann, L, Guénel, P, Teoman, A, Milne, R L, Garcia, J J, Cox, A, Shridhar, V, Burwinkel, B, Marme, F, Hein, R, Sawyer, E J, Haiman, C A, Wang-Gohrke, S, Andrulis, I L, Moysich, K B, Hopper, J L, Odunsi, K, Lindblom, A, Giles, G G, Brenner, H, Simard, J, Lurie, G, Fasching, P A, Carney, M E, Radice, P, Wilkens, L R, Swerdlow, A, Goodman, M T, Brauch, H, Garcia-Closas, M, Hillemanns, P, Winqvist, R, Dürst, M, Devilee, P, Runnebaum, I, Jakubowska, A, Lubinski, J, Mannermaa, A, Butzow, R, Bogdanova, N V, Dörk, T, Pelttari, L M, Zheng, W, Leminen, A, Anton-Culver, H, Bunker, C H, Kristensen, V, Ness, R B, Muir, K, Edwards, R, Meindl, A, Heitz, F, Matsuo, K, Du Bois, A, Wu, A H, Harter, P, Teo, S H, Schwaab, I, Shu, X O, Blot, W, Hosono, S, Kang, D, Nakanishi, T, Hartman, M, Yatabe, Y, Hamann, U, Karlan, B Y, Sangrajrang, S, Kjaer, S K, Gaborieau, V, Jensen, A, Eccles, D, Høgdall, E, Shen, C Y, Brown, J, Woo, Y L, Shah, M, Azmi, M A N, Luben, R, Omar, S Z, Czene, K, Vierkant, R A, Nordestgaard, B G, Flyger, H, Vachon, C, Olson, J E, Wang, X, Levine, D A, Rudolph, A, Weber, R P, Flesch-Janys, D, Iversen, E, Nickels, S, Schildkraut, J M, Silva, I D S, Cramer, D W, Gibson, L, Terry, K L, Fletcher, O, Vitonis, A F, Van Der Schoot, C E, Poole, E M, Hogervorst, F B L, Tworoger, S S, Liu, J, Bandera, E V, Li, J, Olson, S H, Humphreys, K, Orlow, I, Blomqvist, C, Rodriguez-Rodriguez, L, Aittomäki, K, Salvesen, H B, Muranen, T A, Wik, E, Brouwers, B, Krakstad, C, Wauters, E, Halle, M K, Wildiers, H, Kiemeney, L A, Mulot, C, Aben, K K, Laurent-Puig, P, Altena, A M, Truong, T, Massuger, L F A G, Benitez, J, Pejovic, T, Perez, J I A, Hoatlin, M, Zamora, M P, Cook, L S, Balasubramanian, S P, Kelemen, L E, Schneeweiss, A, Le, N D, Sohn, C, Brooks-Wilson, A, Tomlinson, I, Kerin, M J, Miller, N, Cybulski, C, Henderson, B E, Menkiszak, J, Schumacher, F, Wentzensen, N, Le Marchand, L, Yang, H P, Mulligan, A M, Glendon, G, Engelholm, S A, Knight, J A, Høgdall, C K, Apicella, C, Gore, M, Tsimiklis, H, Song, H, Southey, M C, Jager, A, Den Ouweland, A M W, Brown, R, Martens, J W M, Flanagan, J M, Kriege, M, Paul, J, Margolin, S, Siddiqui, N, Severi, G, Whittemore, A S, Baglietto, L, McGuire, V, Stegmaier, C, Sieh, W, Müller, H, Arndt, V, Labrèche, F, Gao, Y T, Goldberg, M S, Yang, G, Dumont, M, McLaughlin, J R, Hartmann, A, Ekici, A B, Beckmann, M W, Phelan, C M, Lux, M P, Permuth-Wey, J, Peissel, B, Sellers, T A, Ficarazzi, F, Barile, M, Ziogas, A, Ashworth, A, Gentry-Maharaj, A, Jones, M, Ramus, S J, Orr, N, Menon, U, Pearce, C L, Brüning, T, Pike, M C, Ko, Y D, Lissowska, J, Figueroa, J, Kupryjanczyk, J, Chanock, S J, Dansonka-Mieszkowska, A, Jukkola-Vuorinen, A, Rzepecka, I K, Pylkäs, K, Bidzinski, M, Kauppila, S, Hollestelle, A, Seynaeve, C, Tollenaar, R A E M, Durda, K, Jaworska, K, Hartikainen, J M, Kosma, V M, Kataja, V, Antonenkova, N N, Long, J, Shrubsole, M, Deming-Halverson, S, Lophatananon, A, Siriwanarangsan, P, Stewart-Brown, S, Ditsch, N, Lichtner, P, Schmutzler, R K, Ito, H, Iwata, H, Tajima, K, Tseng, C