Corine Gartioux

1.5k total citations
23 papers, 419 citations indexed

About

Corine Gartioux is a scholar working on Molecular Biology, Cell Biology and Immunology and Allergy. According to data from OpenAlex, Corine Gartioux has authored 23 papers receiving a total of 419 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 6 papers in Cell Biology and 6 papers in Immunology and Allergy. Recurrent topics in Corine Gartioux's work include Muscle Physiology and Disorders (15 papers), Cell Adhesion Molecules Research (6 papers) and Nuclear Structure and Function (6 papers). Corine Gartioux is often cited by papers focused on Muscle Physiology and Disorders (15 papers), Cell Adhesion Molecules Research (6 papers) and Nuclear Structure and Function (6 papers). Corine Gartioux collaborates with scholars based in France, Italy and Belgium. Corine Gartioux's co-authors include Valérie Allamand, Pascale Guicheney, Alain Krol, Alain Lescure, Pascale Richard, C. Ledeuil, Meral Topçu, J. Beckmann, Ana Ferreiro and Meral Özgüç and has published in prestigious journals such as Nucleic Acids Research, SHILAP Revista de lepidopterología and Diabetes.

In The Last Decade

Corine Gartioux

21 papers receiving 408 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Corine Gartioux France	10	321	68	67	67	55	23	419
Simona Frateschi Switzerland	10	343 1.1×	53 0.8×	19 0.3×	44 0.7×	34 0.6×	15	499
Paula Iughetti Brazil	7	244 0.8×	45 0.7×	37 0.6×	18 0.3×	51 0.9×	9	297
L. Scot Bastian United States	9	155 0.5×	41 0.6×	43 0.6×	19 0.3×	22 0.4×	9	352
Cristina Dias United Kingdom	11	172 0.5×	19 0.3×	143 2.1×	11 0.2×	30 0.5×	16	359
Janine Altmueller Germany	11	477 1.5×	22 0.3×	43 0.6×	16 0.2×	39 0.7×	14	605
Ndona N. Nsumu United States	11	440 1.4×	38 0.6×	47 0.7×	6 0.1×	59 1.1×	12	585
Aurélien Trimouille France	12	237 0.7×	65 1.0×	121 1.8×	14 0.2×	143 2.6×	25	427
Sergio A. Cuevas‐Covarrubias Mexico	11	280 0.9×	18 0.3×	167 2.5×	11 0.2×	37 0.7×	41	418
Eileen Sweezer United States	5	363 1.1×	21 0.3×	82 1.2×	4 0.1×	39 0.7×	8	443
Dylan J. M. Bergen United Kingdom	9	199 0.6×	42 0.6×	81 1.2×	14 0.2×	123 2.2×	14	371

Countries citing papers authored by Corine Gartioux

Since Specialization

Citations

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

Fields of papers citing papers by Corine Gartioux

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Corine Gartioux

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

All Works

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20 of 20 papers shown

Stojkovic, Tanya, Marion Masingue, Corinne Métay, et al.. (2022). LAMA2-Related Muscular Dystrophy: The Importance of Accurate Phenotyping and Brain Imaging in the Diagnosis of LGMD. Journal of Neuromuscular Diseases. 10(1). 125–133.

Mazancourt, Philippe de, Corinne Métay, Robert Carlier, et al.. (2021). A novel COL1A1 variant in a family with clinical features of hypermobile Ehlers‐Danlos syndrome that proved to be a COL1‐related overlap disorder. SHILAP Revista de lepidopterología. 9(9). e04128–e04128. 6 indexed citations

Deev, R. V, Valérie Allamand, Corine Gartioux, et al.. (2020). Intrafamilial Phenotypic Variability of Collagen VI-Related Myopathy Due to a New Mutation in the COL6A1 Gene. Journal of Neuromuscular Diseases. 8(2). 273–285. 5 indexed citations

Gallardo, Eduard, Alix de Becdelièvre, Corine Gartioux, et al.. (2016). Bethlem Myopathy Phenotypes and Follow Up: Description of 8 Patients at the Mildest End of the Spectrum. Journal of Neuromuscular Diseases. 3(2). 267–274. 8 indexed citations

Gallardo, Eduard, Alix de Becdelièvre, Corine Gartioux, et al.. (2016). Bethlem myopathy phenotypes and follow up: Description of 8 patients in the mildest end of the spectrum. Neuromuscular Disorders. 26. S187–S188. 1 indexed citations

