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Neurobiology of Aging|December 14, 2011
Exome sequencing reveals an unexpected genetic cause of disease: NOTCH3 mutation in a Turkish family with Alzheimer's diseaseRita João Guerreiro, Ebba Lohmann, Emma Kinsella, et al.Neurobiology of Aging|June 24, 2021
Frequency of frontotemporal dementia-related gene variants in TurkeySevilhan Artan, Ebru Erzurumluoglu Gokalp, Bedia Samanci, et al.Annals of Clinical and Translational Neurology|July 20, 2026
Stage-Dependent β-Synuclein Links MRI and Cognitive Decline in Alzheimer's DiseaseUlaş Ay, Merve Alaylioglu, Erdi Sahin, et al.Journal of Alzheimer'S Disease : JAD|January 11, 2021
The Right Temporal Variant of Frontotemporal Dementia Is Not Genetically Sporadic: A Case SeriesHulya Ulugut Erkoyun, Sven J van der Lee, Bas Nijmeijer, et al.Neurobiology of Aging|December 31, 2022
TREX1 p.A129fs and p.Y305C variants in a large multi-ethnic cohort of CADASIL-like unrelated patientsMarco Foddis, Sonja Blumenau, Manuel Holtgrewe, et al.Annals of Neurology|October 13, 2020
Characterization of Recessive Parkinson Disease in a Large Multicenter StudySuzanne Lesage, Ariane Lunati, Marion Houot, et al.Scientific Reports|March 17, 2021
PHACTR1 genetic variability is not critical in small vessel ischemic disease patients and PcomA recruitment in C57BL/6J miceClemens Messerschmidt, Marco Foddis, Sonja Blumenau, et al.American Journal of Human Genetics|March 5, 2016
Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent MitophagySuzanne Lesage, Valérie Drouet, Elisa Majounie, et al.Pageof 6