Élise Lebigot

598 total citations
18 papers, 219 citations indexed

About

Élise Lebigot is a scholar working on Clinical Biochemistry, Molecular Biology and Neurology. According to data from OpenAlex, Élise Lebigot has authored 18 papers receiving a total of 219 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Clinical Biochemistry, 11 papers in Molecular Biology and 2 papers in Neurology. Recurrent topics in Élise Lebigot's work include Metabolism and Genetic Disorders (13 papers), Mitochondrial Function and Pathology (9 papers) and ATP Synthase and ATPases Research (3 papers). Élise Lebigot is often cited by papers focused on Metabolism and Genetic Disorders (13 papers), Mitochondrial Function and Pathology (9 papers) and ATP Synthase and ATPases Research (3 papers). Élise Lebigot collaborates with scholars based in France, Netherlands and Türkiye. Élise Lebigot's co-authors include Patrice Thérond, Audrey Boutron, Pauline Gaignard, Abdelhamid Slama, Marie‐Pierre Golinelli‐Cohen, Pascale de Lonlay, Manuel Schiff, Anaïs Brassier, Mokhtar Zater and François Feillet and has published in prestigious journals such as Brain, Clinical Chemistry and European Journal of Endocrinology.

In The Last Decade

Élise Lebigot

17 papers receiving 216 citations

Peers

Countries citing papers authored by Élise Lebigot

Since Specialization

Citations

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

Fields of papers citing papers by Élise Lebigot

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Élise Lebigot

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

All Works

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18 of 18 papers shown

#	Work	Indexed citations
1	Circulatory response to exercise relative to oxygen uptake assessed in the follow‐up of patients with fatty acid beta‐oxidation disorders 2024 ·Journal of Inherited Metabolic Disease ·Apolline Imbard, Hortense de Calbiac, (unknown), Pascal Laforêt, Manuel Schiff, Anaïs Brassier, (unknown), Clément Pontoizeau, (unknown), Chris Ottolenghi, Élise Lebigot, Pauline Gaignard, Stéphanie Gobin, Cécile Acquaviva, Jean‐François Benoist, (unknown), Antoine Legendre, Pascale de Lonlay	2
2	A novel mutation in the NR3C1 gene associated with reversible glucocorticoid resistance 2024 ·European Journal of Endocrinology ·(unknown), Emmanuelle Kuhn, Jérôme Bouligand, Larbi Amazit, (unknown), Élise Lebigot, Peter Kamenický, Marc Lombès, Jérôme Fagart, Say Viengchareun, Laëtitia Martinerie	3
3	UQCRC2-related mitochondrial complex III deficiency, about 7 patients 2022 ·Mitochondrion ·(unknown), Pauline Gaignard, Élise Lebigot, Didier Eyer, Geoffroy Delplancq, (unknown), K. Mazodier, (unknown), Cécile Rouzier, Konstantina Fragaki, (unknown), Christophe Philippe, Ange‐Line Bruel, Laurence Faivre, François Feillet, (unknown)	7
4	Fructose 1,6 bisphosphatase deficiency: outcomes of patients in a single center in Turkey and identification of novel splice site and indel mutations in FBP1 2022 ·Journal of Pediatric Endocrinology and Metabolism ·(unknown), (unknown), Ayşe Kılıç, (unknown), (unknown), İlyas Okur, Leyla Tümer, Élise Lebigot, Fatih Süheyl Ezgü	3
5	MPC2variants disrupt mitochondrial pyruvate metabolism and cause an early-onset mitochondriopathy 2022 ·Brain ·Claire Pujol, Élise Lebigot, Pauline Gaignard, Saïd Galaï, Ichraf Kraoua, (unknown), Rodolphe Dard, (unknown), (unknown), Audrey Boutron, Timothy Wai, Abdelhamid Slama	5
6	Movement disorders in valine métabolism diseases caused by HIBCH and ECHS1 deficiencies 2022 ·European Journal of Neurology ·(unknown), Élise Lebigot, Emmanuel Roze, (unknown), Claude Cancés, Léna Damaj, Caroline Espil, Joël Fluss, Pascale de Lonlay, Ilse Kern, Guy Lenaers, Arnold Munnich, Pierre Meyer, Marie‐Aude Spitz, (unknown), Diane Doummar, Guy Touati, Nicolas Leboucq, Agathe Roubertie	11
