C. Labasse

461 total citations
11 papers, 101 citations indexed

About

C. Labasse is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Genetics. According to data from OpenAlex, C. Labasse has authored 11 papers receiving a total of 101 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 4 papers in Cardiology and Cardiovascular Medicine and 4 papers in Genetics. Recurrent topics in C. Labasse's work include Muscle Physiology and Disorders (4 papers), Cardiomyopathy and Myosin Studies (4 papers) and Nuclear Structure and Function (3 papers). C. Labasse is often cited by papers focused on Muscle Physiology and Disorders (4 papers), Cardiomyopathy and Myosin Studies (4 papers) and Nuclear Structure and Function (3 papers). C. Labasse collaborates with scholars based in France, Argentina and Chile. C. Labasse's co-authors include Norma B. Romero, Jocelyn Laporte, Isabelle Marty, Sandra Donkervoort, Johann Böhm, Vandana Gupta, Carsten G. Bönnemann, Michel Fardeau, Xavière Lornage and Raphaël Schneider and has published in prestigious journals such as Acta Neuropathologica, eLife and Journal of Neuropathology & Experimental Neurology.

In The Last Decade

C. Labasse

11 papers receiving 100 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
C. Labasse France	5	75	44	26	22	18	11	101
S. Makri France	5	140 1.9×	27 0.6×	43 1.7×	19 0.9×	23 1.3×	8	156
Edoardo Malfatti France	6	61 0.8×	44 1.0×	17 0.7×	12 0.5×	12 0.7×	11	87
Benjamin M. Nash Australia	7	152 2.0×	39 0.9×	26 1.0×	18 0.8×	38 2.1×	17	200
Carola Hedberg Sweden	7	158 2.1×	97 2.2×	30 1.2×	25 1.1×	29 1.6×	9	216
F. Fortunato Italy	6	102 1.4×	14 0.3×	18 0.7×	11 0.5×	21 1.2×	12	122
Elise Valkanas United States	6	89 1.2×	29 0.7×	32 1.2×	8 0.4×	50 2.8×	6	125
Samantha J. Bryen Australia	6	99 1.3×	19 0.4×	10 0.4×	17 0.8×	26 1.4×	13	117
Plavi Mittal United States	4	109 1.5×	20 0.5×	31 1.2×	14 0.6×	21 1.2×	7	126
Mai Thao Bui France	5	59 0.8×	10 0.2×	23 0.9×	47 2.1×	8 0.4×	10	108
C. Bouchet-Séraphin France	6	194 2.6×	29 0.7×	47 1.8×	34 1.5×	26 1.4×	11	211

Countries citing papers authored by C. Labasse

Since Specialization

Citations

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

Fields of papers citing papers by C. Labasse

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of C. Labasse

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

All Works

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11 of 11 papers shown

Bui, Mai Thao, Gorka Fernández‐Eulate, Teresinha Evangelista, et al.. (2024). Relevance of muscle biopsies in the neonatal and early infantile period: a 52 years retrospective study in the gene-sequencing era. Acta Neuropathologica Communications. 12(1). 191–191. 1 indexed citations

Lainé, Jeanne, Marion Benoist, Gilles Moulay, et al.. (2023). Caveolae and Bin1 form ring-shaped platforms for T-tubule initiation. eLife. 12. 13 indexed citations

Bauché, Stéphanie, Damien Sternberg, A. Seferian, et al.. (2023). Pathogenic DPAGT1 variants in limb‐girdle congenital myasthenic syndrome (LG‐CMS) associated with tubular aggregates and ORAI1 hypoglycosylation. Neuropathology and Applied Neurobiology. 50(1). e12952–e12952. 5 indexed citations

Bevilacqua, Jorge A., Edoardo Malfatti, C. Labasse, et al.. (2022). Congenital Nemaline Myopathy with Dense Protein Masses. Journal of Neuropathology & Experimental Neurology. 81(4). 304–307. 1 indexed citations

Girard, Emmanuelle, Karine Poulard, Guy Brochier, et al.. (2021). CONGENITAL MYOPATHIES – NEMALINE MYOPATHIES. Neuromuscular Disorders. 31. S61–S62. 1 indexed citations

Küsters, Benno, Josine M. de Winter, Guy Brochier, et al.. (2021). NEM6, KBTBD13-Related Congenital Myopathy: Myopathological Analysis in 18 Dutch Patients Reveals Ring Rods Fibers, Cores, Nuclear Clumps, and Granulo-Filamentous Protein Material. Journal of Neuropathology & Experimental Neurology. 80(4). 366–376. 4 indexed citations

Lornage, Xavière, Norma B. Romero, Sandra Donkervoort, et al.. (2019). ACTN2 mutations cause “Multiple structured Core Disease” (MsCD). Acta Neuropathologica. 137(3). 501–519. 35 indexed citations

Garibaldi, Matteo, John Rendu, Julie Brocard, et al.. (2019). ‘Dusty core disease’ (DuCD): expanding morphological spectrum of RYR1 recessive myopathies. Acta Neuropathologica Communications. 7(1). 3–3. 33 indexed citations

Monges, Soledad, Edoardo Malfatti, Fabiana Lubieniecki, et al.. (2018). Sarcomeric disorganization and nemaline bodies in muscle biopsies of patients with EXOSC3‐related type 1 pontocerebellar hypoplasia. Muscle & Nerve. 59(1). 137–141. 6 indexed citations

10.

Malfatti, Edoardo, Evelyne Goillot, Nathalie Streichenberger, et al.. (2017). Autophagy impairment in muscle biopsies from debranching enzyme deficiency (GSDIII) patients: pinpointing novel therapeutic perspectives. Neuromuscular Disorders. 27. S205–S206. 1 indexed citations

11.

Garibaldi, Matteo, Fabiana Fattori, Beatrice Riva, et al.. (2016). Tubular aggregate myopathy with miosis caused by a novel mutation in ORAI1. Neuromuscular Disorders. 26. S193–S193. 1 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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