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European Journal of Human Genetics : EJHG|January 18, 2007
Progranulin mutations in Dutch familial frontotemporal lobar degenerationIraad F Bronner, Patrizia Rizzu, Harro Seelaar, et al.
Acta Neuropathologica Communications|April 16, 2016
C9orf72 is differentially expressed in the central nervous system and myeloid cells and consistently reduced in C9orf72, MAPT and GRN mutation carriersPatrizia Rizzu, Cornelis Blauwendraat, Sasja Heetveld, et al.
Neurobiology of Aging|November 3, 2015
Pilot whole-exome sequencing of a German early-onset Alzheimer's disease cohort reveals a substantial frequency of PSEN2 variantsCornelis Blauwendraat, Carlo Wilke, Iris E Jansen, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 1, 2008
Genotypic and phenotypic characteristics of Dutch patients with early onset Parkinson's diseaseMaria G Macedo, Dagmar Verbaan, Yue Fang, et al.
EJNMMI Research|October 17, 2012
Blood-brain barrier P-glycoprotein function in healthy subjects and Alzheimer's disease patients: effect of polymorphisms in the ABCB1 geneDaniëlle Me van Assema, Mark Lubberink, Patrizia Rizzu, et al.
Genome Medicine|June 12, 2016
Comprehensive promoter level expression quantitative trait loci analysis of the human frontal lobeCornelis Blauwendraat, Margherita Francescatto, J Raphael Gibbs, et al.
Cell Death & Disease|November 14, 2025
Chr:17q21.31 locus risk haplotype H1 susceptibility to ferroptosis is mediated by endolysosomal pathwayEldem Sadikoglou, Daniel Domingo-Fernández, Natalia Savytska, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 28, 2017
The wide genetic landscape of clinical frontotemporal dementia: systematic combined sequencing of 121 consecutive subjectsCornelis Blauwendraat, Carlo Wilke, Javier Simón-Sánchez, et al.
Annals of Neurology|January 6, 2004
DJ-1 colocalizes with tau inclusions: a link between parkinsonism and dementiaPatrizia Rizzu, David A Hinkle, Victoria Zhukareva, et al.
Molecular Neurobiology|January 6, 2019
Antisense Transcription in Loci Associated to Hereditary Neurodegenerative DiseasesSilvia Zucchelli, Stefania Fedele, Paolo Vatta, et al.
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