Marina Moraitou

TMEM199 Deficiency Is a Disorder of Golgi Homeostasis Characterized by Elevated Aminotransferases, Alkaline Phosphatase, and Cholesterol and Abnormal Glycosylation

Jos C. Jansen, Sharita Timal, Monique van Scherpenzeel et al. · The American Journal of Human Genetics · 2016 · 89 citations · Full text

Autoimmune Disease, Disease Mechanism, Abnormal Glycosylation +9

Lysosomal alterations in peripheral blood mononuclear cells of Parkinson's disease patients

Nikolaos Papagiannakis, Maria Xilouri, Christos Koros et al. · Movement Disorders · 2015 · 67 citations

Genetic assessment of familial and early‐onset Parkinson's disease in a Greek population

Maria Bozi, Dimitra Papadimitriou, Roubina Antonellou et al. · European Journal of Neurology · 2013 · 65 citations

Evidence of an association between the scavenger receptor class B member 2 gene and Parkinson's disease

Helen Michelakakis, Georgia Xiromerisiou, Efthimios Dardiotis et al. · Movement Disorders · 2012 · 64 citations

Genetics, Neurotransmitter, Genetic Epidemiology +20

Circulating Brain‐Enriched MicroRNAs for Detection and Discrimination of Idiopathic and Genetic Parkinson's Disease

Stylianos Ravanidis, Anastasia Bougea, Nikolaos Papagiannakis et al. · Movement Disorders · 2019 · 56 citations