Zobrazeno 1 - 3
of 3
pro vyhledávání: '"van Roozendaal, Cornelis E P"'
Autor:
Antoniou, Antonis C, Sinilnikova, Olga M, McGuffog, Lesley, Healey, Sue, Nevanlinna, Heli, Heikkinen, Tuomas, Simard, Jacques, Spurdle, Amanda B, Beesley, Jonathan, Chen, Xiaoqing, Kathleen Cuningham Foundation Consortium, for Research into Familial Breast Cancer, Neuhausen, Susan L, Ding, Yuan C, Couch, Fergus J, Wang, Xianshu, Fredericksen, Zachary, Peterlongo, Paolo, Peissel, Bernard, Bonanni, Bernardo, Viel, Alessandra, Bernard, Loris, Radice, Paolo, Szabo, Csilla I, Foretova, Lenka, Zikan, Michal, Claes, Kathleen, Greene, Mark H, Mai, Phuong L, Rennert, Gad, Lejbkowicz, Flavio, Andrulis, Irene L, Ozcelik, Hilmi, Glendon, Gord, Group, OCGN, Gerdes, Anne-Marie, Thomassen, Mads, Sunde, Lone, Caligo, Maria A, Laitman, Yael, Kontorovich, Tair, Cohen, Shimrit, Kaufman, Bella, Dagan, Efrat, Baruch, Ruth Gershoni, Friedman, Eitan, Harbst, Katja, Barbany-Bustinza, Gisela, Rantala, Johanna, Ehrencrona, Hans, Karlsson, Per, Domchek, Susan M, Nathanson, Katherine L, Osorio, Ana, Blanco, Ignacio, Lasa, Adriana, Benítez, Javier, Hamann, Ute, Hogervorst, Frans B L, Rookus, Matti A, Collee, J Margriet, Devilee, Peter, Ligtenberg, Marjolijn J, van der Luijt, Rob B, Aalfs, Cora M, Waisfisz, Quinten, Wijnen, Juul, van Roozendaal, Cornelis E P, Group, HEBON, Peock, Susan, Cook, Margaret, Frost, Debra, Oliver, Clare, Platte, Radka, Evans, D Gareth, Lalloo, Fiona, Eeles, Rosalind, Izatt, Louise, Davidson, Rosemarie, Chu, Carol, Eccles, Diana, Cole, Trevor, Hodgson, Shirley, Group, EMBRACE, Godwin, Andrew K, Stoppa-Lyonnet, Dominique, Buecher, Bruno, Léoné, Mélanie, Bressac-de Paillerets, Brigitte, Remenieras, Audrey, Caron, Olivier, Lenoir, Gilbert M, Sevenet, Nicolas, Longy, Michel, Ferrer, Sandra Fert, Prieur, Fabienne, Group, GEMO, Goldgar, David, Miron, Alexander, John, Esther M, Buys, Saundra S, Daly, Mary B, Hopper, John L, Terry, Mary Beth, Yassin, Yosuf, Family Registry, Breast Cancer, Singer, Christian, Gschwantler-Kaulich, Daphne, Staudigl, Christine, Hansen, Thomas v O, Barkardottir, Rosa Bjork, Kirchhoff, Tomas, Pal, Prodipto, Kosarin, Kristi, Offit, Kenneth, Piedmonte, Marion, Rodriguez, Gustavo C, Wakeley, Katie, Boggess, John F, Basil, Jack, Schwartz, Peter E, Blank, Stephanie V, Toland, Amanda E, Montagna, Marco, Casella, Cinzia, Imyanitov, Evgeny N, Allavena, Anna, Schmutzler, Rita K, Versmold, Beatrix, Engel, Christoph, Meindl, Alfons, Ditsch, Nina, Arnold, Norbert, Niederacher, Dieter, Deissler, Helmut, Fiebig, Britta, Suttner, Christian, Schönbuchner, Ines, Gadzicki, Dorothea, Caldes, Trinidad, de la Hoya, Miguel, Pooley, Karen A, Easton, Douglas F, Chenevix-Trench, Georgia, Group, CIMBA
Publikováno v:
