Treffer 1 - 20 von 21 für Suche 'Culver, J.P.', Suchdauer: 0,88s Treffer weiter einschränken
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    Rare germline copy number variants (CNVs) and breast cancer risk von Dennis, J., Tyrer, J.P., Walker, L.C., Michailidou, K., Dorling, L., Bolla, M.K., Andrulis, I.L., Anton-Culver, H., Arndt, V., Aronson, K.J., Freeman, L.E.B., Behrens, S., Benitez, J., Bermisheva, M., Bogdanova, N.V., Bojesen, S.E., Brenner, H., Castelao, J.E., Chenevix-Trench, G., Clarke, C.L., Collee, J.M., Cox, A., Cross, S.S., Czene, K., Dork, T., Dossus, L., Eliassen, A.H., Eriksson, M., Evans, D.G., Figueroa, J., Fletcher, O., Flyger, H., Fritschi, L., Gabrielson, M., Gago-Dominguez, M., Garcia-Closas, M., Giles, G.G., Gonzalez-Neira, A., Haiman, C.A., Hall, P., Hollestelle, A., Hoppe, R., Howell, A., Jager, A., Jakubowska, A., John, E.M., Johnson, N., Jones, M.E., Jung, A., Kaaks, R., Keeman, R., Kitahara, C.M., Ko, Y.D., Kosma, V.M., Koutros, S., Kraft, P., Kristensen, V.N., Kubelka-Sabit, K., Lacey, J.V., Larson, N.L., Linet, M., Ogrodniczak, A., Mannermaa, A., Manoukian, S., Margolin, S., Mavroudis, D., Milne, R.L., Murphy, R.A., Nevanlinna, H., Olson, J.E., Olsson, H., Perou, C.M., Peterlongo, P., Plaseska-Karanfilska, D., Rennert, G., Saloustros, E., Sandler, D.P., Sawyer, E.J., Schmidt, M.K., Schmutzler, R.K., Shibli, R., Smeets, A., Soucy, P., Southey, M.C., Taylor, J.A., Teras, L.R., Terry, M.B., Tomlinson, I., Troester, M.A., Truong, T., Vachon, C.M., Wendt, C., Winqvist, R., Wolk, A., Yang, X.H.R., Zheng, W., Ziogas, A., Simard, J., Dunning, A.M., Pharoah, P.D.P.

    Veröffentlicht in Communications Biology
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  14. 14

    Polygenic risk modeling for prediction of epithelial ovarian cancer risk von Dareng, E.O., Barnes, D.R., Jones, M.R., Andrulis, I.L., Anton-Culver, H., Arun, B.K., Augustinsson, A., Barkardottir, R.B., Beckmann, M.W., Bermisheva, M., Bjorge, L., Black, A., Bonanni, B., Buys, S.S., Caligo, M.A., Campbell, I., Cassingham, H., Chanock, S.J., Chiew, Y.E., Daly, M.B., Dao, F., Davies, E., Bois, A. du, Engel, C., Fasching, P.A., Flanagan, J.M., Machackova, E., Garber, J., Gensini, F., Godwin, A.K., Greene, M.H., Group, O.S., Hakansson, N., Hamann, U., Hartman, M., Hogdall, E., Hopper, J.L., Imyanitov, E.N., Jensen, A., John, E.M., Kang, D., Kelemen, L.E., Khusnutdinova, E., Kurian, A.W., Lambrechts, D., Leslie, G., Lester, J., Levine, D.A., Lu, K.H., Manoukian, S., Marks, J.R., May, T., McGuffog, L., McNeish, I.A., Menon, U., Modugno, F., Montagna, M., Munro, E., Yie, J.N.Y., Olbrecht, S., Olopade, O.I., Olsson, H., Parsons, M.T., Pedersen, I.S., Permuth, J.B., Peterlongo, P., Rantala, J., Sandler, D.P., Schmutzler, R.K., Song, H., Teixeira, M.R., Teo, S.H., BethTerry, M., Thomassen, M., Thomsen, L.C.V., Thull, D.L., Toland, A.E., Torres, D., Trabert, B., Travis, R., Tung, N., Tworoger, S.S., Valen, E., Altena, A.M. van, Nieuwenhuysen, E., Rensburg, E.J. van, Webb, P.M., Weinberg, C.R., Weitzel, J.N., White, E., Woo, Y.L., Wu, A.H., Yannoukakos, D., Zorn, K.K., Easton, D., Lawrenson, K., Monteiro, A.N., Cunningham, J., Goode, E.L., Berchuck, A.

