Cécile Acquaviva

4.8k total citations
110 papers, 2.7k citations indexed

About

Cécile Acquaviva is a scholar working on Molecular Biology, Clinical Biochemistry and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Cécile Acquaviva has authored 110 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 70 papers in Molecular Biology, 54 papers in Clinical Biochemistry and 26 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Cécile Acquaviva's work include Metabolism and Genetic Disorders (54 papers), Mitochondrial Function and Pathology (36 papers) and Kidney Stones and Urolithiasis Treatments (19 papers). Cécile Acquaviva is often cited by papers focused on Metabolism and Genetic Disorders (54 papers), Mitochondrial Function and Pathology (36 papers) and Kidney Stones and Urolithiasis Treatments (19 papers). Cécile Acquaviva collaborates with scholars based in France, United Kingdom and United States. Cécile Acquaviva's co-authors include Christine Vianey‐Saban, Jérôme Harambat, Pierre Cochat, Justine Bacchetta, Sonia Fargue, Jacques Élion, Gill Rumsby, Hélène Cavé, Érick Denamur and Nathalie Guffon and has published in prestigious journals such as Cell, SHILAP Revista de lepidopterología and Blood.

In The Last Decade

Cécile Acquaviva

103 papers receiving 2.6k citations

Peers

Countries citing papers authored by Cécile Acquaviva

Since Specialization

Citations

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

Fields of papers citing papers by Cécile Acquaviva

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Cécile Acquaviva

This figure shows the co-authorship network connecting the top 25 collaborators of Cécile Acquaviva. A scholar is included among the top collaborators of Cécile Acquaviva 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 Cécile Acquaviva. Cécile Acquaviva 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

