- TRIM25 mutation (p.C168*), coding for an E3 ubiquitin ligase, is a cause of early-onset autosomal dominant dementia with amyloid load and parkinsonism(2023)
Auteurs: Estrella Gomez-Tortosa, Yalda Baradaran Heravi, Lubina Dillen, Nila Roy Choudhury, Pablo Aguero Rabes, Julian Perez-Perez, Cemile Kocoglu, M. Jose Sainz, Alicia Ruiz Gonzalez, Raquel Tellez, et al.
Pagina's: 2805 - 2815
- Family-based exome sequencing identifies RBM45 as a possible candidate gene for frontotemporal dementia and amyotrophic lateral sclerosis(2021)
Auteurs: Julie van der Zee, Lubina Dillen, Yalda Baradaran Heravi, Helena Gossye, Cemile Kocoglu, Ivy Cuijt, Bart Dermaut, Anne Sieben, Jonathan Baets, Peter De Jonghe, et al.
- Stress granule mediated protein aggregation and underlying gene defects in the FTD-ALS spectrum(2020)
Auteurs: Yalda Baradaran Heravi, Christine Van Broeckhoven, Julie van der Zee
- Presence of tau astrogliopathy in frontotemporal dementia caused by a novel Grn nonsense (Trp2*) mutation(2019)
Auteurs: Estrella Gómez-Tortosa, Yalda Baradaran Heravi, Valentina González Alvarez, María José Sainz, Cristina Prieto-Jurczynska, Rosa Guerrero-López, Pablo Agüero Rabes, Christine Van Broeckhoven, Julie van der Zee, Alberto Rábano Gutiérrez
Pagina's: 214e11 - 214e15
- Hunting for novel frontotemporal dementia genes(2019)
Auteurs: Yalda Baradaran Heravi, Julie van der Zee, Christine Van Broeckhoven
Aantal pagina's: 169
- Deleterious ABCA7 mutations and transcript rescue mechanisms in early onset Alzheimer's disease(2017)
Auteurs: Arne De Roeck, Tobi Van den Bossche, Julie van der Zee, Jan Verheijen, Wouter De Coster, Jasper Van Dongen, Lubina Dillen, Yalda Baradaran Heravi, Bavo Heeman, Raquel Sanchez-Valle, et al.
Pagina's: 475 - 487