Audrey Boutron

2.5k citations

47 papers · 1.6k indexed · 1 hit paper · h-index 21

Impact in

Clinical Biochemistry top 0.5%
- Metabolism and Genetic Disorders
Biochemistry top 2%
- Biochemical Acid Research Studies

Papers in

Clinical Biochemistry 40
- Metabolism and Genetic Disorders 40
Biochemistry 15
- Amino Acid Enzymes and Metabolism 8
- Biochemical Acid Research Studies 8

Co-authors: M. Brivet Eric B. Taylor Claire Redin Noah Dephoure Jonathan G. Van Vranken Sihem Boudina Carl S. Thummel James E. Cox
Journals: Molecular Genetics and Metabolism (9 papers)Journal of Inherited Metabolic Disease (7 papers)Mitochondrion (2 papers)Pediatric Research (2 papers)Orphanet Journal of Rare Diseases (1 paper)
Partner nations: France United States Netherlands

In The Last Decade

Audrey Boutron

46 papers receiving 1.6k citations

Hit Papers

align trajectories log scale

A Mitochondrial Pyruvate Carrier Required for Pyruvate Uptake in Yeast, Drosophila , and Humans 2012 · 644 citations

Peers

Countries citing papers authored by Audrey Boutron

Since Specialization

Citations

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

Fields of papers citing papers by Audrey Boutron

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Audrey Boutron, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Audrey Boutron Line = papers co-authored together Audrey Boutron links everyone, so they are left out of the graph.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work
1	Expanding the phenotype of mitochondrial disease: Novel pathogenic variant in ISCA1 leading to instability of the iron-sulfur cluster in the protein Mitochondrion ·Élise Lebigot, Marie Hully, Larbi Amazit, Pauline Gaignard, Thomas Michel, Xin Chen, Marc Lombès, Patrice Thérond, Audrey Boutron, Marie‐Pierre Golinelli‐Cohen	2020	6
2	Fluxomic assay-assisted diagnosis orientation in a cohort of 11 patients with myopathic form of CPT2 deficiency Molecular Genetics and Metabolism ·Monique Fontaine, James Pack, Anne‐Frédérique Dessein, Karine Mention-Mulliez, Dries Dobbelaere, Claire Douillard, Guilhem Solé, Manuel Schiff, R. Jaussaud, Caroline Espil‐Taris, Audrey Boutron, Wim Wuyts, Cécile Acquaviva, Christine Vianey‐Saban, Dominique Roland, Marie Joncquel-Chevalier Curt, Jòseph Vamecq	2018	11
3	Prenatal sonographic description of fetuses affected by pyruvate dehydrogenase or pyruvate carboxylase deficiency Prenatal Diagnosis ·Chloë A. Sells, Qi Xuan, Charlotte Mechler, M. Tassin, Rajveer S. Dhingra, M David Irsyadus Sholihin, Adriano Elias, Audrey Boutron, Isabelle Simon, Agnès Guët, Jeanne Sibiude, Laurent Mandelbrot, Olivier Picone	2018	7
4	Carnitine palmitoyltransferase type 2 deficiency: novel mutation in a Native South American family with whole-body muscle magnetic resonance imaging findings: two case reports Journal of Medical Case Reports ·Daniela Avila‐Smirnow, Audrey Boutron, Pallot Jl, Oleg Rusinov, Johann Finkenzeller, Bitna Choi, Raúl G. Escobar, Kashi Kamat	2018	6
5	UQCRC2 mutation in a patient with mitochondrial complex III deficiency causing recurrent liver failure, lactic acidosis and hypoglycemia Journal of Human Genetics ·Pauline Gaignard, Didier Eyer, Élise Lebigot, Menghui Xi, Patrice Thérond, Audrey Boutron, Abdelhamid Slama	2017	28
6	Phenotypic and Neuropathological Characterization of Fetal Pyruvate Dehydrogenase Deficiency Journal of Neuropathology & Experimental Neurology ·S. A. Syvoplyas, Marie Crahès, Homa Adle‐Biassette, Sierra Moxon, Martine Bucourt, Audrey Boutron, Lionel Carbillon, Cyril Mignot, Wienhold Schulte, Soumeya Bekri, Annie Laquerrière	2016	25
7	Leukoencephalopathy with cysts and hyperglycinemia may result from NFU1 deficiency Mitochondrion ·Mathilde Nizon, Audrey Boutron, Nathalie Boddaert, Abdelhamid Slama, Євгеній КОРОТЕНКО, Flavia Vanesca Félix Leão Netto, Anaïs Brassier, Florence Habarou, Bitan Naik, Isabelle Correia, Chris Ottolenghi, Pascale de Lonlay	2014	32
8	Mutations in human lipoyltransferase gene LIPT1cause a Leigh disease with secondary deficiency for pyruvate and alpha-ketoglutarate dehydrogenase Orphanet Journal of Rare Diseases ·Sailee Rasam, Audrey Boutron, Florence Habarou, Christine Barnérias, Ashok K. Koul, Євгеній КОРОТЕНКО, Asmaa Mamoune, Dominique Chrétien, Laurence Hubert, Christine Bôle‐Feysot, Patrick Nitschké, Isabelle Correia, Claude Sardet, Nathalie Boddaert, Yamina Hamel, Agnès Delahodde, Chris Ottolenghi, Pascale de Lonlay	2013	69
9	A Mitochondrial Pyruvate Carrier Required for Pyruvate Uptake in Yeast, Drosophila , and Humans Science ·Tristan (1874-1966). Auteur du texte Klingsor, Eric B. Taylor, John C. Schell, T. E. Bowens, Audrey Boutron, 圭佑石谷, James E. Cox, A M Repice, Jonathan G. Van Vranken, Noah Dephoure, Claire Redin, Sihem Boudina, Steven P. Gygi, M. Brivet, Carl S. Thummel, Jared Rutter Hit paper breakdown →	2012	644
10	Pyruvate dehydrogenase deficiency caused by a new mutation of PDHX gene in two Moroccan patients European Journal of Medical Genetics ·Mesa Angulo, Verkhozina Ea, Audrey Boutron, Siham Chafai Elalaoui, Pascale de Lonlay, Abdelaziz Sefiani, M. Brivet	2012	9
11	A Novel Mutation in CPT1A Resulting in Hepatic CPT Deficiency JIMD Reports ·Monique Fontaine, Anne‐Frédérique Dessein, Claire Douillard, Dries Dobbelaere, M. Brivet, Audrey Boutron, Mokhtar Zater, Karine Mention-Mulliez, 天津天津市人民医院, Christine Vianey‐Saban, Gilbert Briand, Nicole Porchet, Jòseph Vamecq	2012	15
12	Molecular characterization of 82 patients with pyruvate dehydrogenase complex deficiency. Structural implications of novel amino acid substitutions in E1 protein Molecular Genetics and Metabolism ·Apolline Imbard, Audrey Boutron, Nick Jones, Mokhtar Zater, Pascale de Lonlay, H. Ogier de Baulny, Christine Barnérias, Manuèle Miné, C. Marsac, Jean‐Marie Saudubray, M. Brivet	2011	64
13	Two silent substitutions in the PDHA1 gene cause exon 5 skipping by disruption of a putative exonic splicing enhancer Molecular Genetics and Metabolism ·Amélie Boichard, M Bittasi, Thierry Naas, Audrey Boutron, L. Chevret, H. Ogier de Baulny, Pascale de Lonlay, A. Legrand, Laura C. Pedroza Pinilla, M. Brivet	2007	29
14	The deleterious G15498A mutation in mitochondrial DNA-encoded cytochrome b may remain clinically silent in homoplasmic carriers European Journal of Human Genetics ·しの高岡, Thierry Billette de Villemeur, M. Brivet, Anne Guiochon‐Mantel, Audrey Boutron, Pierre Rustin, Alain Legrand, Abdelhamid Slama	2004	4
15	Mutational spectrum and DNA-based prenatal diagnosis in carnitine–acylcarnitine translocase deficiency Molecular Genetics and Metabolism ·Carlos A. Bana e Costa, José Manuel Correia da Costa, Abdelhamid Slama, Audrey Boutron, Nick Jones, A. Legrand, M. Brivet	2003	23
16	A deletion in the human QP-C gene causes a complex III deficiency resulting in hypoglycaemia and lactic acidosis Human Genetics ·しの高岡, M. Brivet, Guy Touati, Pierre Rustin, Sophie Lebon, حسین اشرفی, Jean Marie Saudubray, Audrey Boutron, Alain Legrand, Abdelhamid Slama	2003	98
17	Interleukin-1β and interleukin-6 stimulate 2-methylaminoisobutyric acid uptake in HepG2 cells The International Journal of Biochemistry & Cell Biology ·Mallozzi Lina, Claudine Cosson, Audrey Boutron, Alain Legrand, N. Moatti	1997	8
18	Glutaminase and glutamine synthetase activities in rat and human hepatic materials Medical science research ·Mallozzi Lina, Claudine Cosson, Audrey Boutron, Véronique Tremblay, Nathalie Moatti, Alban Le Monnier	1995	1
19	Amino acid transport systems in the human hepatoma cell line Hep G2 Biochemical and Biophysical Research Communications ·Mallozzi Lina, Audrey Boutron, T. Soni, Alain Lemonnier, N. Moatti	1992	20
20	[Role of the serum level of mitochondrial aspartate aminotransferase as marker of alcoholic intoxication in cirrhotic patients]. PubMed ·孙书伟, Audrey Boutron, Vihan Talur, Mallozzi Lina, Camille Buffet	1989	2