#	Work	Indexed citations
1	Mitochondrial disorders are associated with morphological neuromuscular junction defects 2024 ·Neuromuscular Disorders ·(unknown), Emmanuelle Girard, Nathalie Streichenberger, Philippe Petiot, Cécile Acquaviva, Cécile Pagan, Peter Mulligan, Françoise Bouhour, Laurent Schaeffer, Arnaud Jacquier	1
2	Fifty years of research on mitochondrial fatty acid oxidation disorders: The remaining challenges 2023 ·Journal of Inherited Metabolic Disease ·Christine Vianey‐Saban, Nathalie Guffon, Alain Fouilhoux, Cécile Acquaviva	10
3	Newborn Screening of Primary Carnitine Deficiency: An Overview of Worldwide Practices and Pitfalls to Define an Algorithm before Expansion of Newborn Screening in France 2023 ·International Journal of Neonatal Screening ·(unknown), François Labarthe, (unknown), Caroline Moreau, (unknown), (unknown), Jean‐Baptiste Arnoux, M. Tardieu, Léna Damaj, Claude Bendavid, Anne‐Frédérique Dessein, Cécile Acquaviva, David Cheillan	9
4	Severe neuromuscular forms of glycogen storage disease type IV: Histological, clinical, biochemical, and molecular findings in a large French case series 2023 ·Journal of Inherited Metabolic Disease ·(unknown), Sophie Collardeau‐Frachon, Nathalie Streichenberger, (unknown), Alix Clémenson, Jérôme Massardier, Fabienne Prieur, Hélène Laurichesse, Fanny Laffargue, Cécile Acquaviva, Roseline Froissart, Magali Pettazzoni	1
5	The effect of lumasiran therapy for primary hyperoxaluria type 1 in small infants 2022 ·Pediatric Nephrology ·(unknown), Anne‐Laure Sellier‐Leclerc, Cécile Acquaviva, Jérôme Harambat, Lise Allard, Justine Bacchetta	20
6	Loss of thymidine phosphorylase activity disrupts adipocyte differentiation and induces insulin-resistant lipoatrophic diabetes 2022 ·BMC Medicine ·Jérémie Gautheron, (unknown), Barış Akıncı, (unknown), Martine Auclair, Sema Kalkan Uçar, Samim Özen, Canan Altay, Bridget E. Bax, Ivan Nemazanyy, Véronique Lenoir, Carina Prip‐Buus, Cécile Acquaviva, Olivier Lascols, Bruno Fève, Corinne Vigouroux, Esther Noël, Isabelle Jéru	8
7	Plasma acetyl-l-carnitine and l-carnitine in major depressive episodes: a case–control study before and after treatment 2021 ·Psychological Medicine ·(unknown), Romain Colle, (unknown), (unknown), Cécile Acquaviva, Denis J. David, Séverine Trabado, Philippe Chanson, Bruno Fève, Laurent Becquemont, Céline Verstuyft, Emmanuelle Corruble	6
8	An Atypical Case of Head Tremor and Extensive White Matter in an Adult Female Caused by 3-Hydroxy-3-methylglutaryl-CoA Lyase Deficiency 2021 ·Diagnostics ·(unknown), (unknown), (unknown), (unknown), Lucie Guyant‐Maréchal, Cécile Acquaviva, (unknown), Soumeya Bekri, Ivana Dabaj, Abdellah Tebani	1
9	Late-onset riboflavin transporter deficiency: a treatable mimic of various motor neuropathy aetiologies 2020 ·Journal of Neurology Neurosurgery & Psychiatry ·(unknown), Charline Benoit, Guido Ahle, Cécile Cauquil, Agathe Roubertie, Timothée Lenglet, Jeremy Cosgrove, Isabelle Meunier, (unknown), Cécile Acquaviva, Yann Nadjar	15
10	Plasma oxalate: comparison of methodologies 2020 ·Urolithiasis ·(unknown), Cécile Acquaviva, Bernd Höppe, John C. Lieske, (unknown), (unknown), Frédéric M. Vaz, Gill Rumsby	14
11	Intrafamilial Variability in <b><i>LPIN1</i></b>-Related Rhabdomyolysis 2020 ·Molecular Syndromology ·Linda Pons, Cécile Acquaviva, (unknown), (unknown), (unknown), Julie Steffann, Stéphanie Gobin, Pascale de Lonlay, Nathalie Guffon, Alain Fouilhoux	1
12	A case report of a mild form of multiple acyl-CoA dehydrogenase deficiency due to compound heterozygous mutations in the ETFA gene 2020 ·BMC Medical Genomics ·(unknown), Cécile Laroche-Raynaud, Anne‐Sophie Lia, (unknown), (unknown), Franck Sturtz, (unknown), (unknown), Cécile Acquaviva, Frédéric Favreau, (unknown)	5
13	Mutations inKARScause a severe neurological and neurosensory disease with optic neuropathy 2019 ·Human Mutation ·Sophie Scheidecker, Séverine Bär, Corinne Stoetzel, Véronique Geoffroy, Béatrice Lannes, Bruno Rinaldi, Frédéric Fischer, H. D. Becker, Valérie Pelletier, Cécile Pagan, Cécile Acquaviva, Stéphane Kremer, Marc Mirande, Christine Tranchant, Jean Muller, Sylvie Friant, Hélène Dollfus	15
14	Asparagine synthetase deficiency: A novel case with an unusual molecular mechanism 2019 ·Molecular Genetics and Metabolism Reports ·(unknown), Anne‐Lise Poulat, Nicolas Chatron, Audrey Labalme, Caroline Schluth‐Bolard, Marianne Till, Christine Vianey‐Saban, Vincent des Portes, Patrick Edery, Damien Sanlaville, Gaëtan Lesca, Cécile Acquaviva	6
15	Fluxomic assay-assisted diagnosis orientation in a cohort of 11 patients with myopathic form of CPT2 deficiency 2018 ·Molecular Genetics and Metabolism ·Monique Fontaine, (unknown), 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	11
16	The genetic basis of classic nonketotic hyperglycinemia due to mutations in GLDC and AMT 2016 ·Genetics in Medicine ·Curtis R. Coughlin, Michael A. Swanson, Kathryn E. Kronquist, Cécile Acquaviva, Tim Hutchin, Pilar Rodríguez‐Pombo, (unknown), Elaine Spector, Geralyn Creadon‐Swindell, (unknown), Elisa Rahikkala, Jukka S. Moilanen, (unknown), Gert Matthijs, (unknown), Celia Pérez‐Cerdá, Magdalena Ugarte, Christine Vianey‐Saban, Gunter Scharer, Johan L.K. Van Hove	56
17	Development of a Tandem Mass Spectrometry Method for Rapid Measurement of Medium- and Very-Long-Chain Acyl-CoA Dehydrogenase Activity in Fibroblasts 2016 ·JIMD Reports ·Damien Bouvier, Christine Vianey‐Saban, (unknown), Cécile Acquaviva	10
18	Submicroscopic bone marrow involvement in isolated extramedullary relapses in childhood acute lymphoblastic leukemia: a more precise definition of “isolated” and its possible clinical implications, a collaborative study of the Resistant Disease Committee of the International BFM study group 2007 ·Blood ·Nikola Hagedorn, Cécile Acquaviva, Eva Froňková, Arend von Stackelberg, Andrea Barth, Udo zur Stadt, André Schrauder, Jan Trka, Nathalie Gaspar, Karl Seeger, Günter Henze, Hélène Cavé, Cornelia Eckert	53
19	Isolated Sulfite Oxidase Deficiency in the Newborn: Lactic Acidaemia and Leukoencephalopathy 2007 ·Neuropediatrics ·(unknown), Paula J. Waters, (unknown), Cécile Acquaviva, (unknown), Kenneth J. Poskitt, Juliette Hukin	18
20	Evolutionary Implications of the Frequent Horizontal Transfer of Mismatch Repair Genes 2000 ·Cell ·Érick Denamur, Guillaume Lecointre, Pierre Darlu, Olivier Tenaillon, Cécile Acquaviva, Chalom Sayada, Ivana Šunjevarić, Rodney Rothstein, Jacques Élion, François Taddéi, Miroslav Radman, Ivan Matić	191

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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