Kateřina Veselá - Concepedia

Author

Kateřina Veselá

Also Known As

K Vesela, K Veselá, K. Vesela, K. Veselá, KATERINA VESELA, Katerina Vesela, Katerina Vesela⁎, Katerina Veselá, Kateřina Veselá, Vesela K

Publications

962

Citations

H-Index

Concepts

All Affiliations

Charles University General University Hospital in Prague Czech Academy of Sciences Czech Academy of Sciences, Institute of Physiology Igenbio (United States)

About

Kateřina Veselá is an author at Charles University specializing in medicine, genetics, and molecular biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	440
2	Natural Sciences	4	4	102
3	Biochemistry	4	4	102
4	Public Health	2	2	195
5	Cell Biology	1	1	30

Kateřina Veselá

Publications

875

Citations

H-Index

Page 1

	Year	Citations
Multiple meiotic errors caused by predivision of chromatids in women of advanced maternal age undergoing in vitro fertilisation Alan H. Handyside, Markus Montag, M. Cristina Magli, European Journal of Human Genetics InfertilityDevelopmental BiologyFertilityOogenesisVitro Fertilisation	2012	165
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
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
Neonatal onset of mitochondrial disorders in 129 patients: clinical and laboratory characteristics and a new approach to diagnosis Tomáš Honzík, Markéta Tesařová, Martin Magner, Journal of Inherited Metabolic Disease	2012	82
<i>SURF1</i> missense mutations promote a mild Leigh phenotype Dorota Piekutowska‐Abramczuk, Martin Magner, Ewa Popowska, Clinical Genetics	2009	39
Clinical picture of S-adenosylhomocysteine hydrolase deficiency resembles phosphomannomutase 2 deficiency Tomáš Honzík, Martin Magner, Jakub Krijt, Molecular Genetics and Metabolism BiochemistryNatural SciencesInherited Metabolic DiseaseMolecular BiologyPathology	2012	36
Transferrin mutations at the glycosylation site complicate diagnosis of congenital disorders of glycosylation type I Maïlys Guillard, Yoshinao Wada, Hana Hansíková, Journal of Inherited Metabolic Disease GlycoproteomicsTryptic PeptidesMendelian DisorderTransferrin MutationsBiochemistry	2011	35
Issues of Projectivity in the Prague Dependency Treebank. Eva Hajičová, Jiří Havelka, Petr Sgall,	2004	31
Clinical, biochemical and molecular analyses of six patients with isolated cytochrome c oxidase deficiency due to mutations in the SCO2 gene Kateřina Veselá, Markéta Tesařová, Pavel Martásek, Acta Paediatrica	2004	30

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