Réda Ouazzani

1.3k total citations
38 papers, 695 citations indexed

About

Réda Ouazzani is a scholar working on Psychiatry and Mental health, Cellular and Molecular Neuroscience and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Réda Ouazzani has authored 38 papers receiving a total of 695 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Psychiatry and Mental health, 12 papers in Cellular and Molecular Neuroscience and 9 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Réda Ouazzani's work include Epilepsy research and treatment (14 papers), Hereditary Neurological Disorders (7 papers) and Pharmacological Effects and Toxicity Studies (7 papers). Réda Ouazzani is often cited by papers focused on Epilepsy research and treatment (14 papers), Hereditary Neurological Disorders (7 papers) and Pharmacological Effects and Toxicity Studies (7 papers). Réda Ouazzani collaborates with scholars based in Morocco, France and Switzerland. Réda Ouazzani's co-authors include Alain Malafosse, Catherine Burési, Ali Benomar, Stylianos E. Antonarakis, Maria D. Lalioti, Armand Bottani, T. Chkili, Ahmed Bouhouche, Manuel C. Peitsch and Colette Rossier and has published in prestigious journals such as Brain, Neurology and Annals of Neurology.

In The Last Decade

Réda Ouazzani

35 papers receiving 683 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Réda Ouazzani Morocco 12 219 214 167 133 112 38 695
Edvige Veneselli Italy 17 190 0.9× 175 0.8× 210 1.3× 306 2.3× 159 1.4× 41 1.1k
Bülent Kara Türkiye 14 178 0.8× 82 0.4× 79 0.5× 115 0.9× 51 0.5× 72 690
Muhammad Mahajnah Israel 16 391 1.8× 117 0.5× 281 1.7× 79 0.6× 56 0.5× 55 831
Teresa Temudo Portugal 16 299 1.4× 128 0.6× 413 2.5× 180 1.4× 69 0.6× 51 1.0k
Amirthagowri Ambalavanan Canada 15 335 1.5× 69 0.3× 348 2.1× 135 1.0× 53 0.5× 31 795
Erika F. Augustine United States 16 209 1.0× 79 0.4× 139 0.8× 108 0.8× 133 1.2× 69 879
Elisa De Grandis Italy 15 153 0.7× 69 0.3× 106 0.6× 173 1.3× 97 0.9× 46 578
J.L. Haines United States 15 247 1.1× 120 0.6× 319 1.9× 52 0.4× 32 0.3× 20 853
Hélène Verhelst Belgium 17 264 1.2× 120 0.6× 84 0.5× 155 1.2× 29 0.3× 45 853
Rosario Domingo‐Jiménez Spain 14 224 1.0× 92 0.4× 145 0.9× 32 0.2× 40 0.4× 48 648