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    A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers von Lush, M., Beesley, J., O'Mara, T.A., Dennis, J., Barnes, D.R., McGuffog, L., Leslie, G., Agata, S., Aittomaki, K., Andrulis, I.L., Anton-Culver, H., Aronson, K.J., Augustinsson, A., Barrowdale, D., Baynes, C., Bojesen, S.E., Borg, A., Brenner, H., Burwinkel, B., Buys, S.S., Chanock, S.J., Chung, W.K., Claes, K.B.M., Clarke, C.L., Conroy, D.M., Czene, K., Diez, O., Domchek, S.M., dos-Santos-Silva, I., Dwek, M., Evans, D.G., Friedman, E., Gapstur, S.M., Garber, J., Garcia-Closas, M., Garcia-Saenz, J.A., Gayther, S.A., Gehrig, A., Georgoulias, V., Goldgar, D.E., Hahnen, E., Hamann, U., He, W., Horcasitas, D.J., Imyanitov, E.N., Jager, A., James, P.A., Jensen, U.B., Jones, M.E., Kaaks, R., Kapoor, P.M., Karlan, B.Y., Kraft, P., Kurian, A.W., Marchand, L. le, Lester, J., Manoukian, S., Margolin, S., Martens, J.W.M., Mebirouk, N., Nathanson, K.L., Nevanlinna, H., Nielsen, F.C., O'Brien, K.M., Olopade, O.I., Ottini, L., Pedersen, I.S., Peterlongo, P., Pharoah, P.D.P., Poppe, B., Presneau, N., Pujana, M.A., Punie, K., Romero, A., Rossing, M., Schmidt, M.K., Scott, C., Sharma, P., Soucy, P., Steinsnyder, Z., Stone, J., Swerdlow, A., Toland, A.E., Trainer, A.H., Truong, T., Tung, N., Vega, A., Vijai, J., Weinberg, C.R., Weitzel, J.N., Wolk, A., Yang, X.H.R., Ziogas, A., Park, S.K., Thomassen, M., Offit, K., Schmutzler, R.K., Couch, F.J., Simard, J., Antoniou, A.C.

    Veröffentlicht in Nature Communications
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    Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes von Beesley, J., Soucy, P., Lemacon, A., Tyrer, J.P., Jiang, X., Alonso, M.R., Anton-Culver, H., Aronson, K.J., Arun, B.K., Auber, B., Balmana, J., Barrowdale, D., Bialkowska, K., Blanco, A.M., Blot, W., Bogdanova, N.V., Bosse, K., Brauch, H., Buys, S.S., Caligo, M.A., Carroll, J.S., Chung, W.K., Cross, S.S., Devilee, P., Dite, G.S., Dubois, S., Duran, M., Eriksson, M., Evans, D.G., Fletcher, O., Gabrielson, M., Gago-Dominguez, M., Gaudet, M.M., Glendon, G., Godwin, A.K., Gonzalez-Neira, A., Greene, M.H., Grip, M., Guenel, P., Hahnen, E., Haiman, C.A., Hall, P., Hamann, U., Hartman, M., Hollestelle, A., Isaacs, C., Iwasaki, M., Jakimovska, M., Jakubowska, A., James, P.A., Janavicius, R., Johnson, N., Jones, M.E., Karlan, B.Y., Kerin, M.J., Kirk, J., Kubelka-Sabit, K., Lubinski, J., MacInnis, R.J., Makalic, E., Mannermaa, A., Manoochehri, M., Manoukian, S., Matsuo, K., Maurer, T., Mayes, R., McLean, C., Meindl, A., Muir, K., Mulligan, A.M., Narod, S.A., Nassir, R., Nathanson, K.L., Nevanlinna, H., Nielsen, F.C., Nikitina-Zake, L., Olopade, O.I., Orr, N., Osorio, A., Pankratz, V.S., Park, S.K., Park-Simon, T.W., Paul, J., Peissel, B., Plaseska-Karanfilska, D., Prajzendanc, K., Prentice, R., Ramus, S.J., Rossing, M., Saloustros, E., Sanchez-Herrero, E., Sandler, D.P., Schurmann, P., Sharma, P., Shen, C.Y., Slavin, T.P., Smichkoska, S., Southey, M.C., Spurdle, A.B., Sutter, C.

    Veröffentlicht in Nature Genetics
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    Shared heritability and functional enrichment across six solid cancers von Jiang, X., Schumacher, F.R., Michailidou, K., Lesseur, C., Casey, G., Gaudet, M.M., Albanes, D., Andrew, A.S., Antoniou, A.C., Antonenkova, N.N., Berndt, S.I., Bickeboller, H., Boccia, S., Brauch, H., Brenton, J.D., Brook, M.N., Buchanan, D.D., Caligo, M.A., Cancel-Tassin, G., Cannon-Albright, L., Chan, A.T., Chang-Claude, J., Chanock, S.J., Cox, A., Cybulski, C., Devilee, P., Donovan, J.L., Dork, T., Duell, E.J., Dunning, A.M., Edlund, C.K., Ferris, R.L., Figueiredo, J.C., Ganz, P.A., Garber, J., Garcia-Saenz, J.A., Godwin, A.K., Goode, E.L., Gronberg, H., Hall, P., Hampe, J., Haugen, A., Hoffmeister, M., Hogdall, E., Houlston, R., Ingles, S.A., Jakubowska, A., Jenkins, M.A., Johansson, M., Joshi, A.D., Kaneva, R., Karlan, B.Y., Kuhl, T., Khusnutdinova, E., Knight, J.A., Kote-Jarai, Z., Koutros, S., Kupryjanczyk, J., Lacko, M., Lam, S., Lester, J., Li, L., Lindor, N.M., Margolin, S., May, T., Middha, P., Montagna, M., Moysich, K.B., Nevanlinna, H., Nielsen, F.C., Nussbaum, R.L., Offit, K., Olshan, A.F., Olsson, H., Phipps, A.I., Plaseska-Karanfilska, D., Prokofyeva, D., Stefansson, K., Raskin, L., Rennert, G., Risch, A., Rosenstein, B.S., Ruyck, K. de, Saloustros, E., Schleutker, J., Schmidt, M.K., Singer, C.F., Slattery, M.L., Sorensen, K.D., Swerdlow, A.J., Tangen, C.M., Taylor, J.A., Teixeira, M.R., Terry, M.B., Terry, K.L., Thibodeau, S.N., Thomassen, M., Tischkowitz, M., Townsend, P.A., Tung, N.

    Veröffentlicht in Nature Communications
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