Viktor Stránecký

3.4k total citations
66 papers, 1.3k citations indexed

About

Viktor Stránecký is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Viktor Stránecký has authored 66 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Molecular Biology, 19 papers in Genetics and 8 papers in Physiology. Recurrent topics in Viktor Stránecký's work include Mitochondrial Function and Pathology (8 papers), RNA modifications and cancer (8 papers) and Genomics and Rare Diseases (7 papers). Viktor Stránecký is often cited by papers focused on Mitochondrial Function and Pathology (8 papers), RNA modifications and cancer (8 papers) and Genomics and Rare Diseases (7 papers). Viktor Stránecký collaborates with scholars based in Czechia, United Kingdom and United States. Viktor Stránecký's co-authors include Stanislav Kmoch, Hana Hartmannová, Lenka Nosková, Anna Přistoupilová, Helena Hůlková, Kateřina Hodaňová, M Jirsa, Veronika Barešová, Martin Hřebı́ček and J Zeman and has published in prestigious journals such as Journal of Clinical Investigation, Blood and PLoS ONE.

In The Last Decade

Viktor Stránecký

62 papers receiving 1.3k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Viktor Stránecký Czechia	18	642	226	225	183	177	66	1.3k
Carol Wadham Australia	23	864 1.3×	167 0.7×	138 0.6×	88 0.5×	262 1.5×	43	1.5k
Jan Hilpert Germany	14	672 1.0×	118 0.5×	186 0.8×	153 0.8×	212 1.2×	25	1.4k
Frédérique Savagner France	24	1.0k 1.6×	176 0.8×	138 0.6×	298 1.6×	53 0.3×	58	2.2k
Martha Konieczkowski United States	24	835 1.3×	116 0.5×	221 1.0×	158 0.9×	140 0.8×	41	1.8k
Jocelyne André France	17	975 1.5×	382 1.7×	351 1.6×	119 0.7×	102 0.6×	26	1.6k
Nathan M. Krah United States	17	1.1k 1.7×	194 0.9×	92 0.4×	51 0.3×	173 1.0×	21	2.2k
Nobuhiro Ban Japan	19	727 1.1×	400 1.8×	149 0.7×	151 0.8×	73 0.4×	24	1.7k
Indrika Ratnayaka United Kingdom	18	537 0.8×	224 1.0×	88 0.4×	81 0.4×	204 1.2×	23	1.0k
Susan C. Kiley United States	23	1.2k 1.9×	221 1.0×	123 0.5×	118 0.6×	240 1.4×	36	1.9k
Paola Concolino Italy	19	757 1.2×	357 1.6×	41 0.2×	220 1.2×	235 1.3×	62	1.4k

Countries citing papers authored by Viktor Stránecký

Since Specialization

Citations

This map shows the geographic impact of Viktor Stránecký'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 Viktor Stránecký with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Viktor Stránecký more than expected).

Fields of papers citing papers by Viktor Stránecký

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Viktor Stránecký. 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 Viktor Stránecký. The network helps show where Viktor Stránecký may publish in the future.

Co-authorship network of co-authors of Viktor Stránecký

This figure shows the co-authorship network connecting the top 25 collaborators of Viktor Stránecký. A scholar is included among the top collaborators of Viktor Stránecký 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 Viktor Stránecký. Viktor Stránecký 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

Mráz, Miloš, Petr Svoboda, Helena Kratochvílová, et al.. (2024). Sodium-glucose cotransporter 2 inhibitors induce anti-inflammatory and anti-ferroptotic shift in epicardial adipose tissue of subjects with severe heart failure. Cardiovascular Diabetology. 23(1). 223–223. 11 indexed citations

Přistoupilová, Anna, Ivana Jedličková, Hana Hartmannová, et al.. (2024). Increased burden of rare protein‐truncating variants in constrained, brain‐specific and synaptic genes in extremely impulsively violent males with antisocial personality disorder. Genes Brain & Behavior. 23(1). e12882–e12882. 5 indexed citations

Škopková, Martina, Viktor Stránecký, Miriam Kolníková, et al.. (2023). ATAD3A-related pontocerebellar hypoplasia: new patients and insights into phenotypic variability. Orphanet Journal of Rare Diseases. 18(1). 92–92. 6 indexed citations

Vlčková, Markéta, Darina Prchalová, Jana Haberlová, et al.. (2023). A new patient with congenital myasthenic syndrome type 20 due to compound heterozygous missense SLC5A7 variants suggests trends in genotype–phenotype correlation. Molecular Genetics & Genomic Medicine. 11(6). e2154–e2154. 1 indexed citations

Jedličková, Ivana, Anna Přistoupilová, Lenka Nosková, et al.. (2020). Spinal muscular atrophy caused by a novel Alu‐mediated deletion of exons 2a‐5 in SMN1 undetectable with routine genetic testing. Molecular Genetics & Genomic Medicine. 8(7). e1238–e1238. 9 indexed citations

