A. Laureys

Handbook of LHC Higgs Cross Sections: 3. Higgs Properties

David J. Miller, S. P. Martin, David J. Miller, 2013, 1307.1347.

Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration

F. Jessen, G. Frisoni, T. Strom, 2014, Acta Neuropathologica.

Phenotypic characteristics of Alzheimer patients carrying an ABCA7 mutation

K. Sleegers, C. van Broeckhoven, S. Engelborghs, 2016, Neurology.

Rare Variants in PLD3 Do Not Affect Risk for Early‐Onset Alzheimer Disease in a European Consortium Cohort

M. Tsolaki, K. Sleegers, C. van Broeckhoven, 2015, Human mutation.