M. Tazir

718 total citations
17 papers, 564 citations indexed

About

M. Tazir is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Infectious Diseases. According to data from OpenAlex, M. Tazir has authored 17 papers receiving a total of 564 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 6 papers in Cellular and Molecular Neuroscience and 4 papers in Infectious Diseases. Recurrent topics in M. Tazir's work include Hereditary Neurological Disorders (6 papers), Bacterial biofilms and quorum sensing (5 papers) and Neurological diseases and metabolism (4 papers). M. Tazir is often cited by papers focused on Hereditary Neurological Disorders (6 papers), Bacterial biofilms and quorum sensing (5 papers) and Neurological diseases and metabolism (4 papers). M. Tazir collaborates with scholars based in Algeria, France and United States. M. Tazir's co-authors include Alexis Brice, Pierre Pollak, Alexandra Dürr, Anne‐Louise Leutenegger, François Tison, Suzanne Lesage, Ebba Lohmann, João Tiago Guimarães, Muriel Bonnet and Yves Agid and has published in prestigious journals such as Neurology, Annals of Neurology and Clinical Microbiology and Infection.

In The Last Decade

M. Tazir

17 papers receiving 544 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
M. Tazir Algeria 13 208 201 157 130 102 17 564
Jordi Corral Spain 16 539 2.6× 143 0.7× 359 2.3× 38 0.3× 46 0.5× 27 750
Traki Benhassine Algeria 10 148 0.7× 115 0.6× 114 0.7× 60 0.5× 15 0.1× 21 414
Kin Ki Jim Netherlands 13 176 0.8× 24 0.1× 51 0.3× 63 0.5× 46 0.5× 20 514
M. Asrafuzzaman Riyadh United States 11 119 0.6× 33 0.2× 94 0.6× 20 0.2× 51 0.5× 13 429
Christopher C. Cheng Canada 11 442 2.1× 62 0.3× 145 0.9× 21 0.2× 24 0.2× 20 791
Joel J. Credle United States 12 388 1.9× 325 1.6× 164 1.0× 76 0.6× 478 4.7× 14 1.0k
Luciana Paoletti Argentina 8 339 1.6× 13 0.1× 33 0.2× 22 0.2× 43 0.4× 12 508
Patrick Adams United States 15 319 1.5× 28 0.1× 107 0.7× 8 0.1× 61 0.6× 19 702
Collin M. Bantle United States 9 134 0.6× 137 0.7× 76 0.5× 95 0.7× 27 0.3× 10 372
Xiangpeng Ren China 10 89 0.4× 119 0.6× 63 0.4× 40 0.3× 11 0.1× 10 404

Countries citing papers authored by M. Tazir

Since Specialization
Citations

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

Fields of papers citing papers by M. Tazir

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. Tazir

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

All Works

17 of 17 papers shown
1.
Bes, Michèle, Anne Tristan, Olivier Dauwalder, et al.. (2016). Phenotypic and genotypic characterization of Staphylococcus aureus strains associated with bovine mastitis and nasal carriage of workers in contact to animals in Algeria.. Pakistan Veterinary Journal. 36(2). 184–188. 13 indexed citations
2.
Vallat, Jean‐Michel, Cyril Goizet, M. Tazir, et al.. (2016). Classifications of neurogenetic diseases: An increasingly complex problem. Revue Neurologique. 172(6-7). 339–349. 17 indexed citations
4.
Belkhelfa, Mourad, Hayet Rafa, Oussama Medjeber, et al.. (2012). P070 IL-17 and nitric oxide pathways are involved in inflammatory response during Alzheimer’s disease: A study in Algerian patients. Cytokine. 59(3). 541–541. 1 indexed citations
5.
Lesage, Suzanne, Christel Condroyer, Mathieu Anheim, et al.. (2011). Mutations in the glucocerebrosidase gene confer a risk for Parkinson disease in North Africa. Neurology. 76(3). 301–303. 35 indexed citations
6.
Verkaik, Nelianne J., Cédric Badiou, M. Bes, et al.. (2010). Immunogenicity of toxins during Staphylococcus aureus infection. 2 indexed citations
7.
Dauwalder, Olivier, Michèle Bes, Gérard Lina, et al.. (2010). High prevalence of methicillin-resistant Staphylococcus aureus clone ST80-IV in hospital and community settings in Algiers. Clinical Microbiology and Infection. 17(4). 526–532. 55 indexed citations
9.
Benouda, A., et al.. (2009). Antimicrobial Resistance of Respiratory Pathogens in North African Countries. Journal of Chemotherapy. 21(6). 627–632. 11 indexed citations
10.
Messai, Yamina, Traki Benhassine, Souhila Alouache, et al.. (2008). Prevalence and characterization of extended-spectrum β-lactamases in Klebsiella pneumoniae in Algiers hospitals (Algeria). Pathologie Biologie. 56(5). 319–325. 71 indexed citations
11.
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
12.
Lesage, Suzanne, Pablo Ibáñez, Ebba Lohmann, et al.. (2005). G2019S LRRK2 mutation in French and North African families with Parkinson's disease. Annals of Neurology. 58(5). 784–787. 152 indexed citations
13.
Bomont, Pascale, Christine Ioos, Cengiz Yalçınkaya, et al.. (2003). Identification of seven novel mutations in theGAN gene. Human Mutation. 21(4). 446–446. 42 indexed citations
14.
Chaouch, M., Annachiara De Sandre‐Giovannoli, J.M. Vallat, et al.. (2002). The phenotypic manifestations of autosomal recessive axonalCharcot–Marie–Tooth due to a mutation in Lamin A/C gene. Neuromuscular Disorders. 13(1). 60–67. 65 indexed citations
15.
Sandre‐Giovannoli, Annachiara De, M. Chaouch, Serguei Kozlov, et al.. (2002). Homozygous Defects In Lmna, Encoding Lamin A/C Nuclear‐Envelope Proteins, Cause Autosomal Recessive Axonal Neuropathy In Human (Charcot‐Marie‐Tooth Disorder Type 2) And Mouse. Journal of the Peripheral Nervous System. 7(3). 205–205. 13 indexed citations
16.
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
17.
Tazir, M., et al.. (1989). [Immunoenzymatic determination of free immunoglobulin light chains in the cerebrospinal fluid: its value in the biological diagnosis of multiple sclerosis].. PubMed. 57. 111–24. 2 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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