E. Boyd
Impact in
- Genetics top 2%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Reproductive Medicine top 5%
- Sperm and Testicular Function
Papers in
- Genetics 30
- Genomic variations and chromosomal abnormalities 18
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 9
- Genetics and Neurodevelopmental Disorders 4
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- Sexual Differentiation and Disorders 6
- RNA modifications and cancer 5
- Co-authors
- M.A. Ferguson‐Smith (15 shared papers)John Tolmie (9 shared papers)Alexander Cooke (7 shared papers)Bernard Lennox (4 shared papers)J. M. Connor (11 shared papers)Nabeel A. Affara (3 shared papers)Norma Morrison (13 shared papers)Bryan D. Young (2 shared papers)
- Journals
- Human Genetics (18 papers)Journal of Medical Genetics (10 papers)The Lancet (5 papers)Clinical Genetics (2 papers)Nucleic Acids Research (2 papers)
- Partner nations
- United KingdomHungaryUnited States
In The Last Decade
E. Boyd
55 papers receiving 1.2k citations
Peers
Comparison fields: 5 of 101
- Genetics 826
- Reproductive Medicine 120
- Pediatrics, Perinatology and Child Health 234
- Molecular Biology 628
- Plant Science 283
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-authors
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
Showing the 20 most-cited of 55 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1990 | 128 | |
| 2 | 1981 | 107 | |
| 3 | 1987 | 70 | |
| 4 | 1960 | 70 | |
| 5 | 1986 | 61 | |
| 6 | 1971 | 56 | |
| 7 | 1998 | 52 | |
| 8 | 1961 | 49 | |
| 9 | 1989 | 44 | |
| 10 | 1961 | 42 | |
| 11 | 1991 | 39 | |
| 12 | 1989 | 39 | |
| 13 | 1999 | 38 | |
| 14 | 1990 | 37 | |
| 15 | 1986 | 36 | |
| 16 | 2001 | 29 | |
| 17 | 1996 | 28 | |
| 18 | 1969 | 27 | |
| 19 | 1986 | 26 | |
| 20 | 1999 | 25 |
About E. Boyd
E. Boyd is a scholar working on Genetics, Molecular Biology, Plant Science, Pediatrics, Perinatology and Child Health and Hematology, having authored 55 papers that have together received 1.4k 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 (826 citations), Reproductive Medicine (120 citations), Pediatrics, Perinatology and Child Health (234 citations), Molecular Biology (628 citations) and Plant Science (283 citations). E. Boyd has collaborated with scholars based in United Kingdom, Hungary and United States. Frequent co-authors include M.A. Ferguson‐Smith, John Tolmie, Alexander Cooke, Bernard Lennox, J. M. Connor, Nabeel A. Affara, Norma Morrison, Bryan D. Young, Stephen Harrap and D.A. Aitken. Their work appears in journals such as Human Genetics, Journal of Medical Genetics, The Lancet, Clinical Genetics and Nucleic Acids Research.
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.