Benoît Funalot

5.5k total citations
87 papers, 2.3k citations indexed

About

Benoît Funalot is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Benoît Funalot has authored 87 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 42 papers in Molecular Biology, 28 papers in Cellular and Molecular Neuroscience and 22 papers in Neurology. Recurrent topics in Benoît Funalot's work include Hereditary Neurological Disorders (20 papers), Mitochondrial Function and Pathology (14 papers) and Amyloidosis: Diagnosis, Treatment, Outcomes (12 papers). Benoît Funalot is often cited by papers focused on Hereditary Neurological Disorders (20 papers), Mitochondrial Function and Pathology (14 papers) and Amyloidosis: Diagnosis, Treatment, Outcomes (12 papers). Benoît Funalot collaborates with scholars based in France, United States and Spain. Benoît Funalot's co-authors include Jean‐Michel Vallat, Philippe Couratier, Franck Sturtz, Laurence Richard, Jean‐Claude Desport, Lev G. Goldfarb, Victor Ionâşescu, Kenneth H. Fischbeck, Nyamkhishig Sambuughin and Anthony Antonellis and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Neuroscience and PLoS ONE.

In The Last Decade

Benoît Funalot

81 papers receiving 2.3k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Benoît Funalot France	26	1.1k	813	657	380	314	87	2.3k
Makito Hirano Japan	29	994 0.9×	884 1.1×	1.4k 2.1×	435 1.1×	377 1.2×	149	3.0k
Carlo Casali Italy	29	1.5k 1.4×	997 1.2×	603 0.9×	142 0.4×	418 1.3×	98	2.8k
Alessandra Tessa Italy	29	1.6k 1.5×	1.0k 1.3×	251 0.4×	280 0.7×	496 1.6×	139	2.5k
Ann C. Price United States	13	747 0.7×	491 0.6×	809 1.2×	277 0.7×	226 0.7×	17	1.8k
Ning Wang China	21	1.2k 1.1×	727 0.9×	406 0.6×	161 0.4×	256 0.8×	137	2.5k
Nobutaka Arai Japan	27	841 0.8×	826 1.0×	977 1.5×	236 0.6×	597 1.9×	129	2.6k
Yael Barhum Israel	32	1.1k 1.0×	746 0.9×	534 0.8×	730 1.9×	273 0.9×	59	2.5k
Mongi Ben Hamida Tunisia	18	1.3k 1.2×	1.0k 1.3×	637 1.0×	442 1.2×	434 1.4×	27	2.4k
Tohru Matsuura Japan	31	2.1k 1.9×	1.5k 1.8×	666 1.0×	244 0.6×	410 1.3×	80	3.1k
Meraida Polak United States	18	1.4k 1.2×	611 0.8×	1.6k 2.5×	1.2k 3.1×	313 1.0×	24	2.8k

Countries citing papers authored by Benoît Funalot

Since Specialization

Citations

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

Fields of papers citing papers by Benoît Funalot

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Benoît Funalot

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Mansour‐Hendili, Lamisse, Cyril Gitiaux, Céline Latouche, et al.. (2024). Recurrent “outsider” intronic variation in the SLC5A6 gene causes severe mixed axonal and demyelinating neuropathy, cyclic vomiting and optic atrophy in 3 families from Maghreb. Frontiers in Genetics. 15. 1352006–1352006. 1 indexed citations

Vidaud, Dominique, Ingrid Laurendeau, Benoît Funalot, et al.. (2024). Prenatal diagnosis for neurofibromatosis type 1 and the pitfalls of germline mosaics. npj Genomic Medicine. 9(1). 2 indexed citations

Zaroui, Amira, Mounira Kharoubi, Mélanie Bézard, et al.. (2024). A phenotypic comparison of the Romanian and French ATTRv cohorts: Glu54Gln founder pathogenic variant vs the most common variants in Western Europe. International Journal of Cardiology. 419. 132714–132714. 1 indexed citations

Grévent, D., Marlène Rio, Isabelle Desguerre, et al.. (2018). High predictive value of brain MRI imaging in primary mitochondrial respiratory chain deficiency. Journal of Medical Genetics. 55(6). 378–383. 12 indexed citations

Sánchez‐Caballero, Laura, Benedetta Ruzzenente, L Bianchi, et al.. (2016). Mutations in Complex I Assembly Factor TMEM126B Result in Muscle Weakness and Isolated Complex I Deficiency. The American Journal of Human Genetics. 99(1). 208–216. 42 indexed citations

