학술논문

The predictive ability of the 313 variant–based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant
Document Type
Article
Author
Lakeman, I.M.M.Devilee, P.van Asperen, C.J.van Asperen, C.J.Schmidt, M.K.van den Broek, A.J.Vos, J.A.M.Barnes, D.R.Barrowdale, D.Perkins, J.Dennis, J.Frost, D.Leslie, G.McGuffog, L.Easton, D.F.Antoniou, A.C.Adlard, J.Andrulis, I.L.Glendon, G.Arason, A.Arnold, N.Arun, B.K.Balmaña, J.Benitez, J.Borg, A.Caldés, T.Caligo, M.A.Chung, W.K.Claes, K.B.M.Collée, J.M.van den Ouweland, A.M.W.Couch, F.J.Daly, M.B.Dhawan, M.Domchek, S.M.Nathanson, K.L.Eeles, R.Engel, C.Evans, D.G.Feliubadaló, L.Teulé, A.Foretova, L.Friedman, E.Ganz, P.A.Garber, J.Gayther, S.A.Gerdes, A.-M.Godwin, A.K.Goldgar, D.E.Hahnen, E.Schmutzler, R.K.Wappenschmidt, B.Hake, C.R.Hamann, U.Hogervorst, F.B.L.Adank, M.A.van der Kolk, L.E.Verhoef, S.Vogel, M.J.Kets, C.M.Hooning, M.J.Heemskerk-Gerritsen, B.A.M.Hollestelle, A.Jager, A.Kriege, M.Hopper, J.L.Phillips, K.-A.Hulick, P.J.Imyanitov, E.N.Isaacs, C.Izatt, L.Jakubowska, A.Lubiński, J.James, P.A.Janavicius, R.Jensen, U.B.Mebirouk, N.Jiao, Y.Lesueur, F.John, E.M.Joseph, V.Offit, K.Karlan, B.Y.Konstantopoulou, I.Kwong, A.Leroux, D.Legrand, C.Loud, J.T.Manoukian, S.Miller, A.Piedmonte, M.Gomes, D.M.Montagna, M.Belotti, M.Buecher, B.Caputo, S.Caux-Moncoutier, V.Colas, C.de Pauw, A.Elan, C.Gauthier-Villars, M.Golmard, L.Laurent, M.Saule, C.Mouret-Fourme, E.Stoppa-Lyonnet, D.Neuhausen, S.L.Nevanlinna, H.Yie, J.N.Y.Olah, E.Olopade, O.I.Park, S.K.Beesley, J.Holland, H.Spurdle, A.B.Parsons, M.T.Chenevix-Trench, G.Peterlongo, P.Radice, P.Rantala, J.Rennert, G.Risch, H.A.Sharma, P.Simard, J.Singer, C.F.Stadler, Z.Robson, M.Sutter, C.Tan, Y.Y.Teixeira, M.R.Teo, S.H.Thomassen, M.Thull, D.L.Tischkowitz, M.Toland, A.E.Tung, N.van Rensburg, E.J.Vega, A.Bernstein, J.L.Dunning, A.M.Harrington, P.A.Rookus, M.A.Fox, S.Ahmed, M.Barwell, J.Brady, A.Brennan, P.Brewer, C.Cook, J.Davidson, R.Donaldson, A.Eason, J.Eccles, D.M.Gregory, H.Hanson, H.Henderson, A.Hodgson, S.Kennedy, M.J.Lalloo, F.Miller, C.Morrison, P.J.Ong, K.-R.O’Shaughnessy-Kirwan, A.Porteous, M.E.Rogers, M.T.Side, L.E.Snape, K.Walker, L.Barouk-Simonet, E.Longy, M.Sevenet, N.Berthet, P.Castera, L.Bignon, Y.-J.Bonadona, V.Lasset, C.Bressac-de Paillerets, B.Caron, O.Collonge-Rame, M.-A.Coupier, I.Pujol, P.Delnatte, C.Faivre, L.Ferrer, S.F.Gesta, P.Giraud, S.Houdayer, C.Mari, V.Mazoyer, S.Mortemousque, I.Prieur, F.Schuster, H.Sobol, H.Sokolowska, J.Venat-Bouvet, L.Aalfs, C.M.Meijers-Heijboer, H.E.J.van Os, T.A.M.Ausems, M.G.E.M.Blok, M.J.Gómez Garcia, E.B.Koppert, L.B.Koudijs, M.van der Luijt, R.B.Mensenkamp, A.R.Mooij, T.M.van der Baan, F.H.Oosterwijk, J.C.van der Hout, A.H.van Deurzen, C.H.M.van Doorn, H.C.van Engelen, K.van Hest, L.P.Wijnen, J.T.Mulligan, A.M.
Source
In: Genetics in Medicine. (Genetics in Medicine, September 2021, 23(9):1726-1737)
Subject
Language
English
ISSN
15300366
10983600