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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- Miscellaneous
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Homozygous and compound heterozygous rare variants in VPS13C contribute to Lewy body diseases

Stefanie Smolders, Stéphanie Philtjens, David Crosiers, Anne Sieben (UGent) , Elisabeth Hens, Bavo Heeman, Sara Van Mossevelde, Philippe Pals, Bob Asselbergh, Roberto Dos Santos Dias, et al.

(2020) Research Square.
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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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Extended FTLD pedigree segregating a Belgian GRN-null mutation : neuropathological heterogeneity in one family

Anne Sieben (UGent) , Sara Van Mossevelde, Eline Wauters, Sebastiaan Engelborghs, Julie van der Zee, Tim Van Langenhove (UGent) , Patrick Santens (UGent) , Marleen Praet (UGent) , Paul Boon (UGent) , Marijke Miatton (UGent) , et al.

(2018) ALZHEIMERS RESEARCH & THERAPY. 10.
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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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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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No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patients

Yalda Baradaran-Heravi, Lubina Dillen, Hung Phuoc Nguyen, Sara Van Mossevelde, Jonathan Baets, Peter De Jonghe, Sebastiaan Engelborghs, Peter P De Deyn, Mathieu Vandenbulcke, Rik Vandenberghe, et al.

(2018) NEUROBIOLOGY OF AGING. 69.
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Cross-modal representation of spoken and written word meaning in left pars triangularis

Antonietta Gabriella Liuzzi, Rose Bruffaerts, Ronald Peeters, Katarzyna Adamczuk, Emmanuel Keuleers (UGent) , Simon De Deyne, Gerrit Storms, Patrick Dupont and Rik Vandenberghe

(2017) NEUROIMAGE. 150. p.292-307

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

Homozygous and compound heterozygous rare variants in VPS13C contribute to Lewy body diseases

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

Extended FTLD pedigree segregating a Belgian GRN-null mutation : neuropathological heterogeneity in one family

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

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

No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patients

Cross-modal representation of spoken and written word meaning in left pars triangularis

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