Emmanuelle Sarzi

2.4k total citations
25 papers, 1.7k citations indexed

About

Emmanuelle Sarzi is a scholar working on Molecular Biology, Clinical Biochemistry and Cellular and Molecular Neuroscience. According to data from OpenAlex, Emmanuelle Sarzi has authored 25 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 14 papers in Clinical Biochemistry and 4 papers in Cellular and Molecular Neuroscience. Recurrent topics in Emmanuelle Sarzi's work include Mitochondrial Function and Pathology (22 papers), Metabolism and Genetic Disorders (14 papers) and ATP Synthase and ATPases Research (12 papers). Emmanuelle Sarzi is often cited by papers focused on Mitochondrial Function and Pathology (22 papers), Metabolism and Genetic Disorders (14 papers) and ATP Synthase and ATPases Research (12 papers). Emmanuelle Sarzi collaborates with scholars based in France, United States and Singapore. Emmanuelle Sarzi's co-authors include Agnès Rötig, Arnold Münnich, Dominique Chrétien, Valérie Serre, Pascale de Lonlay, Guy Lenaers, Véronique Paquis‐Flucklinger, Limor Minai, Yusuke Nakamura and Hirofumi Arakawa and has published in prestigious journals such as Nature Genetics, PLoS ONE and Brain.

In The Last Decade

Emmanuelle Sarzi

25 papers receiving 1.7k citations

Peers

Countries citing papers authored by Emmanuelle Sarzi

Since Specialization

Citations

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

Fields of papers citing papers by Emmanuelle Sarzi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Emmanuelle Sarzi