C, Stram, D O, Van Den Berg, D, Yip, C H, Ikram, M K, Teh, Y C, Cai, H, Lu, W, Signorello, L B, Cai, Q, Noh, D Y, Yoo, K Y, Miao, H, Iau, P T C, Teo, Y Y, McKay, J, Shapiro, C, Ademuyiwa, F, Fountzilas, G, Hsiung, C N, Yu, J C, Hou, M F, Healey, C S, Luccarini, C, Peock, S, Stoppa-Lyonnet, D, Peterlongo, P, Rebbeck, T R, Piedmonte, M, Singer, C F, Friedman, E, Thomassen, M, Offit, K, Hansen, T V O, Neuhausen, S L, Szabo, C I, Blanco, I, Garber, J, Narod, S A, Weitzel, J N, Montagna, M, Olah, E, Godwin, A K, Yannoukakos, D, Goldgar, D E, Caldes, T, Imyanitov, E N, Tihomirova, L, Arun, B K, Campbell, I, Mensenkamp, A R, Van Asperen, C J, Van Roozendaal, K E P, Meijers-Heijboer, H, Collée, J M, Oosterwijk, J C, Hooning, M J, Rookus, M A, Van Der Luijt, R B, Os, T A M, Evans, D G, Frost, D, Fineberg, E, Barwell, J, Walker, L, Kennedy, M J, Platte, R, Davidson, R, Ellis, S D, Cole, T, Bressac-De Paillerets, B, Buecher, B, Damiola, F, Faivre, L, Frenay, M, Sinilnikova, O M, Caron, O, Giraud, S, Mazoyer, S, Bonadona, V, Caux-Moncoutier, V, Toloczko-Grabarek, A, Gronwald, J, Byrski, T, Spurdle, A B, Bonanni, B, Zaffaroni, D, Giannini, G, Bernard, L, Dolcetti, R, Manoukian, S, Arnold, N, Engel, C, Deissler, H, Rhiem, K, Niederacher, D, Plendl, H, Sutter, C, Wappenschmidt, B, Borg, Å, Melin, B, Rantala, J, Soller, M, Nathanson, K L, Domchek, S M, Rodriguez, G C, Salani, R, Kaulich, D G, Tea, M K, Paluch, S S, Laitman, Y, Skytte, A B, Kruse, T A, Jensen, U B, Robson, M, Gerdes, A M, Ejlertsen, B, Foretova, L, Savage, S A, Lester, J, Soucy, P, Kuchenbaecker, K B, Olswold, C, Cunningham, J M, Slager, S, Pankratz, V S, Dicks, E, Lakhani, S R, Couch, F J, Hall, P, Monteiro, A N A, Gayther, S A, Pharoah, P D P, Reddel, R R, Goode, E L, Greene, M H, Easton, D F, Berchuck, A, Antoniou, A C, Chenevix-Trench, G, Dunning, A M, Dork, T, Hogdall, E, Silva Idos, S, Aittomaki, K, Hogdall, C K & Pylkas, K 2013, ' Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer ', Nature Genetics, vol. 45, no. 4, pp. 371-384 . https://doi.org/10.1038/ng.2566
    Bojesen, S E, Pooley, K A, Johnatty, S E, Beesley, J, Michailidou, K, Tyrer, J P, Edwards, S L, Pickett, H A, Shen, H C, Smart, C E, Hillman, K M, Mai, P L, Lawrenson, K, Stutz, M D, Lu, Y, Karevan, R, Woods, N, Johnston, R L, French, J D, Chen, X, Weischer, M, Nielsen, S F, Maranian, M J, Ghoussaini, M, Ahmed, S, Baynes, C, Bolla, M K, Wang, Q, Dennis, J, McGuffog, L, Barrowdale, D, Lee, A R, Healey, S, Lush, M, Tessier, D C, Vincent, D, Bacot, F, Vergote, I, Lambrechts, S, Despierre, E, Risch, H A, González-Neira, A, Rossing, M A, Pita, G, Doherty, J A, Alvarez, N, Jensen, A, Hansen, T V O, Skytte, A-B, Jensen, U B & Australian Cancer Study 2013, ' Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer ', Nature Genetics, vol. 45, no. 4, pp. 371-84 . https://doi.org/10.1038/ng.2566
  • 27 . Academic Journal
    Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 women
    저자
    by Dieter Niederacher; Beth Y. Karlan; Steve Ellis; Paolo Radice; Caroline Seynaeve, et al. 
