Hamid Azzedine

2.4k total citations
24 papers, 1.1k citations indexed

About

Hamid Azzedine is a scholar working on Cellular and Molecular Neuroscience, Neurology and Molecular Biology. According to data from OpenAlex, Hamid Azzedine has authored 24 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Cellular and Molecular Neuroscience, 14 papers in Neurology and 10 papers in Molecular Biology. Recurrent topics in Hamid Azzedine's work include Hereditary Neurological Disorders (19 papers), Neurological diseases and metabolism (14 papers) and Genetic Neurodegenerative Diseases (7 papers). Hamid Azzedine is often cited by papers focused on Hereditary Neurological Disorders (19 papers), Neurological diseases and metabolism (14 papers) and Genetic Neurodegenerative Diseases (7 papers). Hamid Azzedine collaborates with scholars based in France, Germany and Switzerland. Hamid Azzedine's co-authors include Roman Chrast, Alexis Brice, Jean‐Jacques Médard, Nathalie Bernard‐Marissal, Éric Leguern, Ahmed Bouhouche, Nazha Birouk, Merle Ruberg, O. Dubourg and Riadh Gouider and has published in prestigious journals such as PLoS ONE, Brain and Neurology.

In The Last Decade

Hamid Azzedine

23 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hamid Azzedine France 17 715 528 342 298 238 24 1.1k
Ahmed Bouhouche Morocco 15 585 0.8× 415 0.8× 264 0.8× 280 0.9× 255 1.1× 44 1.0k
Shawna Feely United States 17 890 1.2× 344 0.7× 326 1.0× 151 0.5× 443 1.9× 32 1.1k
A. Dürr France 9 600 0.8× 580 1.1× 274 0.8× 107 0.4× 273 1.1× 12 963
Khalid Hamid El Hachimi France 18 449 0.6× 455 0.9× 251 0.7× 211 0.7× 189 0.8× 28 963
Jean‐Jacques Médard Switzerland 16 450 0.6× 571 1.1× 131 0.4× 184 0.6× 154 0.6× 24 962
Nathalie Verpoorten Belgium 8 526 0.7× 391 0.7× 231 0.7× 327 1.1× 254 1.1× 9 1.0k
James M. Polke United Kingdom 21 1.1k 1.5× 668 1.3× 416 1.2× 200 0.7× 651 2.7× 47 1.7k
Francesca Cavalcanti Italy 20 1.0k 1.4× 974 1.8× 150 0.4× 178 0.6× 408 1.7× 43 1.3k
Tarik Hamadouche France 15 410 0.6× 221 0.4× 177 0.5× 163 0.5× 178 0.7× 19 630
Coro Paisán‐Ruiz United States 19 322 0.5× 479 0.9× 291 0.9× 223 0.7× 472 2.0× 34 1.1k

Countries citing papers authored by Hamid Azzedine

Since Specialization
Citations

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

Fields of papers citing papers by Hamid Azzedine

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hamid Azzedine

This figure shows the co-authorship network connecting the top 25 collaborators of Hamid Azzedine. A scholar is included among the top collaborators of Hamid Azzedine 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 Hamid Azzedine. Hamid Azzedine 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.
Nguyen, Thi Thanh Huong, et al.. (2021). Leukoencephalopathy and conduction blocks in PLEKHG5-associated intermediate CMT disease. Neuromuscular Disorders. 31(8). 756–764. 5 indexed citations
2.
Weis, Joachim, Kristl G. Claeys, Andreas Roos, et al.. (2016). Towards a functional pathology of hereditary neuropathies. Acta Neuropathologica. 133(4). 493–515. 41 indexed citations
3.
Azzedine, Hamid, Ahmet Bozkurt, Marcus J. Moeller, et al.. (2016). Underestimated associated features in CMT neuropathies: clinical indicators for the causative gene?. Brain and Behavior. 6(4). e00451–e00451. 29 indexed citations
4.
Bernard‐Marissal, Nathalie, Jean‐Jacques Médard, Hamid Azzedine, & Roman Chrast. (2015). Dysfunction in endoplasmic reticulum-mitochondria crosstalk underlies SIGMAR1 loss of function mediated motor neuron degeneration. Brain. 138(4). 875–890. 191 indexed citations
5.
AlDrees, Abdulmajeed, Salah A. Elmalik, Hamdy H. Hassan, et al.. (2014). Ophthalmic features ofPLA2G6-related paediatric neurodegeneration with brain iron accumulation. British Journal of Ophthalmology. 98(7). 889–893. 9 indexed citations
6.
Salih, Mustafa A., Emeline Mundwiller, Arif O. Khan, et al.. (2013). New Findings in a Global Approach to Dissect the Whole Phenotype of PLA2G6 Gene Mutations. PLoS ONE. 8(10). e76831–e76831. 38 indexed citations
7.
Kruer, Michael C., Mustafa A. Salih, Catherine Mooney, et al.. (2013). C19orf12 mutation leads to a pallido-pyramidal syndrome. Gene. 537(2). 352–356. 22 indexed citations
8.
Salih, Mustafa A., Emeline Mundwiller, Arif O. Khan, et al.. (2013). Correction: New Findings in a Global Approach to Dissect the Whole Phenotype of PLA2G6 Gene Mutations. PLoS ONE. 8(11). 6 indexed citations
9.
Azzedine, Hamid, Jan Senderek, Carlo Rivolta, & Roman Chrast. (2012). Molecular Genetics of Charcot-Marie-Tooth Disease: From Genes to Genomes. Molecular Syndromology. 3(5). 204–214. 39 indexed citations
10.
Klebe, Stephan, Alexandra Dürr, Naïma Bouslam, et al.. (2007). Spastic paraplegia 5: Locus refinement, candidate gene analysis and clinical description. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 144B(7). 854–861. 14 indexed citations
11.
Bouslam, Naïma, Ahmed Bouhouche, Ali Benomar, et al.. (2007). A novel locus for autosomal recessive spastic ataxia on chromosome 17p. Human Genetics. 121(3-4). 413–420. 21 indexed citations
12.
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
13.
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
14.
Bouslam, Naïma, Ali Benomar, Hamid Azzedine, et al.. (2005). Mapping of a new form of pure autosomal recessive spastic paraplegia (SPG28). Annals of Neurology. 57(4). 567–571. 43 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.
Azzedine, Hamid, Alessandra Bolino, Nazha Birouk, et al.. (2003). Mutations in MTMR13, a New Pseudophosphatase Homologue of MTMR2 and Sbf1, in Two Families with an Autosomal Recessive Demyelinating Form of Charcot-Marie-Tooth Disease Associated with Early-Onset Glaucoma. The American Journal of Human Genetics. 72(5). 1141–1153. 226 indexed citations
17.
18.
Stévanin, Giovanni, Naïma Bouslam, Stéphane Thobois, et al.. (2003). Spinocerebellar ataxia with sensory neuropathy (SCA25) maps to chromosome 2p. Annals of Neurology. 55(1). 97–104. 54 indexed citations
19.
Azzedine, Hamid, Salima Assami, Jean‐Michel Vallat, et al.. (2000). Charcot–Marie–Tooth 2-like presentation of an Algerian family with giant axonal neuropathy. Neuromuscular Disorders. 10(8). 592–598. 33 indexed citations
20.
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

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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