Ghent University Academic Bibliography

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

Eline Wauters, Sara Van Mossevelde, Kristel Sleegers, Julie van der Zee, Sebastiaan Engelborghs, Anne Sieben, Rik Vandenberghe, Stephanie Philtjens, Marleen Van den Broeck, Karin Peeters, et al.

(2018) NEUROBIOLOGY OF AGING. 67. p.84-94
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Clinical evidence of disease anticipation in families segregating a C9orf72 repeat expansion

Sara Van Mossevelde, Julie van der Zee, Ilse Gijselinck, Kristel Sleegers, Jan De Bleecker (UGent) , Anne Sieben, Rik Vandenberghe, Tim Van Langenhove (UGent) , Jonathan Baets, Olivier Deryck, et al.

(2017) JAMA NEUROLOGY. 74(4). p.445-452
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Clinical features of TBK1 carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohort

Sara Van Mossevelde, Julie van der Zee, Ilse Gijselinck, Sebastiaan Engelborghs, Anne Sieben, Tim Van Langenhove (UGent) , Jan De Bleecker (UGent) , Jonathan Baets, Mathieu Vandenbulcke, Koen Van Laere, et al.

(2016) BRAIN. 139(2). p.452-467
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Phenotypic characteristics of Alzheimer patients carrying an ABCA7 mutation

Tobi Van den Bossche, Kristel Sleegers, Elise Cuyvers, Sebastiaan Engelborghs, Anne Sieben, Arne De Roeck, Caroline Van Cauwenberghe, Steven Vermeulen, Marleen Van den Broeck, Annelies Laureys, et al.

(2016) NEUROLOGY. 86(23). p.2126-2133
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Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohort

Ilse Gijselinck, Sara Van Mossevelde, Julie van der Zee, Anne Sieben, Stephanie Philtjens, Bavo Heeman, Sebastiaan Engelborghs, Mathieu Vandenbulcke, Greet De Baets, Veerle Baumer, et al.

(2015) NEUROLOGY. 85(24). p.2116-2125
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Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration

Julie van der Zee, Tim Van Langenhove (UGent) , Gabor G Kovacs, Lubina Dillen, William Deschamps, Sebastiaan Engelborghs, Radoslav Matěj, Mathieu Vandenbulcke, Anne Sieben, Bart Dermaut (UGent) , et al.

(2014) ACTA NEUROPATHOLOGICA. 128(3). p.397-410
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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, Jan Versijpt, Adrian Ivanoiu, et al.

(2013) JAMA NEUROLOGY. 70(3). p.365-373
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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).
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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
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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

Academic Bibliography

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

Clinical evidence of disease anticipation in families segregating a C9orf72 repeat expansion

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

Phenotypic characteristics of Alzheimer patients carrying an ABCA7 mutation

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

Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration

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

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

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

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