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20072024

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  • 2018

    Reconsidering the causality of TIA1 mutations in ALS

    van der Spek, R. A., van Rheenen, W., Pulit, S. L., Kenna, K. P., Ticozzi, N., Kooyman, M., Mclaughlin, R. L., Moisse, M., van Eijk, K. R., van Vugt, J. J. F. A., Iacoangeli, A., Andersen, P., Blair, I., de Carvalho, M., Chio, A., Corcia, P., Couratier, P., Drory, V. E., Glass, J. D., Hardiman, O., & 16 othersMora, J. S., Morrison, K. E., Mitne-Neto, M., Robberecht, W., Shaw, P. J., Panadés, M. P., van Damme, P., Silani, V., Gotkine, M., Weber, M., van Es, M. A., Landers, J. E., Al-Chalabi, A., van den Berg, L. H., Veldink, J. H. & Project MinE ALS Sequencing Consortium, 2 Jan 2018, In: Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 19, 1-2, p. 1-3 3 p.

    Research output: Contribution to journalEditorialpeer-review

    19 Citations (Scopus)