Nazha Birouk

2.0k total citations
47 papers, 1.3k citations indexed

About

Nazha Birouk is a scholar working on Cellular and Molecular Neuroscience, Neurology and Molecular Biology. According to data from OpenAlex, Nazha Birouk has authored 47 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Cellular and Molecular Neuroscience, 17 papers in Neurology and 10 papers in Molecular Biology. Recurrent topics in Nazha Birouk's work include Hereditary Neurological Disorders (26 papers), Peripheral Neuropathies and Disorders (10 papers) and Genetic Neurodegenerative Diseases (7 papers). Nazha Birouk is often cited by papers focused on Hereditary Neurological Disorders (26 papers), Peripheral Neuropathies and Disorders (10 papers) and Genetic Neurodegenerative Diseases (7 papers). Nazha Birouk collaborates with scholars based in France, Morocco and Tunisia. Nazha Birouk's co-authors include Alexis Brice, Éric Leguern, Riadh Gouider, P. Bouché, Thierry Maisonobe, Sandrine Tardieu, Ahmed Bouhouche, O. Dubourg, T. Chkili and Hamid Azzedine and has published in prestigious journals such as SHILAP Revista de lepidopterología, Brain and Neurology.

In The Last Decade

Nazha Birouk

41 papers receiving 1.3k citations

Peers

Nazha Birouk
Alessandro Filla Italy
H. Skre Norway
A. Löfgren Belgium
Thomas Van Winkle United States
Radim Mazanec Czechia
Pascale Bomont France
Karen Krajewski United States
Peter Van den Bergh Belgium
Kamel Ben Othmane United States
Shawna Feely United States
Alessandro Filla Italy
Nazha Birouk
Citations per year, relative to Nazha Birouk Nazha Birouk (= 1×) peers Alessandro Filla

Countries citing papers authored by Nazha Birouk

Since Specialization
Citations

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

Fields of papers citing papers by Nazha Birouk

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nazha Birouk

This figure shows the co-authorship network connecting the top 25 collaborators of Nazha Birouk. A scholar is included among the top collaborators of Nazha Birouk 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 Nazha Birouk. Nazha Birouk 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.
Ratbi, Ilham, Siham Chafai Elalaoui, Imane Cherkaoui Jaouad, et al.. (2023). Early diagnosis of congenital muscular pathologies using next-generation sequencing: experiences from a tertiary center in Morocco. SHILAP Revista de lepidopterología. 24(1).
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Bouhouche, Ahmed, Nazha Birouk, Yamna Kriouile, et al.. (2016). Clinical and genetic data of Huntington disease in Moroccan patients. African Health Sciences. 15(4). 1232–1232. 4 indexed citations
5.
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
6.
Malfatti, Edoardo, Nazha Birouk, Norma B. Romero, et al.. (2012). Juvenile-onset permanent weakness in muscle phosphofructokinase deficiency. Journal of the Neurological Sciences. 316(1-2). 173–177. 11 indexed citations
7.
Birouk, Nazha. (2009). La maladie de Charcot-Marie-Tooth. La Presse Médicale. 38(2). 200–209. 1 indexed citations
8.
Birouk, Nazha, et al.. (2008). Neuropathie amyloïde liée à une protéine non identifiée. La Revue de Médecine Interne. 30(3). 277–278.
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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
11.
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
12.
Senouci, Karima, et al.. (2006). Pseudo-aïnhum et neuropathie axonale. Annales de Dermatologie et de Vénéréologie. 133(10). 791–794. 1 indexed citations
13.
Dubourg, O., Hamid Azzedine, Christophe Verny, et al.. (2006). Autosomal-recessive forms of demyelinating Charcot-Marie-Tooth disease. NeuroMolecular Medicine. 8(1-2). 75–85. 66 indexed citations
14.
Birouk, Nazha, et al.. (2005). Profil autonomique des patients migraineux. Neurophysiologie Clinique. 35(4). 127–134. 15 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.
Dubourg, O., Hamid Azzedine, Nazha Birouk, et al.. (2000). Phenotypic and genetic study of a family with hereditary sensory neuropathy and prominent weakness. Muscle & Nerve. 23(10). 1508–1514. 16 indexed citations
17.
Bouhouche, Ahmed, Ali Benomar, Nazha Birouk, et al.. (1999). A Locus for an Axonal Form of Autosomal Recessive Charcot-Marie-Tooth Disease Maps to Chromosome 1q21.2-q21.3. The American Journal of Human Genetics. 65(3). 722–727. 68 indexed citations
18.
Leguern, Éric, Riadh Gouider, Dominique Mabin, et al.. (1997). Patients homozygous for the 17p 11.2 duplication in charcot‐marie‐tooth type 1A Disease. Annals of Neurology. 41(1). 104–108. 25 indexed citations
19.
Rouger, H, Éric Leguern, Nazha Birouk, et al.. (1997). Charcot-Marie-Tooth disease with intermediate motor nerve conduction velocities: Characterization of 14 C×32 mutations in 35 families. Human Mutation. 10(6). 443–450. 51 indexed citations
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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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