Antoniou, A C, Sinilnikova, O M, McGuffog, L, Healey, S, Nevanlinna, H, Heikkinen, T, Simard, J, Spurdle, A B, Beesley, J, Chen, X, Neuhausen, S L, Ding, Y, Couch, F J, Wang, X, Fredericksen, Z, Peterlongo, P, Peissel, B, Bonanni, B, Viel, A, Bernard, L, Radice, P, Szabo, C, Foretova, L, Zikan, M, Claes, K, Greene, M H, Mai, P L, Rennert, G, Lejbkowicz, F, Andrulis, I L, Ozcelik, H, Glendon, G, Gerdes, A M, Thomassen, M, Sunde, L, Caligo, M A, Laitman, Y, Kontorovich, T, Cohen, S J, Kaufman, B, Dagan, E, Baruch, R G, Friedman, E, Harbst, K, Barbany-Bustinza, G, Rantala, J, Ehrencrona, H, Karlsson, P S, Domchek, S M, Nathanson, K L, Osorio, A, Blanco, I, Lasa, A, Benitez, J, Hamann, U, Hogervorst, FB, Rookus, M A, Collee, J M, Devilee, P, Ligtenberg, M J L, van der Luijt, R, Aalfs, C M, Waisfisz, Q, Wijnen, J G, van Roozendaal, C E P, Peock, S, Cook, M, Frost, D, Oliver, C, Platte, R, Evans, D, Lalloo, F, Eeles, R, Izatt, L, Davidson, R, Chu, C, Eccles, D, Cole, T, Hodgson, SV, Godwin, A K, Stoppa-Lyonnet, D, Buecher, B, Leone, M, Bressac-de Paillerets, B, Remenieras, A, Caron, O, Lenoir, G M, Sevenet, N, Longy, M, Ferrer, S F, Prieur, F, Goldgar, D, Miron, A, John, E M, Buys, S G M & Daly, M 2009, ' Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers ', Human Molecular Genetics, vol. 18, no. 22, pp. 4442-4456 . https://doi.org/10.1093/hmg/ddp372
Human Molecular Genetics, 18(22), 4442-4456. Oxford University Press
Antoniou, A C, Sinilnikova, O M, McGuffog, L, Healey, S, Nevanlinna, H, Heikkinen, T, Simard, J, Spurdle, A B, Beesley, J, Chen, X, Kathleen Cuningham Foundation Consortium, F R I F B C, Neuhausen, S L, Ding, Y C, Couch, F J, Wang, X, Fredericksen, Z, Peterlongo, P, Peissel, B, Bonanni, B, Viel, A, Bernard, L, Radice, P, Szabo, C I, Foretova, L, Zikan, M, Claes, K, Greene, M H, Mai, P L, Rennert, G, Lejbkowicz, F, Andrulis, I L, Ozcelik, H, Glendon, G, Group, OCGN, Gerdes, A-M, Thomassen, M, Sunde, L, Caligo, M A, Laitman, Y, Kontorovich, T, Cohen, S, Kaufman, B, Dagan, E, Baruch, R G, Friedman, E, Harbst, K, Barbany-Bustinza, G, Rantala, J, Ehrencrona, H, Karlsson, P, Domchek, S M, Nathanson, K L, Osorio, A, Blanco, I, Lasa, A, Benítez, J, Hamann, U, Hogervorst, F B L, Rookus, M A, Collee, J M, Devilee, P, Ligtenberg, M J, van der Luijt, R B, Aalfs, C M, Waisfisz, Q, Wijnen, J, van Roozendaal, C E P, Group, HEBON, Peock, S, Cook, M, Frost, D, Oliver, C, Platte, R, Evans, D G, Lalloo, F, Eeles, R, Izatt, L, Davidson, R, Chu, C, Eccles, D, Cole, T, Hodgson, S, Group, EMBRACE, Godwin, A K, Stoppa-Lyonnet, D, Buecher, B, Léoné, M, Bressac-de Paillerets, B, Remenieras, A, Caron, O, Lenoir, G M, Sevenet, N, Longy, M, Ferrer, S F, Prieur, F, Group, GEMO, Goldgar, D, Miron, A, John, E M, Buys, S S, Daly, M B, Hopper, J L, Terry, M B, Yassin, Y, Family Registry, B C, Singer, C, Gschwantler-Kaulich, D, Staudigl, C, Hansen, T V O, Barkardottir, R B, Kirchhoff, T, Pal, P, Kosarin, K, Offit, K, 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 N, Allavena, A, Schmutzler, R K, Versmold, B, Engel, C, Meindl, A, Ditsch, N, Arnold, N, Niederacher, D, Deissler, H, Fiebig, B, Suttner, C, Schönbuchner, I, Gadzicki, D, Caldes, T, de la Hoya, M, Pooley, K A, Easton, D F, Chenevix-Trench, G & Group, CIMBA 2009, ' Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers ', Human Molecular Genetics, vol. 18, no. 22, pp. 4442-56 . https://doi.org/10.1093/hmg/ddp372
