Hana Hansíková
Charles University(CZ)
Publications by Year
Research Areas
Mitochondrial Function and Pathology, Metabolism and Genetic Disorders, ATP Synthase and ATPases Research, Genetic Neurodegenerative Diseases, Glycosylation and Glycoproteins Research
Most-Cited Works
- → TMEM70 mutations cause isolated ATP synthase deficiency and neonatal mitochondrial encephalocardiomyopathy(2008)197 cited
- → Molecular diagnosis in mitochondrial complex I deficiency using exome sequencing(2012)184 cited
- → Neuroinflammation, mitochondrial defects and neurodegeneration in mucopolysaccharidosis III type C mouse model(2015)144 cited
- → Mutation of Nogo-B Receptor, a Subunit of cis-Prenyltransferase, Causes a Congenital Disorder of Glycosylation(2014)139 cited
- → Congenital disorders of glycosylation: Still “hot” in 2020(2020)131 cited
- → A Transgenic Minipig Model of Huntington's Disease(2013)105 cited
- → Novel insights into the assembly and function of human nuclear-encoded cytochromeoxidase subunits 4, 5a, 6a, 7a and 7b