    소스
    Breast Cancer Res
    Recercat. Dipósit de la Recerca de Catalunya
    instname
    Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
    Consejería de Sanidad de la Comunidad de Madrid
    Dipòsit Digital de la UB
    Universidad de Barcelona
    Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))
    Rebbeck, T R, Friebel, T M, Mitra, N, Wan, F, Chen, S, Andrulis, I L, Apostolou, P, Arnold, N, Arun, B K, Barrowdale, D, Benítez, J, Berger, R, Berthet, P, Borg, A, Buys, S, Caldes, T, Carter, J, Chiquette, J, Claes, K B M, Couch, F J, Cybulski, C, Daly, M B, de la Hoya, M, Díez, O, Domchek, S M, Nathanson, K L, Durda, K, Ellis, S, Evans, D G, Foretova, L, Friedman, E, Frost, D, Ganz, P A, Garber, J, Glendon, G, Godwin, A K, Greene, M H, Gronwald, J, Hahnen, E, Hallberg, E, Hamann, U, Imyanitov, E N, Isaacs, C, Jakubowska, A, Janavicius, R, Jaworska-Bieniek, K, John, E M, Karlan, B Y, Kaufman, B, Thomassen, M & EMBRACE 2016, ' Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 women ', Breast Cancer Research (Online), vol. 18, 112 . https://doi.org/10.1186/s13058-016-0768-3
    Rebbeck, T R, Friebel, T M, Mitra, N, Wan, F, Chen, S, Andrulis, I L, Apostolou, P, Arnold, N, Arun, B K, Barrowdale, D, Benitez, J, Berger, R, Berthet, P, Borg, A, Buys, S S, Caldes, T, Carter, J, Chiquette, J, Claes, K B M, Couch, F J, Cybulski, C, Daly, M B, de la Hoya, M, Diez, O, Domchek, S M, Nathanson, K L, Durda, K, Ellis, S, Evans, D G, Foretova, L, Friedman, E, Frost, D, Ganz, P A, Garber, J, Glendon, G, Godwin, A K, Greene, M H, Gronwald, J, Hahnen, E, Hallberg, E, Hamann, U, Hansen, T V O, Imyanitov, E N, Isaacs, C, Jakubowska, A, Janavicius, R, Jaworska-Bieniek, K, John, E M, Karlan, B Y, Kaufman, B & EMBRACE 2016, ' Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 women ', Breast Cancer Research, vol. 18, no. 1, pp. 112 . https://doi.org/10.1186/s13058-016-0768-3
    BREAST CANCER RESEARCH
  • 27 . Academic Journal
    Evaluation of chromosome 6p22 as a breast cancer risk modifier locus in a follow-up study of BRCA2 mutation carriers
    저자
    by Marion Piedmonte; Ute Hamann; Maria A. Caligo; Xianshu Wang; Douglas F. Easton, et al. 
    소스
    Stevens, K N, Wang, X, Fredericksen, Z, Pankratz, V S, Greene, M H, Andrulis, I L, Thomassen, M, Caligo, M, Nathanson, K L, Jakubowska, A, Osorio, A, Hamann, U, Godwin, A K, Stoppa-Lyonnet, D, Southey, M, Buys, S S, Singer, C F, Hansen, T V O, Arason, A, Offit, K, Piedmonte, M, Montagna, M, Imyanitov, E, Tihomirova, L, Sucheston, L, Beattie, M, Neuhausen, S L, Szabo, C I, Simard, J, Spurdle, A B, Healey, S, Chen, X, Rebbeck, T R, Easton, D F, Chenevix-Trench, G, Antoniou, A C, Couch, F J & Swedish Breast Cancer Study, Sweden (SWE-BRCA) 2012, ' Evaluation of chromosome 6p22 as a breast cancer risk modifier locus in a follow-up study of BRCA2 mutation carriers ', Breast Cancer Research and Treatment, vol. 136, no. 1, pp. 295-302 . https://doi.org/10.1007/s10549-012-2255-6
  • 27 . Academic Journal
    Common Variants at the 19p13.1 and ZNF365 Loci Are Associated with ER Subtypes of Breast Cancer and Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers
    저자
    by Javier Benitez; Finn Cilius Nielsen; Isabelle Coupier; Henry T. Lynch; Lesley McGuffog, et al. 
