CARDIOLIPIN CONTENT OF WILD TYPE AND MUTANT YEASTS IN RELATION TO MITOCHONDRIAL FUNCTION AND DEVELOPMENT

por Jakovcic, S., Getz, G. S., Rabinowitz, M., Jakob, H., Swift, H.
Publicado 1971

Outcome signature genes in breast cancer: is there a unique set?

por Kela, I, Ein-Dor, L, Getz, G, Givol, D, Domany, E
Publicado 2005

Distinct mutational signatures characterize concurrent loss of polymerase proofreading and mismatch repair

por Haradhvala, N. J., Kim, J., Maruvka, Y. E., Polak, P., Rosebrock, D., Livitz, D., Hess, J. M., Leshchiner, I., Kamburov, A., Mouw, K. W., Lawrence, M. S., Getz, G.
Publicado 2018

Whole-genome sequencing reveals activation-induced cytidine deaminase signatures during indolent chronic lymphocytic leukaemia evolution

por Kasar, S., Kim, J., Improgo, R., Tiao, G., Polak, P., Haradhvala, N., Lawrence, M. S., Kiezun, A., Fernandes, S. M., Bahl, S., Sougnez, C., Gabriel, S., Lander, E. S., Kim, H. T., Getz, G., Brown, J. R.
Publicado 2015

Whole-exome sequencing of cell-free DNA and circulating tumor cells in multiple myeloma

por Manier, S., Park, J., Capelletti, M., Bustoros, M., Freeman, S. S., Ha, G., Rhoades, J., Liu, C. J., Huynh, D., Reed, S. C., Gydush, G., Salem, K. Z., Rotem, D., Freymond, C., Yosef, A., Perilla-Glen, A., Garderet, L., Van Allen, E. M., Kumar, S., Love, J. C., Getz, G., Adalsteinsson, V. A., Ghobrial, I. M.
Publicado 2018

Exome sequencing of pleuropulmonary blastoma reveals frequent biallelic loss of TP53 and two hits in DICER1 resulting in retention of 5p-derived miRNA hairpin loop sequences

por Pugh, T J, Yu, W, Yang, J, Field, A L, Ambrogio, L, Carter, S L, Cibulskis, K, Giannikopoulos, P, Kiezun, A, Kim, J, McKenna, A, Nickerson, E, Getz, G, Hoffher, S, Messinger, Y H, Dehner, L P, Roberts, C W M, Rodriguez-Galindo, C, Williams, G M, Rossi, C T, Meyerson, M, Hill, D A
Publicado 2014

Characterizing genomic alterations in cancer by complementary functional associations

por Kim, J. W., Botvinnik, O. B., Abudayyeh, O., Birger, C., Rosenbluh, J., Shrestha, Y., Abazeed, M. E., Hammerman, P. S., DiCara, D., Konieczkowski, D. J., Johannessen, C. M., Liberzon, A., Alizad-Rahvar, A. R., Alexe, G., Aguirre, A., Ghandi, M., Greulich, H., Vazquez, F., Weir, B. A., Van Allen, E. M., Tsherniak, A., Shao, D. D., Zack, T. I., Noble, M., Getz, G., Beroukhim, R., Garraway, L. A., Ardakani, M., Romualdi, C., Sales, G., Barbie, D. A., Boehm, J. S., Hahn, W. C., Mesirov, J. P., Tamayo, P.
Publicado 2016

P1282: DISEASE-SPECIFIC U1 SPLICEOSOMAL RNA MUTATIONS IN MATURE B-CELL NEOPLASMS

por Nadeu, F., Shuai, S., Clot, G., Hilton, L. K., Diaz-Navarro, A., Martín, S., Royo, R., Baumann, T., Kulis, M., López-Oreja, I., Cossio, M., Lu, J., Ljungström, V., Young, E., Plevova, K., Knisbacher, B. A., Lin, Z., Hahn, C. K., Bousquets, P., Alcoceba, M., González, M., Colado, E., Aymerich, M., Terol, M. J., Rivas-Delgado, A., Enjuanes, A., Ruiz-Gaspà, S., Chatzikonstantinou, T., Hägerstrand, D., Jylhä, C., Skaftason, A., Mansouri, L., Stranska, K., Doubek, M., van Gastel-Mol, E. J., Davis, Z., Walewska, R., Scarfò, L., Trentin, L., Visentin, A., Parikh, S. A., Rabe, K. G., Moia, R., Armand, M., Rossi, D., Davi, F., Gaidano, G., Kay, N. E., Shanafelt, T., Ghia, P., Oscier, D., Langerak, A. W., Beà, S., López-Guillermo, A., Neuberg, D., Wu, C. J., Getz, G., Pospisilova, S., Stamatopoulos, K., Rosenquist, R., Huber, W., Zenz, T., Colomer, D., Martín-Subero, J. I., Delgado, J., Morin, R. D., Stein, L. D., Puente, X. S., Campo, E.
Publicado 2022