Patrizia Amati‐Bonneau

7.4k total citations
72 papers, 3.3k citations indexed

About

Patrizia Amati‐Bonneau is a scholar working on Molecular Biology, Clinical Biochemistry and Cellular and Molecular Neuroscience. According to data from OpenAlex, Patrizia Amati‐Bonneau has authored 72 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 59 papers in Molecular Biology, 19 papers in Clinical Biochemistry and 12 papers in Cellular and Molecular Neuroscience. Recurrent topics in Patrizia Amati‐Bonneau's work include Mitochondrial Function and Pathology (55 papers), ATP Synthase and ATPases Research (30 papers) and Metabolism and Genetic Disorders (19 papers). Patrizia Amati‐Bonneau is often cited by papers focused on Mitochondrial Function and Pathology (55 papers), ATP Synthase and ATPases Research (30 papers) and Metabolism and Genetic Disorders (19 papers). Patrizia Amati‐Bonneau collaborates with scholars based in France, Singapore and Morocco. Patrizia Amati‐Bonneau's co-authors include Pascal Reynier, Dominique Bonneau, Vincent Procaccio, Guy Lenaers, Arnaud Chevrollier, Dan Miléa, Marc Ferré, Naïg Guéguen, Christophe Verny and Cécile Delettre and has published in prestigious journals such as Brain, Neurology and Annals of Neurology.

In The Last Decade

Patrizia Amati‐Bonneau

71 papers receiving 3.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Patrizia Amati‐Bonneau France 34 2.7k 812 550 329 315 72 3.3k
Marcela Votruba United Kingdom 30 3.3k 1.3× 816 1.0× 438 0.8× 878 2.7× 189 0.6× 85 4.0k
Laetitia Pelloquin France 16 2.6k 1.0× 769 0.9× 309 0.6× 131 0.4× 134 0.4× 26 2.9k
Dmitry Ivanov United States 27 1.6k 0.6× 107 0.1× 275 0.5× 468 1.4× 461 1.5× 62 2.4k
Christophe Verny France 20 853 0.3× 205 0.3× 578 1.1× 115 0.3× 285 0.9× 51 1.9k
Juha Kuja‐Panula Finland 17 1.0k 0.4× 666 0.8× 320 0.6× 19 0.1× 187 0.6× 22 1.9k
Galina Dvoriantchikova United States 26 1.1k 0.4× 100 0.1× 260 0.5× 492 1.5× 469 1.5× 52 1.9k
Myung‐Hoon Chun South Korea 32 2.1k 0.8× 63 0.1× 1.3k 2.4× 691 2.1× 413 1.3× 116 3.1k
Yun-Zheng Le United States 21 1.3k 0.5× 104 0.1× 232 0.4× 888 2.7× 233 0.7× 53 1.9k
Marcel V. Alavi Germany 16 995 0.4× 167 0.2× 163 0.3× 143 0.4× 79 0.3× 25 1.2k
Nobushige Tanaka Japan 12 544 0.2× 422 0.5× 397 0.7× 135 0.4× 67 0.2× 19 1.4k

Countries citing papers authored by Patrizia Amati‐Bonneau

Since Specialization
Citations

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

Fields of papers citing papers by Patrizia Amati‐Bonneau

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Patrizia Amati‐Bonneau. 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 Patrizia Amati‐Bonneau. The network helps show where Patrizia Amati‐Bonneau may publish in the future.

