Items where authors include "Simons, C."

Article

Jackson, A. orcid.org/0000-0002-3674-3960, Thaker, N. orcid.org/0009-0006-7025-8842, Blakes, A. orcid.org/0000-0002-0260-7020 et al. (20 more authors) (2025) Analysis of R-loop forming regions identifies RNU2-2 and RNU5B-1 as neurodevelopmental disorder genes. Nature Genetics, 57 (6). pp. 1362-1366. ISSN 1061-4036

Chen, Y. orcid.org/0000-0001-5593-6920, Dawes, R. orcid.org/0000-0003-2135-0117, Kim, H.C. orcid.org/0000-0001-5877-5456 et al. (116 more authors) (2024) De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome. Nature, 632. pp. 832-840. ISSN 0028-0836

Piena, M.A., Kroep, S., Simons, C. et al. (4 more authors) (2022) An innovative approach to modelling the optimal treatment sequence for patients with relapsing–remitting multiple sclerosis : implementation, validation, and impact of the decision-making approach. Advances in Therapy, 39 (2). pp. 892-908. ISSN 0741-238X