Isabelle Valnot

1.5k total citations
10 papers, 1.1k citations indexed

About

Isabelle Valnot is a scholar working on Molecular Biology, Clinical Biochemistry and Surgery. According to data from OpenAlex, Isabelle Valnot has authored 10 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 6 papers in Clinical Biochemistry and 1 paper in Surgery. Recurrent topics in Isabelle Valnot's work include Mitochondrial Function and Pathology (9 papers), Metabolism and Genetic Disorders (6 papers) and ATP Synthase and ATPases Research (4 papers). Isabelle Valnot is often cited by papers focused on Mitochondrial Function and Pathology (9 papers), Metabolism and Genetic Disorders (6 papers) and ATP Synthase and ATPases Research (4 papers). Isabelle Valnot collaborates with scholars based in France, United Kingdom and United States. Isabelle Valnot's co-authors include Pierre Rustin, Agnès Rötig, Arnold Münnich, Jan‐Willem Taanman, Alexander Tzagoloff, Antoni Barrientos, Jeanne Amiel, Nadine Gigarel, Jean‐Paul Bonnefont and Valérie Cormier‐Daire and has published in prestigious journals such as Journal of Biological Chemistry, Nature Genetics and The American Journal of Human Genetics.

In The Last Decade

Isabelle Valnot

10 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Isabelle Valnot France 8 1.0k 508 108 58 52 10 1.1k
Lukáš Stibůrek Czechia 13 556 0.5× 148 0.3× 63 0.6× 29 0.5× 63 1.2× 15 660
Hana Hansı́ková Czechia 11 482 0.5× 207 0.4× 49 0.5× 23 0.4× 39 0.8× 13 549
Alena Vojtı́šková Czechia 14 498 0.5× 167 0.3× 19 0.2× 46 0.8× 98 1.9× 15 639
Ichiro Matsuda Japan 8 189 0.2× 188 0.4× 47 0.4× 92 1.6× 49 0.9× 9 408
Alba Timón‐Gómez United States 9 437 0.4× 72 0.1× 57 0.5× 16 0.3× 54 1.0× 14 573
E.G. van Grunsven Netherlands 12 684 0.7× 343 0.7× 26 0.2× 15 0.3× 171 3.3× 15 843
Yasuhiro Horibata Japan 17 546 0.5× 60 0.1× 100 0.9× 31 0.5× 124 2.4× 46 983
Natalie Lassen United States 11 441 0.4× 91 0.2× 24 0.2× 22 0.4× 90 1.7× 18 775
M J Bawden Australia 13 767 0.7× 43 0.1× 97 0.9× 48 0.8× 147 2.8× 16 1.0k
Hana Nůsková Czechia 16 452 0.4× 158 0.3× 23 0.2× 23 0.4× 74 1.4× 26 747

Countries citing papers authored by Isabelle Valnot

Since Specialization
Citations

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

Fields of papers citing papers by Isabelle Valnot

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Isabelle Valnot

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

All Works

10 of 10 papers shown
1.
Williams, Siôn L., Isabelle Valnot, Pierre Rustin, & Jan‐Willem Taanman. (2004). Cytochrome c Oxidase Subassemblies in Fibroblast Cultures from Patients Carrying Mutations in COX10, SCO1, or SURF1. Journal of Biological Chemistry. 279(9). 7462–7469. 117 indexed citations
2.
Barrientos, Antoni, Mário H. Barros, Isabelle Valnot, et al.. (2002). Cytochrome oxidase in health and disease. Gene. 286(1). 53–63. 161 indexed citations
3.
Lonlay, Pascale de, Isabelle Valnot, Marina S. Gorbatyuk, et al.. (2001). Mutations in BCS1, a mitochondrial respiratory chain assembly gene, are responsible for complex III deficiency in patients with tubulopathy, encephalopathy and liver failure.. UCL Discovery (University College London). 3 indexed citations
4.
Lonlay, Pascale de, Isabelle Valnot, Antoni Barrientos, et al.. (2001). A mutant mitochondrial respiratory chain assembly protein causes complex III deficiency in patients with tubulopathy, encephalopathy and liver failure. Nature Genetics. 29(1). 57–60. 232 indexed citations
5.
Amiel, Jeanne, Nadine Gigarel, Paule Bénit, et al.. (2001). Prenatal diagnosis of respiratory chain deficiency by direct mutation screening. Prenatal Diagnosis. 21(7). 602–604. 8 indexed citations
6.
Rötig, Agnès, Isabelle Valnot, Claude Mugnier, Pierre Rustin, & Arnold Münnich. (2000). Screening Human EST Database for Identification of Candidate Genes in Respiratory Chain Deficiency. Molecular Genetics and Metabolism. 69(3). 223–232. 3 indexed citations
7.
Valnot, Isabelle, Nadine Gigarel, Jeanne Amiel, et al.. (2000). Mutations of the SCO1 Gene in Mitochondrial Cytochrome c Oxidase Deficiency with Neonatal-Onset Hepatic Failure and Encephalopathy. The American Journal of Human Genetics. 67(5). 1104–1109. 273 indexed citations
8.
Valnot, Isabelle. (2000). A mutation in the human heme A:farnesyltransferase gene (COX10 ) causes cytochrome c oxidase deficiency. Human Molecular Genetics. 9(8). 1245–1249. 226 indexed citations
9.
Valnot, Isabelle, Nadine Gigarel, Jeanne Amiel, et al.. (2000). Mutations of theSCO1Gene in Mitochondrial CytochromecOxidase Deficiency with Neonatal‐Onset Hepatic Failure and Encephalopathy. The American Journal of Human Genetics. 67(5). 1104–1109. 40 indexed citations
10.
Valnot, Isabelle, Dominique Chrétien, Pascale de Lonlay, et al.. (1999). A mitochondrial cytochrome b mutation but no mutations of nuclearly encoded subunits in ubiquinol cytochrome c reductase (complex III) deficiency. Human Genetics. 104(6). 460–466. 81 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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