Houda Benrahma

876 total citations
26 papers, 311 citations indexed

About

Houda Benrahma is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism and Epidemiology. According to data from OpenAlex, Houda Benrahma has authored 26 papers receiving a total of 311 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 8 papers in Endocrinology, Diabetes and Metabolism and 7 papers in Epidemiology. Recurrent topics in Houda Benrahma's work include Diabetes, Cardiovascular Risks, and Lipoproteins (6 papers), Adipokines, Inflammation, and Metabolic Diseases (4 papers) and Hearing, Cochlea, Tinnitus, Genetics (3 papers). Houda Benrahma is often cited by papers focused on Diabetes, Cardiovascular Risks, and Lipoproteins (6 papers), Adipokines, Inflammation, and Metabolic Diseases (4 papers) and Hearing, Cochlea, Tinnitus, Genetics (3 papers). Houda Benrahma collaborates with scholars based in Morocco, Tunisia and France. Houda Benrahma's co-authors include Abdelhamid Barakat, Hassan Rouba, Hicham Charoute, Omar Abidi, Sonia Abdelhak, Redouane Boulouiz, Khaled Lasram, Majida Charif, Asma Chadli and Mounia Oudghiri and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and BioMed Research International.

In The Last Decade

Houda Benrahma

24 papers receiving 300 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Houda Benrahma Morocco 12 114 79 71 54 54 26 311
Molka Chaieb Tunisia 9 88 0.8× 106 1.3× 94 1.3× 45 0.8× 77 1.4× 17 338
Pegah Ghandil Iran 11 99 0.9× 82 1.0× 45 0.6× 48 0.9× 14 0.3× 30 352
Patinut Buranasupkajorn Thailand 9 58 0.5× 51 0.6× 91 1.3× 60 1.1× 15 0.3× 19 222
Ai‐Ru Hsieh Taiwan 10 77 0.7× 71 0.9× 36 0.5× 24 0.4× 12 0.2× 40 301
Martin S. Cramer United States 9 179 1.6× 71 0.9× 24 0.3× 44 0.8× 21 0.4× 13 433
Monique G. Zaahl South Africa 12 68 0.6× 87 1.1× 49 0.7× 174 3.2× 16 0.3× 20 401
Eeva Sliz Finland 9 58 0.5× 59 0.7× 67 0.9× 25 0.5× 24 0.4× 16 348
Shuilian Yu China 13 63 0.6× 32 0.4× 18 0.3× 51 0.9× 157 2.9× 33 401
Mauro Sérgio Martins Marrocos Brazil 5 64 0.6× 37 0.5× 50 0.7× 42 0.8× 23 0.4× 10 311
Young‐Lim Shin South Korea 11 140 1.2× 121 1.5× 94 1.3× 124 2.3× 24 0.4× 29 400

