T. Chkili

1.0k total citations
32 papers, 721 citations indexed

About

T. Chkili is a scholar working on Neurology, Cellular and Molecular Neuroscience and Molecular Biology. According to data from OpenAlex, T. Chkili has authored 32 papers receiving a total of 721 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Neurology, 10 papers in Cellular and Molecular Neuroscience and 6 papers in Molecular Biology. Recurrent topics in T. Chkili's work include Peripheral Neuropathies and Disorders (6 papers), Hereditary Neurological Disorders (5 papers) and Glycogen Storage Diseases and Myoclonus (4 papers). T. Chkili is often cited by papers focused on Peripheral Neuropathies and Disorders (6 papers), Hereditary Neurological Disorders (5 papers) and Glycogen Storage Diseases and Myoclonus (4 papers). T. Chkili collaborates with scholars based in Morocco, France and Switzerland. T. Chkili's co-authors include Alexis Brice, Nazha Birouk, Éric Leguern, Ahmed Bouhouche, Ali Benomar, Riadh Gouider, M. Yahyaoui, A. Mrabet, Marco Di Duca and T. Hammadouche and has published in prestigious journals such as Nature Genetics, Annals of Neurology and The American Journal of Human Genetics.

In The Last Decade

T. Chkili

32 papers receiving 700 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
T. Chkili Morocco 11 400 363 191 146 93 32 721
M G Sweeney United Kingdom 18 314 0.8× 1.0k 2.9× 128 0.7× 41 0.3× 68 0.7× 21 1.2k
R. M. Chalmers United Kingdom 13 273 0.7× 733 2.0× 180 0.9× 85 0.6× 147 1.6× 16 1.1k
Lorenzo Nanetti Italy 15 491 1.2× 400 1.1× 270 1.4× 84 0.6× 129 1.4× 51 721
S. A. Sørensen Denmark 14 423 1.1× 264 0.7× 325 1.7× 91 0.6× 139 1.5× 29 888
Omar Dabbagh Saudi Arabia 10 152 0.4× 255 0.7× 479 2.5× 99 0.7× 148 1.6× 19 737
Luba Kalaydjieva Bulgaria 9 203 0.5× 267 0.7× 42 0.2× 79 0.5× 113 1.2× 15 530
Afagh Alavi Iran 13 143 0.4× 236 0.7× 134 0.7× 64 0.4× 146 1.6× 60 535
Savine Vicart France 16 418 1.0× 637 1.8× 125 0.7× 51 0.3× 36 0.4× 29 789
Sarah Camargos Brazil 14 269 0.7× 167 0.5× 452 2.4× 39 0.3× 85 0.9× 51 712
Dong-Hui Chen United States 9 277 0.7× 370 1.0× 127 0.7× 39 0.3× 39 0.4× 10 579

Countries citing papers authored by T. Chkili

Since Specialization
Citations

This map shows the geographic impact of T. Chkili'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 T. Chkili with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites T. Chkili more than expected).

Fields of papers citing papers by T. Chkili

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of T. Chkili

This figure shows the co-authorship network connecting the top 25 collaborators of T. Chkili. A scholar is included among the top collaborators of T. Chkili 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 T. Chkili. T. Chkili 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.
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
2.
Aidi, Saadia, et al.. (2006). Troubles cognitifs dus à l’intoxication oxycarbonée: étude neuropsychologique et IRM de 5 cas. Revue Neurologique. 162(12). 1240–1247. 4 indexed citations
3.
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
4.
Allali, F., et al.. (2004). Behçet's disease in Moroccan children: a report of 12 cases. Scandinavian Journal of Rheumatology. 33(5). 362–363. 12 indexed citations
5.
Benomar, Ali, et al.. (2004). Hypertension intracrânienne bénigne. Revue Neurologique. 160(12). 1187–1190. 5 indexed citations
6.
Aidi, Saadia, et al.. (2004). Syndrome catatonique traité par zolpidem et bromocriptine quatre observations. Revue Neurologique. 160(10). 960–960. 1 indexed citations
7.
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
8.
Jiddane, Mohamed, et al.. (2002). [Chronic inflammatory demyelinating polyradiculoneuropathy with hypertrophy of spinal roots, brachial plexus and cranial nerves].. PubMed. 158(8-9). 819–23. 8 indexed citations
9.
Aidi, Saadia, et al.. (2002). La maladie de Wilson. Étude clinique, thérapeutique et évolutive de 21 cas. La Revue de Médecine Interne. 23(5). 419–431. 9 indexed citations
10.
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
11.
Benomar, Ali, et al.. (1999). Vitamin E deficiency ataxia associated with adenoma. Journal of the Neurological Sciences. 162(1). 97–101. 7 indexed citations
12.
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
13.
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
14.
Benomar, Ali, Giovanni Stévanin, Géraldine Cancel‐Tassin, et al.. (1995). The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12–p21.1. Nature Genetics. 10(1). 84–88. 126 indexed citations
15.
Maghraoui, A. El, et al.. (1995). [Fahr syndrome and dysparathyroidism. 3 cases].. PubMed. 24(28). 1301–4. 32 indexed citations
16.
Benomar, Ali, E. Le Guern, Alexandra Dürr, et al.. (1994). Autosomal‐dominant cerebellar ataxia with retinal degeneration (ADCA type II) is genetically different from ADCA type I. Annals of Neurology. 35(4). 439–444. 47 indexed citations
17.
Slassi, I., et al.. (1994). [Dermatomyositis and Wilson disease].. PubMed. 150(5). 391–2. 1 indexed citations
18.
Chkili, T., et al.. (1994). [Alexia without agraphia in the Arabic language. Neurolinguistic and and MRI study].. PubMed. 150(11). 771–5. 5 indexed citations
19.
Yahyaoui, M., et al.. (1990). [Amyotrophic lateral sclerosis syndrome of syphilitic origin. 5 cases].. PubMed. 146(1). 41–4. 5 indexed citations
20.
Chkili, T., et al.. (1976). [Puerperal psychoses in the Moroccan milieu. (apropos of 100 cases)].. PubMed. 53(6). 375–91. 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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