Kevin Kenna

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Kevin Kenna

dr.

    • Heidelberglaan 100, UMC Utrecht

      3584 CX Utrecht

      Netherlands

    20112024

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    • Considerations in the search for epistasis

      Balvert, M., Cooper-Knock, J., Stamp, J., Byrne, R. P., Mourragui, S., van Gils, J., Benonisdottir, S., Schlüter, J., Kenna, K., Abeln, S., Iacoangeli, A., Daub, J. T., Browning, B. L., Taş, G., Hu, J., Wang, Y., Alhathli, E., Harvey, C., Pianesi, L. & Schulte, S. C. & 21 others, González-Domínguez, J., Garrisson, E., Pasanuic, B., Zhang, S., Vorbrugg, S., van Bemmelen, J., Dandinasivara, R., Markowska, M., Koyuturk, M., Guarracino, A., Bonizzoni, P., Bolognini, D., von Berg, J., Baaijens, J., Cartes, J. A., Al-Chalabi, A., Snyder, M. P., Schönhuth, A., Sng, L. M. F., Twine, N. A., 19 Nov 2024, In: Genome Biology. 25, 1, 296.

      Research output: Contribution to journal › Review article › peer-review

      Open Access
      File

    • Mechanism-free repurposing of drugs for C9orf72-related ALS/FTD using large-scale genomic data

      Saez-Atienzar, S., Souza, C. D. S., Chia, R., Beal, S. N., Lorenzini, I., Huang, R., Levy, J., Burciu, C., Ding, J., Gibbs, J. R., Jones, A., Dewan, R., Pensato, V., Peverelli, S., Corrado, L., van Vugt, J. J. F. A., van Rheenen, W., Tunca, C., Bayraktar, E. & Xia, M. & 4 others, 13 Nov 2024, In: Cell genomics. 4, 11, 100679.

      Research output: Contribution to journal › Article › Academic › peer-review

      Open Access
      File
      1 Downloads (Pure)

    • Rare and common genetic determinants of mitochondrial function determine severity but not risk of amyotrophic lateral sclerosis

      Harvey, C., Weinreich, M., Lee, J. A. K., Shaw, A. C., Ferraiuolo, L., Mortiboys, H., Zhang, S., Hop, P. J., Zwamborn, R. A. J., van Eijk, K., Julian, T. H., Moll, T., Iacoangeli, A., Al Khleifat, A., Quinn, J. P., Pfaff, A. L., Kõks, S., Poulton, J., Battle, S. L. & Arking, D. E. & 6 others, Snyder, M. P., Veldink, J. H., Kenna, K. P., Shaw, P. J., Cooper-Knock, J., 15 Feb 2024, In: Heliyon. 10, 3, e24975.

      Research output: Contribution to journal › Article › Academic › peer-review

      Open Access
      File

    • Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson’s disease

      Jul 2024, In: Nature Genetics. 56, 7, p. 1371-1376 6 p.

      Research output: Contribution to journal › Letter › Academic › peer-review

      Open Access
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    • Genetic variability in sporadic amyotrophic lateral sclerosis

      Van Daele, S. H., Moisse, M., van Vugt, J. J. F. A., Zwamborn, R. A. J., van der Spek, R., van Rheenen, W., Van Eijk, K., Kenna, K., Corcia, P., Vourc'h, P., Couratier, P., Hardiman, O., McLaughin, R., Gotkine, M., Drory, V., Ticozzi, N., Silani, V., Ratti, A., de Carvalho, M. & Mora Pardina, J. S. & 14 others, Povedano, M., Andersen, P. M., Weber, M., Başak, N. A., Shaw, C., Shaw, P. J., Morrison, K. E., Landers, J. E., Glass, J. D., van Es, M., van den Berg, L. H., Al-Chalabi, A., Veldink, J. & Van Damme, P., 1 Sept 2023, In: Brain : a journal of neurology. 146, 9, p. 3760-3769 10 p.

      Research output: Contribution to journal › Article › Academic › peer-review

      Open Access
      File
      14 Downloads (Pure)
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