• Source: Scopus
  • Calculated based on no. of publications stored in Pure and citations from Scopus

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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 others, Mora, 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 journalEditorial

    9 Citations (Scopus)