Combined risk factors for melanoma in a Mediterranean population

por Landi, M T, Baccarelli, A, Calista, D, Pesatori, A, Fears, T, Tucker, M A, Landi, G
Publicado 2001

A common founder for the V126D CDKN2A mutation in seven North American melanoma-prone families

por Goldstein, A M, Liu, L, Shennan, M G, Hogg, D, Tucker, M A, Struewing, J P
Publicado 2001

The debrisoquine metabolic phenotype and DNA-based assays: implications of misclassification for the association of lung cancer and the debrisoquine metabolic phenotype.

por Caporaso, N E, Shields, P G, Landi, M T, Shaw, G L, Tucker, M A, Hoover, R, Sugimura, H, Weston, A, Harris, C C
Publicado 1992

Mutation testing in melanoma families: INK4A, CDK4 and INK4D

por Newton Bishop, J A, Harland, M, Bennett, D C, Bataille, V, Goldstein, A M, Tucker, M A, Ponder, B A J, Cuzick, J, Selby, P, Bishop, D T
Publicado 1999

Breast cancer risk after radiotherapy for heritable and non-heritable retinoblastoma: a US–UK study

por Little, M P, Schaeffer, M L, Reulen, R C, Abramson, D H, Stovall, M, Weathers, R, de Vathaire, F, Diallo, I, Seddon, J M, Hawkins, M M, Tucker, M A, Kleinerman, R A
Publicado 2014

ASASSN-18ey: The Rise of a New Black-Hole X-ray Binary

por Tucker, M.A., Shappee, B.J., Holoien, T.W.-S., Auchettl, K., Strader, J., Stanek, K.Z., Kochanek, C.S., Bahramian, A., Dong, Subo, Prieto, J.L., Shields, J., Thompson, Todd A., Beacom, John F., Chomiuk, L., Denneau, L., Flewelling, H., Heinze, A.N., Smith, K.W., Stalder, B., Tonry, J.L., Weiland, H., Rest, A., Huber, M.E., Rowan, D.M., Dage, K.
Publicado 2018

Common genetic variants in the 9p21 region and their associations with multiple tumours

por Gu, F, Pfeiffer, R M, Bhattacharjee, S, Han, S S, Taylor, P R, Berndt, S, Yang, H, Sigurdson, A J, Toro, J, Mirabello, L, Greene, M H, Freedman, N D, Abnet, C C, Dawsey, S M, Hu, N, Qiao, Y-L, Ding, T, Brenner, A V, Garcia-Closas, M, Hayes, R, Brinton, L A, Lissowska, J, Wentzensen, N, Kratz, C, Moore, L E, Ziegler, R G, Chow, W-H, Savage, S A, Burdette, L, Yeager, M, Chanock, S J, Chatterjee, N, Tucker, M A, Goldstein, A M, Yang, X R
Publicado 2013

Association of MC1R Variants and Host Phenotypes With Melanoma Risk in CDKN2A Mutation Carriers: A GenoMEL Study

por Demenais, F., Mohamdi, H., Chaudru, V., Goldstein, A. M., Newton Bishop, J. A., Bishop, D. T., Kanetsky, P. A., Hayward, N. K., Gillanders, E., Elder, D. E., Avril, M. F., Azizi, E., van Belle, P., Bergman, W., Bianchi-Scarrà, G., Bressac-de Paillerets, B., Calista, D., Carrera, C., Hansson, J., Harland, M., Hogg, D., Höiom, V., Holland, E. A., Ingvar, C., Landi, M. T., Lang, J. M., Mackie, R. M., Mann, G. J., Ming, M. E., Njauw, C. J., Olsson, H., Palmer, J., Pastorino, L., Puig, S., Randerson-Moor, J., Stark, M., Tsao, H., Tucker, M. A., van der Velden, P., Yang, X. R., Gruis, N.
Publicado 2010

Germline ATM variants predispose to melanoma: a joint analysis across the GenoMEL and MelaNostrum consortia

por Dalmasso, B., Pastorino, L., Nathan, V., Shah, N. N., Palmer, J. M., Howlie, M., Johansson, P. A., Freedman, N. D., Carter, B. D., Beane-Freeman, L., Hicks, B., Molven, A., Helgadottir, H., Sankar, A., Tsao, H., Stratigos, A. J., Helsing, P., Van Doorn, R., Gruis, N. A., Visser, M., Wadt, K. A. W., Mann, G., Holland, E. A., Nagore, E., Potrony, M., Puig, S., Menin, C., Peris, K., Fargnoli, M. C., Calista, D., Soufir, N., Harland, M., Bishop, T., Kanetsky, P. A., Elder, D. E., Andreotti, V., Vanni, I., Bruno, W., Höiom, V., Tucker, M. A., Yang, X. R., Andresen, P. A., Adams, D. J., Landi, M. T., Hayward, N. K., Goldstein, A. M., Ghiorzo, P.
Publicado 2021