Hana Antonická

5.1k citations
42 papers · 3.1k · h-index 25

Impact in

  • Clinical Biochemistry top 0.2%
    • Metabolism and Genetic Disorders
  • Molecular Biology top 2%
    • Mitochondrial Function and Pathology
    • ATP Synthase and ATPases Research
    • RNA modifications and cancer
    • RNA and protein synthesis mechanisms
    • RNA Research and Splicing
    • Photosynthetic Processes and Mechanisms
    • Genomics and Phylogenetic Studies

Papers in

  • Molecular Biology 42
    • Mitochondrial Function and Pathology 33
    • ATP Synthase and ATPases Research 22
    • RNA modifications and cancer 13
    • RNA and protein synthesis mechanisms 12
    • RNA Research and Splicing 8
    • Ubiquitin and proteasome pathways 2
  • Clinical Biochemistry 17
    • Metabolism and Genetic Disorders 17
Co-authors
Eric A. Shoubridge (32 shared papers)Florin Sasarman (16 shared papers)Nancy G. Kennaway (3 shared papers)Woranontee Weraarpachai (11 shared papers)Tamiko Nishimura (3 shared papers)Catherine Brunel‐Guitton (3 shared papers)Anne‐Claude Gingras (4 shared papers)Timothy Wai (1 shared paper)
Journals
Human Molecular Genetics (7 papers)The American Journal of Human Genetics (6 papers)Nucleic Acids Research (4 papers)Biochemical Journal (4 papers)Cell Reports (2 papers)
Partner nations
CanadaUnited StatesUnited Kingdom

In The Last Decade

Hana Antonická

41 papers receiving 3.1k citations

Peers

Hana Antonická
Comparison fields: 5 of 91
  • Clinical Biochemistry 935
  • Molecular Biology 2.7k
  • Aging 19
  • Cancer Research 134
  • Cell Biology 128
Replace Florin Sasarman with:
Florin Sasarman Canada
Takehiro Yasukawa Japan
Sjoerd Wanrooij Sweden
Benedetta Ruzzenente Sweden
Alexis A. Jourdain Switzerland
Elena J. Tucker Australia
Eva Richard Spain
Joshua M. Baughman United States
Teresa Rizza Italy
Cassandra Obie United States
Hana Antonická relative to Florin Sasarman Canada Florin Sasarman's profile →
Citations per field
00.5×1.5×1.8×
Florin Sasarman · 1×
Citations per year

