ASXL1 and DNMT3A mutation in a cytogenetically normal B3 thymoma

por Belani, R, Oliveira, G, Erikson, G A, Ra, S, Schechter, M S, Lee, J K, Shipman, W J, Haaser, S M, Torkamani, A
Publicado 2014

Large-scale pathway specific polygenic risk and transcriptomic community network analysis identifies novel functional pathways in Parkinson disease

por Bandres-Ciga, S., Saez-Atienzar, S., Kim, J. J., Makarious, M. B., Faghri, F., Diez-Fairen, M., Iwaki, H., Leonard, H., Botia, J., Ryten, M., Hernandez, D., Gibbs, J. R., Ding, J., Gan-Or, Z., Noyce, A., Pihlstrom, L., Torkamani, A., Soltis, A. R., Dalgard, C. L., Scholz, S. W., Traynor, B. J., Ehrlich, D., Scherzer, C. R., Bookman, M., Cookson, M., Blauwendraat, C., Nalls, M. A., Singleton, A. B.
Publicado 2020

Correction to: Large‑scale pathway specific polygenic risk and transcriptomic community network analysis identifies novel functional pathways in Parkinson disease

por Bandres-Ciga, S., Saez-Atienzar, S., Kim, J. J., Makarious, M. B., Faghri, F., Diez-Fairen, M., Iwaki, H., Leonard, H., Botia, J., Ryten, M., Hernandez, D., Gibbs, J. R., Ding, J., Gan-Or, Z., Noyce, A., Pihlstrom, L., Torkamani, A., Soltis, A. R., Dalgard, C. L., Scholz, S. W., Traynor, B. J., Ehrlich, D., Scherzer, C. R., Bookman, M., Cookson, M., Blauwendraat, C., Nalls, M. A., Singleton, A. B.
Publicado 2021

Evidence for the role of EPHX2 gene variants in anorexia nervosa

por Scott-Van Zeeland, A A, Bloss, C S, Tewhey, R, Bansal, V, Torkamani, A, Libiger, O, Duvvuri, V, Wineinger, N, Galvez, L, Darst, B F, Smith, E N, Carson, A, Pham, P, Phillips, T, Villarasa, N, Tisch, R, Zhang, G, Levy, S, Murray, S, Chen, W, Srinivasan, S, Berenson, G, Brandt, H, Crawford, S, Crow, S, Fichter, M M, Halmi, K A, Johnson, C, Kaplan, A S, La Via, M, Mitchell, J E, Strober, M, Rotondo, A, Treasure, J, Woodside, D B, Bulik, C M, Keel, P, Klump, K L, Lilenfeld, L, Plotnicov, K, Topol, E J, Shih, P B, Magistretti, P, Bergen, A W, Berrettini, W, Kaye, W, Schork, N J
Publicado 2014