M. Chaouch

606 total citations
8 papers, 295 citations indexed

About

M. Chaouch is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cell Biology. According to data from OpenAlex, M. Chaouch has authored 8 papers receiving a total of 295 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 4 papers in Cellular and Molecular Neuroscience and 2 papers in Cell Biology. Recurrent topics in M. Chaouch's work include Hereditary Neurological Disorders (4 papers), Nuclear Structure and Function (4 papers) and RNA Research and Splicing (3 papers). M. Chaouch is often cited by papers focused on Hereditary Neurological Disorders (4 papers), Nuclear Structure and Function (4 papers) and RNA Research and Splicing (3 papers). M. Chaouch collaborates with scholars based in France, Algeria and United States. M. Chaouch's co-authors include Kevin P. Campbell, Michel Fardeau, France Leturcq, F.M.S. Tomé, Djamel Grid, Annachiara De Sandre‐Giovannoli, M. Tazir, Nicolas Lévy, K. Azibi and T. Hammadouche and has published in prestigious journals such as Neurology, Human Molecular Genetics and Annals of Human Genetics.

In The Last Decade

M. Chaouch

8 papers receiving 289 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
M. Chaouch France	6	244	128	68	53	42	8	295
Satu Sandell Finland	10	232 1.0×	89 0.7×	41 0.6×	114 2.2×	56 1.3×	21	313
Christopher M. Chamberlain United States	9	335 1.4×	173 1.4×	43 0.6×	70 1.3×	16 0.4×	9	387
Ana Buj‐Bello France	9	325 1.3×	86 0.7×	108 1.6×	68 1.3×	84 2.0×	19	369
Luigi Fulizio Italy	8	397 1.6×	193 1.5×	197 2.9×	148 2.8×	56 1.3×	9	476
T Maríková Czechia	8	252 1.0×	173 1.4×	60 0.9×	24 0.5×	19 0.5×	16	294
Virginie François France	8	236 1.0×	110 0.9×	10 0.1×	56 1.1×	26 0.6×	8	310
Irene Warlo Germany	11	396 1.6×	81 0.6×	171 2.5×	201 3.8×	103 2.5×	15	466
Jana Haberlová Czechia	10	176 0.7×	97 0.8×	39 0.6×	45 0.8×	125 3.0×	24	305
Annalisa Onori Italy	12	274 1.1×	48 0.4×	23 0.3×	21 0.4×	22 0.5×	18	329
Rumi Kurokawa Japan	11	366 1.5×	48 0.4×	84 1.2×	31 0.6×	23 0.5×	12	401

Countries citing papers authored by M. Chaouch

Since Specialization

Citations

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

Fields of papers citing papers by M. Chaouch

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. Chaouch

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

All Works

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8 of 8 papers shown

Hamadouche, Tarik, Yannick Poitelon, Emmanuelle Génin, et al.. (2008). Founder Effect and Estimation of the Age of the c.892C>T (p.Arg298Cys) Mutation in LMNA Associated to Charcot‐Marie‐Tooth Subtype CMT2B1 in Families from North Western Africa. Annals of Human Genetics. 72(5). 590–597. 21 indexed citations

Delague, Valérie, Arnaud Jacquier, Tarik Hamadouche, et al.. (2007). G.O.3 Mutations in FGD4 encoding the Rho GDP/GTP exchange factor FRABIN cause autosomal recessive Charcot-Marie-Tooth type 4H. Neuromuscular Disorders. 17(9-10). 767–767. 3 indexed citations

Chaouch, M., Annachiara De Sandre‐Giovannoli, J.M. Vallat, et al.. (2002). The phenotypic manifestations of autosomal recessive axonalCharcot–Marie–Tooth due to a mutation in Lamin A/C gene. Neuromuscular Disorders. 13(1). 60–67. 65 indexed citations

Sandre‐Giovannoli, Annachiara De, M. Chaouch, Serguei Kozlov, et al.. (2002). Homozygous Defects In Lmna, Encoding Lamin A/C Nuclear‐Envelope Proteins, Cause Autosomal Recessive Axonal Neuropathy In Human (Charcot‐Marie‐Tooth Disorder Type 2) And Mouse. Journal of the Peripheral Nervous System. 7(3). 205–205. 13 indexed citations

Eymard, B., Norma B. Romero, France Leturcq, et al.. (1997). Primary adhalinopathy (α‐sarcoglycanopathy). Neurology. 48(5). 1227–1234. 95 indexed citations

Kaplan, Josseline, Fédérica Piccolo, K. Azibi, et al.. (1996). Genetic, allelic and phenotypic heterogeneity of muscular dystrophies with primary and secondary involvement of adhalin (alpha-sarcoglycan). Neuromuscular Disorders. 6(2). S8–S8. 1 indexed citations

Yamada, Hirotsugu, I. Higuchi, H Kawai, et al.. (1995). Laminin abnormality in severe childhood autosomal recessive muscular dystrophy.. PubMed. 72(6). 715–22. 18 indexed citations

Bachner, L, J. Beckmann, M. Chaouch, et al.. (1993). Severe childhood autosomal recessive muscular dystrophy with the deficiency of the 50 kDa dystrophin-associated glycoprotein maps to chromosome 13q12. Human Molecular Genetics. 2(9). 1423–1428. 79 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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