Ghent University Academic Bibliography

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Your filters: cql: keyword exact "hexanucleotide repeat" cql: author exact 801000620352 or (type exact bookEditor and editor exact 801000620352)

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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 (UGent) , Rik Vandenberghe, Stephanie Philtjens, Marleen Van den Broeck, Karin Peeters, et al.

(2018) NEUROBIOLOGY OF AGING. 67. p.84-94
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TBK1 mutation spectrum in an extended European patient cohort with frontotemporal dementia and amyotrophic lateral sclerosis

Julie van der Zee, Ilse Gijselinck, Sara Van Mossevelde, Federica Perrone, Lubina Dillen, Bavo Heeman, Veerle Bäumer, Sebastiaan Engelborghs, Jan De Bleecker (UGent) , Jonathan Baets, et al.

(2017) HUMAN MUTATION. 38(3). p.297-309
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Investigating the role of ALS genes CHCHD10 and TUBA4A in Belgian FTD-ALS spectrum patients

Federica Perrone, Hung Phuoc Nguyen, Sara Van Mossevelde, Matthieu Moisse, Anne Sieben (UGent) , Patrick Santens (UGent) , Jan De Bleecker (UGent) , Mathieu Vandenbulcke, Sebastiaan Engelborghs, Jonathan Baets, et al.

(2017) NEUROBIOLOGY OF AGING. 51. p.177.e9-177.e16
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The C9orf72 repeat size correlates with onset age of disease, DNA methylation and transcriptional downregulation of the promoter

I Gijselinck, S Van Mossevelde, J van der Zee, Anne Sieben (UGent) , S Engelborghs, Jan De Bleecker (UGent) , A Ivanoiu, O Deryck, D Edbauer, M Zhang, et al.

(2016) MOLECULAR PSYCHIATRY. 21(8). p.1112-1124
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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 (UGent) , 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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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

Academic Bibliography

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

TBK1 mutation spectrum in an extended European patient cohort with frontotemporal dementia and amyotrophic lateral sclerosis

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

The C9orf72 repeat size correlates with onset age of disease, DNA methylation and transcriptional downregulation of the promoter

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

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