Ali Hellani
Impact in
-
- Prenatal Screening and Diagnostics
- Assisted Reproductive Technology and Twin Pregnancy
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Forensic and Genetic Research
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Hemoglobinopathies and Related Disorders
Papers in
- Genetics 13
- Genomic variations and chromosomal abnormalities 9
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
-
- Prenatal Screening and Diagnostics 10
- Co-authors
- Khaled K. Abu‐Amero (28 shared papers)Serdar Coşkun (8 shared papers)Saad S. M. Hassan (3 shared papers)Thomas M. Bosley (15 shared papers)Pinar T. Ozand (3 shared papers)Ali Al‐Odaib (2 shared papers)Nadia Sakati (1 shared paper)Moncef Benkhalifa (1 shared paper)
- Journals
- Ophthalmic Genetics (7 papers)Reproductive BioMedicine Online (5 papers)Prenatal Diagnosis (2 papers)Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques (2 papers)Molecular Human Reproduction (1 paper)
- Partner nations
- Saudi ArabiaUnited StatesSouth Africa
In The Last Decade
Ali Hellani
39 papers receiving 804 citations
Peers
Comparison fields: 5 of 71
- Pediatrics, Perinatology and Child Health 270
- Genetics 324
- Reproductive Medicine 62
- Genetics 54
- Anatomy 7
Countries citing papers authored by Ali Hellani
This map shows the geographic impact of Ali Hellani'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 Ali Hellani with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ali Hellani more than expected).
Fields of papers citing papers by Ali Hellani
This network shows the impact of papers produced by Ali Hellani. 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 Ali Hellani. The network helps show where Ali Hellani may publish in the future.
Co-authors
The 25 scholars most cited alongside Ali Hellani, 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 39 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2004 | 107 | |
| 2 | 2008 | 104 | |
| 3 | 2009 | 76 | |
| 4 | 2014 | 75 | |
| 5 | 2005 | 68 | |
| 6 | 2006 | 50 | |
| 7 | 2008 | 42 | |
| 8 | Down-regulation of OPA1 in patients with primary open angle glaucoma. | 2011 | 28 |
| 9 | 2010 | 27 | |
| 10 | 2009 | 26 | |
| 11 | 2003 | 22 | |
| 12 | 2010 | 15 | |
| 13 | 2009 | 14 | |
| 14 | 2011 | 14 | |
| 15 | High-resolution analysis of DNA copy number alterations in patients with isolated sporadic keratoconus. | 2011 | 13 |
| 16 | 2014 | 12 | |
| 17 | 2004 | 12 | |
| 18 | 2020 | 11 | |
| 19 | 2008 | 11 | |
| 20 | 2011 | 11 |
About Ali Hellani
Ali Hellani is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Surgery and Pathology and Forensic Medicine, having authored 39 papers that have together received 844 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (10 papers), Genomic variations and chromosomal abnormalities (9 papers), Ophthalmology and Eye Disorders (3 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers), Mitochondrial Function and Pathology (2 papers), Chromosomal and Genetic Variations (2 papers), Congenital Anomalies and Fetal Surgery (2 papers) and Congenital limb and hand anomalies (2 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (270 citations), Genetics (324 citations), Reproductive Medicine (62 citations), Genetics (54 citations) and Anatomy (7 citations). Ali Hellani has collaborated with scholars based in Saudi Arabia, United States and South Africa. Frequent co-authors include Khaled K. Abu‐Amero, Serdar Coşkun, Saad S. M. Hassan, Thomas M. Bosley, Pinar T. Ozand, Ali Al‐Odaib, Nadia Sakati, Moncef Benkhalifa, Ana González and Vicente M. Cabrera. Their work appears in journals such as Ophthalmic Genetics, Reproductive BioMedicine Online, Prenatal Diagnosis, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques and Molecular Human Reproduction.
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.