Majida Charif

1.6k total citations
51 papers, 617 citations indexed

About

Majida Charif is a scholar working on Molecular Biology, Sensory Systems and Neurology. According to data from OpenAlex, Majida Charif has authored 51 papers receiving a total of 617 indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 15 papers in Sensory Systems and 13 papers in Neurology. Recurrent topics in Majida Charif's work include Mitochondrial Function and Pathology (17 papers), Hearing, Cochlea, Tinnitus, Genetics (15 papers) and Metabolism and Genetic Disorders (8 papers). Majida Charif is often cited by papers focused on Mitochondrial Function and Pathology (17 papers), Hearing, Cochlea, Tinnitus, Genetics (15 papers) and Metabolism and Genetic Disorders (8 papers). Majida Charif collaborates with scholars based in Morocco, France and Tunisia. Majida Charif's co-authors include Guy Lenaers, Abdelhamid Barakat, Hassan Rouba, Omar Abidi, Redouane Boulouiz, Mostafa Kandil, Vincent Procaccio, Agathe Roubertie, Hicham Charoute and Patrizia Amati‐Bonneau and has published in prestigious journals such as PLoS ONE, Brain and Scientific Reports.

In The Last Decade

Majida Charif

49 papers receiving 610 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Majida Charif Morocco 17 417 167 114 105 88 51 617
Polona Le Quesne Stabej United Kingdom 14 348 0.8× 123 0.7× 167 1.5× 44 0.4× 29 0.3× 18 535
Yosra Bouyacoub Tunisia 12 222 0.5× 85 0.5× 103 0.9× 40 0.4× 14 0.2× 27 381
Piotr Stawiński Poland 15 514 1.2× 42 0.3× 203 1.8× 48 0.5× 119 1.4× 58 782
Matthew A. Lines Canada 19 634 1.5× 36 0.2× 283 2.5× 17 0.2× 217 2.5× 35 919
Franco Carrara Italy 20 1.6k 3.9× 47 0.3× 126 1.1× 58 0.6× 894 10.2× 28 1.8k
Wendy Hutchison Australia 13 540 1.3× 55 0.3× 124 1.1× 27 0.3× 302 3.4× 20 785
H Dahl Australia 9 300 0.7× 69 0.4× 158 1.4× 19 0.2× 104 1.2× 12 459
Sigrid Fuchs Germany 16 584 1.4× 10 0.1× 148 1.3× 43 0.4× 76 0.9× 35 790
Morad Khayat Israel 16 422 1.0× 26 0.2× 162 1.4× 28 0.3× 115 1.3× 50 664

