Anett Illés

Mitochondrial dysfunction and autism: comprehensive genetic analyses of children with autism and mtDNA deletion

Noémi Ágnes Varga, Klára Pentelényi, Péter Balicza et al. · Behavioral and Brain Functions · 2018 · 57 citations · Full text

Broadening the phenotype of the TWNK gene associated Perrault syndrome

Bálint Fekete, Klára Pentelényi, Gábor Rudas et al. · BMC Medical Genetics · 2019 · 23 citations · Full text

NKX2-1 New Mutation Associated With Myoclonus, Dystonia, and Pituitary Involvement

Péter Balicza, Zoltán Grosz, Viktor Molnár et al. · Frontiers in Genetics · 2018 · 20 citations · Full text

Analysis of GJB2 mutations and the clinical manifestation in a large Hungarian cohort

Nóra Kecskeméti, Magdolna Szönyi, Anita Gáborján et al. · European Archives of Oto-Rhino-Laryngology · 2018 · 18 citations

Large Hungarian Cohort, Genetic Disorder, Medicine +10

The Role of Genetic Testing in the Clinical Practice and Research of Early-Onset Parkinsonian Disorders in a Hungarian Cohort: Increasing Challenge in Genetic Counselling, Improving Chances in Stratification for Clinical Trials

Anett Illés, Dóra Csabán, Zoltán Grosz et al. · Frontiers in Genetics · 2019 · 16 citations · Full text