Assessing biases of information contained in pedigrees for the classification of BRCA-genetic variants: a study arising from the ENIGMA analytical working group

por Kerkhofs, C. H. H., Spurdle, A. B., Lindsey, P. J., Goldgar, D. E., Gómez-García, E. B.
Publicado 2016

Efficiency of BRCAPRO and Myriad II mutation probability thresholds versus cancer history criteria alone for BRCA1/2 mutation detection

por van Harssel, J. J. T., van Roozendaal, C. E. P., Detisch, Y., Brandão, R. D., Paulussen, A. D. C., Zeegers, M., Blok, M. J., Gómez García, E. B.
Publicado 2009

Occult Breast Cancer due to Multiple Calcified Hamartomas in a Patient with Cowden Syndrome

por Gómez García, E. B., Lobbes, M. B. I., van de Vijver, K., Keymeulen, K., van der Ent, F., Yntema, H. G., Tjan-Heijnen, V. C., Boetes, C.
Publicado 2012

A white raven detected by imaging

por Baur, L.H.B., Schreurs, W.M.J., van Leeuwen-Wintjes, H.R., Berendsen, C.L., Willems, R., Winkens, R.A.G., Vliegen, R., Theunissen, P., Gomez Garcia, E.B.
Publicado 2015

Regular surveillance for Li-fraumeni syndrome: advice, adherence and perceived benefits

por Lammens, C. R. M., Bleiker, E. M. A., Aaronson, N. K., Wagner, A., Sijmons, R. H., Ausems, M. G. E. M., Vriends, A. H. J. T., Ruijs, M. W. G., van Os, T. A. M., Spruijt, L., Gómez García, E. B., Cats, A., Nagtegaal, T., Verhoef, S.
Publicado 2010

Colorectal cancer risk variants at 8q23.3 and 11q23.1 are associated with disease phenotype in APC mutation carriers

por Ghorbanoghli, Z., Nieuwenhuis, M. H., Houwing-Duistermaat, J. J., Jagmohan-Changur, S., Hes, F. J., Tops, C. M., Wagner, A., Aalfs, C. M., Verhoef, S., Gómez García, E. B., Sijmons, R. H., Menko, F. H., Letteboer, T. G., Hoogerbrugge, N., van Wezel, T., Vasen, H. F. A., Wijnen, J. T.
Publicado 2016