Elisabeth Hens

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

B. Bergmans, K. Sleegers, C. van Broeckhoven, 2020, Alzheimer's Research & Therapy.

ZCWPW1 loss-of-function variants in Alzheimer's Disease

K. Sleegers, C. van Broeckhoven, J. Lambert, 2021, medRxiv.

Premature termination codon mutations in ABCA7 contribute to Alzheimer's disease risk in Belgian patients

C. van Broeckhoven, S. Engelborghs, R. Vandenberghe, 2021, Neurobiology of Aging.

Investigation of the role of matrix metalloproteinases in the genetic etiology of Alzheimer's disease

C. van Broeckhoven, S. Engelborghs, J. van der Zee, 2021, Neurobiology of Aging.

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

B. Asselbergh, C. van Broeckhoven, S. Engelborghs, 2021, Acta Neuropathologica Communications.

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

P. Deyn, B. Asselbergh, S. Engelborghs, 2020 .

Contribution of homozygous and compound heterozygous missense mutations in VWA2 to Alzheimer’s disease

P. Deyn, B. Bergmans, C. Broeckhoven, 2020, Neurobiology of Aging.