E. Boyd
- Genetics top 2%
- Genomic variations and chromosomal abnormalities 18
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 9
- Genetics and Neurodevelopmental Disorders 4
- Reproductive Medicine top 5%
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- Prenatal Screening and Diagnostics 10
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- Sexual Differentiation and Disorders 6
- RNA modifications and cancer 5
- Plant Science top 10%
- Chromosomal and Genetic Variations 12
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- Neuroblastoma Research and Treatments 4
- Co-authors
- M.A. Ferguson‐SmithJohn TolmieAlexander CookeBryan D. YoungJ. M. ConnorBernard LennoxNabeel A. AffaraNorma Morrison
- Partner nations
- United KingdomUnited StatesHungary
In The Last Decade
E. Boyd
55 papers receiving 1.2k citations
Peers
Comparison fields: 5 of 102
- Genetics 804
- Reproductive Medicine 117
- Pediatrics, Perinatology and Child Health 233
- Molecular Biology 623
- Plant Science 304
Countries citing papers authored by E. Boyd
This map shows the geographic impact of E. Boyd'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. Boyd with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites E. Boyd more than expected).
Fields of papers citing papers by E. Boyd
This network shows the impact of papers produced by E. Boyd. 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. Boyd. The network helps show where E. Boyd may publish in the future.
Co-authorship network
The 25 scholars most cited alongside E. Boyd, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2001 | 28 | |
| 2 | 1997 | 9 | |
| 3 | 1996 | 6 | |
| 4 | 1996 | 11 | |
| 5 | 1995 | 4 | |
| 6 | 1994 | 8 | |
| 7 | 1992 | 14 | |
| 8 | 1990 | 19 | |
| 9 | 1990 | 15 | |
| 10 | 1990 | 96 | |
| 11 | 1989 | 20 | |
| 12 | 1989 | 19 | |
| 13 | 1989 | 37 | |
| 14 | 1989 | 3 | |
| 15 | 1987 | 21 | |
| 16 | 1987 | 67 | |
| 17 | 1982 | 4 | |
| 18 | 1981 | 3 | |
| 19 | 1971 | 49 | |
| 20 | 1961 | 42 |
About E. Boyd
E. Boyd is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Developmental Biology, Hematology and Plant Science, having authored 55 papers that have together received 1.3k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (18 papers), Chromosomal and Genetic Variations (12 papers), Prenatal Screening and Diagnostics (10 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (9 papers), Sexual Differentiation and Disorders (6 papers), RNA modifications and cancer (5 papers), Neuroblastoma Research and Treatments (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). The work is most often cited by research in Genetics (804 citations), Reproductive Medicine (117 citations), Pediatrics, Perinatology and Child Health (233 citations), Molecular Biology (623 citations) and Plant Science (304 citations). E. Boyd has collaborated with scholars based in United Kingdom, United States and Hungary. Frequent co-authors include M.A. Ferguson‐Smith, John Tolmie, Alexander Cooke, Bryan D. Young, J. M. Connor, Bernard Lennox, Nabeel A. Affara, Norma Morrison, Peter C. Harris and Stephen Harrap. Their work appears in journals such as Human Genetics, Journal of Medical Genetics, The Lancet, Cytogenetic and Genome Research and Clinical Genetics.
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.