Christensen, J., Trabjerg, B. B., Wagner, R. G., Newton, C. R., Kwon, C.-S., Aaberg, K. M., Trinka, E., Wiebe, S., Cross, J. H., Vegrim, H. M., Vos, T., Steinmetz, J., & Dreier, J. W. (2024). Prevalence of epilepsy: a population-based cohort study in Denmark with comparison to Global Burden of Disease (GBD) prevalence estimates. Journal of Neurology, Neurosurgery & Psychiatry, 96(5), 480–488. https://doi.org/10.1136/jnnp-2024-334547

Goldberg, T. E., Lee, S., Devanand, D. P., & Schneider, L. S. (2023). Comparison of relative change with effect size metrics in Alzheimer’s disease clinical trials. Journal of Neurology, Neurosurgery & Psychiatry, 95(1), 2–7. https://doi.org/10.1136/jnnp-2023-331941

O’Connor, A., Rice, H., Barnes, J., Ryan, N. S., Liu, K. Y., Allegri, R. F., Berman, S., Ringman, J. M., Cruchaga, C., Farlow, M. R., Hassenstab, J., Lee, J.-H., Perrin, R. J., Xiong, C., Gordon, B., Levey, A. I., Goate, A., Graff-Radford, N., Levin, J., … Fox, N. C. (2022). First presentation with neuropsychiatric symptoms in autosomal dominant Alzheimer’s disease: the Dominantly Inherited Alzheimer’s Network Study. Journal of Neurology, Neurosurgery & Psychiatry, 94(5), 403–405. https://doi.org/10.1136/jnnp-2022-329843

Schiava, M., Ikenaga, C., Villar-Quiles, R. N., Caballero-Ávila, M., Topf, A., Nishino, I., Kimonis, V., Udd, B., Schoser, B., Zanoteli, E., Souza, P. V. S., Tasca, G., Lloyd, T., Lopez-de Munain, A., Paradas, C., Pegoraro, E., Nadaj-Pakleza, A., De Bleecker, J., Badrising, U., … Diaz-Manera, J. (2022). Genotype–phenotype correlations in valosin-containing protein disease: a retrospective muticentre study. Journal of Neurology, Neurosurgery & Psychiatry, 93(10), 1099–1111. https://doi.org/10.1136/jnnp-2022-328921

Grunseich, C., Sarkar, N., Lu, J., Owen, M., Schindler, A., Calabresi, P. A., Sumner, C. J., Roda, R. H., Chaudhry, V., Lloyd, T. E., Crawford, T. O., Subramony, S. H., Oh, S. J., Richardson, P., Tanji, K., Kwan, J. Y., Fischbeck, K. H., & Mankodi, A. (2021). Improving the efficacy of exome sequencing at a quaternary care referral centre: novel mutations, clinical presentations and diagnostic challenges in rare neurogenetic diseases. Journal of Neurology, Neurosurgery & Psychiatry, 92(11), 1186–1196. https://doi.org/10.1136/jnnp-2020-325437