H Houst'ková

728 total citations
21 papers, 548 citations indexed

About

H Houst'ková is a scholar working on Molecular Biology, Clinical Biochemistry and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, H Houst'ková has authored 21 papers receiving a total of 548 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 10 papers in Clinical Biochemistry and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in H Houst'ková's work include Mitochondrial Function and Pathology (16 papers), ATP Synthase and ATPases Research (11 papers) and Metabolism and Genetic Disorders (10 papers). H Houst'ková is often cited by papers focused on Mitochondrial Function and Pathology (16 papers), ATP Synthase and ATPases Research (11 papers) and Metabolism and Genetic Disorders (10 papers). H Houst'ková collaborates with scholars based in Czechia, Netherlands and Slovakia. H Houst'ková's co-authors include J Zeman, J Houštěk, Hana Hansı́ková, Petr Pecina, Petr Klement, Coby Van den Bogert, Markéta Tesařová, Hana Hansíková, Dorota Piekutowska‐Abramczuk and Hanna Mierzewska and has published in prestigious journals such as Biochemical Journal, Frontiers in Immunology and Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease.

In The Last Decade

H Houst'ková

21 papers receiving 541 citations

Peers

Countries citing papers authored by H Houst'ková

Since Specialization

Citations

This map shows the geographic impact of H Houst'ková's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by H Houst'ková with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites H Houst'ková more than expected).

Fields of papers citing papers by H Houst'ková

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by H Houst'ková. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by H Houst'ková. The network helps show where H Houst'ková may publish in the future.

