A. Saad
Impact in
- Reproductive Medicine top 10%
- Sperm and Testicular Function
-
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Papers in
- Genetics 9
- Genomic variations and chromosomal abnormalities 4
- Genomics and Rare Diseases 2
-
- Congenital heart defects research 2
- Co-authors
- Lamia Saïd (2 shared papers)Serge Carreau (2 shared papers)Hatem Elghezal (4 shared papers)Moez Gribaa (2 shared papers)Damien Sanlaville (3 shared papers)A. Chaïeb (1 shared paper)Soumaya Mougou-Zerelli (3 shared papers)I. Galeraud-Denis (1 shared paper)
- Journals
- Andrologia (3 papers)Cytogenetic and Genome Research (2 papers)Clinical Genetics (2 papers)Placenta (1 paper)Medical Oncology (1 paper)
- Partner nations
- TunisiaFranceUnited Kingdom
In The Last Decade
A. Saad
19 papers receiving 249 citations
Peers
Comparison fields: 5 of 48
- Reproductive Medicine 59
- Genetics 112
- Public Health, Environmental and Occupational Health 69
- Pediatrics, Perinatology and Child Health 39
- Genetics 22
Countries citing papers authored by A. Saad
This map shows the geographic impact of A. Saad'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 A. Saad with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites A. Saad more than expected).
Fields of papers citing papers by A. Saad
This network shows the impact of papers produced by A. Saad. 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 A. Saad. The network helps show where A. Saad may publish in the future.
Co-authors
The 25 scholars most cited alongside A. Saad, 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 24 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2015 | 58 | |
| 2 | 2008 | 37 | |
| 3 | 2007 | 27 | |
| 4 | 2016 | 21 | |
| 5 | 2013 | 20 | |
| 6 | 2017 | 18 | |
| 7 | 2015 | 13 | |
| 8 | 2012 | 11 | |
| 9 | 2013 | 9 | |
| 10 | 2018 | 9 | |
| 11 | 2019 | 8 | |
| 12 | 2015 | 8 | |
| 13 | 1998 | 7 | |
| 14 | 2011 | 6 | |
| 15 | [Diagnostic strategy of beta-thalassemic mutation in a Tunisian family, application in prenatal diagnosis]. | 2003 | 5 |
| 16 | 2010 | 4 | |
| 17 | 2005 | 1 | |
| 18 | 2010 | 1 | |
| 19 | 1994 | 1 | |
| 20 | 2010 | 0 |
About A. Saad
A. Saad is a scholar working on Genetics, Molecular Biology, Public Health, Environmental and Occupational Health, Pediatrics, Perinatology and Child Health and Hematology, having authored 24 papers that have together received 264 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (5 papers), Sperm and Testicular Function (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Reproductive Biology and Fertility (4 papers), Reproductive biology and impacts on aquatic species (2 papers), Congenital heart defects research (2 papers), Acute Myeloid Leukemia Research (2 papers) and Genomics and Rare Diseases (2 papers). The work is most often cited by research in Reproductive Medicine (59 citations), Genetics (112 citations), Public Health, Environmental and Occupational Health (69 citations), Pediatrics, Perinatology and Child Health (39 citations) and Genetics (22 citations). A. Saad has collaborated with scholars based in Tunisia, France and United Kingdom. Frequent co-authors include Lamia Saïd, Serge Carreau, Hatem Elghezal, Moez Gribaa, Damien Sanlaville, A. Chaïeb, Soumaya Mougou-Zerelli, I. Galeraud-Denis, Soumaya Mougou and Nadia Boutry‐Kryza. Their work appears in journals such as Andrologia, Cytogenetic and Genome Research, Clinical Genetics, Placenta and Medical Oncology.
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.