Rémi Bellance

1.2k total citations
16 papers, 213 citations indexed

About

Rémi Bellance is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Rémi Bellance has authored 16 papers receiving a total of 213 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 4 papers in Genetics and 4 papers in Clinical Biochemistry. Recurrent topics in Rémi Bellance's work include Muscle Physiology and Disorders (5 papers), Metabolism and Genetic Disorders (4 papers) and Neurogenetic and Muscular Disorders Research (4 papers). Rémi Bellance is often cited by papers focused on Muscle Physiology and Disorders (5 papers), Metabolism and Genetic Disorders (4 papers) and Neurogenetic and Muscular Disorders Research (4 papers). Rémi Bellance collaborates with scholars based in France, Martinique and Guadeloupe. Rémi Bellance's co-authors include Norma B. Romero, Annick Labarre‐Vila, Rakesh Patel, Kathryn N. North, Edward S. Johnson, Michael Fahey, Esther Lim, Danielle E. Dye, Nigel F. Clarke and Hanna Kolski and has published in prestigious journals such as Circulation, Annals of Neurology and International Journal of Molecular Sciences.

In The Last Decade

Rémi Bellance

13 papers receiving 211 citations

Peers

Rémi Bellance

MB

CCM

GENET

IMMUN

CMN

Lucie Gueneau France

Tomohiko Kayashima Japan

Michaela Yuen Australia

Daniel Prins United Kingdom

Hayley Goullée Australia

Arnaud Jollet France

Hélène Polvèche France

Adam Bournazos Australia

Agnieszka Madej‐Pilarczyk Poland

Katherine R. Chao United States

Lucie Gueneau France

Rémi Bellance

216 ×1.4

MB

92 ×0.9

CCM

40 ×0.6

GENET

16 ×0.5

IMMUN

18 ×0.8

CMN

Citations per year, relative to Rémi Bellance Rémi Bellance (= 1×) peers Lucie Gueneau

Countries citing papers authored by Rémi Bellance

Since Specialization

Citations

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

Fields of papers citing papers by Rémi Bellance

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rémi Bellance

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

All Works

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16 of 16 papers shown

1.

Duclos, Sophie, et al.. (2025). A Late-Onset and Mild Phenotype of Mitochondrial Complex I Deficiency Due to a Novel Reported Variant Within the ACAD9 Gene. International Journal of Molecular Sciences. 26(15). 7128–7128. 1 indexed citations

2.

Fergelot, Patricia, Caroline Rooryck, Dominique P. Germain, et al.. (2024). Prevalence of Fabry disease in patients with chronic pain: Lessons from the DOUFAB and DOUFABIS studies. European Journal of Pain. 29(1). e4708–e4708.

3.

Felix, A., Fréderique Delion, Rémi Bellance, et al.. (2023). Juvenile Dermatomyositis in Afro-Caribbean children: a cohort study in the French West Indies. Pediatric Rheumatology. 21(1). 113–113. 3 indexed citations

4.

Morin, Stéphanie, et al.. (2020). Gossypetin Derivatives are also Putative Inhibitors of SARS-COV 2: Results of a Computational Study. Zenodo (CERN European Organization for Nuclear Research). 1(6). 201–212. 4 indexed citations

5.

Chaussenot, Annabelle, Sylvie Bannwarth, Sabrina Sacconi, et al.. (2020). Single‐fiber studies for assigning pathogenicity of eight mitochondrial DNA variants associated with mitochondrial diseases. Human Mutation. 41(8). 1394–1406. 4 indexed citations

6.

Barp, Andrea, Rémi Bellance, Edoardo Malfatti, et al.. (2019). Late Onset Multiple Acyl-CoA Dehydrogenase Deficiency (MADD) Myopathy Misdiagnosed as Polymyositis. JCR Journal of Clinical Rheumatology. 1–1. 2 indexed citations

7.

Barp, Andrea, Rémi Bellance, Edoardo Malfatti, et al.. (2019). Late Onset Multiple Acyl-CoA Dehydrogenase Deficiency (MADD) Myopathy Misdiagnosed as Polymyositis. JCR Journal of Clinical Rheumatology. 26(5). e125–e127. 7 indexed citations

8.

Sarrazin, Elisabeth, et al.. (2018). La dystrophie musculaire de Duchenne en Martinique. médecine/sciences. 34. 45–48.

9.

Corcia, Philippe, Patrick Vourc’h, Hélène Blasco, et al.. (2018). Phenotypic and genotypic studies of ALS cases in ALS-SMA families. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 19(5-6). 432–437. 7 indexed citations

10.

Bellance, Rémi. (2015). Le Centre de Référence Caribéen des maladies neuromusculaires et neurologiques rares. médecine/sciences. 31. 45–47.

11.

Malfatti, Edoardo, et al.. (2015). Cylindrical spirals associated with severe congenital muscle weakness and epileptic encephalopathy. Muscle & Nerve. 52(5). 895–899. 5 indexed citations

12.

Terrier, Benjamin, A. Bérezné, Guillaume Bussone, et al.. (2013). Antisignal Recognition Particle Antibodies–Related Cardiomyopathy. Circulation. 127(5). e434–6. 10 indexed citations

13.

Deschamps, Romain, Odile Béra, Agnès Lézin, et al.. (2010). Absence of consistent association between human leukocyte antigen-I and -II alleles and human T-lymphotropic virus type 1 (HTLV-1)-associated myelopathy/tropical spastic paraparesis risk in an HTLV-1 French Afro-Caribbean population. International Journal of Infectious Diseases. 14(11). e986–e990. 10 indexed citations

14.

Clarke, Nigel F., Hanna Kolski, Danielle E. Dye, et al.. (2008). Mutations in TPM3 are a common cause of congenital fiber type disproportion. Annals of Neurology. 63(3). 329–337. 102 indexed citations

15.

Béroud, Christophe, Alain Carrié, Chérif Beldjord, et al.. (2003). Dystrophinopathy caused by mid-intronic substitutions activating cryptic exons in the DMD gene. Neuromuscular Disorders. 14(1). 10–18. 42 indexed citations

16.

Tangy, Frédéric, Laurent Coscoy, Rémi Bellance, et al.. (1995). A search for human T‐cell leukemia virus type I in the lesions of patients with tropical spastic paraparesis and polymyositis. Annals of Neurology. 38(3). 454–460. 16 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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