Mathis, Stéphane, Benoît Funalot, Olivia Boyer, et al.. (2014). Neuropathologic Characterization ofINF2-Related Charcot-Marie-Tooth Disease: Evidence for a Schwann Cell Actinopathy. Journal of Neuropathology & Experimental Neurology. 73(3). 223–233. 25 indexed citations

Mathis, Stéphane, Pascal Cintas, Geneviève de Saint Basile, et al.. (2014). Motor neuronopathy in Chediak–Higashi syndrome. Journal of the Neurological Sciences. 344(1-2). 203–207. 7 indexed citations

Mollard, Séverine, Hao Qiu, Laurence Richard, et al.. (2014). In vitro 3D angiogenesis assay in egg white matrix: comparison to Matrigel, compatibility to various species, and suitability for drug testing. Laboratory Investigation. 94(3). 340–349. 29 indexed citations

Cassereau, Julien, Philippe Codron, & Benoît Funalot. (2014). Inherited peripheral neuropathies due to mitochondrial disorders. Revue Neurologique. 170(5). 366–374. 15 indexed citations

10.

Lia-Baldini, Anne-Sophie, Corinne Magdelaine, Jean‐Pierre Salles, et al.. (2012). Two novel mutations of the calcium-sensing receptor gene affecting the same amino acid position lead to opposite phenotypes and reveal the importance of p.N802 on receptor activity. European Journal of Endocrinology. 168(2). K27–K34. 13 indexed citations

11.

Mollard, Séverine, Karine Durand, Laurence Richard, et al.. (2011). Fingolimod potentiates the effects of sunitinib malate in a rat breast cancer model. Breast Cancer Research and Treatment. 134(1). 31–40. 25 indexed citations

12.

Vézain, Myriam, Bénédicte Gérard, Séverine Drunat, et al.. (2011). A leaky splicing mutation affecting SMN1 exon 7 inclusion explains an unexpected mild case of spinal muscular atrophy. Human Mutation. 32(9). 989–994. 17 indexed citations

13.

Coulpier, Fanny, Laurence Decker, Benoît Funalot, et al.. (2010). CNS/PNS Boundary Transgression by Central Glia in the Absence of Schwann Cells or Krox20/Egr2 Function. Journal of Neuroscience. 30(17). 5958–5967. 43 indexed citations

14.

Funalot, Benoît, Corinne Magdelaine, Franck Sturtz, Robert Ouvrier, & Jean‐Michel Vallat. (2009). Anomalies ultrastructurales des mitochondries axonales chez des patients atteints de formes précoces de maladie de Charcot-Marie-Tooth dues à des mutations de la mitofusine 2. Bulletin de l Académie Nationale de Médecine. 193(1). 151–161. 8 indexed citations

15.

Ouvrier, Robert, John D. Pollard, Corinne Magdelaine, et al.. (2008). Histopathological Findings in Hereditary Motor and Sensory Neuropathy of Axonal Type With Onset in Early Childhood Associated WithMitofusin 2Mutations. Journal of Neuropathology & Experimental Neurology. 67(11). 1097–1102. 70 indexed citations

16.

Funalot, Benoît, et al.. (2007). [Exogenous risk factors in sporadic ALS: a review of the literature]. HAL (Le Centre pour la Communication Scientifique Directe). 1 indexed citations

17.

Jeanneteau, Freddy, Benoît Funalot, Joseph Jankovic, et al.. (2006). A functional variant of the dopamine D ₃ receptor is associated with risk and age-at-onset of essential tremor. Proceedings of the National Academy of Sciences. 103(28). 10753–10758. 151 indexed citations

18.

Funalot, Benoît, William C. Nichols, Jordi Pérez‐Tur, Géraldine Mercier, & G Lucotte. (2006). Genetic Screening for Two LRRK2 Mutations in French Patients with Idiopathic Parkinson's Disease. Genetic Testing. 10(4). 290–293. 14 indexed citations

19.

Antonellis, Anthony, Rachel E. Ellsworth, Nyamkhishig Sambuughin, et al.. (2003). Glycyl tRNA Synthetase Mutations in Charcot-Marie-Tooth Disease Type 2D and Distal Spinal Muscular Atrophy Type V. The American Journal of Human Genetics. 72(5). 1293–1299. 420 indexed citations

20.

Funalot, Benoît, Pascal Reynier, Alain Vighetto, et al.. (2002). Leigh‐like encephalopathy complicating Leber's hereditary optic neuropathy. Annals of Neurology. 52(3). 374–377. 53 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.

Explore authors with similar magnitude of impact