Lubina Dillen

A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study

Ilse Gijselinck, Tim Van Langenhove, Julie van der Zee et al. · The Lancet Neurology · 2011 · 628 citations

Life Sciences, Genetics, Molecular Genetics +16

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 · 117 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

<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 · 103 citations · Full text

Life Sciences, Genetics, Neurology +17

Distinct Clinical Characteristics of C9orf72 Expansion Carriers Compared With GRN, MAPT, and Nonmutation Carriers in a Flanders-Belgian FTLD Cohort

Tim Van Langenhove, Julie van der Zee, Ilse Gijselinck et al. · JAMA Neurology · 2013 · 95 citations

Medicine, Genetics, Neurology +17

Plasma phosphorylated TDP-43 levels are elevated in patients with frontotemporal dementia carrying a C9orf72 repeat expansion or a GRN mutation

Marc Suárez‐Calvet, Oriol Dols‐Icardo, Albert Lladó et al. · Journal of Neurology Neurosurgery & Psychiatry · 2013 · 76 citations

Life Sciences, Neurology, Neuroscience +15