    소스
    Digital.CSIC. Repositorio Institucional del CSIC
    Consejo Superior de Investigaciones Científicas (CSIC)
    instname
    Cancer Epidemiology Biomarkers & Prevention; Vol 21
    Couch, F J, Gaudet, M M, Antoniou, A C, Ramus, S J, Kuchenbaecker, K B, Soucy, P, Beesley, J, Chen, X Q, Wang, X S, Kirchhoff, T, McGuffog, L, Barrowdale, D, Lee, A, Healey, S, Sinilnikova, O M, Andrulis, I L, Ozcelik, H, Mulligan, A M, Thomassen, M, Gerdes, A M, Jensen, U B, Skytte, A B, Kruse, T A, Caligo, M A, von Wachenfeldt, A, Barbany-Bustinza, G, Loman, N, Soller, M, Ehrencrona, H, Karlsson, P, Nathanson, K L, Rebbeck, T R, Domchek, S M, Jakubowska, A, Lubinski, J, Jaworska, K, Durda, K, Zlowocka, E, Huzarski, T, Byrski, T, Gronwald, J, Cybulski, C, Gorski, B, Osorio, A, Duran, M, Tejada, M I, Benitez, J, Hamann, U, Hogervorst, F B L, Os, T A, van Leeuwen, F E, Meijers-Heijboer, E J, van Wijnen, J, Blok, M J, Kets, M, Hooning, M J, Oldenburg, R A, Ausems, M G E M, Peock, S, Frost, D, Ellis, S D, Platte, R, Fineberg, E, Evans, D G, Jacobs, C, Eeles, R A, Adlard, J, Davidson, R, Eccles, D M, Cole, T, Cook, J, Paterson, J, Brewer, C, Douglas, F, Hodgson, SV, Morrison, P J, Walker, L, Porteous, M E, Kennedy, M J, Side, L E, Bove, B, Godwin, A K, Stoppa-Lyonnet, D, Fassy-Colcombet, M, Castera, L, Cornelis, F, Mazoyer, S, Leone, M, Boutry-Kryza, N, Bressac-de Paillerets, B, Caron, O, Pujol, P, Coupier, I, Delnatte, C, Akloul, L, Lynch, H T, Snyder, C L, Buys, S S & Daly, M B 2012, ' Common Variants at the 19p13.1 and ZNF365 Loci Are Associated with ER Subtypes of Breast Cancer and Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers ', Cancer Epidemiology Biomarkers and Prevention, vol. 21, no. 4, pp. 645-657 . https://doi.org/10.1158/1055-9965.EPI-11-0888
    Cancer Epidemiology, Biomarkers & Prevention, 21, 4, pp. 645-57
    Couch, F J, Gaudet, M M, Antoniou, A C, Ramus, S J, Kuchenbaecker, K B, Soucy, P, Beesley, J, Chen, X, Wang, X, Kirchhoff, T, McGuffog, L, Barrowdale, D, Lee, A, Healey, S, Sinilnikova, O M, Andrulis, I L, Ozcelik, H, Mulligan, A M, Thomassen, M, Gerdes, A-M, Jensen, U B, Skytte, A-B, Kruse, T A, Caligo, M A, von Wachenfeldt, A, Barbany-Bustinza, G, Loman, N, Soller, M, Ehrencrona, H, Karlsson, P, Nathanson, K L, Rebbeck, T R, Domchek, S M, Jakubowska, A, Lubinski, J, Jaworska, K, Durda, K, Zlowocka, E, Huzarski, T, Byrski, T, Gronwald, J, Cybulski, C, Górski, B, Osorio, A, Durán, M, Tejada, M I, Benitez, J, Hamann, U, Hogervorst, F B L, van Os, T A & OCGN 2012, ' Common variants at the 19p13.1 and ZNF365 loci are associated with ER subtypes of breast cancer and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers ', Cancer Epidemiology, Biomarkers & Prevention, vol. 21, no. 4, pp. 645-57 . https://doi.org/10.1158/1055-9965.EPI-11-0888
    Couch, F J, Gaudet, M M, Antoniou, A C, Ramus, S J, Kuchenbaecker, K B, Soucy, P, Beesley, J, Chen, X, Wang, X, Kirchhoff, T, McGuffog, L, Barrowdale, D, Lee, A, Healey, S, Sinilnikova, O M, Andrulis, I L, Ozcelik, H, Mulligan, A M, Thomassen, M, Gerdes, A M, Jensen, U B, Skytte, A B, Kruse, T A, Caligo, M A, Von Wachenfeldt, A, Barbany-Bustinza, G, Loman, N, Soller, M, Ehrencrona, H, Karlsson, P, Nathanson, K, Rebbeck, T R, Domchek, S M, Jakubowska, A, Lubinski, J, Jaworska, K, Durda, K, Zołwocka, E, Huzarski, T, Byrski, T, Gronwald, J, Cybulski, C, Goŕski, B, Osorio, A, Durań, M, Tejada, M