Tarik Hamadouche

958 total citations
19 papers, 630 citations indexed

About

Tarik Hamadouche is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Cell Biology. According to data from OpenAlex, Tarik Hamadouche has authored 19 papers receiving a total of 630 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Cellular and Molecular Neuroscience, 7 papers in Molecular Biology and 6 papers in Cell Biology. Recurrent topics in Tarik Hamadouche's work include Hereditary Neurological Disorders (13 papers), Genetic Neurodegenerative Diseases (6 papers) and Neurological diseases and metabolism (4 papers). Tarik Hamadouche is often cited by papers focused on Hereditary Neurological Disorders (13 papers), Genetic Neurodegenerative Diseases (6 papers) and Neurological diseases and metabolism (4 papers). Tarik Hamadouche collaborates with scholars based in France, Algeria and Lebanon. Tarik Hamadouche's co-authors include Mériem Tazir, Sonia Nouioua, Jean‐Michel Vallat, Nicolas Lévy, Djamel Grid, Alexis Brice, Yannick Poitelon, Valérie Delague, Salima Assami and Stéphane Mathis and has published in prestigious journals such as Neurology, The American Journal of Human Genetics and Journal of the Neurological Sciences.

In The Last Decade

Tarik Hamadouche

19 papers receiving 622 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tarik Hamadouche France 15 410 221 178 177 163 19 630
Yo‐Tsen Liu Taiwan 13 392 1.0× 315 1.4× 294 1.7× 198 1.1× 103 0.6× 30 792
G Fabrizi Italy 14 347 0.8× 323 1.5× 192 1.1× 140 0.8× 156 1.0× 23 706
Vincenzo Lupo Spain 17 363 0.9× 328 1.5× 94 0.5× 175 1.0× 117 0.7× 34 633
Gerard W. Hensels Netherlands 12 663 1.6× 349 1.6× 253 1.4× 273 1.5× 167 1.0× 12 923
Claudia Stendel Germany 9 279 0.7× 223 1.0× 84 0.5× 75 0.4× 102 0.6× 17 443
R. Ionasescu United States 17 617 1.5× 327 1.5× 234 1.3× 196 1.1× 96 0.6× 31 808
Ilaria Cabrini Italy 9 282 0.7× 146 0.7× 147 0.8× 123 0.7× 154 0.9× 12 447
Esra Battaloğlu Türkiye 14 229 0.6× 231 1.0× 85 0.5× 126 0.7× 58 0.4× 33 457
A.D. Roses United States 13 289 0.7× 338 1.5× 160 0.9× 92 0.5× 53 0.3× 24 656
Katharina Cosker United Kingdom 11 268 0.7× 417 1.9× 46 0.3× 140 0.8× 185 1.1× 12 737

Countries citing papers authored by Tarik Hamadouche

Since Specialization
Citations

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

Fields of papers citing papers by Tarik Hamadouche

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tarik Hamadouche

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

All Works

19 of 19 papers shown
1.
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
2.
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
3.
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
4.
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
5.
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
6.
Poitelon, Yannick, С. В. Козлов, Jérôme Devaux, et al.. (2012). Behavioral and Molecular Exploration of the AR-CMT2A Mouse Model Lmna R298C/R298C. NeuroMolecular Medicine. 14(1). 40–52. 15 indexed citations
7.
Kwasigroch, Jean Marc, et al.. (2012). Modelling and Bioinformatics Analysis of the Dimeric Structure of House Dust Mite Allergens from Families 5 and 21: Der f 5 Could Dimerize as Der p 5. Journal of Biomolecular Structure and Dynamics. 29(4). 663–675. 17 indexed citations
8.
Poitelon, Yannick, et al.. (2012). Two novel missense mutations in FGD4/FRABIN cause Charcot‐Marie‐Tooth type 4H (CMT4H). Journal of the Peripheral Nervous System. 17(2). 141–146. 17 indexed citations
9.
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
10.
Belarbi, Soreya, Suzanne Lesage, Traki Benhassine, et al.. (2010). LRRK2 G2019S mutation in Parkinson’s disease: A neuropsychological and neuropsychiatric study in a large Algerian cohort. Parkinsonism & Related Disorders. 16(10). 676–679. 64 indexed citations
11.
Tazir, Mériem, Sonia Nouioua, Laurent Magy, et al.. (2009). Phenotypic variability in giant axonal neuropathy. Neuromuscular Disorders. 19(4). 270–274. 40 indexed citations
12.
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
13.
Delague, Valérie, Arnaud Jacquier, Tarik Hamadouche, et al.. (2007). G.O.3 Mutations in FGD4 encoding the Rho GDP/GTP exchange factor FRABIN cause autosomal recessive Charcot-Marie-Tooth type 4H. Neuromuscular Disorders. 17(9-10). 767–767. 3 indexed citations
14.
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
15.
Echaniz‐Laguna, Andoni, Bertrand Degos, Céline Bonnet, et al.. (2006). NDRG1-linked Charcot-Marie-Tooth disease (CMT4D) with central nervous system involvement. Neuromuscular Disorders. 17(2). 163–168. 36 indexed citations
16.
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
17.
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
18.
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
19.
Salih, Mustafa A., Thierry Maisonobe, Mohammad M. Kabiraj, et al.. (2000). Autosomal recessive hereditary neuropathy with focally folded myelin sheaths and linked to chromosome 11q23: a distinct and homogeneous entity. Neuromuscular Disorders. 10(1). 10–15. 12 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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