Catherine Antar

413 total citations
11 papers, 288 citations indexed

About

Catherine Antar is a scholar working on Molecular Biology, Neurology and Clinical Biochemistry. According to data from OpenAlex, Catherine Antar has authored 11 papers receiving a total of 288 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 5 papers in Neurology and 4 papers in Clinical Biochemistry. Recurrent topics in Catherine Antar's work include Amyotrophic Lateral Sclerosis Research (5 papers), Metabolomics and Mass Spectrometry Studies (4 papers) and Metabolism and Genetic Disorders (4 papers). Catherine Antar is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (5 papers), Metabolomics and Mass Spectrometry Studies (4 papers) and Metabolism and Genetic Disorders (4 papers). Catherine Antar collaborates with scholars based in France, Sweden and Australia. Catherine Antar's co-authors include Christian Andrés, William Camu, Patrick Vourc’h, Hélène Blasco, Jean‐Michel Halimi, Bertrand de Toffol, P. Corcia, Bruno Giraudeau, Frédéric Laumonnier and Jamel Chelly and has published in prestigious journals such as Neurology, Analytical Biochemistry and Molecular Psychiatry.

In The Last Decade

Catherine Antar

11 papers receiving 286 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Catherine Antar France 9 194 100 95 36 32 11 288
Cinzia Bertolin Italy 10 191 1.0× 105 1.1× 105 1.1× 37 1.0× 14 0.4× 21 317
Anna Maija Saukkonen Finland 9 148 0.8× 83 0.8× 72 0.8× 20 0.6× 33 1.0× 12 250
Claire Guissart France 12 174 0.9× 65 0.7× 40 0.4× 73 2.0× 35 1.1× 22 301
Abigail L. Pfaff Australia 11 178 0.9× 84 0.8× 42 0.4× 57 1.6× 21 0.7× 33 276
Anna Szuto Canada 10 219 1.1× 160 1.6× 110 1.2× 57 1.6× 52 1.6× 20 361
Janel O. Johnson United States 10 153 0.8× 163 1.6× 73 0.8× 58 1.6× 66 2.1× 11 364
Mustafa Batbayli Denmark 9 235 1.2× 129 1.3× 38 0.4× 51 1.4× 49 1.5× 10 411
M. Kéfi Tunisia 10 211 1.1× 92 0.9× 24 0.3× 28 0.8× 20 0.6× 14 326
Maartje Pennings Netherlands 10 134 0.7× 48 0.5× 31 0.3× 76 2.1× 44 1.4× 21 272
Zoltán Grosz Hungary 8 81 0.4× 33 0.3× 50 0.5× 18 0.5× 44 1.4× 20 170

Countries citing papers authored by Catherine Antar

Since Specialization
Citations

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

Fields of papers citing papers by Catherine Antar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Catherine Antar

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

All Works

11 of 11 papers shown
1.
Veyrat‐Durebex, Charlotte, Isabelle Benz‐de Bretagne, Clément Bruno, et al.. (2021). Quality consideration for the validation of urine TMA and TMAO measurement by nuclear magnetic resonance spectroscopy in Fish Odor Syndrome. Analytical Biochemistry. 630. 114330–114330. 1 indexed citations
2.
Fatet, Alice, Lydie Nadal‐Desbarats, Catherine Antar, et al.. (2021). Characterization of serum metabolome changes during the 5 weeks prior to breeding in female goat kids. Livestock Science. 250. 104572–104572. 2 indexed citations
3.
Veyrat‐Durebex, Charlotte, Christelle Debeissat, Hélène Blasco, et al.. (2017). Hyperphenylalaninemia Correlated with Global Decrease of Antioxidant Genes Expression in White Blood Cells of Adult Patients with Phenylketonuria. JIMD Reports. 37. 73–83. 10 indexed citations
4.
Blasco, Hélène, Charlotte Veyrat‐Durebex, Marylène Bertrand, et al.. (2016). A Multiplatform Metabolomics Approach to Characterize Plasma Levels of Phenylalanine and Tyrosine in Phenylketonuria. JIMD Reports. 69–79. 20 indexed citations
5.
Blasco, Hélène, Lydie Nadal‐Desbarats, Pierre‐François Pradat, et al.. (2014). Untargeted1H-NMR metabolomics in CSF. Neurology. 82(13). 1167–1174. 32 indexed citations
6.
Blasco, Hélène, Nathalie Bernard‐Marissal, Patrick Vourc’h, et al.. (2013). A Rare Motor Neuron Deleterious Missense Mutation in theDPYSL3(CRMP4) Gene is Associated with ALS. Human Mutation. 34(7). 953–960. 28 indexed citations
7.
Corcia, Philippe, Caroline Ingre, Hélène Blasco, et al.. (2012). Homozygous SMN2 deletion is a protective factor in the Swedish ALS population. European Journal of Human Genetics. 20(5). 588–591. 19 indexed citations
8.
Blasco, Hélène, Catherine Antar, F. Labarthe, et al.. (2009). Filter paper saturated by urine sample in metabolic disorders detection by proton magnetic resonance spectroscopy. Analytical and Bioanalytical Chemistry. 396(3). 1205–1211. 10 indexed citations
9.
Laumonnier, Frédéric, Cheryl Shoubridge, Catherine Antar, et al.. (2009). Mutations of the UPF3B gene, which encodes a protein widely expressed in neurons, are associated with nonspecific mental retardation with or without autism. Molecular Psychiatry. 15(7). 767–776. 89 indexed citations
10.
Martin, Isabelle, Patrick Vourc’h, Catherine Antar, et al.. (2009). Association study of the ubiquitin conjugating enzyme gene UBE2H in sporadic ALS. Amyotrophic Lateral Sclerosis. 10(5-6). 432–435. 9 indexed citations
11.
Corcia, P., William Camu, Jean‐Michel Halimi, et al.. (2006). SMN1 gene, but not SMN2 , is a risk factor for sporadic ALS. Neurology. 67(7). 1147–1150. 68 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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