Dóra Csabán

Optimising the mutation screening strategy in Marfan syndrome and identifying genotypes with more severe aortic involvement

Roland Stengl, András Bors, Bence Ágg et al. · Orphanet Journal of Rare Diseases · 2020 · 38 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

Novel dominant MPAN family with a complex genetic architecture as a basis for phenotypic variability

Péter Balicza, Renáta Bencsik, András Lengyel et al. · Neurology Genetics · 2020 · 17 citations · Full text

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

Positive association and future perspectives of mitochondrial DNA copy number and telomere length – a pilot twin study

Dóra Melicher, Anett Illés, Levente Littvay et al. · Archives of Medical Science · 2019 · 10 citations · Full text