I, Benitez, J, Hamann, U, Hogervorst, F B L, Van Os, T A, Van Leeuwen, F E, Meijers-Heijboer, H E J, Wijnen, J, Blok, M J, Kets, M, Hooning, M J, Oldenburg, R A, Ausems, M G E M, Peock, S, Frost, D, Ellis, S D, Platte, R, Fineberg, E, Evans, D G, Jacobs, C, Eeles, R A, Adlard, J, Davidson, R, Eccles, D M, Cole, T, Cook, J, Paterson, J, Brewer, C, Douglas, F, Hodgson, S V, Morrison, P J, Walker, L, Porteous, M E, Kennedy, M J, Side, L E, Bove, B, Godwin, A K, Stoppa-Lyonnet, D, Fassy-Colcombet, M, Castera, L, Cornelis, F, Mazoyer, S, Leóne, M, Boutry-Kryza, N, Bressac-de Paillerets, B, Caron, O, Pujol, P, Coupier, I, Delnatte, C, Akloul, L, Lynch, H T, Snyder, C L, Buys, S S, Daly, M B, Terry, M, Chung, W K, John, E M, Miron, A, Southey, M C, Hopper, J L, Goldgar, D E, Singer, C F, Rappaport, C, Tea, M K M, Fink-Retter, A, Hansen, T V O, Nielsen, F C, Arason, A, Vijai, J, Shah, S, Sarrel, K, Robson, M E, Piedmonte, M, Phillips, K, Basil, J, Rubinstein, W S, Boggess, J, Wakeley, K, Ewart-Toland, A, Montagna, M, Agata, S, Imyanitov, E N, Isaacs, C, Janavicius, R, Lazaro, C, Blanco, I, Feliubadalo, L, Brunet, J, Gayther, S A, Pharoah, P P D, Odunsi, K O, Karlan, B Y, Walsh, C S, Olah, E, Teo, S H, Ganz, P A, Beattie, M S, Van Rensburg, E J, Dorfling, C M, Diez, O, Kwong, A, Schmutzler, R K, Wappenschmidt, B, Engel, C, Meindl, A, Ditsch, N, Arnold, N, Heidemann, S, Niederacher, D, Preisler-Adams, S, Gadzicki, D, Varon-Mateeva, R, Deissler, H, Gehrig, A, Sutter, C, Kast, K, Fiebig, B, Heinritz, W, Caldes, T, De La Hoya, M, Muranen, T A, Nevanlinna, H, Tischkowitz, M D, Spurdle, A B, Neuhausen, S L, Ding, Y C, Lindor, N M, Fredericksen, Z, Pankratz, V S, Peterlongo, P, Manoukian, S, Peissel, B, Zaffaroni, D, Barile, M, Bernard, L, Viel, A, Giannini, G, Varesco, L, Radice, P, Greene, M H, Mai, P L, Easton, D F, Chenevix-Trench, G, Offit, K & Simard, J 2012, ' Common variants at the 19p13.1 and ZNF365 loci are associated with ER subtypes of breast cancer and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers ', Cancer Epidemiology Biomarkers and Prevention, vol. 21, no. 4, pp. 645-657 . https://doi.org/10.1158/1055-9965.EPI-11-0888
    Couch, F J, Gaudet, M M, Antoniou, A C, Ramus, S J, Kuchenbaecker, K B, Soucy, P, Beesley, J, Chen, X, Wang, X, Kirchhoff, T, McGuffog, L, Barrowdale, D, Lee, A R, Healey, S, Sinilnikova, O M, Andrulis, I L, Ozcelik, H, Mulligan, A M, Thomassen, M, Gerdes, A-M A, Jensen, U B, Skytte, A-B S, Kruse, T A, Caligo, M A, von Wachenfeldt, A, Barbany-Bustinza, G, Loman, N, Soller, M, Ehrencrona, H, Karlsson, P W, Nathanson, K L, Rebbeck, T R, Domchek, S M, Jakubowska, A, Lubinski, J, Jaworska, K, Durda, K, Zlowocka, E, Huzarski, T, Byrski, T, Gronwald, J, Cybulski, C, Górski, B, Osorio, A, Durán, M, Tejada, M I, Benitez, J, Hamann, U, Hogervorst, F B L, van Os, T A & OCGN 2012, ' Common variants at the 19p13.1 and ZNF365 loci are associated with ER subtypes of breast cancer and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers ', Cancer Epidemiology, Biomarkers & Prevention, vol. 21, no. 4, pp. 645-57 . https://doi.org/10.1158/1055-9965.EPI-11-0888
  • 27 . Academic Journal
    Ovarian cancer susceptibility alleles and risk of ovarian cancer inBRCA1andBRCA2mutation carriers
    저자
    by Susan J. Ramus; Antonis C. Antoniou; Karoline B. Kuchenbaecker; Penny Soucy; Jonathan Beesley, et al. 