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-authors

The 25 scholars most cited alongside Hana Antonická, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Hana Antonická Line = papers co-authored together Hana Antonická links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 42 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Mutations in COX15 Produce a Defect in the Mitochondrial Heme Biosynthetic Pathway, Causing Early-Onset Fatal Hypertrophic Cardiomyopathy
The American Journal of Human Genetics ·Hana Antonická, André Mattman, Christopher G. Carlson, D. Moira Glerum, Kristen C. Hoffbuhr, Scot C. Leary, Nancy G. Kennaway, Eric A. Shoubridge
2003241
2
Mutation in TACO1, encoding a translational activator of COX I, results in cytochrome c oxidase deficiency and late-onset Leigh syndrome
Nature Genetics ·Woranontee Weraarpachai, Hana Antonická, Florin Sasarman, Jürgen Seeger, Bertold Schrank, Jill E. Kolesar, Hanns Lochmüller, Mario Chevrette, Brett A. Kaufman, Rita Horváth, Eric A. Shoubridge
2009232
3
Mitochondrial RNA Granules Are Centers for Posttranscriptional RNA Processing and Ribosome Biogenesis
Cell Reports ·Hana Antonická, Eric A. Shoubridge
2015224
4
LRPPRC and SLIRP Interact in a Ribonucleoprotein Complex That Regulates Posttranscriptional Gene Expression in Mitochondria
Molecular Biology of the Cell ·Florin Sasarman, Catherine Brunel‐Guitton, Hana Antonická, Timothy Wai, Eric A. Shoubridge
2010219
5
Mutations in COX10 result in a defect in mitochondrial heme A biosynthesis and account for multiple, early-onset clinical phenotypes associated with isolated COX deficiency
Human Molecular Genetics ·Hana Antonická
2003195
6
The Mitochondrial RNA-Binding Protein GRSF1 Localizes to RNA Granules and Is Required for Posttranscriptional Mitochondrial Gene Expression
Cell Metabolism ·Hana Antonická, Florin Sasarman, Tamiko Nishimura, Vincent Paupe, Eric A. Shoubridge
2013183
7
Identification and Characterization of a Common Set of Complex I Assembly Intermediates in Mitochondria from Patients with Complex I Deficiency
Journal of Biological Chemistry ·Hana Antonická, Isla Ogilvie, Tanja Taivassalo, Roberto P. Anitori, Ronald G. Haller, John Vissing, Nancy G. Kennaway, Eric A. Shoubridge
2003158
8
Mutant Mitochondrial Elongation Factor G1 and Combined Oxidative Phosphorylation Deficiency
New England Journal of Medicine ·Marieke J. H. Coenen, Hana Antonická, Cristina Ugalde, Florin Sasarman, (unknown), J. G. A. M. Heister, Robert F. Newbold, Frans J.M. Trijbels, Lambert P. van den Heuvel, Eric A. Shoubridge, Jan Smeıtınk
2004153
9
Distinct Clinical Phenotypes Associated with a Mutation in the Mitochondrial Translation Elongation Factor EFTs
The American Journal of Human Genetics ·Jan Smeıtınk, Orly Elpeleg, Hana Antonická, Heleen Diepstra, Ann Saada, P. Smits, Florin Sasarman, Gert Vriend, Jasmine Jacob‐Hirsch, Avraham Shaag, Gideon Rechavi, Brigitte Welling, Jürgen Horst, Richard J. Rodenburg, Bert van den Heuvel, Eric A. Shoubridge
2006144
10
A pseudouridine synthase module is essential for mitochondrial protein synthesis and cell viability
EMBO Reports ·Hana Antonická, Karine Choquet, Zhen‐Yuan Lin, Anne‐Claude Gingras, Claudia L. Kleinman, Eric A. Shoubridge
2016129
11
A High-Density Human Mitochondrial Proximity Interaction Network
Cell Metabolism ·Hana Antonická, Zhen‐Yuan Lin, Alexandre Janer, Mari J. Aaltonen, Woranontee Weraarpachai, Anne‐Claude Gingras, Eric A. Shoubridge
2020122
12
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 ·Florin Sasarman, Hana Antonická, Eric A. Shoubridge
2008117
13
Mutations in C12orf65 in Patients with Encephalomyopathy and a Mitochondrial Translation Defect
The American Journal of Human Genetics ·Hana Antonická, Elsebet Østergaard, Florin Sasarman, Woranontee Weraarpachai, Flemming Wibrand, Anne Marie B. Pedersen, Richard J. Rodenburg, Marjo S. van der Knaap, Jan Smeıtınk, Zofia M. Chrzanowska‐Lightowlers, Eric A. Shoubridge
2010116
14
The molecular basis for tissue specificity of the oxidative phosphorylation deficiencies in patients with mutations in the mitochondrial translation factor EFG1
Human Molecular Genetics ·Hana Antonická, Florin Sasarman, Nancy G. Kennaway, Eric A. Shoubridge
2006112
15
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 ·Woranontee Weraarpachai, Florin Sasarman, Tamiko Nishimura, Hana Antonická, Karine Auré, Agnès Rötig, Anne Lombès, Eric A. Shoubridge
201281
16
The 3′ addition of CCA to mitochondrial tRNASer(AGY) is specifically impaired in patients with mutations in the tRNA nucleotidyl transferase TRNT1
Human Molecular Genetics ·Florin Sasarman, Isabelle Thiffault, Woranontee Weraarpachai, Steven Salomon, Catalina Maftei, Julie D. Gauthier, Benjamin Ellazam, Neil Webb, Hana Antonická, Alexandre Janer, Catherine Brunel‐Guitton, Orly Elpeleg, Grant A. Mitchell, Eric A. Shoubridge
201556
17
An RMND1 Mutation Causes Encephalopathy Associated with Multiple Oxidative Phosphorylation Complex Deficiencies and a Mitochondrial Translation Defect
The American Journal of Human Genetics ·Alexandre Janer, Hana Antonická, Emilie Lalonde, Tamiko Nishimura, Florin Sasarman, Garry K. Brown, Ruth M. Brown, Jacek Majewski, Eric A. Shoubridge
201255
18
ATAD3A has a scaffolding role regulating mitochondria inner membrane structure and protein assembly
Cell Reports ·Tania Arguello, Susana Peralta, Hana Antonická, Gabriel Gaidosh, Francisca Díaz, Ya-Ting Tu, Sofía García, Ramin Shiekhattar, Antonio Barrientos, Carlos T. Moraes
202153
19
The 2-thiouridylase function of the human MTU1 (TRMU) enzyme is dispensable for mitochondrial translation
Human Molecular Genetics ·Florin Sasarman, Hana Antonická, Rita Horváth, Eric A. Shoubridge
201146
20
Whole-exome sequencing identifies novel ECHS1 mutations in Leigh syndrome
Human Genetics ·Martine Tétreault, Somayyeh Fahiminiya, Hana Antonická, Grant A. Mitchell, Michael T. Geraghty, Matthew A. Lines, Kym M. Boycott, Eric A. Shoubridge, John J. Mitchell, Jacques L. Michaud, Jacek Majewski
201545

About Hana Antonická

Hana Antonická is a scholar working on Molecular Biology, Clinical Biochemistry, Cellular and Molecular Neuroscience, Genetics and Renewable Energy, Sustainability and the Environment, having authored 42 papers that have together received 3.1k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (33 papers), ATP Synthase and ATPases Research (22 papers), Metabolism and Genetic Disorders (17 papers), RNA modifications and cancer (13 papers), RNA and protein synthesis mechanisms (12 papers), RNA Research and Splicing (8 papers), Metalloenzymes and iron-sulfur proteins (2 papers) and Ubiquitin and proteasome pathways (2 papers). The work is most often cited by research in Clinical Biochemistry (935 citations), Molecular Biology (2.7k citations), Aging (19 citations), Cancer Research (134 citations) and Cell Biology (128 citations). Hana Antonická has collaborated with scholars based in Canada, United States and United Kingdom. Frequent co-authors include Eric A. Shoubridge, Florin Sasarman, Nancy G. Kennaway, Woranontee Weraarpachai, Tamiko Nishimura, Catherine Brunel‐Guitton, Anne‐Claude Gingras, Timothy Wai, Zhen‐Yuan Lin and Alexandre Janer. Their work appears in journals such as Human Molecular Genetics, The American Journal of Human Genetics, Nucleic Acids Research, Biochemical Journal and Cell Reports.

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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