Výsledky vyhledávání - "Allavena, Anna"

Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers

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

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

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