Hana Hansı́ková - Concepedia

Author

Hana Hansı́ková

Czech Academy of Sciences, Institute of Physiology ORCID

Also Known As

H Hansikova, H Hansíková, H. Hansikova, H. Hansíková, Hana HANSÍKOVÁ, Hana Hansikova, Hana Hansíková, Hana Hansı́ková, Handl, Jiri

Publications

672

Citations

H-Index

Concepts

All Affiliations

Czech Academy of Sciences, Institute of Physiology Czech Academy of Sciences Charles University

About

Hana Hansı́ková is an author at Czech Academy of Sciences, Institute of Physiology specializing in medicine, molecular genetics, and molecular biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	308
2	Molecular Biology	4	4	199
3	Natural Sciences	3	3	177
4	Biochemistry	2	2	157
5	Biology	1	1	20

Hana Hansı́ková

Publications

597

Citations

H-Index

Page 1

	Year	Citations
Retrospective, Multicentric Study of 180 Children with Cytochrome c Oxidase Deficiency Marek Böhm, Ewa Pronicka, Elżbieta Karczmarewicz, Pediatric Research Multicentric StudyPediatric HematologyInherited Metabolic DiseaseHematologyPediatrics	2005	109
Altered properties of mitochondrial ATP-synthase in patients with a T → G mutation in the ATPase 6 (subunit a) gene at position 8993 of mtDNA J Houštěk, Petr Klement, Jana Heřmanská, Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease Mitochondrial BiogenesisMitochondrial FunctionBiochemistryNatural SciencesGenetics	1995	105
Tissue-specific cytochrome <i>c</i> oxidase assembly defects due to mutations in <i>SCO2</i> and <i>SURF1</i> Lukáš Stibůrek, Kateřina Veselá, Hana Hansı́ková, Biochemical Journal	2005	100
Loss of function of Sco1 and its interaction with cytochrome <i>c</i> oxidase Lukáš Stibůrek, Kateřina Veselá, Hana Hansı́ková, American Journal of Physiology-Cell Physiology	2009	98
Diminished synthesis of subunit a (ATP6) and altered function of ATP synthase and cytochrome <i>c</i> oxidase due to the mtDNA 2 bp microdeletion of TA at positions 9205 and 9206 Pavel Ješina, Markéta Tesařová, Daniela Fornůsková, Biochemical Journal	2004	60
Functional alteration of cytochrome c oxidase by SURF1 mutations in Leigh syndrome Petr Pecina, Markéta Čapková, Subir Roy Chowdhury, Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease Functional AlterationBiochemistryMitochondrial FunctionNatural SciencesGenetics	2003	52
Noninvasive diagnostics of mitochondrial disorders in isolated lymphocytes with high resolution respirometry Petr Pecina, H Houst'ková, Tomáš Mráček, BBA Clinical	2014	31
A Novel Mutation in SURF1 Causes Skipping of Exon 8 in a Patient with Cytochrome c Oxidase-Deficient Leigh Syndrome and Hypertrichosis Siôn L. Williams, Jan‐Willem Taanman, Hana Hansı́ková, Molecular Genetics and Metabolism Mendelian DisorderGenetic DisorderGeneticsMolecular BiologyPathology	2001	22
Segregation pattern and biochemical effect of the G3460A mtDNA mutation in 27 members of LHON family Vilma Kaplanová, J Zeman, Hana Hansı́ková, Journal of the Neurological Sciences BiologyG3460a Mtdna MutationGenome InstabilityDna SequencingDna	2004	20

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