I. Pénisson-Besnier

2.4k total citations
55 papers, 1.2k citations indexed

About

I. Pénisson-Besnier is a scholar working on Molecular Biology, Neurology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, I. Pénisson-Besnier has authored 55 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Molecular Biology, 12 papers in Neurology and 9 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in I. Pénisson-Besnier's work include Muscle Physiology and Disorders (13 papers), Mitochondrial Function and Pathology (12 papers) and Cardiomyopathy and Myosin Studies (9 papers). I. Pénisson-Besnier is often cited by papers focused on Muscle Physiology and Disorders (13 papers), Mitochondrial Function and Pathology (12 papers) and Cardiomyopathy and Myosin Studies (9 papers). I. Pénisson-Besnier collaborates with scholars based in France, Finland and Sweden. I. Pénisson-Besnier's co-authors include Frédéric Dubas, Frédéric Dubas, J Emile, J.M. de Bray, Pascal Reynier, Pascal Laforêt, Michel Fardeau, Y. Gandon, Peter Hackman and Anna Vihola and has published in prestigious journals such as Neurology, The FASEB Journal and Human Molecular Genetics.

In The Last Decade

I. Pénisson-Besnier

54 papers receiving 1.1k citations

Peers

I. Pénisson-Besnier

CCM

NEURO

GENET

CMN

J. Mendell United States

Carlo P. Trevisan Italy

W. Mortier Germany

Olavo M. Vasconcelos United States

Hui Xiong China

Anna Mazzeo Italy

Claudio Bruno Italy

Yasushi Oya Japan

Madoka Mori‐Yoshimura Japan

Marina Pedemonte Italy

J. Mendell United States

I. Pénisson-Besnier

770 ×1.1

218 ×0.7

CCM

276 ×1.2

NEURO

142 ×0.9

GENET

301 ×2.0

CMN

Citations per year, relative to I. Pénisson-Besnier I. Pénisson-Besnier (= 1×) peers J. Mendell

Countries citing papers authored by I. Pénisson-Besnier

Since Specialization

Citations

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

Fields of papers citing papers by I. Pénisson-Besnier

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by I. Pénisson-Besnier. 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 I. Pénisson-Besnier. The network helps show where I. Pénisson-Besnier may publish in the future.

Co-authorship network of co-authors of I. Pénisson-Besnier

This figure shows the co-authorship network connecting the top 25 collaborators of I. Pénisson-Besnier. A scholar is included among the top collaborators of I. Pénisson-Besnier 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 I. Pénisson-Besnier. I. Pénisson-Besnier 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

Laforêt, Pascal, Benjamin Granger, Dalil Hamroun, et al.. (2013). The French Pompe registry. Baseline characteristics of a cohort of 126 patients with adult Pompe disease. Revue Neurologique. 169(8-9). 595–602. 39 indexed citations

Pénisson-Besnier, I.. (2013). Distal myopathies. Revue Neurologique. 169(8-9). 534–545. 1 indexed citations

Ochala, Julien, David S. Gokhin, I. Pénisson-Besnier, et al.. (2012). Congenital myopathy-causing tropomyosin mutations induce thin filament dysfunction via distinct physiological mechanisms. Human Molecular Genetics. 21(20). 4473–4485. 36 indexed citations

Gentil, Christel, France Leturcq, Rabah Ben Yaou, et al.. (2012). Variable phenotype of del45-55 Becker patients correlated with nNOSµ mislocalization and RYR1 hypernitrosylation. Human Molecular Genetics. 21(15). 3449–3460. 39 indexed citations

Lindqvist, Johan, I. Pénisson-Besnier, Hiroyuki Iwamoto, et al.. (2012). A myopathy-related actin mutation increases contractile function. Acta Neuropathologica. 123(5). 739–746. 16 indexed citations

Letournel, Franck, et al.. (2010). Nemaline bodies as unique pathological feature in the course of treated dermatomyositis. Clinical Neuropathology. 29(11). 357–360. 5 indexed citations

