Hicham Charoute

839 total citations
68 papers, 480 citations indexed

About

Hicham Charoute is a scholar working on Molecular Biology, Genetics and Sensory Systems. According to data from OpenAlex, Hicham Charoute has authored 68 papers receiving a total of 480 indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 18 papers in Genetics and 11 papers in Sensory Systems. Recurrent topics in Hicham Charoute's work include Hearing, Cochlea, Tinnitus, Genetics (11 papers), SARS-CoV-2 and COVID-19 Research (6 papers) and Diabetes, Cardiovascular Risks, and Lipoproteins (6 papers). Hicham Charoute is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (11 papers), SARS-CoV-2 and COVID-19 Research (6 papers) and Diabetes, Cardiovascular Risks, and Lipoproteins (6 papers). Hicham Charoute collaborates with scholars based in Morocco, France and Tunisia. Hicham Charoute's co-authors include Abdelhamid Barakat, Hassan Rouba, Houda Benrahma, Majida Charif, Guy Lenaers, Sonia Abdelhak, Abderrahim Malki, M’hammed Sarih, Khadija Akarid and Rachid Saı̈le and has published in prestigious journals such as PLoS ONE, Gene and American Journal of Tropical Medicine and Hygiene.

In The Last Decade

Hicham Charoute

59 papers receiving 473 citations

Peers

Hicham Charoute
YF Liu China
Alexandra Evagelidis Canada
Hideo Sasai Japan
Mayerson Thompson Brazil
Kamaldeen Muili United States
Marie Garcia France
S. Baba Japan
Sandra A. Rebuffat France
Sangeeta Amladi India
Samuel A. Molina United States
YF Liu China
Hicham Charoute
Citations per year, relative to Hicham Charoute Hicham Charoute (= 1×) peers YF Liu

Countries citing papers authored by Hicham Charoute

Since Specialization
Citations

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

Fields of papers citing papers by Hicham Charoute

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hicham Charoute

This figure shows the co-authorship network connecting the top 25 collaborators of Hicham Charoute. A scholar is included among the top collaborators of Hicham Charoute 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 Hicham Charoute. Hicham Charoute 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.
Charoute, Hicham, et al.. (2025). In silico analysis of missense SNPs in APPL1 gene: implications on APPL1–AKT2 complex and its relation to MODY 14. Journal of Biomolecular Structure and Dynamics. 1–25.
2.
Charoute, Hicham, et al.. (2025). A Case–Control Study of the Association Between GSTP1 Gene Polymorphisms (rs1695 and rs1138272) and the Susceptibility to Male Infertility in the Moroccan Population. Genetic Testing and Molecular Biomarkers. 29(2). 21–31. 1 indexed citations
3.
Charoute, Hicham, Pascal Pineau, M’hammed Sarih, et al.. (2025). Genomic surveillance in Morocco tracks SARS-CoV-2 variant shift from Alpha to Omicron sublineage JN1. PubMed. 3(1). 63–63.
4.
Bouhouche, Ahmed, et al.. (2024). Novel WFS1 Variants in Two Moroccan Families with Wolfram Syndrome. Genetic Testing and Molecular Biomarkers. 28(6). 257–262. 1 indexed citations
5.
Charoute, Hicham, et al.. (2024). Virological characterization of Hepatitis B virus infection in Morocco: A ten-years study (2014 – 2023). Diagnostic Microbiology and Infectious Disease. 110(4). 116502–116502.
6.
Charoute, Hicham, Jalal Nourlil, M’hammed Sarih, et al.. (2024). Report of SARS-CoV-2 JN.1 variant in Morocco. Microbiology Resource Announcements. 13(9). e0055924–e0055924. 1 indexed citations
7.
Charoute, Hicham, et al.. (2023). Exploring the impact of CYP11A1’s missense SNPs on the interaction between CYP11A1 and cholesterol: A comprehensive structural analysis and MD simulation study. Computational Biology and Chemistry. 106. 107937–107937. 2 indexed citations
8.
Charoute, Hicham, et al.. (2022). Anti-SARS-CoV-2 Antibody Responses 5 Months Post Complete Vaccination of Moroccan Healthcare Workers. Vaccines. 10(3). 465–465. 9 indexed citations
9.
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
10.
Charoute, Hicham, et al.. (2022). Association between G2677T/A polymorphism in ABCB1 gene and the risk of drug resistance epilepsy: An updated systematic review and meta-analysis. Epilepsy Research. 185. 106977–106977. 2 indexed citations
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Charoute, Hicham, et al.. (2019). Cytogenetic profile of patients with clinical spectrum of ambiguous genitalia, amenorrhea, and Turner phenotype: A 21‐year single‐center experience. American Journal of Medical Genetics Part A. 179(8). 1516–1524. 2 indexed citations
15.
Charoute, Hicham, et al.. (2019). Further Evidence for the Implication of the <b><i>MET</i></b> Gene in Non-Syndromic Autosomal Recessive Deafness. Human Heredity. 84(3). 109–116. 3 indexed citations
16.
Charoute, Hicham, Hassan Rouba, Mostafa Kabine, et al.. (2018). A novel mutation in SLITRK6 causes deafness and myopia in a Moroccan family. Gene. 659. 89–92. 3 indexed citations
17.
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
18.
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
19.
Charoute, Hicham, et al.. (2016). Compound heterozygous SLC29A3 mutation causes H syndrome in a Moroccan patient: A case report. Current Research in Translational Medicine. 64(2). 65–68. 9 indexed citations
20.
Dehbi, Hind, et al.. (2016). Intra-familial phenotypic variability in a Moroccan family with hearing loss and palmoplantar keratoderma (PPK). Current Research in Translational Medicine. 64(2). 61–64. 4 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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