Ridha Mrad
Impact in
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genomics and Rare Diseases
- Genetic Syndromes and Imprinting
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- Sexual Differentiation and Disorders
- Connexins and lens biology
Papers in
-
- Sexual Differentiation and Disorders 7
- Genetics 41
- Genetics and Neurodevelopmental Disorders 12
- Genomic variations and chromosomal abnormalities 9
- BRCA gene mutations in cancer 6
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 5
- Co-authors
- Habiba Chaâbouni (24 shared papers)Faouzi Mâazoul (33 shared papers)Maher Kharrat (14 shared papers)Lamia Ben Jemâa (10 shared papers)Nizar Smaoui (4 shared papers)Roy Soetikno (1 shared paper)Spilios D. Fassois (4 shared papers)Leslie Lenert (1 shared paper)
- Journals
- European Journal of Medical Genetics (4 papers)International Journal of Pediatric Otorhinolaryngology (2 papers)Journal of vibration and acoustics (2 papers)Clinical Genetics (2 papers)Pediatric Nephrology (2 papers)
- Partner nations
- TunisiaFranceUnited States
In The Last Decade
Ridha Mrad
84 papers receiving 971 citations
Peers
Comparison fields: 5 of 111
- Genetics 486
- Molecular Biology 601
- Cognitive Neuroscience 116
- Endocrinology, Diabetes and Metabolism 95
- Clinical Biochemistry 38
Countries citing papers authored by Ridha Mrad
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
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-authors
The 25 scholars most cited alongside Ridha Mrad, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 89 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2006 | 135 | |
| 2 | 2004 | 87 | |
| 3 | 2004 | 74 | |
| 4 | 1997 | 58 | |
| 5 | 2006 | 42 | |
| 6 | 1991 | 32 | |
| 7 | 2018 | 31 | |
| 8 | 2007 | 30 | |
| 9 | 2013 | 25 | |
| 10 | 2010 | 24 | |
| 11 | 2018 | 24 | |
| 12 | 2011 | 23 | |
| 13 | 2001 | 22 | |
| 14 | [A clinic and a paraclinic study of Tunisian population of children with autism. About 63 cases]. | 2006 | 19 |
| 15 | 2009 | 18 | |
| 16 | 1991 | 17 | |
| 17 | 2018 | 16 | |
| 18 | 2018 | 16 | |
| 19 | 2008 | 14 | |
| 20 | 2016 | 13 |
About Ridha Mrad
Ridha Mrad is a scholar working on Molecular Biology, Genetics, Pathology and Forensic Medicine, Cell Biology and Cognitive Neuroscience, having authored 89 papers that have together received 1.0k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (12 papers), Genomic variations and chromosomal abnormalities (9 papers), Autism Spectrum Disorder Research (8 papers), Sexual Differentiation and Disorders (7 papers), BRCA gene mutations in cancer (6 papers), Biomedical Research and Pathophysiology (6 papers), Hormonal and reproductive studies (5 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers). The work is most often cited by research in Genetics (486 citations), Molecular Biology (601 citations), Cognitive Neuroscience (116 citations), Endocrinology, Diabetes and Metabolism (95 citations) and Clinical Biochemistry (38 citations). Ridha Mrad has collaborated with scholars based in Tunisia, France and United States. Frequent co-authors include Habiba Chaâbouni, Faouzi Mâazoul, Maher Kharrat, Lamia Ben Jemâa, Nizar Smaoui, Roy Soetikno, Spilios D. Fassois, Leslie Lenert, A. Belhadj and J. Fielding Hejtmancik. Their work appears in journals such as European Journal of Medical Genetics, International Journal of Pediatric Otorhinolaryngology, Journal of vibration and acoustics, Clinical Genetics and Pediatric Nephrology.
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.