Geert Joris

发表

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

K. Sleegers, C. van Broeckhoven, S. Engelborghs, 2011, Brain : a journal of neurology.

Cellular ageing, increased mortality and FTLD‐TDP‐associated neuropathology in progranulin knockout mice

S. Pereson, C. van Broeckhoven, P. D. De Deyn, 2012, The Journal of pathology.

Increased caspase activation and decreased TDP‐43 solubility in progranulin knockout cortical cultures

C. van Broeckhoven, J. Timmermans, S. Kumar-Singh, 2010, Journal of neurochemistry.

TDP-43 transgenic mice develop spastic paralysis and neuronal inclusions characteristic of ALS and frontotemporal lobar degeneration

S. Pereson, C. van Broeckhoven, S. Kumar-Singh, 2010, Proceedings of the National Academy of Sciences.

Overexpression of ALS-Associated p.M337V Human TDP-43 in Mice Worsens Disease Features Compared to Wild-type Human TDP-43 Mice

C. van Broeckhoven, S. Kumar-Singh, J. Janssens, 2013, Molecular Neurobiology.

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.

Whole‐exome rare‐variant analysis of Alzheimer's disease and related biomarker traits

P. Scheltens, F. Barkhof, G. Frisoni, 2022, Alzheimer's & dementia : the journal of the Alzheimer's Association.

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

C. van Broeckhoven, S. Engelborghs, M. Cruts, 2010, Archives of neurology.

Progranulin expression correlates with dense‐core amyloid plaque burden in Alzheimer disease mouse models

S. Pereson, C. van Broeckhoven, M. Hutton, 2009, The Journal of pathology.

Investigating the Role of Chromatin Remodeler FOXA1 in Ferroptotic Cell Death

W. V. Berghe, K. Laukens, B. Cuypers, 2021, bioRxiv.

Overexpression of ALS-Associated p.M337V Human TDP-43 in Mice Worsens Disease Features Compared to Wild-type Human TDP-43 Mice

C. van Broeckhoven, S. Kumar-Singh, J. Janssens, 2013, Molecular Neurobiology.

Rare variants in IFFO1, DTNB and NLRC3 associate with Alzheimer's disease CSF profile of neuronal injury and inflammation

P. Scheltens, F. Barkhof, G. Frisoni, 2021, medRxiv.

Methylmap: visualization of modified nucleotides for large cohort sizes

D. Dickson, Wouter De Coster, M. Strazisar, 2022, bioRxiv.

Rare variants in IFFO1, DTNB, NLRC3 and SLC22A10 associate with Alzheimer’s disease CSF profile of neuronal injury and inflammation

P. Scheltens, F. Barkhof, G. Frisoni, 2022, Molecular Psychiatry.

Reduced brain volumes in mice expressing APP-Austrian mutation but not in mice expressing APP-Swedish–Austrian mutations

Annemie Van der Linden, Jean-Pierre Timmermans, Samir Kumar-Singh, 2008, Neuroscience Letters.

The European Reference Genome Atlas: piloting a decentralised approach to equitable biodiversity genomics

Robert P. Davey, Robert M. Waterhouse, Peter W. Harrison, 2024, bioRxiv.

Rare variants in IFFO1, DTNB, NLRC3 and SLC22A10 associate with Alzheimerâ€TMs disease CSF profile of neuronal injury and inflammation

C. Broeckhoven, K. Sleegers, O. Blin, 2022 .