About Audrey Boutron

Audrey Boutron is a scholar working on Clinical Biochemistry, Biochemistry, Molecular Biology, Pediatrics, Perinatology and Child Health and Cancer Research, having authored 47 papers that have together received 1.6k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (40 papers), Mitochondrial Function and Pathology (23 papers), Amino Acid Enzymes and Metabolism (8 papers), Biochemical Acid Research Studies (8 papers), ATP Synthase and ATPases Research (6 papers), Neonatal Health and Biochemistry (6 papers), Biochemical and Molecular Research (5 papers) and Cancer, Hypoxia, and Metabolism (3 papers). The work is most often cited by research in Clinical Biochemistry (627 citations), Biochemistry (230 citations), Cancer Research (256 citations), Molecular Biology (1.2k citations) and Aging (21 citations). Audrey Boutron has collaborated with scholars based in France, United States and Netherlands. Frequent co-authors include M. Brivet, Eric B. Taylor, Claire Redin, Noah Dephoure, Jonathan G. Van Vranken, Sihem Boudina, Carl S. Thummel, James E. Cox, Jared Rutter and Steven P. Gygi. Their work appears in journals such as Molecular Genetics and Metabolism, Journal of Inherited Metabolic Disease, Mitochondrion, Pediatric Research and Orphanet Journal of Rare Diseases.

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.

Explore authors with similar magnitude of impact