Bennett, Craig L., and La Spada, Albert R. (2015) Unwinding the role of senataxin in neurodegeneration. Discovery Medicine, 19 (103). pp. 127-136.

Bennett, Craig L., Chen, Yingzhang, Vignali, Marissa, Lo, Russell S., Mason, Amanda G., Unal, Asli, Saifee, Nabiha P. Huq, Fields, Stanley, and La Spada, Albert R. (2013) Protein interaction analysis of senataxin and the ALS4 L389S mutant yields insights into senataxin post-translational modification and uncovers mutant-specific binding with a brain cytoplasmic RNA-encoded peptide. PLoS ONE, 8 (11). e78837. pp. 1-10.

Zhu, Hong, Guariglia, Sara, Yu, Raymond Y.L., Li, Wenjing, Brancho, Deborah, Peinado, Hector, Lyden, David, Salzer, James, Bennett, Craig, and Chow, Chi-Wing (2013) Mutation of SIMPLE in Charcot-Marie-Tooth 1C alters production of exosomes. Molecular Biology of the Cell, 24 (11). pp. 1619-1637.

Baird, Fiona J., and Bennett, Craig L. (2013) Microtubule defects and neurodegeneration. Journal of Genetic Syndromes & Gene Therapy, 4 (11). 1000203. pp. 1-7.

Chen, Yi-zhi, Gao, Qing, Zhao, Zue-zhi, Chen, Ying-zhang, Bennett, Craig L., Xiong, Xi-shan, Mei, Chang-lin , Shi, Yong-quan, and Chen, Xiang-mei (2010) Systematic review of TCF2 anomalies in renal cysts and diabetes syndrome/maturity onset diabetes of the young type 5. Chinese Medical Journal, 123 (22). pp. 3326-3333.

Chakrabarti, Lisa , Zahra, Rabaab, Jackson, Stephen M., Kazemi-Esfarjani, Parsa, Sopher, Bryce L., Mason, Amanda G., Toneff, Thomas , Ryu, Soyoung, Shaffer, Scott, Kansy, Janice W., Eng, Jeremiah, Merrihew, Gennifer, MacCoss, Michael J., Murphy, Anne, Goodlett, David R., Hook, Vivian, Bennett, Craig L., Pallanck, Leo J., and La Spada, Albert R. (2010) Mitochondrial dysfunction in NnaD mutant flies and Purkinje cell degeneration mice reveals a role for Nna proteins in neuronal bioenergetics. Neuron, 66 (6). pp. 835-847.

Travaglini, Lorena, Brancati, Francesco., Attie-Bitach, Tania, Audollent, Sophie, Bertini, Enrico, Kaplan, Josseline, Perrault, Isabelle, Iannicelli, Miriam, Mancuso, Brunella, Rigoli, Luciana, Rozet, Jean-Michel, Swistun, Dominika, Tolentino, Jerlyn, Dallapiccola, Bruno, Gleeson, Joseph G., Valente, Enza Maria, Zankl, A., Leventer, R., Grattan-Smith, P., Janecke, A., D'Hooghe, M., Sznajer, Y., Van Coster, R., Demerleir, L., Dias, K., Moco, C., Moreira, A., Ae Kim, C., Maegawa, G., Petkovic, D., Abdel-Salam, G.M.H., Abdel-Aleem, A., Zaki, M.S., Marti, I., Quijano-Roy, S., Sigaudy, S., De Lonlay, P., Romano, S., Touraine, R., Koenig, M., Lagier-Tourenne, C., Messer, J., Collignon, P., Wolf, N., Philippi, H., Kitsiou Tzeli, S., Halldorsson, S., Johannsdottir, J., Ludvigsson, P., Phadke, S.R., Udani, V., Stuart, B., Magee, A., Lev, D., Michelson, M., Ben-Zeev, B., Fischetto, R., Benedicenti, F., Stanzial, F., Borgatti, R., Accorsi, P., Battaglia, S., Fazzi, E., Giordano, L., Pinelli, L., Boccone, L., Bigoni, S., Ferlini, A., Donati, M.A., Caridi, G., Divizia, M.T., Faravelli, F., Ghiggeri, G., Pessagno, A., Briguglio, M., Briuglia, S., Salpietro, C.D., Tortorella, G., Adami, A., Castorina, P., Lalatta, F., Marra, G., Riva, D., Scelsa, B., Spaccini, L., Uziel, G., Del Giudice, E., Laverda, A.M., Ludwig, K., Permunian, A., Suppiej, A., Signorini, S., Uggetti, C., Battini, R., Di Giacomo, M., Cilio, M.R., Di Sabato, M.L., Leuzzi, V., Parisi, P., Pollazzon, M., Silengo, M., De Vescovi, R., Greco, D., Romano, C., Cazzagon, M., Simonati, A., Al-Tawari, A.A., Bastaki, L., Megabane, A., Sabolic Avramovska, V., De Jong, M.M., Stromme, P., Koul, R., Rajab, A., Azam, M., Barbot, C., Martorell Sampol, L., Rodriguez, B., Pascual-Castroviejo, I, Teber, S., Anlar, B., Comu, S., Karaca, E., Kayserili, H., Yuksel, A., Akcakus, M., Al Gazali, L., Sztriha, L., Nicholl, D., Woods, C.G., Bennett, Craig, Hurst, J., Sheridan, E., Barnicoat, A., Hennekam, R., Lees, M., Blair, E., Bernes, S., Sanchez, H., Clark, A.E., DeMarco, E., Donahue, C., Sherr, E., Hahn, J., Sanger, T.D., Gallager, T.E., Dobyns, W.B., Daugherty, C., Krishnamoorthy, K.S., Sarco, D., Walsh, C.A., McKanna, T., Milisa, J., Chung, W.K., De Vivo, D.C., Raynes, H., Schubert, R., Seward, A., Brooks, D.G., Goldstein, A., Caldwell, J., Finsecke, E., Maria, B.L., Holden, K., Cruse, R.P., Swoboda, K.J., and Viskochil, D. (2009) Expanding CEP290 mutational spectrumin ciliopathies. American Journal of Medical Genetics: Part A, 149 (10). pp. 2173-2180.

Bennett, Craig L., Chen, Yingzhang, Hahn, Sihoun, Glass, Ian A., and Gospe Jr, Sidney M. (2009) Prevalence of ALDH7A1 mutations in 18 North American pyridoxine-dependent seizure (PDS) patients. Epilepsia, 50 (5). pp. 1167-1175.