Co-authorship network of co-authors of Patrizia Amati‐Bonneau

This figure shows the co-authorship network connecting the top 25 collaborators of Patrizia Amati‐Bonneau. A scholar is included among the top collaborators of Patrizia Amati‐Bonneau 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 Patrizia Amati‐Bonneau. Patrizia Amati‐Bonneau 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.
Charif, Majida, Patrizia Amati‐Bonneau, Agnès Guichet, et al.. (2025). Two Cases of ROSAH-Like Syndrome Restricted to the Ophthalmologic Presentation. Ocular Immunology and Inflammation. 33(5). 849–853. 1 indexed citations
2.
Ferré, Marc, Valérie Desquiret‐Dumas, Alexis Descatha, et al.. (2024). Genetic susceptibility to optic neuropathy in patients with alcohol use disorder. Journal of Translational Medicine. 22(1). 495–495.
3.
Charif, Majida, Arnaud Chevrollier, Naïg Guéguen, et al.. (2022). Next-Generation Sequencing Identifies Novel PMPCA Variants in Patients with Late-Onset Dominant Optic Atrophy. Genes. 13(7). 1202–1202. 1 indexed citations
4.
Charif, Majida, Ichraf Kraoua, Valérie Desquiret‐Dumas, et al.. (2022). Next-generation sequencing of Tunisian Leigh syndrome patients reveals novel variations: impact for diagnosis and treatment. Bioscience Reports. 42(9). 4 indexed citations
5.
Charif, Majida, Yvette C. Wong, Soojin Kim, et al.. (2021). Dominant mutations in MIEF1 affect mitochondrial dynamics and cause a singular late onset optic neuropathy. Molecular Neurodegeneration. 16(1). 12–12. 13 indexed citations
6.
Bris, Céline, Vincent Procaccio, Patrizia Amati‐Bonneau, et al.. (2019). Deciphering exome sequencing data: Bringing mitochondrial DNA variants to light. Human Mutation. 40(12). 2430–2443. 7 indexed citations
7.
Sfaihi, L., Majida Charif, Valérie Desquiret‐Dumas, et al.. (2018). Next generation sequencing in family with MNGIE syndrome associated to optic atrophy: Novel homozygous POLG mutation in the C-terminal sub-domain leading to mtDNA depletion. Clinica Chimica Acta. 488. 104–110. 14 indexed citations
8.
Leruez, Stéphanie, Christophe Verny, Dominique Bonneau, et al.. (2018). Cyclosporine A does not prevent second-eye involvement in Leber’s hereditary optic neuropathy. Orphanet Journal of Rare Diseases. 13(1). 33–33. 13 indexed citations
9.
Gerber, S., Xavier Gérard, Klaus Zwicker, et al.. (2016). Compound heterozygosity for severe and hypomorphic NDUFS2 mutations cause non-syndromic LHON-like optic neuropathy. Journal of Medical Genetics. 54(5). 346–356. 38 indexed citations
10.
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
11.
Leruez, Stéphanie, Patrizia Amati‐Bonneau, Christophe Verny, et al.. (2014). Mitochondrial dysfunction affecting visual pathways. Revue Neurologique. 170(5). 344–354. 11 indexed citations
12.
Bombelli, Francesco, Tanya Stojkovic, O. Dubourg, et al.. (2014). Charcot-Marie-Tooth Disease Type 2A. JAMA Neurology. 71(8). 1036–1036. 95 indexed citations
13.
Chevrollier, Arnaud, Julien Cassereau, Marc Ferré, et al.. (2012). Standardized mitochondrial analysis gives new insights into mitochondrial dynamics and OPA1 function. The International Journal of Biochemistry & Cell Biology. 44(6). 980–988. 35 indexed citations
14.
Guillet, Virginie, Arnaud Chevrollier, Julien Cassereau, et al.. (2009). Ethambutol-induced optic neuropathy linked to OPA1 mutation and mitochondrial toxicity. Mitochondrion. 10(2). 115–124. 38 indexed citations
15.
Miléa, Dan, Patrizia Amati‐Bonneau, Pascal Reynier, & Dominique Bonneau. (2009). Genetically determined optic neuropathies. Current Opinion in Neurology. 23(1). 24–28. 26 indexed citations
16.
Chevrollier, Arnaud, Virginie Guillet, Dominique Loiseau, et al.. (2008). Hereditary optic neuropathies share a common mitochondrial coupling defect. Annals of Neurology. 63(6). 794–798. 94 indexed citations
17.
Verny, Christophe, Patrizia Amati‐Bonneau, Franck Letournel, et al.. (2008). Mitochondrial DNA A3243G mutation involved in familial diabetes, chronic intestinal pseudo-obstruction and recurrent pancreatitis. Diabetes & Metabolism. 34(6). 620–626. 22 indexed citations
18.
Hudson, Gavin, Patrizia Amati‐Bonneau, Emma L. Blakely, et al.. (2007). Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: a novel disorder of mtDNA maintenance. Brain. 131(2). 329–337. 304 indexed citations
19.
Amati‐Bonneau, Patrizia, Agnès Guichet, Aurélien Olichon, et al.. (2005). OPA1 R445H mutation in optic atrophy associated with sensorineural deafness. Annals of Neurology. 58(6). 958–963. 120 indexed citations
20.
Verny, Christophe, Patrizia Amati‐Bonneau, Frédéric Dubas, et al.. (2005). Atrophie optique, cataracte et signes extra-pyramidaux par mutation du gène OPA3. Revue Neurologique. 161(4). 451–454. 13 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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