Daniela Záhoráková

Diagnostic exome sequencing in early‐onset Parkinson's disease confirms <i>VPS13C</i> as a rare cause of autosomal‐recessive Parkinson's disease

Barbara Schormair, David Kemlink, Brit Mollenhauer et al. · Clinical Genetics · 2017 · 91 citations · Full text

Genetic Testing, Exome Sequencing, Genetics +18

Polymorphisms in Serotonin-Related Genes in Anorexia Nervosa. The First Study in Czech Population and Meta-analyses with Previously Performed Studies

D. Martásková, Lenka Šlachtová, David Kemlink et al. · Folia Biologica · 2009 · 35 citations · Full text

Genetics, Genetic Epidemiology, Human Polymorphism +19

Brain iron accumulation in Wilson's disease: A longitudinal imaging case study during anticopper treatment using 7.0T MRI and transcranial sonography

Petr Dušek, David Školoudík, Jana Mašková et al. · Journal of Magnetic Resonance Imaging · 2017 · 33 citations · Full text

Mutation analysis of the MECP2 gene in patients of Slavic origin with Rett syndrome: novel mutations and polymorphisms

Daniela Záhoráková, R. Rosipal, Jan Hadač et al. · Journal of Human Genetics · 2007 · 25 citations · Full text

Genetic Disorder, Rett Syndrome, Genetics +8

Comparison of transcranial sonography-magnetic resonance fusion imaging in Wilson's and early-onset Parkinson's diseases

Jana Mašková, David Školoudík, Andrea Burgetová et al. · Parkinsonism & Related Disorders · 2016 · 18 citations

Medical Imaging, Corticobasal Degeneration, Neurological Disorder +11