Hana Antonická

5.0k total citations
42 papers, 3.0k citations indexed

About

Hana Antonická is a scholar working on Molecular Biology, Clinical Biochemistry and Cellular and Molecular Neuroscience. According to data from OpenAlex, Hana Antonická has authored 42 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 42 papers in Molecular Biology, 17 papers in Clinical Biochemistry and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in Hana Antonická's work include Mitochondrial Function and Pathology (33 papers), ATP Synthase and ATPases Research (22 papers) and Metabolism and Genetic Disorders (17 papers). Hana Antonická is often cited by papers focused on Mitochondrial Function and Pathology (33 papers), ATP Synthase and ATPases Research (22 papers) and Metabolism and Genetic Disorders (17 papers). Hana Antonická collaborates with scholars based in Canada, United States and United Kingdom. Hana Antonická's co-authors include Eric A. Shoubridge, Florin Sasarman, Nancy G. Kennaway, Woranontee Weraarpachai, Tamiko Nishimura, Catherine Brunel‐Guitton, Anne‐Claude Gingras, Timothy Wai, Jan Smeıtınk and Zhen‐Yuan Lin and has published in prestigious journals such as New England Journal of Medicine, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Hana Antonická

40 papers receiving 3.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hana Antonická Canada 25 2.8k 1.0k 150 150 142 42 3.0k
Sjoerd Wanrooij Sweden 23 2.2k 0.8× 930 0.9× 134 0.9× 102 0.7× 143 1.0× 42 2.4k
Florin Sasarman Canada 26 2.3k 0.8× 831 0.8× 109 0.7× 120 0.8× 124 0.9× 33 2.5k
Roel Smeets Netherlands 22 1.9k 0.7× 1.0k 1.0× 129 0.9× 160 1.1× 95 0.7× 33 2.1k
Alexis A. Jourdain Switzerland 20 1.7k 0.6× 286 0.3× 90 0.6× 204 1.4× 187 1.3× 31 2.0k
Cassandra Obie United States 16 1.4k 0.5× 345 0.3× 171 1.1× 163 1.1× 185 1.3× 22 1.7k
Eva Richard Spain 23 820 0.3× 609 0.6× 104 0.7× 85 0.6× 87 0.6× 61 1.2k
Benedetta Ruzzenente Sweden 18 1.7k 0.6× 377 0.4× 68 0.5× 207 1.4× 114 0.8× 27 1.8k
Celia Pérez‐Cerdá Spain 30 1.8k 0.7× 1.3k 1.3× 325 2.2× 47 0.3× 412 2.9× 119 2.5k
Majbrit Hjerrild Denmark 8 1.4k 0.5× 238 0.2× 81 0.5× 104 0.7× 165 1.2× 8 1.6k
Simona Reina Italy 25 1.5k 0.6× 266 0.3× 38 0.3× 144 1.0× 206 1.5× 47 1.8k

