Ridha Mrad

1.5k total citations
89 papers, 1.0k citations indexed

About

Ridha Mrad is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Ridha Mrad has authored 89 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Molecular Biology, 41 papers in Genetics and 10 papers in Pathology and Forensic Medicine. Recurrent topics in Ridha Mrad's work include Genetics and Neurodevelopmental Disorders (12 papers), Genomic variations and chromosomal abnormalities (9 papers) and Autism Spectrum Disorder Research (8 papers). Ridha Mrad is often cited by papers focused on Genetics and Neurodevelopmental Disorders (12 papers), Genomic variations and chromosomal abnormalities (9 papers) and Autism Spectrum Disorder Research (8 papers). Ridha Mrad collaborates with scholars based in Tunisia, France and United States. Ridha Mrad's co-authors include Habiba Chaâbouni, Faouzi Mâazoul, Maher Kharrat, Lamia Ben Jemâa, Nizar Smaoui, Leslie Lenert, Spilios D. Fassois, Roy Soetikno, A. Belhadj and J. Fielding Hejtmancik and has published in prestigious journals such as SHILAP Revista de lepidopterología, American Journal of Psychiatry and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Ridha Mrad

84 papers receiving 971 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ridha Mrad Tunisia 17 601 486 116 95 75 89 1.0k
Bernd Frank Germany 24 748 1.2× 228 0.5× 55 0.5× 42 0.4× 124 1.7× 48 1.5k
Algirdas Utkus Lithuania 17 368 0.6× 425 0.9× 29 0.3× 40 0.4× 51 0.7× 112 1.0k
Iben Bache Denmark 15 254 0.4× 341 0.7× 62 0.5× 72 0.8× 16 0.2× 29 731
Julie S. Cohen United States 22 617 1.0× 578 1.2× 76 0.7× 20 0.2× 203 2.7× 44 1.4k
Giovanni Sorge Italy 22 486 0.8× 553 1.1× 60 0.5× 27 0.3× 45 0.6× 75 1.3k
Michael Freilinger Austria 19 447 0.7× 206 0.4× 106 0.9× 48 0.5× 95 1.3× 42 1.2k
Charu Deshpande United Kingdom 13 436 0.7× 344 0.7× 40 0.3× 23 0.2× 53 0.7× 24 1.1k
Salvatore Savasta Italy 23 542 0.9× 366 0.8× 38 0.3× 25 0.3× 148 2.0× 120 1.6k
Takeo Kato Japan 17 741 1.2× 254 0.5× 51 0.4× 20 0.2× 68 0.9× 60 1.3k
Siddharth Gupta United States 19 291 0.5× 200 0.4× 76 0.7× 24 0.3× 128 1.7× 45 858

