L. Dillen

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TBK 1 Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis

F. Jessen, C. Broeckhoven, K. Sleegers, 2019 .

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

F. Jessen, G. Frisoni, B. Bergmans, 2017, Human mutation.

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

Giuliano Binetti, Alberto Lleó, Juan Fortea, 2016, Acta Neuropathologica.

Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration

F. Jessen, G. Frisoni, T. Strom, 2014, Acta Neuropathologica.

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

C. van Broeckhoven, S. Engelborghs, R. Vandenberghe, 2013, JAMA neurology.

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

B. Bergmans, C. van Broeckhoven, S. Engelborghs, 2018, Neurobiology of Aging.

Rapidly progressive frontotemporal dementia and bulbar amyotrophic lateral sclerosis in Portuguese patients with C9orf72 mutation

C. van Broeckhoven, M. de Carvalho, A. de Mendonça, 2013, Amyotrophic lateral sclerosis & frontotemporal degeneration.

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

P. Deyn, C. Broeckhoven, S. Engelborghs, 2013, Neurobiology of Aging.

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

S. Pereson, C. Broeckhoven, K. Sleegers, 2012, The Lancet Neurology.

No association of CpG SNP rs9357140 with onset age in Belgian C9orf72 repeat expansion carriers

P. Deyn, C. Broeckhoven, K. Sleegers, 2020, Neurobiology of Aging.

A Pan-European Study of the C9orf72 Repeat Associated with FTLD: Geographic Prevalence, Genomic Instability, and Intermediate Repeats

F. Jessen, G. Frisoni, K. Sleegers, 2012, Human mutation.

Elimination of micronucleated cells by apoptosis after treatment with inhibitors of microtubules.

M. Kirsch‐Volders, I. Decordier, E. Cundari, 2002, Mutagenesis.

C9orf72 G4C2 repeat expansions in Alzheimer's disease and mild cognitive impairment

P. Deyn, C. Broeckhoven, K. Sleegers, 2013, Neurobiology of Aging.

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

Patrick Santens, Mathieu Vandenbulcke, Adrian Ivanoiu, 2015, Acta neuropathologica communications.

Sporadic Creutzfeldt-Jakob Disease and Other Proteinopathies in Comorbidity

C. van Broeckhoven, J. van der Zee, R. Rusina, 2020, Frontiers in Neurology.

Outcome of very old patients admitted to the ICU for sepsis: A systematic review

M. Hamaker, D. Dijk, L. Haas, 2017 .

C9orf72 G4C2 repeat expansions in Alzheimer's disease and mild cognitive impairment

P. Deyn, C. Broeckhoven, K. Sleegers, 2013, Neurobiology of Aging.

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

M. Tsolaki, K. Sleegers, C. van Broeckhoven, 2017, Acta Neuropathologica.

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

G. Frisoni, C. Broeckhoven, S. Engelborghs, 2018, Neurobiology of Aging.

Common and rare TBK1 variants in early-onset Alzheimer disease in a European cohort

C. Broeckhoven, M. Tsolaki, K. Sleegers, 2018, Neurobiology of Aging.

NEK1 genetic variability in a Belgian cohort of ALS and ALS-FTD patients

C. Broeckhoven, S. Engelborghs, R. Vandenberghe, 2018, Neurobiology of Aging.

Family-based exome sequencing identifies RBM45 as a possible candidate gene for frontotemporal dementia and amyotrophic lateral sclerosis

P. Deyn, C. Broeckhoven, S. Engelborghs, 2021, Neurobiology of Disease.

Plasma phosphorylated TDP-43 levels are elevated in patients with frontotemporal dementia carrying a C9orf72 repeat expansion or a GRN mutation

J. Molinuevo, C. van Broeckhoven, J. Clarimón, 2013, Journal of Neurology, Neurosurgery & Psychiatry.

Mutated CTSF in adult-onset neuronal ceroid lipofuscinosis and FTD

C. van Broeckhoven, S. Engelborghs, J. Verhoeven, 2016, Neurology: Genetics.

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

M. Tsolaki, K. Sleegers, C. van Broeckhoven, 2015, Human mutation.

TRIM25 mutation (p.C168*), coding for an E3 ubiquitin ligase, is a cause of early‐onset autosomal dominant dementia with amyloid load and parkinsonism

C. van Broeckhoven, J. van der Zee, E. Gómez-Tortosa, 2022, Alzheimer's & dementia : the journal of the Alzheimer's Association.

Genetic variability in SQSTM1 and risk of early-onset Alzheimer dementia: a European early-onset dementia consortium study

G. Frisoni, C. Broeckhoven, K. Sleegers, 2015, Neurobiology of Aging.

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

C. van Broeckhoven, S. Engelborghs, R. Vandenberghe, 2013, JAMA neurology.