Hervé Testard

904 total citations
9 papers, 289 citations indexed

About

Hervé Testard is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Hervé Testard has authored 9 papers receiving a total of 289 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 3 papers in Pediatrics, Perinatology and Child Health and 3 papers in Genetics. Recurrent topics in Hervé Testard's work include Genomic variations and chromosomal abnormalities (2 papers), Amino Acid Enzymes and Metabolism (1 paper) and Genomics and Rare Diseases (1 paper). Hervé Testard is often cited by papers focused on Genomic variations and chromosomal abnormalities (2 papers), Amino Acid Enzymes and Metabolism (1 paper) and Genomics and Rare Diseases (1 paper). Hervé Testard collaborates with scholars based in France, United Kingdom and Spain. Hervé Testard's co-authors include Jean Aicardi, Nathalie Bednarek, John B.P. Stephenson, Françoise Goutières, V. V. Smith, Orvar Eeg‐Olofsson, Frances Elmslie, C D Ferrie, David A. Griesemer and Martin Kirkpatrick and has published in prestigious journals such as Blood, Neurology and Annals of Neurology.

In The Last Decade

Hervé Testard

7 papers receiving 276 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hervé Testard France 7 186 96 76 34 34 9 289
Eduardo López‐Laso Spain 12 224 1.2× 93 1.0× 42 0.6× 27 0.8× 16 0.5× 40 453
Tomohiro Kumada Japan 13 168 0.9× 36 0.4× 85 1.1× 26 0.8× 34 1.0× 44 398
Elly F. Ippel Netherlands 9 139 0.7× 96 1.0× 51 0.7× 16 0.5× 18 0.5× 10 254
Anna-Kaisa Anttonen Finland 3 151 0.8× 69 0.7× 128 1.7× 13 0.4× 75 2.2× 3 286
Noboru Fueki Japan 10 207 1.1× 31 0.3× 49 0.6× 29 0.9× 14 0.4× 24 356
Anna Marcé‐Grau Spain 10 139 0.7× 63 0.7× 20 0.3× 26 0.8× 24 0.7× 19 284
Anne-Marie Childs United Kingdom 6 232 1.2× 32 0.3× 32 0.4× 37 1.1× 24 0.7× 6 400
Clara DM van Karnebeek Canada 7 190 1.0× 49 0.5× 39 0.5× 9 0.3× 28 0.8× 7 349
Xixiang Ma China 9 177 1.0× 72 0.8× 96 1.3× 23 0.7× 8 0.2× 17 284
Megumi Tsuji Japan 9 111 0.6× 55 0.6× 31 0.4× 10 0.3× 20 0.6× 25 285

Countries citing papers authored by Hervé Testard

Since Specialization
Citations

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

Fields of papers citing papers by Hervé Testard

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hervé Testard

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

All Works

9 of 9 papers shown
1.
Spitz, Marie‐Aude, Sylvain Roche, Bénédicte Héron, et al.. (2016). Chronic Diarrhea in l-Amino Acid Decarboxylase (AADC) Deficiency: A Prominent Clinical Finding Among a Series of Ten French Patients. JIMD Reports. 31. 85–93. 13 indexed citations
2.
Testard, Hervé, et al.. (2011). Anhidrotic ectodermal dysplasia. SpringerReference. 48(5). 343–5.
3.
Jung, Julien, Hervé Testard, Elisabeth Tournier‐Lasserve, et al.. (2010). Phenotypic Variability of Episodic Ataxia Type 2 Mutations: A Family Study. European Neurology. 64(2). 114–116. 17 indexed citations
4.
Ville, Dorothée, Julitta de Bellescize, Hervé Testard, et al.. (2009). Ring 14 chromosome presenting as early‐onset isolated partial epilepsy. Developmental Medicine & Child Neurology. 51(11). 917–922. 14 indexed citations
5.
Ferrie, C D, Jean Aicardi, Nathalie Bednarek, et al.. (2007). Paroxysmal extreme pain disorder (previously familial rectal pain syndrome). Neurology. 69(6). 586–595. 124 indexed citations
6.
Krahn, Martin, Adolfo López de Munaín, Nathalie Streichenberger, et al.. (2006). CAPN3 mutations in patients with idiopathic eosinophilic myositis. Annals of Neurology. 59(6). 905–911. 75 indexed citations
7.
8.
9.
Aitken, Celia, James C. Booth, M Booth, et al.. (1996). Molecular epidemiology and significance of a cluster of cases of CMV infection occurring on a special care baby unit. Journal of Hospital Infection. 34(3). 183–189. 1 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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2026