Countries citing papers authored by Ridha Mrad

Since Specialization
Citations

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

Fields of papers citing papers by Ridha Mrad

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ridha Mrad

This figure shows the co-authorship network connecting the top 25 collaborators of Ridha Mrad. A scholar is included among the top collaborators of Ridha Mrad 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 Ridha Mrad. Ridha Mrad 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.
Kâaroud, H., et al.. (2023). Primary Hyperoxaluria Type 1: Clinical, Paraclinical, and Evolutionary Aspects in Adults from One Nephrology Center. International Journal of Nephrology. 2023. 1–5. 1 indexed citations
2.
Mrad, Ridha, et al.. (2023). Phenotype Spectrum in Tunisian Population with NPHP1 Deletion. Indian Journal of Nephrology. 33(6). 426–431. 1 indexed citations
3.
4.
Kharrat, Maher, et al.. (2022). Novel RAB3GAP1 Mutation in the First Tunisian Family With Warburg Micro Syndrome. Journal of Clinical Neurology. 18(2). 214–214. 1 indexed citations
5.
Chérif, M., et al.. (2022). Li–Fraumeni syndrome in Tunisian carriers with different and rare tumor phenotype: genotype–phenotype correlation. BMC Medical Genomics. 15(1). 44–44. 4 indexed citations
6.
Ouertani, Inès, et al.. (2022). 3M syndrome: A Tunisian seven-cases series. European Journal of Medical Genetics. 65(3). 104448–104448. 5 indexed citations
7.
Kraoua, Ichraf, Nadège Calmels, Cathy Obringer, et al.. (2022). Heterogeneous clinical features in Cockayne syndrome patients and siblings carrying the same CSA mutations. Orphanet Journal of Rare Diseases. 17(1). 121–121. 7 indexed citations
8.
Chehida, Amel Ben, Lilia Kraoua, Heather Etchevers, et al.. (2019). A severe clinical phenotype of Noonan syndrome with neonatal hypertrophic cardiomyopathy in the second case worldwide withRAF1S259Y neomutation. Genetics Research. 101. e6–e6. 3 indexed citations
9.
10.
Kraoua, Lilia, Inès Ouertani, Faouzi Mâazoul, et al.. (2018). WDR73-related galloway mowat syndrome with collapsing glomerulopathy. European Journal of Medical Genetics. 62(9). 103550–103550. 6 indexed citations
11.
Kraoua, Lilia, Alexandre Atkinson, Valérie Delague, et al.. (2018). Novel ALPK3 mutation in a Tunisian patient with pediatric cardiomyopathy and facio-thoraco-skeletal features. Journal of Human Genetics. 63(10). 1077–1082. 16 indexed citations
12.
Fradj, Mohamed Kacem Ben, Lilia Kraoua, Faouzi Mâazoul, et al.. (2018). <b><i>TOP3B</i></b>: A Novel Candidate Gene in Juvenile Myoclonic Epilepsy?. Cytogenetic and Genome Research. 154(1). 1–5. 16 indexed citations
13.
Mâazoul, Faouzi, Lilia Kraoua, Inès Ouertani, et al.. (2017). Novel PAX3 mutations causing Waardenburg syndrome type 1 in Tunisian patients. International Journal of Pediatric Otorhinolaryngology. 103. 14–19. 3 indexed citations
14.
Mrad, Ridha, et al.. (2014). Bathing suit ichthyosis caused by a TGM1 mutation in a Tunisian child. International Journal of Dermatology. 53(12). 1478–1480. 5 indexed citations
15.
Mâazoul, Faouzi, Myriam Châabouni, Inès Ouertani, et al.. (2012). Epidemiologic and clinical characteristics of 458 Tunisian patients with intellectual deficiency and a reconsidered diagnostic strategy. European Journal of Medical Genetics. 56(1). 13–19. 1 indexed citations
16.
Kharrat, Maher, et al.. (2011). Non-syndromic autosomal recessive mental retardation in Tunisian families : exclusion of GRIK2 and TUSC3 genes.. PubMed. 89(5). 479–84. 2 indexed citations
17.
Petit, François, Stéphane Bezieau, Vincent Gajdos, et al.. (2008). The Tunisian population history through the Crigler–Najjar type I syndrome. European Journal of Human Genetics. 16(7). 848–853. 12 indexed citations
18.
Laumonnier, Frédéric, Sébastien Roger, Pascaline Guérin, et al.. (2006). Association of a Functional Deficit of the BK Ca Channel, a Synaptic Regulator of Neuronal Excitability, With Autism and Mental Retardation. American Journal of Psychiatry. 163(9). 1622–1629. 135 indexed citations
19.
Mrad, Ridha, et al.. (2005). Épidermolyse bulleuse jonctionnelle congénitale, aplasie cutanée et atrésie pylorique. Annales de Dermatologie et de Vénéréologie. 132(3). 298–299.
20.
Jemâa, Lamia Ben, Vincent des Portes, Ramzi Zemni, et al.. (1999). Refined 2.7 centimorgan locus in Xp21.3-22.1 for a nonspecific X-linked mental retardation gene (MRX54). American Journal of Medical Genetics. 85(3). 276–282. 7 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Bernd Frank Breakdown of academic impact, for papers by Algirdas Utkus Breakdown of academic impact, for papers by Iben Bache Breakdown of academic impact, for papers by Julie S. Cohen Breakdown of academic impact, for papers by Giovanni Sorge Breakdown of academic impact, for papers by Michael Freilinger Breakdown of academic impact, for papers by Charu Deshpande Breakdown of academic impact, for papers by Salvatore Savasta Breakdown of academic impact, for papers by Takeo Kato Breakdown of academic impact, for papers by Siddharth Gupta
Rankless by CCL
2026