Julie van der Zee guest prof. external funds - associate professor - guest professor

Publications Julie van der Zee

Investigation of the role of miRNA variants in neurodegenerative brain diseases

Source
Frontiers in genetics - ISSN 1664-8021-16 (2025) p. 1-10
Author(s)

Genome-wide analyses reveal a potential role for the MAPT, MOBP, and APOE loci in sporadic frontotemporal dementia

Source
The American journal of human genetics - ISSN 0002-9297-111:7 (2024) p. 1316-1329
Author(s)
    Claudia Manzoni, Demis A. Kia, Raffaele Ferrari, Ganna Leonenko, Beatrice Costa, Valentina Saba, Edwin Jabbari, Manuela M. X. Tan, Diego Albani, Victoria Alvarez, Ignacio Alvarez, Ole A. Andreassen, Antonella Angiolillo, Andrea Arighi, Matt Baker, Luisa Benussi, Valentina Bessi, Giuliano Binetti, Daniel J. Blackburn, Merce Boada, Bradley F. Boeve, Sergi Borrego-Ecija, Barbara Borroni, Geir Brathen, William S. Brooks, Amalia C. Bruni, Paola Caroppo, Sara Bandres-Ciga, Jordi Clarimon, Rosanna Colao, Carlos Cruchaga, Adrian Danek, Sterre C. M. de Boer, Itziar de Rojas, Alfonso di Costanzo, Dennis W. Dickson, Janine Diehl-Schmid, Carol Dobson-Stone, Oriol Dols-Icardo, Aldo Donizetti, Elise Dopper, Elisabetta Durante, Camilla Ferrari, Gianluigi Forloni, Francesca Frangipane, Laura Fratiglioni, Rosa Rademakers, Christine Van Broeckhoven, Julie van der Zee, Valentina Escott-Price

Subclinical epileptiform activity in the Alzheimer continuum : association with disease, cognition and detection method

Source
Alzheimer's research & therapy - ISSN 1758-9193-16:1 (2024) p. 1-20
Author(s)
    Amber Nous, Laura Seynaeve, Odile Feys, Vincent Wens, Xavier De Tiege, Pieter Van Mierlo, Amir G. Baroumand, Koenraad Nieboer, Gert-Jan Allemeersch, Shana Mangelschots, Veronique Michiels, Julie van der Zee, Christine Van Broeckhoven, Annemie Ribbens, Ruben Houbrechts, Sara De Witte, Mandy Wittens, Maria Bjerke, Caroline Vanlersberghe, Sarah Ceyssens, Guy Nagels, Ilse Smolders, Sebastiaan Engelborghs

TRIM25 mutation (p.C168*), coding for an E3 ubiquitin ligase, is a cause of early-onset autosomal dominant dementia with amyloid load and parkinsonism

Source
Alzheimer's & dementia - ISSN 1552-5260-19:7 (2023) p. 2805-2815
Author(s)
    Estrella Gomez-Tortosa, Yalda Baradaran Heravi, Lobke Dillen, Nila Roy Choudhury, Pablo Aguero Rabes, Julian Perez-Perez, Cemile Koçoğlu, M. Jose Sainz, Alicia Ruiz Gonzalez, Raquel Tellez, Lucia Cremades-Jimeno, Blanca Cardaba, Christine Van Broeckhoven, Gracjan Michlewski, Julie van der Zee