    소스
    Recercat. Dipósit de la Recerca de Catalunya
    instname
    Articles publicats en revistes (Patologia i Terapèutica Experimental)
    Dipòsit Digital de la UB
    Universidad de Barcelona
    Human Mutation; Vol 33
    Human Mutation, 33, 4, pp. 690-702
    Human Mutation
    Human Mutation, Wiley, 2012, 33, pp.690-702. ⟨10.1002/humu.22025⟩
    Ramus, S J, Antoniou, A C, Kuchenbaecker, K B, Soucy, P, Beesley, J, Chen, X, McGuffog, L, Sinilnikova, O M, Healey, S, Barrowdale, D, Lee, A, Thomassen, M, Gerdes, A-M, Kruse, T A, Jensen, U B, Skytte, A-B, Caligo, M A, Liljegren, A, Lindblom, A, Olsson, H, Kristoffersson, U, Stenmark-Askmalm, M, Melin, B, Domchek, S M, Nathanson, K L, Rebbeck, T R, Jakubowska, A, Lubinski, J, Jaworska, K, Durda, K, Złowocka, E, Gronwald, J, Huzarski, T, Byrski, T, Cybulski, C, Toloczko-Grabarek, A, Osorio, A, Benitez, J, Duran, M, Tejada, M-I, Hamann, U, Rookus, M, van Leeuwen, F E, Aalfs, C M, Meijers-Heijboer, H E J, van Asperen, C J, van Roozendaal, K E P, Hoogerbrugge, N, Collée, J M, Kriege, M & SWE-BRCA 2012, ' Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers ', Human Mutation, vol. 33, no. 4, pp. 690-702 . https://doi.org/10.1002/humu.22025
    Evans, G, Ramus, S J, Antoniou, A C, Kuchenbaecker, K B, Soucy, P, Beesley, J, Chen, X, Mcguffog, L, Sinilnikova, O M, Healey, S, Barrowdale, D, Lee, A & Thomassen, M 2012, ' Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers ', Human Mutation, vol. 33, no. 4, pp. 690-702 . https://doi.org/10.1002/humu.22025
    Human Mutation, 2012, 33, pp.690-702. ⟨10.1002/humu.22025⟩
    Ramus, S J, Antoniou, A C, Kuchenbaecker, K B, Soucy, P, Beesley, J, Chen, X, McGuffog, L, Sinilnikova, O M, Healey, S, Barrowdale, D, Lee, A R, Thomassen, M, Gerdes, A-M A, Kruse, T A, Jensen, U B, Skytte, A-B S, Caligo, M A, Liljegren, A, Lindblom, A, Olsson, H, Kristoffersson, U, Stenmark-Askmalm, M, Melin, B, Domchek, S M, Nathanson, K L, Rebbeck, T R, Jakubowska, A, Lubinski, J, Jaworska, K, Durda, K, Złowocka, E, Gronwald, J, Huzarski, T, Byrski, T, Cybulski, C, Toloczko-Grabarek, A, Osorio, A, Benitez, J, Duran, M, Tejada, M-I, Hamann, U, Rookus, M, van Leeuwen, F E, Aalfs, C M, Meijers-Heijboer, H E J, van Asperen, C J, van Roozendaal, K E P, Hoogerbrugge, N, Collée, J M, Hansen, T V O & SWE-BRCA 2012, ' Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers ', Human Mutation, vol. 33, no. 4, pp. 690-702 . https://doi.org/10.1002/humu.22025
  • 27 . Academic Journal
    Common Breast Cancer Susceptibility Alleles and the Risk of Breast Cancer for BRCA1 and BRCA2 Mutation Carriers: Implications for Risk Prediction
    저자
    by Tomas Kirchhoff; Tomasz Huzarski; Esther M. John; Frans B. L. Hogervorst; Javier Godino, et al. 
