Ghent University Academic Bibliography

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

Cemile Koçoğlu, Helena Gossye, Lubina Dillen, Sara Van Mossevelde, Jan De Bleecker (UGent) , Rik Vandenberghe, Peter P. De Deyn, Kristel Sleegers, Patrick Cras, Sebastiaan Engelborghs, et al.

(2021) NEUROBIOLOGY OF AGING. 97. p.145.e1-145.e4
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Amyloid-β1–43 cerebrospinal fluid levels and the interpretation of APP, PSEN1 and PSEN2 mutations

Federica Perrone, Maria Bjerke, Elisabeth Hens, Anne Sieben (UGent) , Maarten Timmers, Arne De Roeck, Rik Vandenberghe, Kristel Sleegers, Jean-Jacques Martin, Peter P. De Deyn, et al.

(2020) ALZHEIMERS RESEARCH & THERAPY. 12(1).
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Loss of DPP6 in neurodegenerative dementia : a genetic player in the dysfunction of neuronal excitability

Rita Cacace, Bavo Heeman, Sara Van Mossevelde, Arne De Roeck, Julie Hoogmartens, Peter De Rijk, Helena Gossye, Kristof De Vos, Wouter De Coster, Mojca Strazisar, et al.

(2019) ACTA NEUROPATHOLOGICA. 137(6). p.901-918
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An intronic VNTR affects splicing of ABCA7 and increases risk of Alzheimer's disease

Arne De Roeck, Lena Duchateau, Jasper Van Dongen, Rita Cacace, Maria Bjerke, Tobi Van den Bossche, Patrick Cras, Rik Vandenberghe, Peter P De Deyn, Sebastiaan Engelborghs, et al.

(2018) ACTA NEUROPATHOLOGICA. 135(6). p.827-837
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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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Male-specific epistasis between WWC1 and TLN2 genes is associated with Alzheimer's disease

Elena S Gusareva, Jean-Claude Twizere, Kristel Sleegers, Pierre Dourlen, Jose F Abisambra, Shelby Meier, Ryan Cloyd, Blaine Weiss, Bart Dermaut (UGent) , Kyrylo Bessonov, et al.

(2018) NEUROBIOLOGY OF AGING. 72.
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Common and rare TBK1 variants in early-onset Alzheimer disease in a European cohort

Jan Verheijen, Julie van der Zee, Ilse Gijselinck, Tobi Van den Bossche, Lubina Dillen, Bavo Heeman, Estrella Gómez-Tortosa, Albert Lladó, Raquel Sanchez-Valle, Caroline Graff, et al.

(2018) NEUROBIOLOGY OF AGING. 62. p.245.e1-245.e7
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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 (UGent) , Rik Vandenberghe, Tim Van Langenhove (UGent) , Jonathan Baets, Olivier Deryck, et al.

(2017) JAMA NEUROLOGY. 74(4). p.445-452
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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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Phenotypic characteristics of Alzheimer patients carrying an ABCA7 mutation

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

(2016) NEUROLOGY. 86(23). p.2126-2133

Academic Bibliography

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

Amyloid-β1–43 cerebrospinal fluid levels and the interpretation of APP, PSEN1 and PSEN2 mutations

Loss of DPP6 in neurodegenerative dementia : a genetic player in the dysfunction of neuronal excitability

An intronic VNTR affects splicing of ABCA7 and increases risk of Alzheimer's disease

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

Male-specific epistasis between WWC1 and TLN2 genes is associated with Alzheimer's disease

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

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

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

Phenotypic characteristics of Alzheimer patients carrying an ABCA7 mutation

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