Radoslav Matěj

Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration

Julie van der Zee, Tim Van Langenhove, Gábor G. Kovács et al. · Acta Neuropathologica · 2014 · 113 citations · Full text

<i>TBK1</i> Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis

Julie van der Zee, Ilse Gijselinck, Sara Van Mossevelde et al. · Human Mutation · 2016 · 102 citations · Full text

Neurogenomics, Neurological Disorder, Genetics +28

Intensity of human prion disease surveillance predicts observed disease incidence

Genevieve M Klug, Handan Wand, Marion Simpson et al. · Journal of Neurology Neurosurgery & Psychiatry · 2013 · 75 citations · Full text

Deleterious ABCA7 mutations and transcript rescue mechanisms in early onset Alzheimer’s disease

Arne De Roeck, Tobi Van den Bossche, Julie van der Zee et al. · Acta Neuropathologica · 2017 · 73 citations · Full text

Relationship between ALS and the degree of cognitive impairment, markers of neurodegeneration and predictors for poor outcome. A prospective study

Robert Rusina, Petr Ridzoň, Petr Kulišťák et al. · European Journal of Neurology · 2009 · 58 citations