University College London Hospitals (UCLH)

Spectral fingerprints or spectral tilt? Evidence for distinct oscillatory signatures of memory formation (2019) Fellner MC, Gollwitzer S, Rampp S, Kreiselmeyr G, Bush D, Diehl B, Axmacher N, et al. Journal article ICAR: endoscopic skull-base surgery (2019) Wang EW, Zanation AM, Gardner PA, Schwartz TH, Eloy JA, Adappa ND, Bettag M, et al. Journal article Machine learning in whole-body MRI: experiences and challenges from an applied study using multicentre data (2019) Lavdas , Glocker B, Rueckert D, Taylor SA, Aboagye EO, Rockall AG Journal article, Review article DNA methylation-based reclassification of olfactory neuroblastoma (2018) Capper D, Engel NW, Stichel D, Lechner M, Gloess S, Schmid S, Koelsche C, et al. Journal article Fumarate hydratase (FH) deficiency in uterine leiomyomas: recognition by histological features versus blind immunoscreening (2018) Siegler L, Erber R, Burghaus S, Brodkorb T, Wachter D, Wilkinson N, Bolton J, et al. Journal article Fully automatic, multiorgan segmentation in normal whole body magnetic resonance imaging (MRI), using classification forests (CFS), convolutional neural networks (CNNs), and a multi-atlas (MA) approach (2017) Lavdas I, Glocker B, Kamnitsas K, Rueckert D, Mair H, Sandhu A, Taylor SA, et al. Journal article The long-term course of temporal lobe epilepsy: From unilateral to bilateral interictal epileptiform discharges in repeated video-EEG monitorings (2017) Gollwitzer S, Scott CA, Farrell F, Bell GS, De Tisi J, Walker MC, Wehner T, et al. Journal article Preclinical transgenic and patient-derived xenograft models recapitulate the radiological features of human adamantinomatous craniopharyngioma (2017) Boult JK, Apps JR, Hölsken A, Hutchinson JC, Carreno G, Danielson LS, Smith LM, et al. Journal article Visual and semiautomated evaluation of epileptogenicity in focal cortical dysplasias - An intracranial EEG study (2016) Gollwitzer S, Valente I, Rodionov R, Scott C, Ritter LM, Wehner T, Hamer H, et al. Journal article Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia (2016) Meyer E, Carss KJ, Rankin J, Nichols JME, Grozeva D, Joseph AP, Mencacci NE, et al. Journal article