Sonia Nouioua

742 total citations
18 papers, 441 citations indexed

About

Sonia Nouioua is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Sonia Nouioua has authored 18 papers receiving a total of 441 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Cellular and Molecular Neuroscience, 6 papers in Molecular Biology and 5 papers in Neurology. Recurrent topics in Sonia Nouioua's work include Hereditary Neurological Disorders (10 papers), Genetic Neurodegenerative Diseases (7 papers) and Neurological diseases and metabolism (5 papers). Sonia Nouioua is often cited by papers focused on Hereditary Neurological Disorders (10 papers), Genetic Neurodegenerative Diseases (7 papers) and Neurological diseases and metabolism (5 papers). Sonia Nouioua collaborates with scholars based in Algeria, France and Australia. Sonia Nouioua's co-authors include Mériem Tazir, Jean‐Michel Vallat, Tarik Hamadouche, Stéphane Mathis, Djamel Grid, Salima Assami, Traki Benhassine, Jean‐Michel Vallat, Michel Kœnig and Laurent Magy and has published in prestigious journals such as Neurology, Journal of Neuropathology & Experimental Neurology and Journal of the Neurological Sciences.

In The Last Decade

Sonia Nouioua

18 papers receiving 435 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sonia Nouioua Algeria 11 298 164 136 124 105 18 441
Claudia Stendel Germany 9 279 0.9× 223 1.4× 102 0.8× 75 0.6× 84 0.8× 17 443
Stefania Magri Italy 13 271 0.9× 296 1.8× 54 0.4× 66 0.5× 115 1.1× 33 477
Yujiro Higuchi Japan 13 381 1.3× 206 1.3× 84 0.6× 161 1.3× 135 1.3× 53 551
Xingyao Wu United States 11 456 1.5× 180 1.1× 115 0.8× 144 1.2× 200 1.9× 20 598
Daniele Galatolo Italy 12 227 0.8× 219 1.3× 57 0.4× 64 0.5× 50 0.5× 28 340
Ana Cuesta Spain 6 373 1.3× 162 1.0× 61 0.4× 153 1.2× 110 1.0× 10 439
Kishin Koh Japan 11 194 0.7× 136 0.8× 51 0.4× 99 0.8× 72 0.7× 38 295
Alleene V. Strickland United States 7 256 0.9× 185 1.1× 105 0.8× 113 0.9× 101 1.0× 7 417
Elena Sánchez-Ferrero Spain 8 164 0.6× 161 1.0× 36 0.3× 101 0.8× 86 0.8× 10 313
Meyke Schouten Netherlands 10 124 0.4× 221 1.3× 64 0.5× 49 0.4× 60 0.6× 19 420

Countries citing papers authored by Sonia Nouioua

Since Specialization
Citations

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

Fields of papers citing papers by Sonia Nouioua

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sonia Nouioua

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

All Works

18 of 18 papers shown
1.
Tazir, Mériem & Sonia Nouioua. (2024). Distal hereditary motor neuropathies. Revue Neurologique. 180(10). 1031–1036. 3 indexed citations
2.
Malfatti, Edoardo, Sonia Nouioua, Emmanuel Fournier, et al.. (2021). A TOR1AIP1 variant segregating with an early onset limb girdle myasthenia—Support for the role of LAP1 in NMJ function and disease. Neuropathology and Applied Neurobiology. 48(1). e12743–e12743. 6 indexed citations
3.
Nouioua, Sonia, et al.. (2021). Un cas de myasthénie congénitale des ceintures résolu grâce à une collaboration tripartite. médecine/sciences. 37. 50–52. 1 indexed citations
4.
Alipacha, Lamia, et al.. (2018). Neuromyélite optique de Devic séropositive à neuro-imagerie normale. Revue Neurologique. 174. S28–S29. 1 indexed citations
5.
Duchesne, Mathilde, Stéphane Mathis, Laurence Richard, et al.. (2017). Nerve Biopsy Is Still Useful in Some Inherited Neuropathies. Journal of Neuropathology & Experimental Neurology. 77(2). 88–99. 13 indexed citations
6.
Nouioua, Sonia, et al.. (2017). Description d’une famille algérienne associant une dysferlinopathie et une merosinopathie primaires. Revue Neurologique. 173. S68–S69. 1 indexed citations
7.
Stöckler‐Ipsiroglu, Sylvia, Roberta Battini, Suzanne D. DeBrosse, et al.. (2015). Arginine:glycine amidinotransferase (AGAT) deficiency: Clinical features and long term outcomes in 16 patients diagnosed worldwide. Molecular Genetics and Metabolism. 116(4). 252–259. 45 indexed citations
8.
Tazir, Mériem, Tarik Hamadouche, Sonia Nouioua, Stéphane Mathis, & Jean‐Michel Vallat. (2014). Hereditary motor and sensory neuropathies or Charcot–Marie–Tooth diseases: An update. Journal of the Neurological Sciences. 347(1-2). 14–22. 66 indexed citations
9.
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
10.
Nouioua, Sonia, et al.. (2013). Creatine deficiency syndrome. A treatable myopathy due to arginine–glycine amidinotransferase (AGAT) deficiency. Neuromuscular Disorders. 23(8). 670–674. 25 indexed citations
11.
Tazir, Mériem, et al.. (2013). Autosomal recessive Charcot‐Marie‐Tooth disease: from genes to phenotypes. Journal of the Peripheral Nervous System. 18(2). 113–129. 53 indexed citations
12.
Nouioua, Sonia, et al.. (2012). Multicenter Transversal Two-Phase Study to Determine a National Prevalence of Epilepsy in Algeria. Neuroepidemiology. 39(2). 131–134. 9 indexed citations
13.
Nouioua, Sonia, Tarik Hamadouche, Benoît Funalot, et al.. (2011). Novel mutations in the PRX and the MTMR2 genes are responsible for unusual Charcot-Marie-Tooth disease phenotypes. Neuromuscular Disorders. 21(8). 543–550. 18 indexed citations
14.
Tazir, Mériem, Sonia Nouioua, Laurent Magy, et al.. (2009). Phenotypic variability in giant axonal neuropathy. Neuromuscular Disorders. 19(4). 270–274. 40 indexed citations
15.
Tazir, Mériem, Lamia Alipacha, Jean‐Pierre Delaunoy, et al.. (2009). Ataxia with oculomotor apraxia type 2: A clinical and genetic study of 19 patients. Journal of the Neurological Sciences. 278(1-2). 77–81. 41 indexed citations
16.
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
17.
Azzedine, Hamid, N. Ravisé, Christophe Verny, et al.. (2006). Spine deformities in Charcot-Marie-Tooth 4C caused by SH3TC2 gene mutations. Neurology. 67(4). 602–606. 76 indexed citations
18.
Tazir, Mériem, Jean-Michel Vallat, Pascale Bomont, et al.. (2002). Genetic heterogeneity in giant axonal neuropathy: an Algerian family not linked to chromosome 16q24.1. Neuromuscular Disorders. 12(9). 849–852. 21 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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