Gill, O. N., Spencer, Y., Richard-Loendt, A., Kelly, C., Brown, D., Sinka, K., . . . Brandner, S. (2020). Prevalence in Britain of abnormal prion protein in human appendices before and after exposure to the cattle BSE epizootic. Acta Neuropathologica. doi:10.1007/s00401-020-02153-7

Louis, D. N., Wesseling, P., Brandner, S., Brat, D. J., Ellison, D. W., Giangaspero, F., . . . Rous, B. (2019). Data Sets for the Reporting of Tumors of the Central Nervous System. Arch Pathol Lab Med. doi:10.5858/arpa.2018-0565-OA

Rudge, P., Jaunmuktane, Z., Hyare, H., Ellis, M., Koltzenburg, M., Collinge, J., . . . Mead, S. (2019). Early neurophysiological biomarkers and spinal cord pathology in inherited prion disease. Brain. doi:10.1093/brain/awy358

Banerjee, G., Adams, M. E., Jaunmuktane, Z., Lammie, G. A., Turner, B., Wani, M., . . . Werring, D. J. (2019). Early onset cerebral amyloid angiopathy following childhood exposure to cadaveric dura. Annals of Neurology. doi:10.1002/ana.25407

Jaunmuktane, Z., Quaegebeur, A., Taipa, R., Mead, S., & Brandner, S. (2019). Human transmission of amyloid-beta cerebral amyloid angiopathy. Presented at: 120th Meeting of the British-Neuropathological-Society (BNS) / Developmental Neuropathology Symposium.

Brandner, S., & Jaunmuktane, Z. (2019). IDH mutant astrocytoma: biomarkers for prognostic stratification and the next frontiers. Neuropathology and Applied Neurobiology. doi:10.1111/nan.12521

Jaunmuktane, Z., Capper, D., Jones, D. T. W., Schrimpf, D., Sill, M., Dutt, M., . . . Brandner, S. (2019). Methylation array profiling of adult brain tumours: diagnostic outcomes in a large, single centre. Acta Neuropathol Commun, 7 (1), 24-?. doi:10.1186/s40478-019-0668-8

Zhang, Y., Pusch, S., Innes, J., Sidlauskas, K., Ellis, M., Lau, J., . . . Brandner, S. (2019). Mutant IDH Sensitizes Gliomas to Endoplasmic Reticulum Stress and Triggers Apoptosis via miR-183-Mediated Inhibition of Semaphorin 3E. Cancer Research. doi:10.1158/0008-5472.CAN-19-0054

Hou, Y., Pinheiro, J., Sahm, F., Reuss, D. E., Schrimpf, D., Stichel, D., . . . Bertero, L. (2019). Papillary glioneuronal tumor (PGNT) exhibits a characteristic methylation profile and fusions involving PRKCA. Acta Neuropathologica. doi:10.1007/s00401-019-01969-2

Sievers, P., Appay, R., Schrimpf, D., Stichel, D., Reuss, D. E., Wefers, A. K., . . . Jones, D. T. W. (2019). Rosette-forming glioneuronal tumors share a distinct DNA methylation profile and mutations in FGFR1, with recurrent co-mutation of PIK3CA and NF1. Acta Neuropathologica. doi:10.1007/s00401-019-02038-4