1983 …2023

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  • Apoptotic cell death in disease—Current understanding of the NCCD 2023

    Vitale, I., Pietrocola, F., Guilbaud, E., Aaronson, S. A., Abrams, J. M., Adam, D., Agostini, M., Agostinis, P., Alnemri, E. S., Altucci, L., Amelio, I., Andrews, D. W., Aqeilan, R. I., Arama, E., Baehrecke, E. H., Balachandran, S., Bano, D., Barlev, N. A., Bartek, J., Bazan, N. G., & 208 othersBecker, C., Bernassola, F., Bertrand, M. J. M., Bianchi, M. E., Blagosklonny, M. V., Blander, J. M., Blandino, G., Blomgren, K., Borner, C., Bortner, C. D., Bove, P., Boya, P., Brenner, C., Broz, P., Brunner, T., Damgaard, R. B., Calin, G. A., Campanella, M., Candi, E., Carbone, M., Carmona-Gutierrez, D., Cecconi, F., Chan, F. K. M., Chen, G. Q., Chen, Q., Chen, Y. H., Cheng, E. H., Chipuk, J. E., Cidlowski, J. A., Ciechanover, A., Ciliberto, G., Conrad, M., Cubillos-Ruiz, J. R., Czabotar, P. E., D’Angiolella, V., Daugaard, M., Dawson, T. M., Dawson, V. L., De Maria, R., De Strooper, B., Debatin, K. M., Deberardinis, R. J., Degterev, A., Del Sal, G., Deshmukh, M., Di Virgilio, F., Diederich, M., Dixon, S. J., Dynlacht, B. D., El-Deiry, W. S., Elrod, J. W., Engeland, K., Fimia, G. M., Galassi, C., Ganini, C., Garcia-Saez, A. J., Garg, A. D., Garrido, C., Gavathiotis, E., Gerlic, M., Ghosh, S., Green, D. R., Greene, L. A., Gronemeyer, H., Häcker, G., Hajnóczky, G., Hardwick, J. M., Haupt, Y., He, S., Heery, D. M., Hengartner, M. O., Hetz, C., Hildeman, D. A., Ichijo, H., Inoue, S., Jäättelä, M., Janic, A., Joseph, B., Jost, P. J., Kanneganti, T. D., Karin, M., Kashkar, H., Kaufmann, T., Kelly, G. L., Kepp, O., Kimchi, A., Kitsis, R. N., Klionsky, D. J., Kluck, R., Krysko, D. V., Kulms, D., Kumar, S., Lavandero, S., Lavrik, I. N., Lemasters, J. J., Liccardi, G., Linkermann, A., Lipton, S. A., Lockshin, R. A., López-Otín, C., Luedde, T., MacFarlane, M., Madeo, F., Malorni, W., Manic, G., Mantovani, R., Marchi, S., Marine, J. C., Martin, S. J., Martinou, J. C., Mastroberardino, P. G., Medema, J. P., Mehlen, P., Meier, P., Melino, G., Melino, S., Miao, E. A., Moll, U. M., Muñoz-Pinedo, C., Murphy, D. J., Niklison-Chirou, M. V., Novelli, F., Núñez, G., Oberst, A., Ofengeim, D., Opferman, J. T., Oren, M., Pagano, M., Panaretakis, T., Pasparakis, M., Penninger, J. M., Pentimalli, F., Pereira, D. M., Pervaiz, S., Peter, M. E., Pinton, P., Porta, G., Prehn, J. H. M., Puthalakath, H., Rabinovich, G. A., Rajalingam, K., Ravichandran, K. S., Rehm, M., Ricci, J. E., Rizzuto, R., Robinson, N., Rodrigues, C. M. P., Rotblat, B., Rothlin, C. V., Rubinsztein, D. C., Rudel, T., Rufini, A., Ryan, K. M., Sarosiek, K. A., Sawa, A., Sayan, E., Schroder, K., Scorrano, L., Sesti, F., Shao, F., Shi, Y., Sica, G. S., Silke, J., Simon, H. U., Sistigu, A., Stephanou, A., Stockwell, B. R., Strapazzon, F., Strasser, A., Sun, L., Sun, E., Sun, Q., Szabadkai, G., Tait, S. W. G., Tang, D., Tavernarakis, N., Troy, C. M., Turk, B., Urbano, N., Vandenabeele, P., Vanden Berghe, T., Vander Heiden, M. G., Vanderluit, J. L., Verkhratsky, A., Villunger, A., von Karstedt, S., Voss, A. K., Vousden, K. H., Vucic, D., Vuri, D., Wagner, E. F., Walczak, H., Wallach, D., Wang, R., Wang, Y., Weber, A., Wood, W., Yamazaki, T., Yang, H. T., Zakeri, Z., Zawacka-Pankau, J. E., Zhang, L., Zhang, H., Zhivotovsky, B., Zhou, W., Piacentini, M., Kroemer, G. & Galluzzi, L., May 2023, In: Cell death and differentiation. 30, 5, p. 1097-1154 58 p.

    Research output: Contribution to journalReview articlepeer-review

    Open Access
  • Atp7b-dependent choroid plexus dysfunction causes transient copper deficit and metabolic changes in the developing mouse brain

    Washington-Hughes, C. L., Roy, S., Seneviratne, H. K., Karuppagounder, S. S., Morel, Y., Jones, J. W., Zak, A., Xiao, T., Boronina, T. N., Cole, R. N., Bumpus, N. N., Chang, C. J., Dawson, T. M. & Lutsenko, S., Jan 10 2023, In: PLoS genetics. 19, 1, e1010558.

    Research output: Contribution to journalArticlepeer-review

    Open Access
  • Bi-allelic TTI1 variants cause an autosomal-recessive neurodevelopmental disorder with microcephaly

    Serey-Gaut, M., Cortes, M., Makrythanasis, P., Suri, M., Taylor, A. M. R., Sullivan, J. A., Asleh, A. N., Mitra, J., Dar, M. A., McNamara, A., Shashi, V., Dugan, S., Song, X., Rosenfeld, J. A., Cabrol, C., Iwaszkiewicz, J., Zoete, V., Pehlivan, D., Akdemir, Z. C., Roeder, E. R., & 29 othersLittlejohn, R. O., Dibra, H. K., Byrd, P. J., Stewart, G. S., Geckinli, B. B., Posey, J., Westman, R., Jungbluth, C., Eason, J., Sachdev, R., Evans, C. A., Lemire, G., VanNoy, G. E., O'Donnell-Luria, A., Mau-Them, F. T., Juven, A., Piard, J., Nixon, C. Y., Zhu, Y., Ha, T., Buckley, M. F., Thauvin, C., Essien Umanah, G. K., Van Maldergem, L., Lupski, J. R., Roscioli, T., Dawson, V. L., Dawson, T. M. & Antonarakis, S. E., Mar 2 2023, In: American journal of human genetics. 110, 3, p. 499-515 17 p.

    Research output: Contribution to journalArticlepeer-review

    Open Access
  • DNA Methylation Signature of Aging: Potential Impact on the Pathogenesis of Parkinson's Disease

    Yazar, V., Dawson, V. L., Dawson, T. M. & Kang, S. U., 2023, In: Journal of Parkinson's Disease. 13, 2, p. 145-164 20 p.

    Research output: Contribution to journalReview articlepeer-review

    Open Access