    소스
    CANCER RESEARCH
    r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
    Institut d’Investigació Biomèdica Sant Pau (IIB Sant Pau)
    instname
    Antoniou, A C, Beesley, J, McGuffog, L, Sinilnikova, O M, Healey, S, Neuhausen, S L, Ding, Y C, Rebbeck, T R, Weitzel, J N, Lynch, H T, Isaacs, C, Ganz, P A, Tomlinson, G, Olopade, O I, Couch, F J, Wang, X S, Lindor, N M, Pankratz, V S, Radice, P, Manoukian, S, Peissel, B, Zaffaroni, D, Barile, M, Viel, A, Allavena, A, Dall'Olio, V, Peterlongo, P, Szabo, C I, Zikan, M, Claes, K, Poppe, B, Foretova, L, Mai, P L, Greene, M H, Rennert, G, Lejbkowicz, F, Glendon, G, Ozcelik, H, Andrulis, I L, Thomassen, M, Gerdes, A M, Sunde, L, Cruger, D, Jensen, U B, Caligo, M, Friedman, E, Kaufman, B, Laitman, Y, Milgrom, R, Dubrovsky, M, Cohen, S, Borg, A, Jernstrom, H, Lindblom, A, Rantala, J, Stenmark-Askmalm, M, Melin, B, Nathanson, K L, Domchek, S, Jakubowska, A, Lubinski, J, Huzarski, T, Osorio, A, Lasa, A, Duran, M, Tejada, M I, Godino, J, Benitez, J, Hamann, U, Kriege, M, Hoogerbrugge, N, van der Luijt, R B, van Asperen, C J, Devilee, P, Meijers-Heijboer, E J, Blok, M J, Aalfs, C M, Hogervorst, F, Rookus, M A, Cook, M, Oliver, C, Frost, D, Conroy, D, Evans, D G, Lalloo, F, Pichert, G, Davidson, R, Cole, T, Cook, J, Paterson, J, Hodgson, S, Morrison, P J, Porteous, M E, Walker, L, Kennedy, M J, Dorkins, H, Peock, S, Godwin, A K & Stoppa-Lyonnet, D A O 2010, ' Common Breast Cancer Susceptibility Alleles and the Risk of Breast Cancer for BRCA1 and BRCA2 Mutation Carriers: Implications for Risk Prediction ', Cancer Research, vol. 70, no. 23, pp. 9742-9754 . https://doi.org/10.1158/0008-5472.CAN-10-1907
    Cancer Research, 70, 23, pp. 9742-54
    Antoniou, A C, Beesley, J, McGuffog, L, Sinilnikova, O M, Healey, S, Neuhausen, S L, Ding, Y C, Rebbeck, T R, Weitzel, J N, Lynch, H T, Isaacs, C, Ganz, P A, Tomlinson, G, Olopade, O I, Couch, F J, Wang, X, Lindor, N M, Pankratz, V S, Radice, P, Manoukian, S, Peissel, B, Zaffaroni, D, Barile, M, Viel, A, Allavena, A, Dall'Olio, V, Peterlongo, P, Szabo, C I, Zikan, M, Claes, K, Poppe, B, Foretova, L, Mai, P L, Greene, M H, Rennert, G, Lejbkowicz, F, Glendon, G, Ozcelik, H, Andrulis, I L, Thomassen, M, Gerdes, A-M A, Sunde, L E M, Cruger, D, Jensen, U B, Caligo, M, Friedman, E, Kaufman, B, Laitman, Y, Milgrom, R, Dubrovsky, M & Ontario Cancer Genetics Network 2010, ' Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers: implications for risk prediction ', Cancer Research Institute Report, vol. 70, no. 23, pp. 9742-54 . https://doi.org/10.1158/0008-5472.CAN-10-1907
    Evans, G, Antoniou, A C, Beesley, J, McGuffog, L, Sinilnikova, O M, Healey, S, Neuhausen, S L, Ding, Y C, Rebbeck, T R, Weitzel, J N, Lynch, H T, Isaacs, C, Ganz, P A, Tomlinson, G, Olopade, O I, Couch, F J, Wang, X, Lindor, N M, Pankratz, V S, Radice, P, Manoukian, S, Peissel, B, Zaffaroni, D, Barile, M, Viel, A, Allavena, A, Dall'Olio, V, Peterlongo, P, Szabo, C I, Zikan, M, Claes, K, Poppe, B, Foretova, L, Mai, P L, Greene, M H, Rennert, G, Lejbkowicz, F, Glendon, G, Ozcelik, H, Andrulis, I