E. Boyd

2.4k citations

55 papers · 1.3k · h-index 22

Impact in

Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination 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
Molecular Biology 21
- 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)Bryan D. Young (2 shared papers)J. M. Connor (11 shared papers)Bernard Lennox (4 shared papers)Nabeel A. Affara (3 shared papers)Norma Morrison (13 shared papers)
Journals: Human Genetics (18 papers)Journal of Medical Genetics (10 papers)The Lancet (5 papers)Cytogenetic and Genome Research (2 papers)Clinical Genetics (2 papers)
Partner nations: United Kingdom United States Hungary

In The Last Decade

E. Boyd

55 papers receiving 1.2k citations

Peers

Countries citing papers authored by E. Boyd

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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.

Border = papers with E. Boyd Line = papers co-authored together E. Boyd links everyone, so they are left out of the graph.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Showing the 20 most-cited of 55 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Genotype-phenotype correlations in XX males and their bearing on current theories of sex determination Human Genetics ·M.A. Ferguson‐Smith, Alexander Cooke, Nabeel A. Affara, E. Boyd, John Tolmie	1990	96
2	High-resolution analysis of human peripheral lymphocyte chromosomes by flow cytometry. Proceedings of the National Academy of Sciences ·Bryan D. Young, M.A. Ferguson‐Smith, R Sillar, E. Boyd	1981	96
3	Mapping the testis determinants by an analysis of Y-specific sequences in males with apparent XX and XO karyotypes and females with XY karyotypes Nucleic Acids Research ·Nabeel A. Affara, M.A. Ferguson‐Smith, R.E. Magenis, John Tolmie, E. Boyd, Alexander Cooke, Derek J. Jamieson, KY Kwok, Michael Mitchell, L. Snadden	1987	67
4	THE XXX SYNDROME The Lancet ·J. Gregory Fraser, Jean Campbell, R. C. MacGillivray, E. Boyd, Bernard Lennox	1960	60
5	Determination of the DNA content of human chromosomes by flow cytometry Cytogenetic and Genome Research ·Peter C. Harris, E. Boyd, Bryan D. Young, M.A. Ferguson‐Smith	1986	58
6	Regional assignment of Y-linked DNA probes by deletion mapping and their homology with X- chromosome and autosomal sequences Nucleic Acids Research ·Nabeel A. Affara, L. Florentin, Norma Morrison, KY Kwok, Michael Mitchell, April Cook, Derek J. Jamieson, L. Glasgow, Linda Meredith, E. Boyd, M.A. Ferguson‐Smith	1986	52
7	A new strategy for cryptic telomeric translocation screening in patients with idiopathic mental retardation. Journal of Medical Genetics ·Saeed Reza Ghaffari, E. Boyd, John Tolmie, Yanick J. Crow, Alison Trainer, J M Connor	1998	51
8	Chromosome Breakage and Ultrasound BMJ ·E. Boyd, U. Abdulla, Ian Donald, J. E. E. Fleming, A. J. Hall, M.A. Ferguson‐Smith	1971	49
9	A CASE OF XXXXY KLINEFELTER'S SYNDROME The Lancet ·J. Gregory Fraser, E. Boyd, Bernard Lennox, W. M. Dennison	1961	42
10	Regional chromosomal assignment of the human glucocorticoid receptor gene to 5q31 Human Genetics ·A. Theriault, E. Boyd, Stephen Harrap, Stanley M. Hollenberg, J. M. Connor	1989	37
11	DAMAGE TO CHROMOSOMES BY THERAPEUTIC DOSES OF RADIOIODINE The Lancet ·E. Boyd, W. Watson Buchanan, Bernard Lennox	1961	37
12	Interstitial deletion of the long arm of chromosome 2 with normal levels of isocitrate dehydrogenase. Journal of Medical Genetics ·Ian A. Glass, C. A. Swindlehurst, D.A. Aitken, W McCrea, E. Boyd	1989	37
13	Analysis of the origin of Turner's syndrome using polymorphic DNA probes. Journal of Medical Genetics ·S. A. R. Loughlin, A. A. Redha, J. McIver, E. Boyd, A D Carothers, J. M. Connor	1991	34
14	Duchenne muscular dystrophy due to familial Xp21 deletion detectable by DNA analysis and flow cytometry Human Genetics ·D.E. Wilcox, Alexander Cooke, J. Coigan, E. Boyd, D.A. Aitken, L.E. Sinclair, L. Glasgow, J Stephenson, M.A. Ferguson‐Smith	1986	34
15	Regional chromosomal assignment of the human mineralocorticoid receptor gene to 4q31.1 Human Genetics ·Norma Morrison, Stephen Harrap, JeffreyL. Arriza, E. Boyd, J. M. Connor	1990	33
16	The application of comparative genomic hybridization as an additional tool in the chromosome analysis of acute myeloid leukemia and myelodysplastic syndromes Cancer Genetics and Cytogenetics ·Mee Hye Kim, Janet Stewart, Caroline Devlin, Young Tae Kim, E. Boyd, Michael Connor	2001	28
17	Prevalence of the Fragile X Syndrome in an Institution for the Mentally Handicapped The British Journal of Psychiatry ·David A. Primrose, Rabia El-Matmati, E. Boyd, