Magalie Barth

4.0k total citations
32 papers, 378 citations indexed

About

Magalie Barth is a scholar working on Molecular Biology, Clinical Biochemistry and Physiology. According to data from OpenAlex, Magalie Barth has authored 32 papers receiving a total of 378 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 17 papers in Clinical Biochemistry and 10 papers in Physiology. Recurrent topics in Magalie Barth's work include Metabolism and Genetic Disorders (17 papers), Mitochondrial Function and Pathology (9 papers) and Diet and metabolism studies (5 papers). Magalie Barth is often cited by papers focused on Metabolism and Genetic Disorders (17 papers), Mitochondrial Function and Pathology (9 papers) and Diet and metabolism studies (5 papers). Magalie Barth collaborates with scholars based in France, United States and United Kingdom. Magalie Barth's co-authors include Dominique Bonneau, Vincent Procaccio, Pascal Reynier, Arnaud Chevrollier, Naïg Guéguen, Patrizia Amati‐Bonneau, Daniel Henrion, Valérie Desquiret‐Dumas, Anne-Sophie Lèbre and Alice Kuster and has published in prestigious journals such as SHILAP Revista de lepidopterología, PEDIATRICS and The Journal of Urology.

In The Last Decade

Magalie Barth

29 papers receiving 375 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Magalie Barth France 12 274 171 92 36 35 32 378
Nastassja Himmelreich Germany 11 244 0.9× 211 1.2× 70 0.8× 51 1.4× 49 1.4× 25 365
Jorida Çoku United States 12 459 1.7× 204 1.2× 37 0.4× 40 1.1× 34 1.0× 18 525
Sabine Grønborg Denmark 11 207 0.8× 74 0.4× 64 0.7× 22 0.6× 69 2.0× 25 330
Tessa van Dijk Netherlands 10 170 0.6× 114 0.7× 60 0.7× 23 0.6× 49 1.4× 18 320
Jaak Jaeken Belgium 9 236 0.9× 123 0.7× 64 0.7× 132 3.7× 59 1.7× 11 350
Nanna Cornelius Denmark 8 423 1.5× 341 2.0× 98 1.1× 71 2.0× 32 0.9× 10 551
Yoichi Wada Japan 13 209 0.8× 113 0.7× 43 0.5× 39 1.1× 39 1.1× 27 372
Lisa Worgan Australia 9 281 1.0× 189 1.1× 35 0.4× 14 0.4× 65 1.9× 14 376
Laura Pollard United States 12 240 0.9× 79 0.5× 137 1.5× 21 0.6× 38 1.1× 43 391
Anke Schumann Germany 11 179 0.7× 149 0.9× 75 0.8× 29 0.8× 64 1.8× 32 379

Countries citing papers authored by Magalie Barth

Since Specialization
Citations

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

Fields of papers citing papers by Magalie Barth

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Magalie Barth

This figure shows the co-authorship network connecting the top 25 collaborators of Magalie Barth. A scholar is included among the top collaborators of Magalie Barth 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 Magalie Barth. Magalie Barth 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.
Lefort, Bruno, Magalie Barth, Naïg Guéguen, et al.. (2025). Pantethine Therapy Dramatically Rescues End-Stage Failing Heart in a Patient with Deficiency of Coenzyme A Biosynthesis. ESC Heart Failure. 12(4). 3195–3199.
2.
Malinge, Marie‐Claire, et al.. (2024). Diagnosis of tuberous sclerosis in the prenatal period: a retrospective study of 240 cases and review of the literature. European Journal of Human Genetics. 32(12). 1590–1598. 3 indexed citations
3.
Prokop, Jeremy W., Charles E. Schwartz, Surender Rajasekaran, et al.. (2023). Two New Cases of Bachmann–Bupp Syndrome Identified through the International Center for Polyamine Disorders. SHILAP Revista de lepidopterología. 11(2). 29–29. 3 indexed citations
4.
5.
Lamireau, Delphine, Pascale de Lonlay, Aude Servais, et al.. (2023). Systemic primary carnitine deficiency induces severe arrhythmia due to shortening of QT interval. Molecular Genetics and Metabolism. 140(4). 107733–107733. 4 indexed citations
6.
Denamur, Sophie, Guy Touati, Léna Damaj, et al.. (2022). Recommended respiratory tests are not routinely performed for mucopolysaccharidosis patients. ERJ Open Research. 8(1). 567–2021. 2 indexed citations
7.
Sevin, Caroline, et al.. (2022). An international study of caregiver-reported burden and quality of life in metachromatic leukodystrophy. Orphanet Journal of Rare Diseases. 17(1). 329–329. 14 indexed citations
8.
Riquin, Élise, Magalie Barth, Estelle Colin, et al.. (2022). Neuropsychological Features of Children and Adolescents With Mitochondrial Disorders: A Descriptive Case Series. Frontiers in Psychiatry. 13. 864445–864445.
9.
Schönewolf‐Greulich, Bitten, Alexandra Afenjar, Magalie Barth, et al.. (2021). Clinical and molecular delineation of PUS3 ‐associated neurodevelopmental disorders. Clinical Genetics. 100(5). 628–633. 26 indexed citations
10.
Alsaif, Hessa S., Eissa Faqeih, Magalie Barth, et al.. (2021). ZNF668 deficiency causes a recognizable disorder of DNA damage repair. Human Genetics. 140(9). 1395–1401. 1 indexed citations
11.
Barth, Magalie, Jérémie Lefranc, Karine Mention, et al.. (2021). West Syndrome Is an Exceptional Presentation of Pyridoxine- and Pyridoxal Phosphate-Dependent Epilepsy: Data From a French Cohort and Review of the Literature. Frontiers in Pediatrics. 9. 621200–621200. 7 indexed citations
12.
Riquin, Élise, Philippe Duverger, Magalie Barth, et al.. (2020). Neuropsychological and Psychiatric Features of Children and Adolescents Affected With Mitochondrial Diseases: A Systematic Review. Frontiers in Psychiatry. 11. 747–747. 13 indexed citations
13.
Dessein, Anne‐Frédérique, Monique Fontaine, Marie Joncquel-Chevalier Curt, et al.. (2017). Fluxomic evidence for impaired contribution of short-chain acyl-CoA dehydrogenase to mitochondrial palmitate β-oxidation in symptomatic patients with ACADS gene susceptibility variants. Clinica Chimica Acta. 471. 101–106. 10 indexed citations
14.
Kuster, Alice, Jean‐Baptiste Arnoux, Magalie Barth, et al.. (2017). Diagnostic approach to neurotransmitter monoamine disorders: experience from clinical, biochemical, and genetic profiles. Journal of Inherited Metabolic Disease. 41(1). 129–139. 11 indexed citations
15.
Desquiret‐Dumas, Valérie, Naïg Guéguen, Céline Bris, et al.. (2016). The addition of ketone bodies alleviates mitochondrial dysfunction by restoring complex I assembly in a MELAS cellular model. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1863(1). 284–291. 45 indexed citations
16.
Leman, Géraldine, Naïg Guéguen, Valérie Desquiret‐Dumas, et al.. (2015). Assembly defects induce oxidative stress in inherited mitochondrial complex I deficiency. The International Journal of Biochemistry & Cell Biology. 65. 91–103. 35 indexed citations
17.
18.
Ziegler, Alban, Agnès Guichet, Magalie Barth, et al.. (2014). Extensive Mongolian spots in 4p16.3 deletion (Wolf–Hirschhorn syndrome). Clinical Dysmorphology. 23(3). 109–110. 1 indexed citations
19.
Tosch, Valérie, Nasim Vasli, Christine Kretz, et al.. (2010). Novel molecular diagnostic approaches for X-linked centronuclear (myotubular) myopathy reveal intronic mutations. Neuromuscular Disorders. 20(6). 375–381. 26 indexed citations
20.
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

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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