This figure shows the co-authorship network connecting the top 25 collaborators of Emmanuelle Sarzi. A scholar is included among the top collaborators of Emmanuelle Sarzi 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 Emmanuelle Sarzi. Emmanuelle Sarzi 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	The human OPA1delTTAG mutation induces adult onset and progressive auditory neuropathy in mice 2024 ·Cellular and Molecular Life Sciences ·(unknown), (unknown), (unknown), (unknown), Majida Charif, Emmanuelle Sarzi, Frédéric Flamant, Romain Guyot, Chantal Cazevieille, Jean‐Luc Puel, Guy Lenaers, Jing Wang	3
2	Optic neuropathy linked to ACAD9 pathogenic variants: A potentially riboflavin-responsive disorder? 2021 ·Mitochondrion ·Naïg Guéguen, (unknown), Emmanuelle Sarzi, (unknown), Gaël Manès, Cécile Delettre, Pascal Amédro, Nicolas Leboucq, M. Kœnig, Pierre Meyer, Isabelle Meunier, Pascal Reynier, Guy Lenaers, Agathe Roubertie	5
3	OPA1 gene therapy prevents retinal ganglion cell loss in a Dominant Optic Atrophy mouse model 2018 ·Scientific Reports ·Emmanuelle Sarzi, Marie Seveno, (unknown), (unknown), Mélanie Quilès, Marie O. Péquignot, Agnès Müller, Christian Hamel, Guy Lenaers, Cécile Delettre	49
4	ACO2 mutations: A novel phenotype associating severe optic atrophy and spastic paraplegia 2018 ·Neurology Genetics ·Cécilia Marelli, Christian Hamel, Mélanie Quilès, Bertrand Carlander, Lise Larrieu, Cécile Delettre, Emmanuelle Sarzi, Dominique Chrétien, Pierre Rustin, M. Kœnig, Claire Guissart	16
5	Optical Coherence Tomography: Imaging Mouse Retinal Ganglion Cells <em>In Vivo</em> 2017 ·Journal of Visualized Experiments ·(unknown), Emmanuelle Sarzi, Mélanie Cavalier, Marie Seveno, (unknown), Christian Hamel, Marie O. Péquignot, Cécile Delettre	9
6	Increased steroidogenesis promotes early-onset and severe vision loss in females withOPA1dominant optic atrophy 2016 ·Human Molecular Genetics ·Emmanuelle Sarzi, Marie Seveno, Claire Angebault, Dan Miléa, Cecilia Rönnbäck, Mélanie Quilès, (unknown), (unknown), (unknown), Annie Lacroux, Christian Lavergne, Pascal Reynier, Michael Larsen, Christian P. Hamel, Guy Lenaers, (unknown)	17
7	OPA1-related disorders: Diversity of clinical expression, modes of inheritance and pathophysiology 2015 ·Neurobiology of Disease ·Juan Manuel Chao de la Barca, Delphine Mirebeau‐Prunier, Patrizia Amati‐Bonneau, Marc Ferré, Emmanuelle Sarzi, Céline Bris, Stéphanie Leruez, Arnaud Chevrollier, Valérie Desquiret‐Dumas, Naïg Guéguen, Christophe Verny, Christian Hamel, Dan Miléa, Vincent Procaccio, Dominique Bonneau, Guy Lenaers, Pascal Reynier	43
8	Neuroradiological findings expand the phenotype of OPA1-related mitochondrial dysfunction 2015 ·Journal of the Neurological Sciences ·Agathe Roubertie, Nicolas Leboucq, Marie Picot, Erika Nogué, Hervé Brunel, Emmanuelle Le Bars, Gaël Manès, (unknown), Catherine Blanchet, Michel Mondain, Hugues Chevassus, Patrizia Amati‐Bonneau, Emmanuelle Sarzi, Michel Pagès, Max Villain, Isabelle Meunier, Guy Lenaers, Christian P. Hamel	20
9	In vivo time-lapse imaging of mitochondria in healthy and diseased peripheral myelin sheath 2015 ·Mitochondrion ·Sergio González, Ruani Fernando, Jade Berthelot, Claire Perrin-Tricaud, Emmanuelle Sarzi, Roman Chrast, Guy Lenaers, Nicolas Tricaud	12
10	Why Mitochondria Must Fuse to Maintain Their Genome Integrity 2013 ·Antioxidants and Redox Signaling ·Sara Vidoni, Claudia Zanna, Michela Rugolo, Emmanuelle Sarzi, Guy Lenaers	42
11	The human OPA1delTTAG mutation induces premature age-related systemic neurodegeneration in mouse 2012 ·Brain ·Emmanuelle Sarzi, Claire Angebault, Marie Seveno, Naïg Guéguen, Benjamin Chaix, Guy Biélicki, Nathalie Boddaert, Anne-Laure Mausset-Bonnefont, Chantal Cazevieille, Valérie Rigau, Jean‐Pierre Renou, Jing Wang, Cécile Delettre, Philippe Brabet, Jean‐Luc Puel, Christian Hamel, Pascal Reynier, Guy Lenaers	78
12	OPA1 links human mitochondrial genome maintenance to mtDNA replication and distribution 2010 ·Genome Research ·Ghizlane Elachouri, Sara Vidoni, Claudia Zanna, Alexandre Pattyn, Hassan Boukhaddaoui, Karen Gaget, Patrick Yu‐Wai‐Man, Giuseppe Gasparre, Emmanuelle Sarzi, Cécile Delettre, Aurélien Olichon, Dominique Loiseau, Pascal Reynier, Patrick F. Chinnery, Agnès Rötig, Valério Carelli, Christian Hamel, Michela Rugolo, Guy Lenaers	178
13	Instabilité du génome mitochondrial et pathologies associées 2010 ·médecine/sciences ·Emmanuelle Sarzi, Agnès Rötig	5
14	The first founder DGUOK mutation associated with hepatocerebral mitochondrial DNA depletion syndrome 2009 ·Molecular Genetics and Metabolism ·N. Brahimi, Marguerite Jambou, Emmanuelle Sarzi, Valérie Serre, Nathalie Boddaert, S. Romano, Pascale de Lonlay, Abdelhamid Slama, Arnold Münnich, Agnès Rötig	26
15	Mutation of RRM2B, encoding p53-controlled ribonucleotide reductase (p53R2), causes severe mitochondrial DNA depletion 2007 ·Nature Genetics ·(unknown), Limor Minai, Valérie Serre, Jean-Philippe Jaı̈s, Emmanuelle Sarzi, Sophie Aubert, Dominique Chrétien, Pascale de Lonlay, Véronique Paquis‐Flucklinger, Hirofumi Arakawa, Yusuke Nakamura, Arnold Münnich, Agnès Rötig	428
16	Twinkle helicase (PEO1) gene mutation causes mitochondrial DNA depletion 2007 ·Annals of Neurology ·Emmanuelle Sarzi, Steffi Goffart, Valérie Serre, Dominique Chrétien, Abdelhamid Slama, Arnold Münnich, Johannes N. Spelbrink, Agnès Rötig	132
17	Mitochondrial DNA Depletion is a Prevalent Cause of Multiple Respiratory Chain Deficiency in Childhood 2007 ·The Journal of Pediatrics ·Emmanuelle Sarzi, (unknown), Dominique Chrétien, (unknown), (unknown), Abdelhamid Slama, Valérie Cormier‐Daire, Pascale de Lonlay, Arnold Münnich, Agnès Rötig	127
18	A novel recurrent mitochondrial DNA mutation in ND3 gene is associated with isolated complex I deficiency causing Leigh syndrome and dystonia 2006 ·American Journal of Medical Genetics Part A ·Emmanuelle Sarzi, Michael D. Brown, Sophie Lebon, Dominique Chrétien, Arnold Münnich, Agnès Rötig, Vincent Procaccio	86
19	MPV17 encodes an inner mitochondrial membrane protein and is mutated in infantile hepatic mitochondrial DNA depletion 2006 ·Nature Genetics ·Antonella Spinazzola, Carlo Viscomi, Erika Fernández‐Vizarra, Franco Carrara, Pio D’Adamo, Sarah E. Calvo, Renè Massimiliano Marsano, Claudia Donnini, Hans Weiher, Pietro Strisciuglio, Rossella Parini, Emmanuelle Sarzi, Alicia Chan, Salvatore DiMauro, Agnès Rötig, Paolo Gasparini, Iliana Ferrero, Vamsi K. Mootha, Valeria Tiranti, Massimo Zeviani	330
20	Molecular diagnostics of mitochondrial disorders 2004 ·Biochimica et Biophysica Acta (BBA) - Bioenergetics ·Agnès Rötig, Sophie Lebon, Elena Zinovieva, (unknown), Emmanuelle Sarzi, Jean‐Paul Bonnefont, Arnold Münnich	28

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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