C. Marsac

4.5k total citations
102 papers, 3.4k citations indexed

About

C. Marsac is a scholar working on Molecular Biology, Clinical Biochemistry and Biochemistry. According to data from OpenAlex, C. Marsac has authored 102 papers receiving a total of 3.4k indexed citations (citations by other indexed papers that have themselves been cited), including 71 papers in Molecular Biology, 59 papers in Clinical Biochemistry and 26 papers in Biochemistry. Recurrent topics in C. Marsac's work include Metabolism and Genetic Disorders (59 papers), Mitochondrial Function and Pathology (45 papers) and Biochemical Acid Research Studies (16 papers). C. Marsac is often cited by papers focused on Metabolism and Genetic Disorders (59 papers), Mitochondrial Function and Pathology (45 papers) and Biochemical Acid Research Studies (16 papers). C. Marsac collaborates with scholars based in France, Germany and United States. C. Marsac's co-authors include Françoise Degoul, G Ponsot, D. François, Bernhard Kadenbach, Peter Seibel, Isabelle Desguerre, S Kantengwa, Claudio Franceschi, Andrea Cossarizza and Barbara S. Polla and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

C. Marsac

101 papers receiving 3.3k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
C. Marsac 2.4k 1.4k 453 445 281 102 3.4k
H.R. Scholte 2.6k 1.1× 1.8k 1.2× 209 0.5× 602 1.4× 351 1.2× 100 3.7k
Elisabeth Holme 3.0k 1.2× 2.0k 1.4× 330 0.7× 404 0.9× 143 0.5× 80 4.1k
Garry K. Brown 2.8k 1.1× 2.2k 1.5× 752 1.7× 363 0.8× 148 0.5× 91 3.8k
S. E. Olpin 1.9k 0.8× 1.5k 1.1× 238 0.5× 548 1.2× 170 0.6× 81 3.0k
R. J. A. Wanders 2.0k 0.8× 1.1k 0.8× 253 0.6× 773 1.7× 250 0.9× 65 2.7k
P. Vreken 3.3k 1.4× 1.2k 0.8× 348 0.8× 594 1.3× 210 0.7× 81 4.5k
Jos P.N. Ruiter 2.5k 1.1× 2.2k 1.5× 263 0.6× 820 1.8× 214 0.8× 98 3.9k
Lambert van den Heuvel 2.9k 1.2× 1.4k 1.0× 205 0.5× 239 0.5× 185 0.7× 62 3.6k
Antònia Ribes 2.5k 1.0× 2.1k 1.5× 610 1.3× 586 1.3× 435 1.5× 175 3.9k
F.A. Hommes 1.2k 0.5× 1.0k 0.7× 332 0.7× 465 1.0× 208 0.7× 118 2.2k