Antoniou, A C, Sinilnikova, O M, McGuffog, L, Healey, S, Nevanlinna, H, Heikkinen, T, Simard, J, Spurdle, A B, Beesley, J, Chen, X, Kathleen Cuningham Foundation Consortium for Research into Familial Breast Cancer, Neuhausen, S L, Ding, Y C, Couch, F J, Wang, X, Fredericksen, Z, Peterlongo, P, Peissel, B, Bonanni, B, Viel, A, Bernard, L, Radice, P, Szabo, C I, Foretova, L, Zikan, M, Claes, K, Greene, M H, Mai, P L, Rennert, G, Lejbkowicz, F, Andrulis, I L, Ozcelik, H, Glendon, G, OCGN, Gerdes, A-M, Thomassen, M, Sunde, L, Caligo, M A, Laitman, Y, Kontorovich, T, Cohen, S, Kaufman, B, Dagan, E, Baruch, R G, Friedman, E, Harbst, K, Barbany-Bustinza, G, Rantala, J, Ehrencrona, H, Karlsson, P, Domchek, S M, Nathanson, K L, HEBON, EMBRACE, GEMO, Breast Cancer Family Registry & CIMBA 2009, ' Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers ', Human Molecular Genetics, vol. 18, no. 22, pp. 4442-56 . https://doi.org/10.1093/hmg/ddp372
Human Molecular Genetics, 18, 22, pp. 4442-56
Human molecular genetics, 18(22), 4442-4456. Oxford University Press
Human Molecular Genetics, 18, 4442-56
Human Molecular Genetics, 18(22), 4442-4456. Oxford University Press
Antoniou, A C, Sinilnikova, O M, McGuffog, L, Healey, S, Nevanlinna, H, Heikkinen, T, Simard, J, Spurdle, A B, Beesley, J, Chen, X, Kathleen Cuningham Foundation Consortium, F R I F B C, Neuhausen, S L, Ding, Y C, Couch, F J, Wang, X, Fredericksen, Z, Peterlongo, P, Peissel, B, Bonanni, B, Viel, A, Bernard, L, Radice, P, Szabo, C I, Foretova, L, Zikan, M, Claes, K, Greene, M H, Mai, P L, Rennert, G, Lejbkowicz, F, Andrulis, I L, Ozcelik, H, Glendon, G, Group, OCGN, Gerdes, A-M, Thomassen, M, Sunde, L, Caligo, M A, Laitman, Y, Kontorovich, T, Cohen, S, Kaufman, B, Dagan, E, Baruch, R G, Friedman, E, Harbst, K, Barbany-Bustinza, G, Rantala, J, Ehrencrona, H, Karlsson, P, Domchek, S M, Nathanson, K L, Osorio, A, Blanco, I, Lasa, A, Benítez, J, Hamann, U, Hogervorst, F B L, Rookus, M A, Collee, J M, Devilee, P, Ligtenberg, M J, van der Luijt, R B, Aalfs, C M, Waisfisz, Q, Wijnen, J, van Roozendaal, C E P, Group, HEBON, Peock, S, Cook, M, Frost, D, Oliver, C, Platte, R, Evans, D G, Lalloo, F, Eeles, R, Izatt, L, Davidson, R, Chu, C, Eccles, D, Cole, T, Hodgson, S, Group, EMBRACE, Godwin, A K, Stoppa-Lyonnet, D, Buecher, B, Léoné, M, Bressac-de Paillerets, B, Remenieras, A, Caron, O, Lenoir, G M, Sevenet, N, Longy, M, Ferrer, S F, Prieur, F, Group, GEMO, Goldgar, D, Miron, A, John, E M, Buys, S S, Daly, M B, Hopper, J L, Terry, M B, Yassin, Y, Family Registry, B C, Singer, C, Gschwantler-Kaulich, D, Staudigl, C, Hansen, T V O, Barkardottir, R B, Kirchhoff, T, Pal, P, Kosarin, K, Offit, K, 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 N, Allavena, A, Schmutzler, R K, Versmold, B, Engel, C, Meindl, A, Ditsch, N, Arnold, N, Niederacher, D, Deissler, H, Fiebig, B, Suttner, C, Schönbuchner, I, Gadzicki, D, Caldes, T, de la Hoya, M, Pooley, K A, Easton, D F, Chenevix-Trench, G & Group, CIMBA 2009, ' Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers ', Human Molecular Genetics, vol. 18, no. 22, pp. 4442-56 . https://doi.org/10.1093/hmg/ddp372