Gaudon, Karen, I. Pénisson-Besnier, B. Chabrol, et al.. (2010). Multiexon deletions account for 15% of congenital myasthenic syndromes with RAPSN mutations after negative DNA sequencing. Journal of Medical Genetics. 47(12). 795–796. 9 indexed citations

Laforêt, Pascal, Cécile Acquaviva, Odile Rigal, et al.. (2009). Diagnostic assessment and long-term follow-up of 13 patients with Very Long-Chain Acyl-Coenzyme A dehydrogenase (VLCAD) deficiency. Neuromuscular Disorders. 19(5). 324–329. 66 indexed citations

Stojkovic, Tanya, Pascale Richard, Adolfo López de Munaín, et al.. (2009). Clinical outcome in 19 French and Spanish patients with valosin-containing protein myopathy associated with Paget’s disease of bone and frontotemporal dementia. Neuromuscular Disorders. 19(5). 316–323. 66 indexed citations

10.

Pénisson-Besnier, I.. (2009). Traitement de la myasthénie auto-immune. Revue Neurologique. 166(4). 400–405. 6 indexed citations

11.

Hackman, Peter, Sylvie Marchand, J. Sarparanta, et al.. (2008). Truncating mutations in C-terminal titin may cause more severe tibial muscular dystrophy (TMD). Neuromuscular Disorders. 18(12). 922–928. 72 indexed citations

12.

Pénisson-Besnier, I., et al.. (2008). Syndrome lymphoprolifératif cutané lié à l’EBV au cours d’une dermatomyosite traitée par immunosuppresseurs. La Revue de Médecine Interne. 30(8). 720–723. 6 indexed citations

13.

Pénisson-Besnier, I., Valérie Biancalana, Pascal Reynier, Mireille Cossée, & Frédéric Dubas. (2007). Diagnosis of myotubular myopathy in the oldest known manifesting female carrier: A clinical and genetic study. Neuromuscular Disorders. 17(2). 180–185. 21 indexed citations

14.

Vézain, Myriam, Pascale Saugier-Véber, Judith Melki, et al.. (2007). A sensitive assay for measuring SMN mRNA levels in peripheral blood and in muscle samples of patients affected with spinal muscular atrophy. European Journal of Human Genetics. 15(10). 1054–1062. 32 indexed citations

15.

Yaou, Rabah Ben, Henri Marc Bécane, L. Demay, et al.. (2005). La dystrophie musculaire des ceintures autosomique dominante associée à des troubles de la conduction cardiaque (LGMD1B). Description de 8 nouvelles familles avec mutations du gène LMNA. Revue Neurologique. 161(1). 42–54. 12 indexed citations

16.

Pénisson-Besnier, I., et al.. (1998). Autosomal dominant late adult onset distal leg myopathy. Neuromuscular Disorders. 8(7). 459–466. 21 indexed citations

17.

Bray, J.M. de, I. Pénisson-Besnier, Frédéric Dubas, & J Emile. (1997). Extracranial and intracranial vertebrobasilar dissections: diagnosis and prognosis. Journal of Neurology Neurosurgery & Psychiatry. 63(1). 46–51. 112 indexed citations

18.

Reynier, Pascal, et al.. (1997). Male infertility associated with multiple mitochondrial DNA rearrangements. Comptes Rendus de l Académie des Sciences - Series III - Sciences de la Vie. 320(8). 629–636. 11 indexed citations

19.

Pénisson-Besnier, I., et al.. (1993). EFFICACITE DE TRIAMTERENE DANS L'HYDROCEPHALIE DE L'ADULTE. La Presse Médicale. 22(5). 224–225. 1 indexed citations

20.

Pénisson-Besnier, I., G. Guy, & Y. Gandon. (1989). Intramedullary epidermoid cyst evaluated by computed tomographic scan and magnetic resonance imaging. Neurosurgery. 25(6). 955–955. 33 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