Countries citing papers authored by C. Marsac

Since Specialization
Citations

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

Fields of papers citing papers by C. Marsac

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of C. Marsac

This figure shows the co-authorship network connecting the top 25 collaborators of C. Marsac. A scholar is included among the top collaborators of C. Marsac 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 C. Marsac. C. Marsac 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.
Miné, Manuèle, et al.. (2006). A novel gross deletion caused by non-homologous recombination of the PDHX gene in a patient with pyruvate dehydrogenase deficiency☆. Molecular Genetics and Metabolism. 89(1-2). 106–110. 10 indexed citations
2.
Miné, Manuèle, M. Brivet, Guy Touati, et al.. (2003). Splicing Error in E1α Pyruvate Dehydrogenase mRNA Caused by Novel Intronic Mutation Responsible for Lactic Acidosis and Mental Retardation. Journal of Biological Chemistry. 278(14). 11768–11772. 41 indexed citations
3.
Fouque, Françoise, et al.. (2003). Differential Effect of DCA Treatment on the Pyruvate Dehydrogenase Complex in Patients with Severe PDHC Deficiency. Pediatric Research. 53(5). 793–799. 28 indexed citations
4.
Marchant, Dominique, Karı̈n Gogat, P. Dureau, et al.. (2002). Use of denaturing HPLC and automated sequencing to screen the VMD2 gene for mutations associated with Best's vitelliform macular dystrophy. Ophthalmic Genetics. 23(3). 167–174. 7 indexed citations
5.
Camand, Olivier, Dominique Marchant, Sandrine Boutboul, et al.. (2001). Mutation analysis of the tyrosinase gene in oculocutaneous albinism. Human Mutation. 17(4). 352–352. 11 indexed citations
6.
Péquignot, Marie O., Runu Dey, Massimo Zeviani, et al.. (2001). Mutations in theSURF1gene associated with Leigh syndrome and cytochromecoxidase deficiency. Human Mutation. 17(5). 374–381. 68 indexed citations
7.
Birch‐Machin, Mark A., et al.. (1999). Riboflavine-response Leigh syndrome and leukodystrophy associated to partial succinate dehydrogenase deficiency. Archives de Pédiatrie. 11 indexed citations
8.
Boitier, Eric, Annie Nicole, C. Marsac, et al.. (1999). Overproduction of Cu/Zn-Superoxide Dismutase or Bcl-2 Prevents the Brain Mitochondrial Respiratory Dysfunction Induced by Glutathione Depletion. Experimental Neurology. 158(2). 428–436. 58 indexed citations
9.
Rouillac, Christelle, Bernard Aral, Dominique Marchant, et al.. (1999). First prenatal diagnosis of defects in theHsPDX1 gene encoding protein X, an additional lipoyl-containing subunit of the human pyruvate dehydrogenase complex. Prenatal Diagnosis. 19(12). 1160–1164. 7 indexed citations
10.
Benelli, Chantal, Ghania Ait‐Ghezala, Mohamed Amessou, et al.. (1997). Mutations in PDX1, the Human Lipoyl-Containing Component X of the Pyruvate Dehydrogenase–Complex Gene on Chromosome 11p1, in Congenital Lactic Acidosis. The American Journal of Human Genetics. 61(6). 1318–1326. 39 indexed citations
11.
Possekel, Stefanie, Eric Boitier, C. Marsac, & Françoise Degoul. (1996). Third International Congress on Human Mitochondrial Pathology (Euromit III): Towards a better understanding of energy metabolism disorders. Neuromuscular Disorders. 6(3). 215–218. 2 indexed citations
12.
Chariot, Patrick, Gisèle Bonne, François‐Jérôme Authier, C. Marsac, & Romain K. Gherardi. (1994). Expression of cytochrome c oxidase subunits encoded by mitochondrial or nuclear DNA in the muscle of patients with zidovudine myopathy. Journal of the Neurological Sciences. 125(2). 190–193. 5 indexed citations
13.
Marsac, C., D. Stansbie, Gisèle Bonne, et al.. (1993). Defect in the lipoyl-bearing protein X subunit of the pyruvate dehydrogenase complex in two patients with encephalomyelopathy. The Journal of Pediatrics. 123(6). 915–920. 27 indexed citations
14.
Bonne, Gisèle, Chantal Benelli, Linda De Meırleır, et al.. (1993). El Pyruvate Dehydrogenase Deficiency in a Child with Motor Neuropathy. Pediatric Research. 33(3). 284–288. 30 indexed citations
15.
Lauber, Jürgen, C. Marsac, Bernhard Kadenbach, & Peter Seibel. (1991). Mutations in mitochondrial tRNA genes: a frequent cause of neuromuscular diseases. Nucleic Acids Research. 19(7). 1393–1397. 74 indexed citations
16.
Romero, Norma B., et al.. (1990). Immunohistochemical demonstration of fibre type-specific isozymes of cytochrome c oxidase in human skeletal muscle. Histochemistry and Cell Biology. 94(2). 211–215. 14 indexed citations
17.
Seibel, Peter, Françoise Degoul, Norma B. Romero, C. Marsac, & Bernhard Kadenbach. (1990). Identification of point mutations by mispairing PCR as exemplified in MERRF disease. Biochemical and Biophysical Research Communications. 173(2). 561–565. 44 indexed citations
18.
Nelson, Isabelle, Françoise Degoul, B. Obermaier–Kusser, et al.. (1989). Mapping of heteroplasmic mitochondrial DNA deletions in Kearns-Sayre syndrome. Nucleic Acids Research. 17(20). 8117–8124. 56 indexed citations
19.
Robinson, B. H., J. Oei, Jean Marie Saudubray, et al.. (1987). The French and North American phenotypes of pyruvate carboxylase deficiency, correlation with biotin containing protein by 3H-biotin incorporation, 35S-streptavidin labeling, and Northern blotting with a cloned cDNA probe.. PubMed. 40(1). 50–9. 32 indexed citations
20.
Saudubray, Jean Marie, C. Marsac, J.M. Limal, et al.. (1981). Variation in plasma ketone bodies during a 24-hour fast in normal and in hypoglycemic children: Relationship to age. The Journal of Pediatrics. 98(6). 904–908. 44 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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