O.S. Alfi
Impact in
-
- Prenatal Screening and Diagnostics
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Papers in
- Genetics 16
- Genomic variations and chromosomal abnormalities 10
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3
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- DNA Repair Mechanisms 4
- Genomics and Chromatin Dynamics 4
- DNA and Nucleic Acid Chemistry 3
- Co-authors
- Ming S. Lin (8 shared papers)George N. Donnell (15 shared papers)David E. Comings (1 shared paper)Ruimin Chang (1 shared paper)G R DeVore (1 shared paper)Barbara F. Crandall (1 shared paper)Roopika Menon (1 shared paper)Greggory R. DeVore (1 shared paper)
- Journals
- PEDIATRICS (2 papers)Chromosoma (2 papers)Journal of Medical Genetics (2 papers)The Journal of Pediatrics (1 paper)Ophthalmology (1 paper)
- Partner nations
- United StatesEgyptUnited Kingdom
In The Last Decade
O.S. Alfi
35 papers receiving 792 citations
Peers
Comparison fields: 5 of 100
- Pediatrics, Perinatology and Child Health 254
- Genetics 354
- Developmental Biology 28
- Genetics 69
- Hepatology 42
Countries citing papers authored by O.S. Alfi
This map shows the geographic impact of O.S. Alfi'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 O.S. Alfi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites O.S. Alfi more than expected).
Fields of papers citing papers by O.S. Alfi
This network shows the impact of papers produced by O.S. Alfi. 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 O.S. Alfi. The network helps show where O.S. Alfi may publish in the future.
Co-authors
The 25 scholars most cited alongside O.S. Alfi, 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 38 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1977 | 144 | |
| 2 | Deletion of the short arm of chromosome no.9 (46,9p-): a new deletion syndrome. | 1973 | 114 |
| 3 | Evidence for genetic control of nondisjunction in man. | 1980 | 90 |
| 4 | 2010 | 86 | |
| 5 | 1976 | 62 | |
| 6 | 1995 | 55 | |
| 7 | The 9p- syndrome. | 1976 | 38 |
| 8 | 1986 | 28 | |
| 9 | 1993 | 23 | |
| 10 | 1973 | 23 | |
| 11 | 1974 | 19 | |
| 12 | Role of amniocentesis in ultrasound-detected fetal malformations. | 1986 | 19 |
| 13 | 1976 | 18 | |
| 14 | Trisomy 19 q. | 1976 | 16 |
| 15 | Trisomy 22: a clinically identifiable syndrome. | 1975 | 16 |
| 16 | 1977 | 14 | |
| 17 | 1995 | 14 | |
| 18 | 46, Del (9) (22:), a new deletion syndrome. | 1974 | 11 |
| 19 | 1976 | 8 | |
| 20 | 1971 | 8 |
About O.S. Alfi
O.S. Alfi is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Plant Science and Surgery, having authored 38 papers that have together received 858 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (12 papers), Genomic variations and chromosomal abnormalities (10 papers), Chromosomal and Genetic Variations (7 papers), Metabolism and Genetic Disorders (5 papers), DNA Repair Mechanisms (4 papers), Genomics and Chromatin Dynamics (4 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers) and DNA and Nucleic Acid Chemistry (3 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (254 citations), Genetics (354 citations), Developmental Biology (28 citations), Genetics (69 citations) and Hepatology (42 citations). O.S. Alfi has collaborated with scholars based in United States, Egypt and United Kingdom. Frequent co-authors include Ming S. Lin, George N. Donnell, David E. Comings, Ruimin Chang, G R DeVore, Barbara F. Crandall, Roopika Menon, Greggory R. DeVore, P. W. Allderdice and Miriam G. Wilson. Their work appears in journals such as PEDIATRICS, Chromosoma, Journal of Medical Genetics, The Journal of Pediatrics and Ophthalmology.
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.