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List of works by Jessie Theuns

-Synuclein gene duplications in sporadic Parkinson disease

article

A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's disease

scientific article

A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants

scientific article

A multicenter study of glucocerebrosidase mutations in dementia with Lewy bodies

scientific article published on June 2013

A novel locus for dementia with Lewy bodies: a clinically and genetically heterogeneous disorder

scientific article

A novel presenilin 1 mutation associated with Pick's disease but not beta-amyloid plaques

scientific article

A pan-European study of the C9orf72 repeat associated with FTLD: geographic prevalence, genomic instability, and intermediate repeats

scientific article published on 4 January 2013

APP and BACE1 miRNA genetic variability has no major role in risk for Alzheimer disease.

scientific article

APP duplication is sufficient to cause early onset Alzheimer's dementia with cerebral amyloid angiopathy

scientific article

Alpha-synuclein repeat variants and survival in Parkinson's disease

scientific article

Alzheimer and Parkinson diagnoses in progranulin null mutation carriers in an extended founder family

scientific article published in October 2007

Alzheimer-associated C allele of the promoter polymorphism -22C>T causes a critical neuron-specific decrease of presenilin 1 expression

scientific article

Amyloid pathology influences aβ1-42 cerebrospinal fluid levels in dementia with lewy bodies

scientific article published in January 2013

Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study ⬇️

scientific article published on 30 August 2011

Comprehensive Genetic and Mutation Analysis of Familial Dementia with Lewy Bodies Linked to 2q35-q36

scientific article published on 01 January 2010

Contribution of VPS35 genetic variability to LBD in the Flanders-Belgian population

scientific article

DLB and PDD: a role for mutations in dementia and Parkinson disease genes?

scientific article published on 26 November 2011

GIGYF2 has no major role in Parkinson genetic etiology in a Belgian population

scientific article published on 24 March 2009

Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update

scientific article

Genetic risk and transcriptional variability of amyloid precursor protein in Alzheimer's disease

scientific article published on 24 August 2006

Genetic variability in the mitochondrial serine protease HTRA2 contributes to risk for Parkinson disease

scientific article published in June 2008

Genetic variant in the HSPB1 promoter region impairs the HSP27 stress response

scientific article

Guanosine triphosphate cyclohydrolase 1 promoter deletion causes dopa-responsive dystonia

scientific article published on 13 September 2012

High-density SNP haplotyping suggests altered regulation of tau gene expression in progressive supranuclear palsy

article

Intraneuronal amyloid beta and reduced brain volume in a novel APP T714I mouse model for Alzheimer's disease.

scientific article published on 16 November 2006

Juvenile dystonia-parkinsonism and dementia caused by a novel ATP13A2 frameshift mutation

scientific article published in February 2011

Large-scale assessment of polyglutamine repeat expansions in Parkinson disease

scientific article

Large-scale replication and heterogeneity in Parkinson disease genetic loci

scientific article

Linkage and association studies identify a novel locus for Alzheimer disease at 7q36 in a Dutch population-based sample

scientific article

Locus-specific mutation databases for neurodegenerative brain diseases

scientific article

Mean age-of-onset of familial alzheimer disease caused by presenilin mutations correlates with both increased Abeta42 and decreased Abeta40.

scientific article published in July 2006

Non-motor symptoms in a Flanders-Belgian population of 215 Parkinson's disease patients as assessed by the Non-Motor Symptoms Questionnaire ⬇️

scientific article published on July 23, 2012

Parkinson disease: insights in clinical, genetic and pathological features of monogenic disease subtypes

scientific article published on 26 July 2011

Population-specific frequencies for LRRK2 susceptibility variants in the Genetic Epidemiology of Parkinson's Disease (GEO-PD) Consortium

scientific article

Promoter mutations that increase amyloid precursor-protein expression are associated with Alzheimer disease

scientific article

Relative contribution of simple mutations vs. copy number variations in five Parkinson disease genes in the Belgian population

scientific article published in July 2009

Role of sepiapterin reductase gene at the PARK3 locus in Parkinson's disease

scientific article published on 22 July 2011

Tau is central in the genetic Alzheimer-frontotemporal dementia spectrum

scientific article

The gene encoding nicastrin, a major gamma-secretase component, modifies risk for familial early-onset Alzheimer disease in a Dutch population-based sample

scientific article

The genetics of dementia with Lewy bodies: what are we missing?

scientific article published on September 2012

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