Ghent University Academic Bibliography

Show Sort by

Your filters: cql: author="Vandenberghe, Rik" or (type any "bookEditor journalEditor issueEditor" and editor="Vanden...

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

Lubina Dillen, Tim Van Langenhove (UGent) , Sebastiaan Engelborghs, Mathieu Vandenbulcke, Stayko Sarafov, Ivailo Tournev, Celine Merlin, Patrick Cras, Rik Vandenberghe, Peter P De Deyn, et al.

(2013) NEUROBIOLOGY OF AGING. 34(6).
Add to list
Distinct clinical characteristics of C9orf72 expansion carriers compared with GRN, MAPT, and nonmutation carriers in a Flanders-Belgian FTLD cohort

Tim Van Langenhove (UGent) , Julie van der Zee, Ilse Gijselinck, Sebastiaan Engelborghs, Rik Vandenberghe, Mathieu Vandenbulcke, Jan De Bleecker (UGent) , Anne Sieben (UGent) , Jan Versijpt, Adrian Ivanoiu, et al.

(2013) JAMA NEUROLOGY. 70(3). p.365-373
Add to list
A pan-European study of the C9orf72 repeat associated with FTLD : geographic prevalence, genomic instability, and intermediate repeats

Julie van der Zee, Ilse Gijselinck, Lubina Dillen, Tim Van Langenhove (UGent) , Jessie Theuns, Sebastiaan Engelborghs, Stéphanie Philtjens, Mathieu Vandenbulcke, Kristel Sleegers, Anne Sieben (UGent) , et al.

(2013) HUMAN MUTATION. 34(2). p.363-373
Add to list
- Conference Paper
- C3
Identification of novel causal genes for frontotemporal lobar degeneration using whole genome sequencing

Stephanie Philtjens, Ilse Gijselinck, Tim Van Langenhove (UGent) , Julie van der Zee, Sebastiaan Engelborgs, Rik Vandenberghe, Matthieu Vandenbulcke, Patrick Santens (UGent) , Peter De Deyn, Christine Van Broeckhoven, et al.

(2012) DEMENTIA AND GERIATRIC COGNITIVE DISORDERS. 33(suppl. 1). p.257-258
Add to list
Ataxin-2 polyQ expansions in FTLD-ALS spectrum disorders in Flanders-Belgian cohorts

Tim Van Langenhove (UGent) , Julie van der Zee, Sebastiaan Engelborghs, Rik Vandenberghe, Patrick Santens (UGent) , Marleen Van den Broeck, Maria Mattheijssens, Karin Peeters, Dirk Nuytten, Patrick Cras, et al.

(2012) NEUROBIOLOGY OF AGING. 33(5).
Add to list
- Conference Paper
- C3
Distinct clinical characteristics of C9orf72 expansion carriers compared to GRN, MAPT and non-mutation carries in a Flanders-Belgian FTLD cohort

Tim Van Langenhove (UGent) , Julie van der Zee, Ilse Gijselinck, Sebastiaan Engelborghs, Rik Vandenberghe, Mathieu Vandenbulcke, Jan De Bleecker (UGent) , Anne Sieben (UGent) , Adrian Ivanoiu, Oliver Deryck, et al.

(2012) DEMENTIA AND GERIATRIC COGNITIVE DISORDERS. 33(suppl. 1). p.226-226
Add to list
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

Ilse Gijselinck, Tim Van Langenhove (UGent) , Julie van der Zee, Kristel Sleegers, Stephanie Philtjens, Gernot Kleinberger, Jonathan Janssens, Karolien Bettens, Caroline Van Cauwenberghe, Sandra Pereson, et al.

(2012) LANCET NEUROLOGY. 11(1). p.54-65
Add to list
TMEM106B is associated with frontotemporal lobar degeneration in a clinically diagnosed patient cohort

Julie van der Zee, Tim Van Langenhove (UGent) , Gernot Kleinberger, Kristel Sleegers, Sebastiaan Engelborghs, Rik Vandenberghe, Patrick Santens (UGent) , Marleen Van Den Broeck, Geert Joris, Jolien Brys, et al.

(2011) BRAIN. 134(3). p.808-815
Add to list
Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALS

Ilse Gijselinck, Kristel Sleegers, Sebastiaan Engelborghs, Wim Robberecht, Jean-Jacques Martin, Rik Vandenberghe, Raf Sciot, Bart Dermaut (UGent) , Dirk Goossens, Julie van der Zee, et al.

(2009) NEUROBIOLOGY OF AGING. 30(8). p.1329-1331
Add to list
- Journal Article
- A1
- open access
CHMP2B C-truncating mutations in frontotemporal lobar degeneration are associated with an aberrant endosomal phenotype in vitro

Julie van der Zee, Hazel Urwin, Sebastiaan Engelborghs, Marc Bruyland, Rik Vandenberghe, Bart Dermaut (UGent) , Tim De Pooter, Karin Peeters, Patrick Santens (UGent) , Peter P De Deyn, et al.

(2008) HUMAN MOLECULAR GENETICS. 17(2). p.313-322

← Previous

Academic Bibliography

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

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

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

Identification of novel causal genes for frontotemporal lobar degeneration using whole genome sequencing

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

Distinct clinical characteristics of C9orf72 expansion carriers compared to GRN, MAPT and non-mutation carries in a Flanders-Belgian FTLD cohort

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

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

Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALS

CHMP2B C-truncating mutations in frontotemporal lobar degeneration are associated with an aberrant endosomal phenotype in vitro

Contents

Support

Contact