Countries citing papers authored by Majida Charif

Since Specialization
Citations

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

Fields of papers citing papers by Majida Charif

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Majida Charif

This figure shows the co-authorship network connecting the top 25 collaborators of Majida Charif. A scholar is included among the top collaborators of Majida Charif 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 Majida Charif. Majida Charif 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.
Charif, Majida, Patrizia Amati‐Bonneau, Agnès Guichet, et al.. (2025). Two Cases of ROSAH-Like Syndrome Restricted to the Ophthalmologic Presentation. Ocular Immunology and Inflammation. 33(5). 849–853. 1 indexed citations
2.
Boulouiz, Redouane, et al.. (2025). Clinical and Molecular Spectrum of Wilson Disease in the Arab World: A Systematic Review. Biochemical Genetics. 63(2). 1198–1218.
3.
Charif, Majida, Saïd Galaï, Lilia Kraoua, et al.. (2024). Expanding the genetic spectrum of mitochondrial diseases in Tunisia: novel variants revealed by whole-exome sequencing. Frontiers in Genetics. 14. 1259826–1259826.
4.
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Charif, Majida, et al.. (2023). Triple-A Syndrome in Morocco: Founder Effect, Age Estimation of the <i>AAAS</i> c.1331+1G&gt;A Variant, and Implications for Genetic Diagnosis. Molecular Syndromology. 15(2). 96–103. 1 indexed citations
7.
Charif, Majida, Farid Mansouri, Mohamed Addi, et al.. (2023). Population structure and genetic diversity of Moroccan cannabis (Cannabis sativa L.) germplasm through simple sequence repeat (SSR) analysis. Genetic Resources and Crop Evolution. 71(5). 2037–2051. 5 indexed citations
8.
Abdelghaffar, Houria, et al.. (2023). Homozygous Missense Variants in FOXI1 and TMPRSS3 Genes Associated with Non-syndromic Deafness in Moroccan Families. Biochemical Genetics. 62(3). 1914–1924. 1 indexed citations
9.
Charif, Majida, Arnaud Chevrollier, Naïg Guéguen, et al.. (2022). Next-Generation Sequencing Identifies Novel PMPCA Variants in Patients with Late-Onset Dominant Optic Atrophy. Genes. 13(7). 1202–1202. 1 indexed citations
10.
Goudenège, David, Simone A. Baechler, Shar-yin N. Huang, et al.. (2022). Cancer/Testis Antigen 55 is required for cancer cell proliferation and mitochondrial DNA maintenance. Mitochondrion. 64. 19–26. 3 indexed citations
11.
Charif, Majida, Hicham Charoute, Hassan Rouba, et al.. (2022). A homozygous nonsense HECW2 variant is associated with neurodevelopmental delay and intellectual disability. European Journal of Medical Genetics. 65(6). 104515–104515. 2 indexed citations
12.
Bonnet, Crystel, Majida Charif, Mostafa Kandil, et al.. (2020). A homozygous MPZL2 deletion is associated with non syndromic hearing loss in a moroccan family. International Journal of Pediatric Otorhinolaryngology. 140. 110481–110481. 6 indexed citations
13.
Boussion, F., Stéphane Triau, Majida Charif, et al.. (2019). Second report of RING finger protein 113A (RNF113A) involvement in a Mendelian disorder. American Journal of Medical Genetics Part A. 182(3). 565–569. 7 indexed citations
14.
Sfaihi, L., Majida Charif, Valérie Desquiret‐Dumas, et al.. (2018). Next generation sequencing in family with MNGIE syndrome associated to optic atrophy: Novel homozygous POLG mutation in the C-terminal sub-domain leading to mtDNA depletion. Clinica Chimica Acta. 488. 104–110. 14 indexed citations
15.
Charif, Majida, et al.. (2017). Homozygous mutations in PJVK and MYO15A genes associated with non-syndromic hearing loss in Moroccan families. International Journal of Pediatric Otorhinolaryngology. 101. 25–29. 15 indexed citations
16.
Charoute, Hicham, et al.. (2017). Novel compound heterozygous mutations in the GPR98 (USH2C) gene identified by whole exome sequencing in a Moroccan deaf family. Molecular Biology Reports. 44(5). 429–434. 10 indexed citations
17.
Charif, Majida, et al.. (2015). Recessive TBC1D24 Mutations Are Frequent in Moroccan Non-Syndromic Hearing Loss Pedigrees. PLoS ONE. 10(9). e0138072–e0138072. 21 indexed citations
18.
Charif, Majida, Omar Abidi, Redouane Boulouiz, et al.. (2013). Analysis of CLDN14 gene in deaf Moroccan patients with non-syndromic hearing loss. Gene. 523(1). 103–105. 8 indexed citations
19.
Abidi, Omar, Majida Charif, Brahim El Houate, et al.. (2012). Association of the MTHFR A1298C Variant with Unexplained Severe Male Infertility. PLoS ONE. 7(3). e34111–e34111. 39 indexed citations
20.
Houate, Brahim El, Omar Abidi, Majida Charif, et al.. (2012). Association of Spermatogenic Failure with the b2/b3 Partial AZFc Deletion. PLoS ONE. 7(4). e34902–e34902. 35 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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