Antoniou, A C, Sinilnikova, O M, McGuffog, L, Healey, S, Nevanlinna, H, Heikkinen, T, Simard, J, Spurdle, A B, Beesley, J, Chen, X, Kathleen Cuningham Foundation Consortium for Research into Familial Breast Cancer, Neuhausen, S L, Ding, Y C, Couch, F J, Wang, X, Fredericksen, Z, Peterlongo, P, Peissel, B, Bonanni, B, Viel, A, Bernard, L, Radice, P, Szabo, C I, Foretova, L, Zikan, M, Claes, K, Greene, M H, Mai, P L, Rennert, G, Lejbkowicz, F, Andrulis, I L, Ozcelik, H, Glendon, G, OCGN, Gerdes, A-M, Thomassen, M, Sunde, L, Caligo, M A, Laitman, Y, Kontorovich, T, Cohen, S, Kaufman, B, Dagan, E, Baruch, R G, Friedman, E, Harbst, K, Barbany-Bustinza, G, Rantala, J, Ehrencrona, H, Karlsson, P, Domchek, S M, Nathanson, K L, HEBON, EMBRACE, GEMO, Breast Cancer Family Registry & CIMBA 2009, ' Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers ', Human Molecular Genetics, vol. 18, no. 22, pp. 4442-56 . https://doi.org/10.1093/hmg/ddp372
Human Molecular Genetics, 18, 22, pp. 4442-56
Human molecular genetics, 18(22), 4442-4456. Oxford University Press
Human Molecular Genetics, 18, 4442-56
Contains fulltext : 81601.pdf (Publisher’s version ) (Closed access) Genome-wide association studies of breast cancer have identified multiple single nucleotide polymorphisms (SNPs) that are associated with increased breast cancer risks in the gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c41be362381a4c8c14eb137f64d605c0
https://doi.org/10.1093/hmg/ddp372
https://doi.org/10.1093/hmg/ddp372
Akademický článek
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Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers.
Autor:
Antoniou AC; Department of Public Health and Primary Care, Cancer Research UK Genetic Epidemiology Unit, University of Cambridge, Cambridge, UK. antonis@srl.cam.ac.uk, Sinilnikova OM, McGuffog L, Healey S, Nevanlinna H, Heikkinen T, Simard J, Spurdle AB, Beesley J, Chen X, Neuhausen SL, Ding YC, Couch FJ, Wang X, Fredericksen Z, Peterlongo P, Peissel B, Bonanni B, Viel A, Bernard L, Radice P, Szabo CI, Foretova L, Zikan M, Claes K, Greene MH, Mai PL, Rennert G, Lejbkowicz F, Andrulis IL, Ozcelik H, Glendon G, Gerdes AM, Thomassen M, Sunde L, Caligo MA, Laitman Y, Kontorovich T, Cohen S, Kaufman B, Dagan E, Baruch RG, Friedman E, Harbst K, Barbany-Bustinza G, Rantala J, Ehrencrona H, Karlsson P, Domchek SM, Nathanson KL, Osorio A, Blanco I, Lasa A, Benítez J, Hamann U, Hogervorst FB, Rookus MA, Collee JM, Devilee P, Ligtenberg MJ, van der Luijt RB, Aalfs CM, Waisfisz Q, Wijnen J, van Roozendaal CE, Peock S, Cook M, Frost D, Oliver C, Platte R, Evans DG, Lalloo F, Eeles R, Izatt L, Davidson R, Chu C, Eccles D, Cole T, Hodgson S, Godwin AK, Stoppa-Lyonnet D, Buecher B, Léoné M, Bressac-de Paillerets B, Remenieras A, Caron O, Lenoir GM, Sevenet N, Longy M, Ferrer SF, Prieur F, Goldgar D, Miron A, John EM, Buys SS, Daly MB, Hopper JL, Terry MB, Yassin Y, Singer C, Gschwantler-Kaulich D, Staudigl C, Hansen Tv, Barkardottir RB, Kirchhoff T, Pal P, Kosarin K, Offit K, Piedmonte M, Rodriguez GC, Wakeley K, Boggess JF, Basil J, Schwartz PE, Blank SV, Toland AE, Montagna M, Casella C, Imyanitov EN, Allavena A, Schmutzler RK, Versmold B, Engel C, Meindl A, Ditsch N, Arnold N, Niederacher D, Deissler H, Fiebig B, Suttner C, Schönbuchner I, Gadzicki D, Caldes T, de la Hoya M, Pooley KA, Easton DF, Chenevix-Trench G
Publikováno v:
Human molecular genetics [Hum Mol Genet] 2009 Nov 15; Vol. 18 (22), pp. 4442-56. Date of Electronic Publication: 2009 Aug 05.