Ghent University Academic Bibliography

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

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Rare ABCA7 mutations in Alzheimer’s disease and cerebral amyloid angiopathy pathology

Elisabeth Hendrickx Van de Craen, Liene Bossaerts, Anne Sieben, Tobi Van den Bossche, Maria Bjerke, Bernard Hanseeuw, Bruno Bergmans (UGent) , Rik Vandenberghe, Peter P. De Deyn, Patrick Cras, et al.

(2026) NEUROBIOLOGY OF AGING. 160. p.33-46
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Biomarker-based diagnosis and care pathways for Alzheimer’s disease in the era of disease-modifying treatments : a consensus statement by Belgian experts

Tim Van Langenhove (UGent) , Sarah Van Mossevelde (UGent) , Marijke Miatton (UGent) , Jan De Lepeleire, Rose Bruffaerts, Jean Christophe Bier, Kurt Segers, Jurn Verschraegen, Mirko Petrovic (UGent) , Manfredi Ventura, et al.

(2026) EUROPEAN JOURNAL OF NEUROLOGY. 33(8).
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Pharmacotherapy for behavioural manifestations in frontotemporal dementia : an expert consensus from the European Reference Network for Rare Neurological Diseases (ERN-RND)

Casper Wittebrood, Marina Boban, Annchiara Cagnin, Sabina Capellari, Francois-Laurent De Winter, Atbin Djamshidian, Manuel Menendez Gonzalez, Lena E. Hjermind, Lenka Krajcovicova, Johanna Krüger, et al.

(2024) EUROPEAN JOURNAL OF NEUROLOGY. 31(12).
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Patients carrying the mutation p.R406W in MAPT present with non-conforming phenotypic spectrum

Helena Gossye, Sarah Van Mossevelde (UGent) , Anne Sieben, Maria Bjerke, Elisabeth Hendrickx Van de Craen, Julie van der Zee, Peter P. De Deyn, Jan De Bleecker (UGent) , Jan Versijpt, Jenneke van den Ende, et al.

(2023) BRAIN. 146(4). p.1624-1636
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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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Family-based exome sequencing identifies RBM45 as a possible candidate gene for frontotemporal dementia and amyotrophic lateral sclerosis

Julie van der Zee, Lubina Dillen, Yalda Baradaran-Heravi, Helena Gossye, Cemile Kocoglu, Ivy Cuyt, Bart Dermaut (UGent) , Anne Sieben, Jonathan Baets, Peter De Jonghe, et al.

(2021) NEUROBIOLOGY OF DISEASE. 156.
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Contribution of rare homozygous and compound heterozygous VPS13C missense mutations to dementia with Lewy bodies and Parkinson’s disease

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

(2021) ACTA NEUROPATHOLOGICA COMMUNICATIONS. 9(1).
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Multivariate analysis reveals anatomical correlates of naming errors in primary progressive aphasia

Rose Bruffaerts, Jolien Schaeverbeke, An-Sofie De Weer, Natalie Nelissen, Eva Dries, Karen Van Bouwel, Anne Sieben, Bruno Bergmans (UGent) , Charlotte Swinnen, Yolande Pijnenburg, et al.

(2020) NEUROBIOLOGY OF AGING. 88. p.71-82
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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, 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, Elisabeth Hens, Bavo Heeman, Sara Van Mossevelde, Philippe Pals, Bob Asselbergh, Roberto Dos Santos Dias, et al.

(2020) Research Square.

Academic Bibliography

Rare ABCA7 mutations in Alzheimer’s disease and cerebral amyloid angiopathy pathology

Biomarker-based diagnosis and care pathways for Alzheimer’s disease in the era of disease-modifying treatments : a consensus statement by Belgian experts

Pharmacotherapy for behavioural manifestations in frontotemporal dementia : an expert consensus from the European Reference Network for Rare Neurological Diseases (ERN-RND)

Patients carrying the mutation p.R406W in MAPT present with non-conforming phenotypic spectrum

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

Family-based exome sequencing identifies RBM45 as a possible candidate gene for frontotemporal dementia and amyotrophic lateral sclerosis

Contribution of rare homozygous and compound heterozygous VPS13C missense mutations to dementia with Lewy bodies and Parkinson’s disease

Multivariate analysis reveals anatomical correlates of naming errors in primary progressive aphasia

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

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