Countries citing papers authored by Réda Ouazzani

Since Specialization
Citations

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

Fields of papers citing papers by Réda Ouazzani

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Réda Ouazzani

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

All Works

20 of 20 papers shown
1.
2.
Souirti, Zouhayr, et al.. (2021). The modern terminology of epilepsy adopted by the Moroccan League Against Epilepsy. Epilepsy & Behavior. 122. 108177–108177.
3.
Alami, Mohammed, Meryem Benjelloun, Najib Kissani, et al.. (2020). Sleep quality and mental health in the context of COVID-19 pandemic and lockdown in Morocco. Sleep Medicine. 74. 248–253. 88 indexed citations
4.
Kuaté, Callixte, et al.. (2018). Clinical aspects, neuroimaging, and electroencephalography of 35 cases of hemiconvulsion-hemiplegia syndrome. Epilepsy & Behavior. 80. 184–190. 6 indexed citations
5.
Ouazzani, Réda. (2013). Epilepsy surgery in Morocco study and long-term follow-up in 51 cases. Journal of the Neurological Sciences. 333. e53–e54. 2 indexed citations
6.
Ouazzani, Réda, et al.. (2013). La chirurgie de l’épilepsie au Maroc, étude et suivi à long terme de 51 patients. 2(2). 1 indexed citations
7.
8.
Salzmann, Annick, Michel Guipponi, Peter J. Lyons, et al.. (2011). Carboxypeptidase A6 gene (CPA6) mutations in a recessive familial form of febrile seizures and temporal lobe epilepsy and in sporadic temporal lobe epilepsy. Human Mutation. 33(1). 124–135. 33 indexed citations
9.
Baulac, Stéphanie, Ahmed Bouhouche, Philippe Couarch, et al.. (2008). A locus for bilateral occipital polymicrogyria maps to chromosome 6q16–q22. Neurogenetics. 10(1). 35–42. 6 indexed citations
10.
11.
Bouhouche, Ahmed, Nazha Birouk, Ali Benomar, et al.. (2007). A Novel GDAP1 Mutation P78L Responsible for CMT4A Disease in Three Moroccan Families. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 34(4). 421–426. 10 indexed citations
12.
Birouk, Nazha, et al.. (2007). Lymphome T révélé par une mononeuropathie multiple : étude d’un cas avec revue de la littérature. Revue Neurologique. 163(4). 462–470. 6 indexed citations
13.
Bouhouche, Ahmed, Ali Benomar, Merle Ruberg, et al.. (2006). Autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2): phenotype-genotype correlations in 13 Moroccan families. Brain. 130(4). 1062–1075. 26 indexed citations
14.
Bouhouche, Ahmed, Ali Benomar, Naïma Bouslam, et al.. (2005). Autosomal recessive mutilating sensory neuropathy with spastic paraplegia maps to chromosome 5p15.31–14.1. European Journal of Human Genetics. 14(2). 249–252. 26 indexed citations
15.
Birouk, Nazha, Hamid Azzedine, O. Dubourg, et al.. (2003). Phenotypical Features of a Moroccan Family With Autosomal Recessive Charcot-Marie-Tooth Disease Associated With the S194X Mutation in the GDAP1 Gene. Archives of Neurology. 60(4). 598–598. 45 indexed citations
16.
Benomar, Ali, Farid Meggouh, Ahmed Bouhouche, et al.. (2002). Clinical comparison between AVED patients with 744 del A mutation and Friedreich ataxia with GAA expansion in 15 Moroccan families. Journal of the Neurological Sciences. 198(1-2). 25–29. 40 indexed citations
17.
Kissani, Najib, et al.. (2001). Comparaison du profil des patients épileptiques au Maroc à plusieurs années d'intervalle. 13(4). 1 indexed citations
18.
Benomar, Ali, et al.. (1999). Vitamin E deficiency ataxia associated with adenoma. Journal of the Neurological Sciences. 162(1). 97–101. 7 indexed citations
19.
Lalioti, Maria D., Hamish S. Scott, Pierre Genton, et al.. (1998). A PCR Amplification Method Reveals Instability of the Dodecamer Repeat in Progressive Myoclonus Epilepsy (EPM1) and No Correlation between the Size of the Repeat and Age at Onset. The American Journal of Human Genetics. 62(4). 842–847. 52 indexed citations
20.
Labauge, Pierre, Réda Ouazzani, A. Mrabet, et al.. (1997). Allelic heterogeneity of mediterranean myoclonus and the cystatin B gene. Annals of Neurology. 41(5). 686–689. 3 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Edvige Veneselli Breakdown of academic impact, for papers by Bülent Kara Breakdown of academic impact, for papers by Muhammad Mahajnah Breakdown of academic impact, for papers by Teresa Temudo Breakdown of academic impact, for papers by Amirthagowri Ambalavanan Breakdown of academic impact, for papers by Erika F. Augustine Breakdown of academic impact, for papers by Elisa De Grandis Breakdown of academic impact, for papers by J.L. Haines Breakdown of academic impact, for papers by Hélène Verhelst Breakdown of academic impact, for papers by Rosario Domingo‐Jiménez
Rankless by CCL
2026