Benoît Funalot

5.5k citations

87 papers · 2.3k indexed · h-index 26

Cellular and Molecular Neuroscience top 2%
- Hereditary Neurological Disorders 20
- Genetic Neurodegenerative Diseases 10
Neurology top 2%
- Neurological diseases and metabolism 10
- Amyotrophic Lateral Sclerosis Research 7
Neurology top 2%
- Neurological diseases and metabolism 10
- Amyotrophic Lateral Sclerosis Research 7
Genetics top 2%
- Neurogenetic and Muscular Disorders Research 8
Clinical Biochemistry top 2%
- Metabolism and Genetic Disorders 8
Molecular Biology
- Mitochondrial Function and Pathology 14
- Amyloidosis: Diagnosis, Treatment, Outcomes 12

Co-authors: Jean‐Michel Vallat Philippe Couratier Franck Sturtz Laurence Richard Jean‐Claude Desport Lev G. Goldfarb Victor Ionâşescu Kenneth H. Fischbeck
Cited by: Cellular and Molecular Neuroscience Neurology Genetics
Journals: Neurology (5 papers)Neuromuscular Disorders (3 papers)Journal of Neuropathology & Experimental Neurology (3 papers)
Partner nations: France United States Spain

In The Last Decade

Benoît Funalot

81 papers receiving 2.3k citations

Peers

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

The 25 scholars most cited alongside Benoît Funalot, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Benoît Funalot Line = papers co-authored together Benoît Funalot links everyone, so they are left out of the graph.