Lainé, Jeanne, Arnaud F. Klein, Lucette Joassard, et al.. (2015). Two novel COLVI long chains in zebrafish that are essential for muscle development. Human Molecular Genetics. 24(23). 6624–6639. 15 indexed citations

Deconinck, Nicolas, Pascale Richard, Valérie Allamand, et al.. (2014). Bethlem myopathy: long-term follow-up identifies COL6 mutations predicting severe clinical evolution. Journal of Neurology Neurosurgery & Psychiatry. 86(12). 1337–1346. 31 indexed citations

Quijano‐Roy, Susana, Clarisse Baumann, Valérie Allamand, et al.. (2014). Congenital muscular dystrophy phenotype with neuromuscular spindles excess in a 5-year-old girl caused by HRAS mutation. Neuromuscular Disorders. 24(11). 993–998.

Pénisson-Besnier, I., Valérie Allamand, Philippe Beurrier, et al.. (2013). Compound heterozygous mutations of the TNXB gene cause primary myopathy. Neuromuscular Disorders. 23(8). 664–669. 32 indexed citations

10.

Bozorgmehr, Bita, Ariana Kariminejad, Shahriar Nafissi, et al.. (2013). Ullrich Congenital Muscular Dystrophy (UCMD): Clinical and Genetic Correlations.. PubMed. 7(3). 15–22. 9 indexed citations

11.

Stojkovic, Tanya, Isabelle Nelson, Juliette Nectoux, et al.. (2013). P.1.15 Clinical heterogeneity of myopathy related to partial merosin deficiency. Neuromuscular Disorders. 23(9-10). 746–746. 1 indexed citations

12.

Perez, Aura, Corine Gartioux, Maud Beuvin, et al.. (2012). G.P.18 Muscle pathology and dysfunction in a novel mouse model of COLVI-myopathy. Neuromuscular Disorders. 22(9-10). 827–828. 2 indexed citations

13.

Castets, Perrine, Svetlana Maugenre, Corine Gartioux, et al.. (2009). Selenoprotein N is dynamically expressed during mouse development and detected early in muscle precursors. BMC Developmental Biology. 9(1). 46–46. 26 indexed citations

14.

Allamand, Valérie, Corine Gartioux, Emmanuelle Lacène, et al.. (2007). C.O.3 Endoplasmic reticulum retention of COL6 chains in Ullrich congenital muscular dystrophy. Neuromuscular Disorders. 17(9-10). 833–833. 1 indexed citations

15.

Rederstorff, Mathieu, Valérie Allamand, Pascale Guicheney, et al.. (2007). Ex vivo correction of selenoprotein N deficiency in rigid spine muscular dystrophy caused by a mutation in the selenocysteine codon. Nucleic Acids Research. 36(1). 237–244. 9 indexed citations

16.

Allamand, Valérie, Laure Bidou, Masayuki Arakawa, et al.. (2007). Drug‐induced readthrough of premature stop codons leads to the stabilization of laminin α2 chain mRNA in CMD myotubes. The Journal of Gene Medicine. 10(2). 217–224. 53 indexed citations

17.

Allamand, Valérie, Pascale Richard, Alain Lescure, et al.. (2006). A single homozygous point mutation in a 3′untranslated region motif of selenoprotein N mRNA causes SEPN1‐related myopathy. EMBO Reports. 7(4). 450–454. 68 indexed citations

18.

Pepe, Guglielmina, Laura Lucarini, Ruizhu Zhang, et al.. (2005). COL6A1 genomic deletions in Bethlem myopathy and Ullrich muscular dystrophy. Annals of Neurology. 59(1). 190–195. 27 indexed citations

19.

Giusti, Betti, Laura Lucarini, S. Lucioli, et al.. (2005). Dominant and recessive COL6A1 mutations in Ullrich scleroatonic muscular dystrophy. Annals of Neurology. 58(3). 400–410. 57 indexed citations

20.

Topçu, Meral, Corine Gartioux, Florence Ribiérre, et al.. (2000). Vacuoliting Megalencephalic Leukoencephalopathy with Subcortical Cysts, Mapped to Chromosome 22qtel. The American Journal of Human Genetics. 66(2). 733–739. 60 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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