Countries citing papers authored by Hana Antonická

Since Specialization
Citations

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

Fields of papers citing papers by Hana Antonická

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hana Antonická

This figure shows the co-authorship network connecting the top 25 collaborators of Hana Antonická. A scholar is included among the top collaborators of Hana Antonická 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 Hana Antonická. Hana Antonická is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Antonická, Hana, et al.. (2024). CHCHD10P80L knock-in zebrafish display a mild ALS-like phenotype. Experimental Neurology. 382. 114945–114945. 2 indexed citations
2.
Zhong, Hui, Alexandre Janer, Oleh Khalimonchuk, et al.. (2023). BOLA3 and NFU1 link mitoribosome iron–sulfur cluster assembly to multiple mitochondrial dysfunctions syndrome. Nucleic Acids Research. 51(21). 11797–11812. 17 indexed citations
3.
Janer, Alexandre, et al.. (2023). The role of the mitochondrial outer membrane protein SLC25A46 in mitochondrial fission and fusion. Life Science Alliance. 6(6). e202301914–e202301914. 18 indexed citations
4.
Arguello, Tania, Susana Peralta, Hana Antonická, et al.. (2021). ATAD3A has a scaffolding role regulating mitochondria inner membrane structure and protein assembly. Cell Reports. 37(12). 110139–110139. 50 indexed citations
5.
Mitsopoulos, Panagiotis, et al.. (2017). Stomatin-like protein 2 deficiency results in impaired mitochondrial translation. PLoS ONE. 12(6). e0179967–e0179967. 16 indexed citations
6.
Antonická, Hana, Karine Choquet, Zhen‐Yuan Lin, et al.. (2016). A pseudouridine synthase module is essential for mitochondrial protein synthesis and cell viability. EMBO Reports. 18(1). 28–38. 127 indexed citations
7.
Janer, Alexandre, Clara DM van Karnebeek, Florin Sasarman, et al.. (2015). RMND1 deficiency associated with neonatal lactic acidosis, infantile onset renal failure, deafness, and multiorgan involvement. European Journal of Human Genetics. 23(10). 1301–1307. 23 indexed citations
8.
Tétreault, Martine, Somayyeh Fahiminiya, Hana Antonická, et al.. (2015). Whole-exome sequencing identifies novel ECHS1 mutations in Leigh syndrome. Human Genetics. 134(9). 981–991. 44 indexed citations
9.
Antonická, Hana & Eric A. Shoubridge. (2015). Mitochondrial RNA Granules Are Centers for Posttranscriptional RNA Processing and Ribosome Biogenesis. Cell Reports. 10(6). 920–932. 220 indexed citations
10.
Antonická, Hana, Florin Sasarman, Tamiko Nishimura, Vincent Paupe, & Eric A. Shoubridge. (2013). The Mitochondrial RNA-Binding Protein GRSF1 Localizes to RNA Granules and Is Required for Posttranscriptional Mitochondrial Gene Expression. Cell Metabolism. 17(3). 386–398. 178 indexed citations
11.
Weraarpachai, Woranontee, Florin Sasarman, Tamiko Nishimura, et al.. (2012). Mutations in C12orf62, a Factor that Couples COX I Synthesis with Cytochrome c Oxidase Assembly, Cause Fatal Neonatal Lactic Acidosis. The American Journal of Human Genetics. 90(1). 142–151. 78 indexed citations
12.
Sasarman, Florin, Hana Antonická, Rita Horváth, & Eric A. Shoubridge. (2011). The 2-thiouridylase function of the human MTU1 (TRMU) enzyme is dispensable for mitochondrial translation. Human Molecular Genetics. 20(23). 4634–4643. 46 indexed citations
13.
Sasarman, Florin, Catherine Brunel‐Guitton, Hana Antonická, Timothy Wai, & Eric A. Shoubridge. (2010). LRPPRC and SLIRP Interact in a Ribonucleoprotein Complex That Regulates Posttranscriptional Gene Expression in Mitochondria. Molecular Biology of the Cell. 21(8). 1315–1323. 215 indexed citations
14.
Smits, P., Hana Antonická, Peter M. van Hasselt, et al.. (2010). Mutation in subdomain G' of mitochondrial elongation factor G1 is associated with combined OXPHOS deficiency in fibroblasts but not in muscle. European Journal of Human Genetics. 19(3). 275–279. 39 indexed citations
15.
Antonická, Hana, Elsebet Østergaard, Florin Sasarman, et al.. (2010). Mutations in C12orf65 in Patients with Encephalomyopathy and a Mitochondrial Translation Defect. The American Journal of Human Genetics. 87(1). 115–122. 115 indexed citations
16.
Sasarman, Florin, Hana Antonická, & Eric A. Shoubridge. (2008). The A3243G tRNALeu(UUR) MELAS mutation causes amino acid misincorporation and a combined respiratory chain assembly defect partially suppressed by overexpression of EFTu and EFG2. Human Molecular Genetics. 17(23). 3697–3707. 116 indexed citations
17.
Smeıtınk, Jan, Orly Elpeleg, Hana Antonická, et al.. (2006). Distinct Clinical Phenotypes Associated with a Mutation in the Mitochondrial Translation Elongation Factor EFTs. The American Journal of Human Genetics. 79(5). 869–877. 142 indexed citations
18.
Coenen, Marieke J. H., Hana Antonická, Cristina Ugalde, et al.. (2004). Mutant Mitochondrial Elongation Factor G1 and Combined Oxidative Phosphorylation Deficiency. New England Journal of Medicine. 351(20). 2080–2086. 152 indexed citations
19.
Antonická, Hana, André Mattman, D. Moira Glerum, et al.. (2003). Mutations in COX15 Produce a Defect in the Mitochondrial Heme Biosynthetic Pathway, Causing Early-Onset Fatal Hypertrophic Cardiomyopathy. The American Journal of Human Genetics. 72(1). 101–114. 237 indexed citations
20.
Houštěk, J, Petr Klement, Hana Antonická, et al.. (1999). Complex approach to prenatal diagnosis of cytochromec oxidase deficiencies. Prenatal Diagnosis. 19(6). 552–558. 11 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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