All Works

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

20 of 20 papers shown

#	Work
1	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 ·Lamisse Mansour‐Hendili,Cyril Gitiaux,廖清高,Céline Latouche,Bénédicte Héron,Tanya Stojkovic,Christopher N. Lewis,Thomas Smol,V. Fábián-Vonsik,Karine Mention,Yann Nadjar,Manuel Schiff,Julie Lemale,Jamal Ghoumid,Frédèric Gottrand,Cécile Talbotec,Agnès Rötig,Benoît Funalot,Isabelle Desguerre	2024	1
2	Prenatal diagnosis for neurofibromatosis type 1 and the pitfalls of germline mosaics npj Genomic Medicine ·学而熊谷,Dominique Vidaud,Severino Cavalcante de Sousa Júnior,Edward A. Walker,Mark Stein,Fabian Bill,Malin Olbers,Ingrid Laurendeau,Geny Syahdiany,Mattias Carlsson Feng,Benoît Funalot,P. Wolkenstein,Michel Vidaud,Alice Goldenberg,Fanny Morice‐Picard,Djihad Hadjadj,Béatrice Parfait,Éric Pasmant	2024	2
3	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 ·忠人及川,Amira Zaroui,Mounira Kharoubi,Mélanie Bézard,Benoît Funalot,Robert Adam,Corinne Donfut,Sorina Bădeliță,L. Magnaterra,清野学,Daniel Coriu,Ruxandra Jurcuţ,Thibaud Damy	2024	1
4	High predictive value of brain MRI imaging in primary mitochondrial respiratory chain deficiency Journal of Medical Genetics ·T.K.Aleyamma fenn,D. Grévent,Marlène Rio,Isabelle Desguerre,Pascale de Lonlay,R. Lévy,Volodia Dangouloff‐Ros,Jean‐Paul Bonnefont,Giulia Barcia,Benoît Funalot,Claude Besmond,Metodi D. Metodiev,Benedetta Ruzzenente,Zahra Assouline,Arnold Münnich,Agnès Rötig,Nathalie Boddaert	2018	12
5	Mutations in Complex I Assembly Factor TMEM126B Result in Muscle Weakness and Isolated Complex I Deficiency The American Journal of Human Genetics ·Laura Sánchez‐Caballero,Benedetta Ruzzenente,L Bianchi,Zahra Assouline,Giulia Barcia,Metodi D. Metodiev,Marlène Rio,Benoît Funalot,Mariël A.M. van den Brand,Sergio Guerrero‐Castillo,J. Molenaar,David A. Koolen,Ulrich Brandt,Richard J. Rodenburg,Leo Nijtmans,Agnès Rötig	2016	42
6	Neuropathologic Characterization ofINF2-Related Charcot-Marie-Tooth Disease: Evidence for a Schwann Cell Actinopathy Journal of Neuropathology & Experimental Neurology ·Stéphane Mathis,Benoît Funalot,Olivia Boyer,Catherine Lacroix,Pascale Marcorelles,Laurent Magy,Laurence Richard,Corinne Antignac,Jean‐Michel Vallat	2014	25
7	Motor neuronopathy in Chediak–Higashi syndrome Journal of the Neurological Sciences ·Stéphane Mathis,Pascal Cintas,Geneviève de Saint Basile,Laurent Magy,Benoît Funalot,J.M. Vallat	2014	7
8	In vitro 3D angiogenesis assay in egg white matrix: comparison to Matrigel, compatibility to various species, and suitability for drug testing Laboratory Investigation ·Mozhgan Mardani‐Talaee,Séverine Mollard,Hao Qiu,Laurence Richard,Raphaël Cazal,D. W. Latham,Nicolas Védrenne,Muyuan Lin,M. Ivova Rikova,Laurent Fourcade,Benoît Funalot,Franck Sturtz	2014	29
9	Inherited peripheral neuropathies due to mitochondrial disorders Revue Neurologique ·Julien Cassereau,Philippe Codron,Benoît Funalot	2014	15
10	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 ·Anne-Sophie Lia-Baldini,Corinne Magdelaine,D. W. Latham,Latifha bint Abdullah AL-KINDI,Jean‐Pierre Salles,Pierre Moulin,Brigitte Delemer,Qisya Nur Basirah Adawiyah1 Abdul Fattah,Benoît Funalot,Franck Sturtz,Anne Lienhardt-Roussie	2012	13
11	Fingolimod potentiates the effects of sunitinib malate in a rat breast cancer model Breast Cancer Research and Treatment ·Mozhgan Mardani‐Talaee,Séverine Mollard,Karine Durand,Laurence Richard,D. W. Latham,Jeanne Cook‐Moreau,M. Ivova Rikova,Hao Qiu,Чугунов Антон Олегович,Laurent Fourcade,Benoît Funalot,Franck Sturtz	2011	25
12	A leaky splicing mutation affecting SMN1 exon 7 inclusion explains an unexpected mild case of spinal muscular atrophy Human Mutation ·Myriam Vézain,Bénédicte Gérard,Séverine Drunat,Benoît Funalot,E. Chretien,R. A. Arlen,Jean‐Michel Vallat,Thierry Frébourg,Mario Tosi,Alexandra Martins,Pascale Saugier-Véber	2011	17
13	CNS/PNS Boundary Transgression by Central Glia in the Absence of Schwann Cells or Krox20/Egr2 Function Journal of Neuroscience ·Fanny Coulpier,Laurence Decker,Benoît Funalot,Jean‐Michel Vallat,F. García-Bragado,Patrick Charnay,Piotr Topilko	2010	43
14	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 ·Benoît Funalot,Corinne Magdelaine,Franck Sturtz,Robert Ouvrier,Jean‐Michel Vallat	2009	8
15	Histopathological Findings in Hereditary Motor and Sensory Neuropathy of Axonal Type With Onset in Early Childhood Associated WithMitofusin 2Mutations Journal of Neuropathology & Experimental Neurology ·Sanchuan Luo,Robert Ouvrier,John D. Pollard,Corinne Magdelaine,Danqing Zhu,Garth A. Nicholson,Aya Shintani,Monique M. Ryan,Benoît Funalot	2008	70
16	[Exogenous risk factors in sporadic ALS: a review of the literature] HAL (Le Centre pour la Communication Scientifique Directe) ·Olga Vorobyova,Benoît Funalot,Tien-Jou Kao,D. M. Murphy,Philippe Couratier	2007	1
17	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 ·Freddy Jeanneteau,Benoît Funalot,Joseph Jankovic,Hao Deng,Jean‐Pierre Lagarde,G Lucotte,Pierre Sokoloff	2006	151
18	Genetic Screening for Two LRRK2 Mutations in French Patients with Idiopathic Parkinson's Disease Genetic Testing ·Benoît Funalot,William C. Nichols,Jordi Pérez‐Tur,Géraldine Mercier,G Lucotte	2006	14
19	Glycyl tRNA Synthetase Mutations in Charcot-Marie-Tooth Disease Type 2D and Distal Spinal Muscular Atrophy Type V The American Journal of Human Genetics ·Anthony Antonellis,Rachel E. Ellsworth,Nyamkhishig Sambuughin,Imke Puls,Annette Abel,Masayo Inagawa‐Ogashiwa,Albena Jordanova,Ivo Kremensky,Kyproula Christodoulou,Lefkos Middleton,Kumaraswamy Sivakumar,Victor Ionâşescu,Benoît Funalot,Jeffery M. Vance,Lev G. Goldfarb,Kenneth H. Fischbeck,Eric D. Green	2003	420
20	Leigh‐like encephalopathy complicating Leber's hereditary optic neuropathy Annals of Neurology ·Benoît Funalot,Pascal Reynier,Alain Vighetto,Danièle Ranoux,Jean‐Paul Bonnefont,Catherine Godinot,Yves Malthièry,Jean‐Louis Mas	2002	53

About Benoît Funalot

Benoît Funalot is a scholar working on Neurology, Cellular and Molecular Neuroscience, Neurology, Clinical Biochemistry and Genetics, having authored 87 papers that have together received 2.3k indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (20 papers), Mitochondrial Function and Pathology (14 papers), Amyloidosis: Diagnosis, Treatment, Outcomes (12 papers), Neurological diseases and metabolism (10 papers), Genetic Neurodegenerative Diseases (10 papers), Metabolism and Genetic Disorders (8 papers), Neurogenetic and Muscular Disorders Research (8 papers) and Amyotrophic Lateral Sclerosis Research (7 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (813 citations), Neurology (657 citations), Neurology (314 citations), Genetics (380 citations) and Clinical Biochemistry (189 citations). Benoît Funalot has collaborated with scholars based in France, United States and Spain. Frequent 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. Their work appears in journals such as Neurology, Neuromuscular Disorders, Journal of Neuropathology & Experimental Neurology, Journal of the Peripheral Nervous System and The American Journal of Human Genetics.

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