Gamze Güven

Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy

Suzanne Lesage, Valérie Drouet, Elisa Majounie et al. · The American Journal of Human Genetics · 2016 · 447 citations · Full text

Life Sciences, Cell Biology, Neuroscience +16

A new F‐box protein 7 gene mutation causing typical Parkinson's disease

Ebba Lohmann, Anne‐Sophie Coquel, Aurélie Honoré et al. · Movement Disorders · 2015 · 66 citations

Life Sciences, Genetics, Molecular Genetics +15

<i>HPCA</i> confirmed as a genetic cause of DYT2‐like dystonia phenotype

Burcu Atasu, Haşmet Hanağası, Meltem Pak et al. · Movement Disorders · 2018 · 39 citations

Life Sciences, Genetics, Neurology +16

Mutation Frequency of the Major Frontotemporal Dementia Genes, MAPT, GRN and C9ORF72 in a Turkish Cohort of Dementia Patients

Gamze Güven, Ebba Lohmann, José Brás et al. · PLoS ONE · 2016 · 32 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Clinical variability in ataxia–telangiectasia

Ebba Lohmann, Stefanie Krüger, Ann‐Kathrin Hauser et al. · Journal of Neurology · 2015 · 27 citations

Life Sciences, Neurology, Neuroscience +11