Edward Orye
Impact in
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Developmental Biology top 10%
Papers in
- Genetics 22
- Genomic variations and chromosomal abnormalities 22
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- Prenatal Screening and Diagnostics 9
- Co-authors
- Margarita Craen (4 shared papers)Cornelis S. Van Der Hooft (4 shared papers)Henri A. Verhaaren (5 shared papers)G. Dacremont (1 shared paper)Dietbrandt Carton (1 shared paper)Jos A. Kint (1 shared paper)Hendrik van Egmond (2 shared papers)Yves Benoît (4 shared papers)
- Journals
- Clinical Genetics (5 papers)Human Genetics (4 papers)Journal of Medical Genetics (3 papers)Human Heredity (2 papers)Archives of Disease in Childhood (1 paper)
- Partner nations
- BelgiumNetherlands
In The Last Decade
Edward Orye
32 papers receiving 548 citations
Peers
Comparison fields: 5 of 58
- Genetics 325
- Developmental Biology 20
- Ophthalmology 73
- Pediatrics, Perinatology and Child Health 131
- Physiology 95
Countries citing papers authored by Edward Orye
This map shows the geographic impact of Edward Orye'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 Edward Orye with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Edward Orye more than expected).
Fields of papers citing papers by Edward Orye
This network shows the impact of papers produced by Edward Orye. 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 Edward Orye. The network helps show where Edward Orye may publish in the future.
Co-authors
The 25 scholars most cited alongside Edward Orye, 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 35 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1973 | 102 | |
| 2 | 1974 | 61 | |
| 3 | 1991 | 52 | |
| 4 | 1971 | 44 | |
| 5 | 1988 | 42 | |
| 6 | 1975 | 41 | |
| 7 | 1983 | 27 | |
| 8 | 1976 | 25 | |
| 9 | 1983 | 25 | |
| 10 | 1972 | 21 | |
| 11 | 1982 | 20 | |
| 12 | 1975 | 19 | |
| 13 | 1983 | 17 | |
| 14 | 1975 | 16 | |
| 15 | 1974 | 14 | |
| 16 | De novo distal trisomy 17q. | 1985 | 12 |
| 17 | Distal trisomy 14q due to tandem duplication (q24 leads to q32). | 1983 | 12 |
| 18 | 1974 | 11 | |
| 19 | Familial D/D and D/G, translocation. | 1967 | 10 |
| 20 | [Ring chromosome 18]. | 1968 | 9 |
About Edward Orye
Edward Orye is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Pathology and Forensic Medicine, Plant Science and Ophthalmology, having authored 35 papers that have together received 630 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (22 papers), Prenatal Screening and Diagnostics (9 papers), Chromosomal and Genetic Variations (9 papers), DNA and Nucleic Acid Chemistry (6 papers), Genetic factors in colorectal cancer (4 papers), Genomics and Chromatin Dynamics (3 papers), DNA Repair Mechanisms (3 papers) and Ocular Oncology and Treatments (3 papers). The work is most often cited by research in Genetics (325 citations), Developmental Biology (20 citations), Ophthalmology (73 citations), Pediatrics, Perinatology and Child Health (131 citations) and Physiology (95 citations). Edward Orye has collaborated with scholars based in Belgium and Netherlands. Frequent co-authors include Margarita Craen, Cornelis S. Van Der Hooft, Henri A. Verhaaren, G. Dacremont, Dietbrandt Carton, Jos A. Kint, Hendrik van Egmond, Yves Benoît, Marleen M. Praet and Marc J. Coppens. Their work appears in journals such as Clinical Genetics, Human Genetics, Journal of Medical Genetics, Human Heredity and Archives of Disease in Childhood.
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.