Stéphanie Philtjens

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

Investigating the role of rare heterozygous TREM2 variants in Alzheimer's disease and frontotemporal dementia

Elise Cuyvers, Karolien Bettens, Stéphanie Philtjens et al. · Neurobiology of Aging · 2013 · 188 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

Loss of <i>TBK1</i> is a frequent cause of frontotemporal dementia in a Belgian cohort

Ilse Gijselinck, Sara Van Mossevelde, Julie van der Zee et al. · Neurology · 2015 · 173 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

Contribution of rare homozygous and compound heterozygous VPS13C missense mutations to dementia with Lewy bodies and Parkinson’s disease

Stefanie Smolders, Stéphanie Philtjens, David Crosiers et al. · Acta Neuropathologica Communications · 2021 · 44 citations · Full text

Life Sciences, Genetics, Neurology +17