Co-authorship network of co-authors of H Houst'ková

This figure shows the co-authorship network connecting the top 25 collaborators of H Houst'ková. A scholar is included among the top collaborators of H Houst'ková based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with H Houst'ková. H Houst'ková is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Anti-IL6 Autoantibodies in an Infant With CRP-Less Septic Shock 2019 ·Frontiers in Immunology ·Markéta Bloomfield, Zuzana Paračková, (unknown), Iva Pospíšilová, (unknown), H Houst'ková, Anna Šedivá	32
2	Noninvasive diagnostics of mitochondrial disorders in isolated lymphocytes with high resolution respirometry 2014 ·PubMed ·Petr Pecina, H Houst'ková, Tomáš Mráček, Alena Pecinová, Hana Nůsková, Markéta Tesařová, Hana Hansı́ková, Jan Janota, J Zeman, J Houštěk	23
3	Novel Mutations in the TAZ Gene in Patients with Barth Syndrome 2013 ·Prague Medical Report ·(unknown), Markéta Tesařová, Martin Magner, H Houst'ková, Hana Hansı́ková, (unknown), Viktor Tomek, (unknown), J Zeman, Tomáš Honzík	15
4	Early onset Alexander disease: a case report with evidence for manifestation of the disorder in neurohypophyseal pituicytes 2008 ·Clinical Neuropathology ·(unknown), Lenka Dvořáková, Lenka Mrázová, H Houst'ková, M. Elleder	3
5	Deficiency of mitochondrial ATP synthase of nuclear genetic origin 2006 ·Neuromuscular Disorders ·Wolfgang Sperl, Pavel Ješina, J Zeman, Johannes A. Mayr, (unknown), (unknown), (unknown), Hana Hansíková, H Houst'ková, Zdeněk Krejčík, Johannes Koch, Joél Smet, Wolfgang Muss, E. Holme, J Houštěk	56
6	Retrospective, Multicentric Study of 180 Children with Cytochrome c Oxidase Deficiency 2005 ·Pediatric Research ·Marek Böhm, Ewa Pronicka, Elżbieta Karczmarewicz, Maciej Pronicki, Dorota Piekutowska‐Abramczuk, Jolanta Sykut‐Cegielska, Hanna Mierzewska, Hana Hansı́ková, Kateřina Veselá, Markéta Tesařová, H Houst'ková, J Houštěk, J Zeman	87
7	Segregation pattern and biochemical effect of the G3460A mtDNA mutation in 27 members of LHON family 2004 ·Journal of the Neurological Sciences ·Vilma Kaplanová, J Zeman, Hana Hansı́ková, (unknown), H Houst'ková, (unknown), J Houštěk	15
8	Genetic defects of cytochrome c oxidase assembly 2004 ·Physiological Research ·Petr Pecina, H Houst'ková, J Zeman, J Houštěk	84
9	Functional alteration of cytochrome c oxidase by SURF1 mutations in Leigh syndrome 2003 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Petr Pecina, (unknown), Subir Roy Chowdhury, Z Drahota, (unknown), Alena Vojtı́šková, Hana Hansı́ková, H Houst'ková, J Zeman, Catherine Godinot, J Houštěk	46
10	[A new missense mutation of 574C>T in the SURF1 gene--biochemical and molecular genetic study in seven children with Leigh syndrome]. 2002 ·PubMed ·(unknown), Hana Hansíková, Catherine Godinot, H Houst'ková, J Houštěk, J Zeman	11
11	[Variation in manifestations of heteroplasmic mtDNA mutation 8993 T>G in two families]. 2002 ·PubMed ·Markéta Tesařová, Hana Hansíková, (unknown), Piroska Klement, H Houst'ková, J Houštěk, J Zeman	1
12	Pulmonary storage with emphysema as a sign of Niemann–Pick type C2 disease (second complementation group). Report of a case 2001 ·Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin ·M. Elleder, H Houst'ková, J Zeman, J. Ledvinová, Helena Poupětová	22
13	A Novel Mutation in SURF1 Causes Skipping of Exon 8 in a Patient with Cytochrome c Oxidase-Deficient Leigh Syndrome and Hypertrichosis 2001 ·Molecular Genetics and Metabolism ·Siôn L. Williams, Jan‐Willem Taanman, Hana Hansı́ková, H Houst'ková, Subir Roy Chowdhury, J Zeman, J Houštěk	20
14	[Various manifestations of the A8344G mtDNA heteroplasmic mutation in 4 families with the MERRF syndrome]. 1999 ·PubMed ·(unknown), J Zeman, H Houst'ková, Hana Hansíková, (unknown), Helena Hůlková, M. Elleder, Evžen Růžička, (unknown), Eva Hrubá, J Houštěk	8
15	Complex approach to prenatal diagnosis of cytochromec oxidase deficiencies 1999 ·Prenatal Diagnosis ·J Houštěk, Petr Klement, (unknown), Hana Antonická, H Houst'ková, (unknown), Ronald J. A. Wanders, J Zeman	11
16	Defective kinetics of cytochrome c oxidase and alteration of mitochondrial membrane potential in fibroblasts and cytoplasmic hybrid cells with the mutation for myoclonus epilepsy with ragged-red fibres (‘MERRF’) at position 8344 nt 1999 ·Biochemical Journal ·Hana Antonická, Daniel Floryk, (unknown), (unknown), (unknown), H Houst'ková, (unknown), Z Drahota, J Zeman, J Houštěk	12
17	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 1995 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·J Houštěk, Petr Klement, (unknown), H Houst'ková, Hana Hansı́ková, Coby Van den Bogert, J Zeman	85
18	Hajdu–Cheney syndrome in a 3 1/2 year old girl 1994 ·Australasian Radiology ·J Zeman, H Houst'ková, K. Kozlowski	8
19	Different restriction fragment pattern of mtDNA indicative of generalized 8993 point mutations in a boy with lactic acidosis 1994 ·Journal of Inherited Metabolic Disease ·Petr Klement, J Zeman, Hana Hansíková, H Houst'ková, (unknown), J Houštěk	4
20	Resin Hemoperfusion in Hepatic Porphyrias 1985 ·Artificial Organs ·Jiří Horák, Pavel Martásek, (unknown), (unknown), M Jirsa, (unknown), H Houst'ková	2

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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