E. V. Davison
Impact in
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- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Genetic and rare skin diseases.
Papers in
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- Prenatal Screening and Diagnostics 13
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- Acute Myeloid Leukemia Research 7
- Co-authors
- D E Rooney (1 shared paper)Jackie Wolstenholme (1 shared paper)M. D. Kilby (3 shared papers)Sarah Hillman (1 shared paper)Eamonn Richard Maher (1 shared paper)Samantha J. Pretlove (1 shared paper)Arri Coomarasamy (1 shared paper)Dominic J. McMullan (1 shared paper)
- Journals
- Prenatal Diagnosis (6 papers)Journal of Medical Genetics (4 papers)Journal of Clinical Pathology (4 papers)Human Genetics (3 papers)Ultrasound in Obstetrics and Gynecology (2 papers)
- Partner nations
- United KingdomIrelandUnited States
In The Last Decade
E. V. Davison
35 papers receiving 791 citations
Peers
Comparison fields: 5 of 59
- Pediatrics, Perinatology and Child Health 370
- Genetics 349
- Ophthalmology 56
- Reproductive Medicine 47
- Developmental Neuroscience 20
Countries citing papers authored by E. V. Davison
This map shows the geographic impact of E. V. Davison'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 E. V. Davison with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites E. V. Davison more than expected).
Fields of papers citing papers by E. V. Davison
This network shows the impact of papers produced by E. V. Davison. 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 E. V. Davison. The network helps show where E. V. Davison may publish in the future.
Co-authors
The 25 scholars most cited alongside E. V. Davison, 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 37 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2010 | 191 | |
| 2 | 1994 | 117 | |
| 3 | 1993 | 74 | |
| 4 | Temporal relationship and reliability of the clinical, hormonal, and ultrasonographic indices of ovulation in infertile women. | 1990 | 61 |
| 5 | 2003 | 46 | |
| 6 | 1997 | 39 | |
| 7 | 1986 | 37 | |
| 8 | 1991 | 29 | |
| 9 | 1994 | 25 | |
| 10 | 1987 | 25 | |
| 11 | 1999 | 25 | |
| 12 | 1988 | 19 | |
| 13 | 1984 | 17 | |
| 14 | 1988 | 17 | |
| 15 | 2006 | 16 | |
| 16 | 1997 | 16 | |
| 17 | 1986 | 15 | |
| 18 | 1979 | 14 | |
| 19 | Meiotic and sperm chromosome analysis in a male carrier of an inverted insertion (3;10)(q13.2;p14p13). | 1992 | 12 |
| 20 | 1989 | 12 |
About E. V. Davison
E. V. Davison is a scholar working on Pediatrics, Perinatology and Child Health, Hematology, Genetics, Ophthalmology and Oncology, having authored 37 papers that have together received 891 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (13 papers), Acute Myeloid Leukemia Research (7 papers), Genomic variations and chromosomal abnormalities (5 papers), Chromosomal and Genetic Variations (5 papers), Sarcoma Diagnosis and Treatment (4 papers), Neuroblastoma Research and Treatments (4 papers), Acute Lymphoblastic Leukemia research (4 papers) and Genetic Syndromes and Imprinting (4 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (370 citations), Genetics (349 citations), Ophthalmology (56 citations), Reproductive Medicine (47 citations) and Developmental Neuroscience (20 citations). E. V. Davison has collaborated with scholars based in United Kingdom, Ireland and United States. Frequent co-authors include D E Rooney, Jackie Wolstenholme, M. D. Kilby, Sarah Hillman, Eamonn Richard Maher, Samantha J. Pretlove, Arri Coomarasamy, Dominic J. McMullan, Michael M. Reid and S. Larkins. Their work appears in journals such as Prenatal Diagnosis, Journal of Medical Genetics, Journal of Clinical Pathology, Human Genetics and Ultrasound in Obstetrics and Gynecology.
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.