Inge de Koning

A Mutation in the Fibroblast Growth Factor 14 Gene Is Associated with Autosomal Dominant Cerebral Ataxia

John C. van Swieten, Esther Brusse, Bianca M. de Graaf et al. · The American Journal of Human Genetics · 2003 · 291 citations · Full text

Mendelian Disorder, Brain Development, Genetic Disorder +7

The clinical and pathological phenotype of C9ORF72 hexanucleotide repeat expansions

Javier Simón‐Sánchez, Elise G.P. Dopper, Petra E. Cohn‐Hokke et al. · Brain · 2012 · 269 citations · Full text

Phenotypic variation in hereditary frontotemporal dementia with tau mutations

John C. van Swieten, M Stevens, Sonia M. Rosso et al. · Annals of Neurology · 1999 · 221 citations

Distinct genetic forms of frontotemporal dementia

Harro Seelaar, Wouter Kamphorst, Sonia M. Rosso et al. · Neurology · 2008 · 215 citations

CSF biomarkers in frontotemporal lobar degeneration with known pathology

H. Bian, John C. van Swieten, Susan Leight et al. · Neurology · 2008 · 213 citations · Full text