L, Thomassen, M, Gerdes, A M, Sunde, L, Cruger, D, Jensen, U B, Caligo, M, Friedman, E, Kaufman, B, Laitman, Y, Milgrom, R, Dubrovsky, M, Cohen, S, Borg, A, Jernström, H, Lindblom, A, Rantala, J, Stenmark-Askmalm, M, Melin, B, Nathanson, K, Domchek, S, Jakubowska, A, Lubinski, J, Huzarski, T, Osorio, A, Lasa, A, Durán, M, Tejada, M I, Godino, J, Benitez, J, Hamann, U, Kriege, M, Hoogerbrugge, N, Van Der Luijt, R B, Van Asperen, C J, Devilee, P, Meijers-Heijboer, E J, Blok, M J, Aalfs, C M, Hogervorst, F, Rookus, M, Cook, M, Oliver, C, Frost, D, Conroy, D, Evans, D G, Lalloo, F, Pichert, G, Davidson, R, Cole, T, Cook, J, Paterson, J, Hodgson, S, Morrison, P J, Porteous, M E, Walker, L, Kennedy, M J, Dorkins, H, Peock, S, Godwin, A K, Stoppa-Lyonnet, D, De Pauw, A, Mazoyer, S, Bonadona, V, Lasset, C, Dreyfus, H, Leroux, D, Hardouin, A, Berthet, P, Faivre, L, Loustalot, C, Noguchi, T, Sobol, H, Rouleau, E, Nogues, C, Frénay, M, Vénat-Bouvet, L, Hopper, J L, Daly, M B, Terry, M B, John, E M, Buys, S S, Yassin, Y, Miron, A, Goldgar, D, Singer, C F, Dressler, A C, Gschwantler-Kaulich, D, Pfeiler, G, Hansen, T V O, Jnson, L, Agnarsson, B A, Kirchhoff, T, Offit, K, Devlin, V, Dutra-Clarke, A, Piedmonte, M, Rodriguez, G C, Wakeley, K, Boggess, J F, Basil, J, Schwartz, P E, Blank, S V, Toland, A E, Montagna, M, Casella, C, Imyanitov, E, Tihomirova, L, Blanco, I, Lazaro, C, Ramus, S J, Sucheston, L, Karlan, B Y, Gross, J, Schmutzler, R, Wappenschmidt, B, Engel, C, Meindl, A, Lochmann, M, Arnold, N, Heidemann, S, Varon-Mateeva, R, Niederacher, D, Sutter, C, Deissler, H, Gadzicki, D, Preisler-Adams, S, Kast, K, Schönbuchner, I, Caldes, T, De La Hoya, M, Aittomäki, K, Nevanlinna, H, Simard, J, Spurdle, A B, Holland, H, Chen, X, Platte, R, Chenevix-Trench, G & Easton, D F 2010, ' Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers: Implications for risk prediction ', Cancer Research, vol. 70, no. 23, pp. 9742-9754 . https://doi.org/10.1158/0008-5472.CAN-10-1907
    Antoniou, A C, Beesley, J, McGuffog, L, Sinilnikova, O M, Healey, S, Neuhausen, S L, Ding, Y C, Rebbeck, T R, Weitzel, J N, Lynch, H T, Isaacs, C, Ganz, P A, Tomlinson, G, Olopade, O I, Couch, F J, Wang, X, Lindor, N M, Pankratz, V S, Radice, P, Manoukian, S, Peissel, B, Zaffaroni, D, Barile, M, Viel, A, Allavena, A, Dall'olio, V, Peterlongo, P, Szabo, C I, Zikan, M, Claes, K, Poppe, B, Foretova, L, Mai, P L, Greene, M H, Rennert, G, Lejbkowicz, F, Glendon, G, Ozcelik, H, Andrulis, I L, for the Ontario Cancer Genetics Network, Thomassen, M, Gerdes, A-M, Sunde, L, Cruger, D, Birk Jensen, U, Caligo, M, Friedman, E, Kaufman, B, Laitman, Y, Milgrom, R, Dubrovsky, M, for SWE-BRCA, for HEBON, for EMBRACE, for GEMO, for GEMO, for the Breast Cancer Family Registry, for kConFab & on behalf of CIMBA 2010, ' Common Breast Cancer Susceptibility Alleles and the Risk of Breast Cancer for BRCA1 and BRCA2 Mutation Carriers: Implications for Risk Prediction ', Cancer Research, vol. 70, no. 23, pp. 9742-9754 . https://doi.org/10.1158/0008-5472.CAN-10-1907
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