Malika Chaouch

1.4k total citations
14 papers, 910 citations indexed

About

Malika Chaouch is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Malika Chaouch has authored 14 papers receiving a total of 910 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 6 papers in Cellular and Molecular Neuroscience and 6 papers in Genetics. Recurrent topics in Malika Chaouch's work include Genetic Neurodegenerative Diseases (4 papers), Genomics and Rare Diseases (3 papers) and Epilepsy research and treatment (3 papers). Malika Chaouch is often cited by papers focused on Genetic Neurodegenerative Diseases (4 papers), Genomics and Rare Diseases (3 papers) and Epilepsy research and treatment (3 papers). Malika Chaouch collaborates with scholars based in Algeria, France and United States. Malika Chaouch's co-authors include Djamel Grid, Nicolas Lévy, Mériem Tazir, Colin L. Stewart, Jean-Michel Vallat, Annachiara De Sandre‐Giovannoli, T. Hammadouche, Serguei Kozlov, Pierre Szepetowski and Antoon Vandenberghe and has published in prestigious journals such as Nature, FEBS Letters and The American Journal of Human Genetics.

In The Last Decade

Malika Chaouch

13 papers receiving 889 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Malika Chaouch Algeria	10	691	275	203	85	83	14	910
Marcella Neri Italy	18	546 0.8×	197 0.7×	121 0.6×	118 1.4×	144 1.7×	37	785
Shuhei Kameya Japan	18	968 1.4×	177 0.6×	135 0.7×	164 1.9×	69 0.8×	56	1.1k
Jorge A. Bevilacqua Chile	18	657 1.0×	279 1.0×	303 1.5×	72 0.8×	225 2.7×	54	928
Pervin Dinçer Türkiye	14	825 1.2×	258 0.9×	313 1.5×	73 0.9×	176 2.1×	45	947
Masaji Tachikawa Japan	9	391 0.6×	197 0.7×	91 0.4×	57 0.7×	33 0.4×	13	547
Rita C.M. Pavanello Brazil	18	899 1.3×	303 1.1×	108 0.5×	154 1.8×	254 3.1×	50	1.0k
Kamel Ben Othmane United States	9	852 1.2×	826 3.0×	267 1.3×	108 1.3×	185 2.2×	10	1.3k
Bas Blits Netherlands	15	550 0.8×	316 1.1×	82 0.4×	176 2.1×	40 0.5×	22	869
Glen B. Banks United States	21	1.0k 1.5×	235 0.9×	154 0.8×	207 2.4×	163 2.0×	28	1.2k
Abigail J. Renoux United States	6	523 0.8×	175 0.6×	89 0.4×	295 3.5×	30 0.4×	12	692

Countries citing papers authored by Malika Chaouch

Since Specialization

Citations

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

Fields of papers citing papers by Malika Chaouch

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Malika Chaouch

This figure shows the co-authorship network connecting the top 25 collaborators of Malika Chaouch. A scholar is included among the top collaborators of Malika 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 Malika Chaouch. Malika 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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14 of 14 papers shown

Navarro, Claire, Charles Marques Lourenço, Nathalie Da Silva, et al.. (2023). A recurrent homozygous LMNA missense variant p.Thr528Met causes atypical progeroid syndrome characterized by mandibuloacral dysostosis, severe muscular dystrophy, and skeletal deformities. American Journal of Medical Genetics Part A. 191(9). 2274–2289. 1 indexed citations

Chaouch, Malika, et al.. (2017). Recherche de variants génétiques de vulnérabilité à l’épilepsie chez des familles Algériennes. 1(1).

Chaouch, Malika, et al.. (2016). Greater improvement in LRRK2 G2019S patients undergoing Subthalamic Nucleus Deep Brain Stimulation compared to non-mutation carriers. BMC Neuroscience. 17(1). 6–6. 26 indexed citations

Chaouch, Malika, et al.. (2015). Consanguinity and epilepsy in Oran, Algeria: A case–control study. Epilepsy Research. 111. 10–17. 18 indexed citations

Hamadouche, Tarik, Jean Muller, Nathalie Drouot, et al.. (2015). Molecular and clinical study of a cohort of 110 Algerian patients with autosomal recessive ataxia. BMC Medical Genetics. 16(1). 36–36. 23 indexed citations

Guipponi, Michel, et al.. (2015). Familial epilepsy in Algeria: Clinical features and inheritance profiles. Seizure. 31. 12–18. 6 indexed citations

Siquier-Pernet, Karine, Christine Bôle‐Feysot, Patrick Nitschké, et al.. (2015). Refining the phenotype associated with CASC5 mutation. Neurogenetics. 17(1). 71–78. 17 indexed citations

Benhassine, Traki, Sonia Nouioua, S. Makri, et al.. (2013). Intragenic deletion patterns of dystrophin gene in Duchenne and Becker muscular dystrophy patients from Algeria. Genes & Genomics. 36(1). 17–24. 1 indexed citations

Langouët, Maéva, Guillaume Rieunier, Sébastien Moutton, et al.. (2013). Mutation in TTI2 Reveals a Role for Triple T Complex in Human Brain Development. Human Mutation. 34(11). 1472–1476. 18 indexed citations

10.

Borck, Guntram, et al.. (2009). Compound heterozygous ASPM mutations associated with microcephaly and simplified cortical gyration in a consanguineous Algerian family. European Journal of Medical Genetics. 52(4). 180–184. 20 indexed citations

11.

Delague, Valérie, Arnaud Jacquier, Tarik Hamadouche, et al.. (2007). Mutations in FGD4 Encoding the Rho GDP/GTP Exchange Factor FRABIN Cause Autosomal Recessive Charcot-Marie-Tooth Type 4H. The American Journal of Human Genetics. 81(1). 1–16. 117 indexed citations

12.

Sandre‐Giovannoli, Annachiara De, Malika 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. The American Journal of Human Genetics. 70(3). 726–736. 417 indexed citations

13.

Jung, Daniel, France Leturcq, Yoshihide Sunada, et al.. (1996). Absence of γ‐sarcoglycan (35 DAG) in autosomal recessive muscular dystrophy linked to chromosome 13q12. FEBS Letters. 381(1-2). 15–20. 46 indexed citations

14.

Matsumura, Kiichiro, F.M.S. Tomé, H. Barry Collin, et al.. (1992). Deficiency of the 50K dystrophin-associated glycoprotein in severe childhood autosomal recessive muscular dystrophy. Nature. 359(6393). 320–322. 200 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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