M. Brivet

4.7k total citations · 1 hit paper
88 papers, 3.3k citations indexed

About

M. Brivet is a scholar working on Clinical Biochemistry, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, M. Brivet has authored 88 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 72 papers in Clinical Biochemistry, 48 papers in Molecular Biology and 21 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in M. Brivet's work include Metabolism and Genetic Disorders (72 papers), Mitochondrial Function and Pathology (33 papers) and Neonatal Health and Biochemistry (20 papers). M. Brivet is often cited by papers focused on Metabolism and Genetic Disorders (72 papers), Mitochondrial Function and Pathology (33 papers) and Neonatal Health and Biochemistry (20 papers). M. Brivet collaborates with scholars based in France, United States and Netherlands. M. Brivet's co-authors include Jean‐Marie Saudubray, Jean‐Paul Bonnefont, Audrey Boutron, Abdelhamid Slama, Daniel Rabier, Pascale de Lonlay, France Demaugre, Christine Vianey‐Saban, Guy Touati and Delphine Martin and has published in prestigious journals such as Science, New England Journal of Medicine and Proceedings of the National Academy of Sciences.

In The Last Decade

M. Brivet

83 papers receiving 3.3k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

A Mitochondrial Pyruvate Carrier Required for Pyruvate Uptake in Yeast, Drosophila , and Humans

2012 644 citations Eric B. Taylor, John C. Schell et al. Science profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
M. Brivet France	28	2.3k	2.0k	671	411	294	88	3.3k
S. E. Olpin United Kingdom	31	1.9k 0.8×	1.5k 0.8×	548 0.8×	267 0.6×	238 0.8×	81	3.0k
Enrico Zammarchi Italy	28	1.7k 0.7×	1.1k 0.5×	626 0.9×	347 0.8×	243 0.8×	101	3.2k
Ute Spiekerkoetter Germany	30	1.5k 0.7×	1.7k 0.8×	787 1.2×	302 0.7×	228 0.8×	111	2.6k
Fatima Djouadi France	30	1.9k 0.8×	661 0.3×	862 1.3×	97 0.2×	193 0.7×	64	2.8k
Akira Ohtake Japan	27	1.9k 0.8×	1.1k 0.6×	226 0.3×	140 0.3×	146 0.5×	138	2.7k
Toshihiro Ohura Japan	27	1.5k 0.6×	1.8k 0.9×	654 1.0×	574 1.4×	575 2.0×	90	3.0k
Rikke Katrine Jentoft Olsen Denmark	25	1.4k 0.6×	1.4k 0.7×	382 0.6×	138 0.3×	232 0.8×	66	2.1k
Alisa Gutman Israel	27	916 0.4×	746 0.4×	411 0.6×	193 0.5×	318 1.1×	84	1.8k
Klaus-Dieter Gerbitz Germany	30	1.7k 0.7×	1.1k 0.5×	305 0.5×	149 0.4×	100 0.3×	71	2.6k
Radha Ananthakrishnan United States	30	1.1k 0.5×	1.1k 0.5×	430 0.6×	112 0.3×	72 0.2×	114	2.8k

Countries citing papers authored by M. Brivet

Since Specialization

Citations

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

Fields of papers citing papers by M. Brivet

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. Brivet

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

All Works

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20 of 20 papers shown

Brivet, M., et al.. (2016). Inherited Metabolic Diseases. SPIRE - Sciences Po Institutional REpository. 8 indexed citations

Taylor, Eric B., John C. Schell, Audrey Boutron, et al.. (2012). A Mitochondrial Pyruvate Carrier Required for Pyruvate Uptake in Yeast, Drosophila , and Humans. Science. 337(6090). 96–100. 644 indexed citations breakdown →

Boutron, Audrey, et al.. (2012). Pyruvate dehydrogenase deficiency caused by a new mutation of PDHX gene in two Moroccan patients. European Journal of Medical Genetics. 55(10). 535–540. 9 indexed citations