Stolařová, Lenka, Eva Macháčková, Petra Zemánková, et al.. (2020). Identification of Germline Mutations in Melanoma Patients with Early Onset, Double Primary Tumors, or Family Cancer History by NGS Analysis of 217 Genes. Biomedicines. 8(10). 404–404. 13 indexed citations

Ondrušková, Nina, Tomáš Honzík, Viktor Stránecký, et al.. (2020). Severe phenotype of ATP6AP1‐CDG in two siblings with a novel mutation leading to a differential tissue‐specific ATP6AP1 protein pattern, cellular oxidative stress and hepatic copper accumulation. Journal of Inherited Metabolic Disease. 43(4). 694–700. 13 indexed citations

Krejčík, Zdeněk, Jǐŕı Kléma, Monika Beličková, et al.. (2020). LncRNA Profiling Reveals That the Deregulation of H19, WT1-AS, TCL6, and LEF1-AS1 Is Associated with Higher-Risk Myelodysplastic Syndrome. Cancers. 12(10). 2726–2726. 21 indexed citations

Ďuďáková, Ľubica, Pavlína Skalická, Olga Ulmanová, et al.. (2020). Pseudodominant Nanophthalmos in a Roma Family Caused by a Novel PRSS56 Variant. Journal of Ophthalmology. 2020. 1–9. 1 indexed citations

10.

Kousal, Bohdan, Tomáš Honzík, Hana Hansíková, et al.. (2019). Review of SRD5A3 Disease-Causing Sequence Variants and Ocular Findings in Steroid 5α-Reductase Type 3 Congenital Disorder of Glycosylation, and a Detailed New Case. Folia Biologica. 65(3). 134–141. 10 indexed citations

11.

Vevera, Jan, Mehdi Zarrei, Hana Hartmannová, et al.. (2018). Rare copy number variation in extremely impulsively violent males. Genes Brain & Behavior. 18(6). e12536–e12536. 10 indexed citations

12.

Lišková, Petra, Ľubica Ďuďáková, Karla E. Rojas López, et al.. (2018). Ectopic GRHL2 Expression Due to Non-coding Mutations Promotes Cell State Transition and Causes Posterior Polymorphous Corneal Dystrophy 4. The American Journal of Human Genetics. 102(3). 447–459. 40 indexed citations

13.

Prchalová, Darina, Markéta Havlovičová, Katalin Štěrbová, et al.. (2017). Analysis of 31-year-old patient with SYNGAP1 gene defect points to importance of variants in broader splice regions and reveals developmental trajectory of SYNGAP1-associated phenotype: case report. BMC Medical Genetics. 18(1). 62–62. 23 indexed citations

14.

Magner, Martin, Viktor Stránecký, Anna Přistoupilová, et al.. (2016). Thymidine kinase 2 and alanyl-tRNA synthetase 2 deficiencies cause lethal mitochondrial cardiomyopathy: case reports and review of the literature. Cardiology in the Young. 27(5). 936–944. 27 indexed citations

15.

Tesařová, Markéta, Viktor Stránecký, Anna Přistoupilová, et al.. (2014). Lipoprotein Lipase Deficiency: Clinical, Biochemical and Molecular Characteristics in Three Patients with Novel Mutations in the LPL Gene. Folia Biologica. 60(5). 235–243. 9 indexed citations

16.

Pecina, Petr, et al.. (2012). Adaptation of respiratory chain biogenesis to cytochrome c oxidase deficiency caused by SURF1 gene mutations. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1822(7). 1114–1124. 26 indexed citations

17.

Hejzlarová, Kateřina, et al.. (2012). Compensatory upregulation of respiratory chain complexes III and IV in isolated deficiency of ATP synthase due to TMEM70 mutation. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1817(7). 1037–1043. 34 indexed citations

18.

Kmoch, Stanislav, Viktor Stránecký, Richard D. Emes, & Hannah M. Mitchison. (2012). Bioinformatic perspectives in the neuronal ceroid lipofuscinoses. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1832(11). 1831–1841. 6 indexed citations

19.

Slany, Robert K., Jiřina Bártková, Viktor Stránecký, et al.. (2012). DNA Damage Response and Inflammatory Signaling Limit the MLL-ENL-Induced Leukemogenesis In Vivo. Cancer Cell. 21(4). 517–531. 53 indexed citations

20.

Nosková, Lenka, Viktor Stránecký, Hana Hartmannová, et al.. (2011). Mutations in DNAJC5, Encoding Cysteine-String Protein Alpha, Cause Autosomal-Dominant Adult-Onset Neuronal Ceroid Lipofuscinosis. The American Journal of Human Genetics. 89(4). 589–589. 10 indexed citations

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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