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Authors whose works are in public domain in at least one jurisdiction

List of works by Patrick Cras

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

scientific article

A comprehensive study of the genetic impact of rare variants in SORL1 in European early-onset Alzheimer's disease

scientific article published on 30 March 2016

A multicenter study of glucocerebrosidase mutations in dementia with Lewy bodies

scientific article published on June 2013

A systematic review comparing the diagnostic value of 14-3-3 protein in the cerebrospinal fluid, RT-QuIC and RT-QuIC on nasal brushing in sporadic Creutzfeldt-Jakob disease

scientific article published on 10 August 2018

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

scientific article published in October 2007

Alzheimer's disease and driving: review of the literature and consensus guideline from Belgian dementia experts and the Belgian road safety institute endorsed by the Belgian Medical Association

scientific article

Ataxin-2 polyQ expansions in FTLD-ALS spectrum disorders in Flanders-Belgian cohorts

scientific article published on 27 October 2011

Clinical Evidence of Disease Anticipation in Families Segregating a C9orf72 Repeat Expansion

scientific article published on 13 February 2017

Clinical features of TBK1 carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohort

scientific article published on 15 December 2015

Clinical variability and onset age modifiers in an extended Belgian GRN founder family

scientific article

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

Deleterious ABCA7 mutations and transcript rescue mechanisms in early onset Alzheimer's disease

scientific article published on 27 April 2017

Diagnostic performance of a CSF-biomarker panel in autopsy-confirmed dementia

scientific article published on 10 April 2007

Diagnostic value of cerebrospinal fluid tau, neurofilament, and progranulin in definite frontotemporal lobar degeneration

scientific article published on 20 March 2018

Distinct clinical characteristics of C9orf72 expansion carriers compared with GRN, MAPT, and nonmutation carriers in a Flanders-Belgian FTLD cohort

scientific article published in March 2013

Explorative genetic study of UBQLN2 and PFN1 in an extended Flanders-Belgian cohort of frontotemporal lobar degeneration patients

scientific article published on 9 January 2013

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

scientific article published on 24 March 2009

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

scientific article published in June 2008

Global investigation and meta-analysis of the C9orf72 (G4C2)n repeat in Parkinson disease

scientific article

Guanosine triphosphate cyclohydrolase 1 promoter deletion causes dopa-responsive dystonia

scientific article published on 13 September 2012

Identification of 2 Loci at chromosomes 9 and 14 in a multiplex family with frontotemporal lobar degeneration and amyotrophic lateral sclerosis

scientific article published in May 2010

Investigating the role of ALS genes CHCHD10 and TUBA4A in Belgian FTD-ALS spectrum patients

scientific article published on 21 December 2016

Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brains

scientific article published on 10 November 2015

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

scientific article published on 9 October 2013

Loss of DPP6 in neurodegenerative dementia: a genetic player in the dysfunction of neuronal excitability.

scientific article

Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohort

scientific article

Mutated CTSF in adult-onset neuronal ceroid lipofuscinosis and FTD.

scientific article published on 16 September 2016

Neuronal RNA oxidation is a prominent feature of familial Alzheimer's disease

scientific article published in October 2004

No added diagnostic value of non-phosphorylated tau fraction (p-taurel) in CSF as a biomarker for differential dementia diagnosis

scientific article

No association of CSF biomarkers with APOEepsilon4, plaque and tangle burden in definite Alzheimer's disease

scientific article published on 22 June 2007

No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patients

article

Phenotypic characteristics of Alzheimer patients carrying an ABCA7 mutation

scientific article published on April 2016

Rare Variants in PLD3 Do Not Affect Risk for Early-Onset Alzheimer Disease in a European Consortium Cohort

scientific article published on 28 September 2015

Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration

scientific article

Rare nonsynonymous variants in SORT1 are associated with increased risk for frontotemporal dementia

scientific article published on 17 February 2018

Redox metals and oxidative abnormalities in human prion diseases

scientific article published on 11 August 2005

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

scientific article published in July 2009

TBK1 Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis

scientific article published on 23 December 2016

TMEM106B is a genetic modifier of frontotemporal lobar degeneration with C9orf72 hexanucleotide repeat expansions

scientific article published on 19 January 2014

TMEM106B is associated with frontotemporal lobar degeneration in a clinically diagnosed patient cohort

scientific article

The genetics and neuropathology of frontotemporal lobar degeneration

scientific article published in September 2012