Nathalie Bonello‐Palot

1.4k total citations
42 papers, 859 citations indexed

About

Nathalie Bonello‐Palot is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Nathalie Bonello‐Palot has authored 42 papers receiving a total of 859 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 16 papers in Cellular and Molecular Neuroscience and 12 papers in Genetics. Recurrent topics in Nathalie Bonello‐Palot's work include Hereditary Neurological Disorders (15 papers), Hemoglobinopathies and Related Disorders (11 papers) and Genetic Neurodegenerative Diseases (10 papers). Nathalie Bonello‐Palot is often cited by papers focused on Hereditary Neurological Disorders (15 papers), Hemoglobinopathies and Related Disorders (11 papers) and Genetic Neurodegenerative Diseases (10 papers). Nathalie Bonello‐Palot collaborates with scholars based in France, Netherlands and Switzerland. Nathalie Bonello‐Palot's co-authors include Nicolas Lévy, B. Chabrol, Catherine Badens, Françoise Dignat‐George, Annie Verschueren, Annabelle Chaussenot, Jean Pouget, Arnaud Chevrollier, Sebastien Arméro and Franck Paganelli and has published in prestigious journals such as Journal of the American College of Cardiology, Brain and Scientific Reports.

In The Last Decade

Nathalie Bonello‐Palot

40 papers receiving 842 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nathalie Bonello‐Palot France 15 357 250 200 117 104 42 859
Mary Blonski United States 11 292 0.8× 57 0.2× 114 0.6× 45 0.4× 52 0.5× 13 835
Brigham B. Hyde United States 6 635 1.8× 53 0.2× 28 0.1× 62 0.5× 56 0.5× 8 883
Monica Y. Lee United States 7 386 1.1× 25 0.1× 117 0.6× 38 0.3× 93 0.9× 7 922
Katalin Komlósi Hungary 15 235 0.7× 22 0.1× 159 0.8× 30 0.3× 32 0.3× 56 566
Tiffany Sharma United States 13 403 1.1× 32 0.1× 72 0.4× 36 0.3× 251 2.4× 19 688
Masakuni Noda Japan 11 317 0.9× 34 0.1× 157 0.8× 21 0.2× 61 0.6× 15 602
Holger Summer Germany 10 324 0.9× 54 0.2× 173 0.9× 15 0.1× 21 0.2× 14 660
Ronan Pendu France 6 135 0.4× 46 0.2× 25 0.1× 39 0.3× 26 0.3× 7 691
Anita K. Stannard United Kingdom 9 194 0.5× 101 0.4× 54 0.3× 9 0.1× 47 0.5× 11 506
Luis A. Carbini United States 14 226 0.6× 67 0.3× 307 1.5× 244 2.1× 18 0.2× 16 595

Countries citing papers authored by Nathalie Bonello‐Palot

Since Specialization
Citations

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

Fields of papers citing papers by Nathalie Bonello‐Palot

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Nathalie Bonello‐Palot. 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 Nathalie Bonello‐Palot. The network helps show where Nathalie Bonello‐Palot may publish in the future.