Forges, Thierry, Patricia Monnier, Bruno Leheup, et al.. (2010). Ovarian tissue cryopreservation and subsequent spontaneous pregnancies in a patient with classic galactosemia. Fertility and Sterility. 95(1). 290.e1–290.e3. 11 indexed citations

Barth, Magalie, Chris Ottolenghi, Laurence Hubert, et al.. (2010). Multiple sources of metabolic disturbance inETHE1‐related ethylmalonic encephalopathy. Journal of Inherited Metabolic Disease. 33(S3). 443–453. 24 indexed citations

Lombès, Anne, et al.. (2009). Rapid screening for nuclear genes mutations in isolated respiratory chain complex I defects. Molecular Genetics and Metabolism. 96(4). 196–200. 33 indexed citations

Brivet, M., et al.. (2005). First characterization of a large deletion of the PDHA1 gene. Molecular Genetics and Metabolism. 86(4). 456–461. 14 indexed citations

Villemeur, Thierry Billette de, M. Brivet, Anne Guiochon‐Mantel, et al.. (2004). The deleterious G15498A mutation in mitochondrial DNA-encoded cytochrome b may remain clinically silent in homoplasmic carriers. European Journal of Human Genetics. 12(3). 220–224. 4 indexed citations

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

10.

Brivet, M.. (2003). Impaired mitochondrial pyruvate importation in a patient and a fetus at risk. Molecular Genetics and Metabolism. 78(3). 186–192. 62 indexed citations

11.

Odièvre, M, et al.. (2002). A secondary respiratory chain defect in a patient with Fanconi–Bickel syndrome. Journal of Inherited Metabolic Disease. 25(5). 379–384. 13 indexed citations

12.

Vianey‐Saban, Christine, P. Divry, M. Brivet, et al.. (1998). Mitochondrial very-long-chain acyl-coenzyme A dehydrogenase deficiency: clinical characteristics and diagnostic considerations in 30 patients. Clinica Chimica Acta. 269(1). 43–62. 124 indexed citations

13.

Morris, A. A. M., S. E. Olpin, M. Brivet, et al.. (1998). A patient with carnitine-acylcarnitine translocase deficiency with a mild phenotype. The Journal of Pediatrics. 132(3). 514–516. 34 indexed citations

14.

Saudubray, Jean‐Marie, Delphine Martin, F Poggi-Travert, et al.. (1997). Clinical presentations of inherited mitochondrial fatty acid oxidation disorders: An update. 12(1). 34–40. 5 indexed citations

15.

Pande, S.V., M. Brivet, Abdelhamid Slama, et al.. (1993). Carnitine-acylcarnitine translocase deficiency with severe hypoglycemia and auriculo ventricular block. Translocase assay in permeabilized fibroblasts.. Journal of Clinical Investigation. 91(3). 1247–1252. 86 indexed citations

16.

Brivet, M., et al.. (1991). Riboflavin responsive ethylmalonic‐adipic aciduria in a 9‐month‐old boy with liver cirrhosis, myopathy and encephalopathy. Journal of Inherited Metabolic Disease. 14(3). 333–337. 2 indexed citations

17.

Birlouez-Aragon, I., et al.. (1990). Lactose intake and lactase activity: two risk factors for senile and diabetic cataract.. 1(2). 74–79. 1 indexed citations

18.

Baptista, Joyce, M. Brivet, N. Kadhom, M Gautier, & Alban Le Monnier. (1989). Cytosolic thymidine kinase activity in cultured human fibroblasts from individuals with galactokinase deficiency. Biochemical Genetics. 27(3-4). 219–228. 1 indexed citations

19.

Brivet, M., et al.. (1989). Effect of lactation in a mother with galactosemia. The Journal of Pediatrics. 115(2). 280–282. 14 indexed citations

20.

Soni, T., et al.. (1988). The Philadelphia variant of galactokinase: Impaired [1-14C]galactose oxidation by intact erythrocytes. Clinica Chimica Acta. 174(1). 101–110. 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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