7	Fructose‐1,6‐bisphosphatase deficiency causes fatty liver disease and requires long‐term hepatic follow‐up 2021 ·Journal of Inherited Metabolic Disease ·(unknown), Élise Lebigot, (unknown), Anaïs Brassier, Aline Cano, Pascale de Lonlay, François Feillet, Claire Gay, F. Labarthe, Marie‐Cécile Nassogne, (unknown), Agathe Roubertie, (unknown), Guy Touati, Pierre Broué	9
8	A Review of Multiple Mitochondrial Dysfunction Syndromes, Syndromes Associated with Defective Fe-S Protein Maturation 2021 ·Biomedicines ·Élise Lebigot, Manuel Schiff, Marie‐Pierre Golinelli‐Cohen	18
9	Mitochondrial dysfunction caused by novel ATAD3A mutations 2020 ·Molecular Genetics and Metabolism ·Nathalie Dorison, Pauline Gaignard, Aurélien Bayot, A. Gélot, (unknown), S. Fourati, Élise Lebigot, Perrine Charles, Timothy Wai, Patrice Thérond, Abdelhamid Slama	20
10	Expanding the phenotype of mitochondrial disease: Novel pathogenic variant in ISCA1 leading to instability of the iron-sulfur cluster in the protein 2020 ·Mitochondrion ·Élise Lebigot, Marie Hully, Larbi Amazit, Pauline Gaignard, Thomas Michel, (unknown), Marc Lombès, Patrice Thérond, Audrey Boutron, Marie‐Pierre Golinelli‐Cohen	6
11	Recurrent Liver Failure in an 11-Year-Old Boy 2020 ·Clinical Chemistry ·(unknown), (unknown), Élise Lebigot, (unknown)	2
12	Human Dermal Fibroblast: A Promising Cellular Model to Study Biological Mechanisms of Major Depression and Antidepressant Drug Response 2019 ·Current Neuropharmacology ·(unknown), Romain Colle, Élise Lebigot, Séverine Trabado, (unknown), Bruno Fève, Laurent Becquemont, Emmanuelle Corruble, Céline Verstuyft	15
13	Les déficits de la chaîne respiratoire : démarche diagnostique des cytopathies mitochondriales 2018 ·Revue Francophone des Laboratoires ·Pauline Gaignard, (unknown), Élise Lebigot, Patrice Thérond, Abdelhamid Slama	0
14	Troponin elevation in other conditions than acute coronary syndromes 2017 ·Annales de biologie clinique ·(unknown), (unknown), (unknown), Khaldoun Ghazal, Élise Lebigot, Claudine Cosson, (unknown), Patrice Thérond	13
15	UQCRC2 mutation in a patient with mitochondrial complex III deficiency causing recurrent liver failure, lactic acidosis and hypoglycemia 2017 ·Journal of Human Genetics ·Pauline Gaignard, Didier Eyer, Élise Lebigot, (unknown), Patrice Thérond, Audrey Boutron, Abdelhamid Slama	28
16	Impact of mutations within the [Fe-S] cluster or the lipoic acid biosynthesis pathways on mitochondrial protein expression profiles in fibroblasts from patients 2017 ·Molecular Genetics and Metabolism ·Élise Lebigot, Pauline Gaignard, Imen Dorboz, Abdelhamid Slama, (unknown), Pascale de Lonlay, Bénédicte Héron, Frédérique Sabourdy, Odile Boespflug‐Tanguy, Ariel R. Cardoso, Florence Habarou, Chris Ottolenghi, Patrice Thérond, Cécile Bouton, Marie‐Pierre Golinelli‐Cohen, Audrey Boutron	40
17	Ketone Bodies as a Possible Adjuvant to Ketogenic Diet in PDHc Deficiency but Not in GLUT1 Deficiency 2017 ·JIMD Reports ·Florence Habarou, Nadia Bahi‐Buisson, Élise Lebigot, Clément Pontoizeau, (unknown), Anaïs Brassier, Kim‐Hanh Le Quan Sang, Christine Broissand, Sandrine Vuillaumier‐Barrot, Agathe Roubertie, Audrey Boutron, Chris Ottolenghi, Pascale de Lonlay	6
18	Fructose 1,6‐bisphosphatase deficiency: clinical, biochemical and genetic features in French patients 2015 ·Journal of Inherited Metabolic Disease ·Élise Lebigot, Anaïs Brassier, Mokhtar Zater, Dilek Imanci, François Feillet, Patrice Thérond, Pascale de Lonlay, Audrey Boutron	31

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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