Countries citing papers authored by Houda Benrahma

Since Specialization
Citations

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

Fields of papers citing papers by Houda Benrahma

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Houda Benrahma

This figure shows the co-authorship network connecting the top 25 collaborators of Houda Benrahma. A scholar is included among the top collaborators of Houda Benrahma 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 Houda Benrahma. Houda Benrahma 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.
Benrahma, Houda, et al.. (2024). Conventional and molecular cytogenetic characterization of a Moroccan patient with WAGR syndrome. SHILAP Revista de lepidopterología. 25(1). 1 indexed citations
2.
Benrahma, Houda, Noureddine Hamamouch, Kamal El Bissati, et al.. (2021). A review on current diagnostic techniques for COVID-19. Expert Review of Molecular Diagnostics. 21(2). 141–160. 21 indexed citations
3.
4.
Diawara, Idrissa, et al.. (2020). A laboratory-based study of COVID-19 in Casablanca, Morocco. Journal of Public Health in Africa. 12(2). 5–5. 2 indexed citations
5.
Charoute, Hicham, et al.. (2017). Association analysis of genetic variants with metabolic syndrome components in the Moroccan population. Current Research in Translational Medicine. 65(3). 121–125. 9 indexed citations
6.
Charoute, Hicham, Rym Kéfi, Houda Benrahma, et al.. (2016). Novel variants of mitochondrial DNA associated with Type 2 diabetes mellitus in Moroccan population. Mitochondrial DNA Part A. 29(1). 9–13. 6 indexed citations
7.
Charoute, Hicham, et al.. (2015). Association analysis of APOA5 rs662799 and rs3135506 polymorphisms with obesity in Moroccan patients. Pathologie Biologie. 63(6). 243–247. 6 indexed citations
8.
Charoute, Hicham, et al.. (2015). Haplotype analysis of the Apolipoprotein A5 gene in Moroccan patients with the metabolic syndrome. Journal of Diabetes & Metabolic Disorders. 14(1). 29–29. 12 indexed citations
9.
Charoute, Hicham, Houda Benrahma, Lilia Romdhane, et al.. (2015). Mediterranean Founder Mutation Database (MFMD): Taking Advantage from Founder Mutations in Genetics Diagnosis, Genetic Diversity and Migration History of the Mediterranean Population. Human Mutation. 36(11). E2441–E2453. 12 indexed citations
10.
Benrahma, Houda, Hicham Charoute, Hassan Rouba, et al.. (2014). TNF A −308G>A polymorphism in Moroccan patients with type 2 diabetes mellitus: a case–control study and meta-analysis. Molecular Biology Reports. 41(9). 5805–5811. 8 indexed citations
11.
Benrahma, Houda, Hicham Charoute, Khaled Lasram, et al.. (2014). Association Analysis of IGF2BP2, KCNJ11, and CDKAL1 Polymorphisms with Type 2 Diabetes Mellitus in a Moroccan Population: A Case–Control Study and Meta-analysis. Biochemical Genetics. 52(9-10). 430–442. 28 indexed citations
12.
Charoute, Hicham, et al.. (2014). Association of APOA5 rs662799 and rs3135506 polymorphisms with arterial hypertension in Moroccan patients. Lipids in Health and Disease. 13(1). 60–60. 24 indexed citations
13.
Benrahma, Houda, et al.. (2014). Vitamin D receptor gene polymorphisms and vitamin D status and susceptibility to type 2 diabetes mellitus in Moroccans patients. 6 indexed citations
14.
Lasram, Khaled, Nizar Ben Halim, Rym Kéfi, et al.. (2014). Evidence for Association of the E23K Variant ofKCNJ11Gene with Type 2 Diabetes in Tunisian Population: Population-Based Study and Meta-Analysis. BioMed Research International. 2014. 1–9. 13 indexed citations
15.
Barakat, Abdelhamid, Majida Charif, Redouane Boulouiz, et al.. (2013). Genetic and molecular analysis of the CLDN14 gene in Moroccan family with non-syndromic hearing loss. Indian journal of human genetics. 19(3). 331–331. 3 indexed citations
16.
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
17.
Abidi, Omar, Houda Benrahma, Mehdi Karkouri, et al.. (2012). Clinicopathological Features and Molecular Analysis of Primary Glioblastomas in Moroccan Patients. Journal of Molecular Neuroscience. 49(3). 567–573. 10 indexed citations
18.
Benrahma, Houda, Omar Abidi, Hassan Rouba, et al.. (2011). Association of the C677T Polymorphism in the Human Methylenetetrahydrofolate Reductase ( MTHFR ) Gene with the Genetic Predisposition for Type 2 Diabetes Mellitus in a Moroccan Population. Genetic Testing and Molecular Biomarkers. 16(5). 383–387. 29 indexed citations
19.
Benrahma, Houda, Majida Charif, Redouane Boulouiz, et al.. (2011). Maternal Effect and Familial Aggregation in a Type 2 Diabetic Moroccan Population. Journal of Community Health. 36(6). 943–948. 17 indexed citations
20.
Charif, Majida, Redouane Boulouiz, Houda Benrahma, et al.. (2010). Prevalence of the mitochondrial A 1555G mutation in Moroccan patients with non-syndromic hearing loss. International Journal of Pediatric Otorhinolaryngology. 74(9). 1071–1074. 18 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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