Co-authorship network of co-authors of Nathalie Bonello‐Palot

This figure shows the co-authorship network connecting the top 25 collaborators of Nathalie Bonello‐Palot. A scholar is included among the top collaborators of Nathalie Bonello‐Palot 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 Nathalie Bonello‐Palot. Nathalie Bonello‐Palot 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.
Bernit, Emmanuelle, Alexander L. Hornung, Anne Charrier, et al.. (2025). A novel red blood cell deformability biomarker is associated with hemolysis and vaso-occlusive crises in sickle cell disease. Scientific Reports. 15(1). 15864–15864. 1 indexed citations
2.
3.
Badens, Catherine, et al.. (2024). Perilipin 1: a systematic review on its functions on lipid metabolism and atherosclerosis in mice and humans. Cardiovascular Research. 120(3). 237–248. 16 indexed citations
4.
Beloribi‐Djefaflia, Sadia, Raúl Juntas Morales, Farzad Fatehi, et al.. (2023). Clinical and genetic features of patients suffering from CMT4J. Journal of Neurology. 271(3). 1355–1365. 6 indexed citations
5.
Bonello‐Palot, Nathalie, Yann Péréon, Andoni Echaniz‐Laguna, et al.. (2023). Clinical and electrophysiological characteristics of women with X‐linked Charcot–Marie–Tooth disease. European Journal of Neurology. 30(10). 3265–3276. 1 indexed citations
6.
Bonello‐Palot, Nathalie, et al.. (2023). Transfusion requirements and complication rate in β‐thalassemia intermedia due to heterozygous β‐globin gene mutation and triplicated α‐globin genes. European Journal Of Haematology. 111(5). 742–747. 2 indexed citations
7.
Bonello‐Palot, Nathalie, Patrice Bourgeois, Nicolas Lévy, et al.. (2021). A Rare Mutation in LMNB2 Associated with Lipodystrophy Drives Premature Cell Senescence. Cells. 11(1). 50–50. 2 indexed citations
8.
Bartoli, Marc, Nathalie Bonello‐Palot, Christophe Pécheux, et al.. (2021). Retrospective analysis and reclassification of DYSF variants in a large French series of dysferlinopathy patients. Genetics in Medicine. 23(8). 1574–1577. 14 indexed citations
9.
Dutour, Anne, Nathalie Bonello‐Palot, Patrice Bourgeois, et al.. (2020). Unraveling LMNA Mutations in Metabolic Syndrome: Cellular Phenotype and Clinical Pitfalls. Cells. 9(2). 310–310. 13 indexed citations
10.
Kouton, Ludivine, Émilien Delmont, Nathalie Martini, et al.. (2020). A New Point Mutation in the PMP22 Gene in a Family Suffering From Atypical HNPP. Journal of Neuromuscular Diseases. 7(4). 505–510. 3 indexed citations
11.
Salort‐Campana, Emmanuelle, Svetlana Gorokhova, Nathalie Bonello‐Palot, et al.. (2020). Refining NGS diagnosis of muscular disorders. Journal of Neurology Neurosurgery & Psychiatry. 92(2). 223–225. 1 indexed citations
12.
Boyer, Anthony, R. Bellance, Martin Krahn, et al.. (2019). Identification of novel pathogenic copy number variations in Charcot-Marie-Tooth disease. Journal of Human Genetics. 65(3). 313–323. 7 indexed citations
13.
Bonello‐Palot, Nathalie, Marc Laine, Thomas Cuisset, et al.. (2019). High prevalence of mutations in perilipin 1 in patients with precocious acute coronary syndrome. Atherosclerosis. 293. 86–91. 3 indexed citations
14.
Orvain, Corentin, Philippe Joly, Serge Pissard, et al.. (2017). Diagnostic approach to hemoglobins with high oxygen affinity: experience from France and Belgium and review of the literature. Annales de biologie clinique. 75(1). 39–51. 9 indexed citations
15.
Gaborit, Bénédicte, Inès Abdesselam, Monique Bernard, et al.. (2016). A Heterozygous ZMPSTE24 Mutation Associated with Severe Metabolic Syndrome, Ectopic Fat Accumulation, and Dilated Cardiomyopathy. Cells. 5(2). 21–21. 27 indexed citations
16.
Bonello‐Palot, Nathalie, Stéphanie Simoncini, Stéphane Robert, et al.. (2014). Prelamin A accumulation in endothelial cells induces premature senescence and functional impairment. Atherosclerosis. 237(1). 45–52. 49 indexed citations
17.
Bonello, Laurent, Sebastien Arméro, Omar Aït Mokhtar, et al.. (2010). Clopidogrel Loading Dose Adjustment According to Platelet Reactivity Monitoring in Patients Carrying the 2C19*2Loss of Function Polymorphism. Journal of the American College of Cardiology. 56(20). 1630–1636. 93 indexed citations
18.
Rotthier, Annelies, Jonathan Baets, Els De Vriendt, et al.. (2009). Genes for hereditary sensory and autonomic neuropathies: a genotype-phenotype correlation. Brain. 132(10). 2699–2711. 116 indexed citations
19.
Latour, Philippe, Véronique Bonnet, Shahram Attarian, et al.. (2009). U1 snRNA mis-binding: a new cause of CMT1B. Neurogenetics. 11(1). 13–19. 16 indexed citations
20.
Bonello, Laurent, Nathalie Bonello‐Palot, Sebastien Arméro, et al.. (2009). Impact of P2Y12-ADP receptor polymorphism on the efficacy of clopidogrel dose-adjustment according to platelet reactivity monitoring in coronary artery disease patients. Thrombosis Research. 125(4). e167–e170. 22 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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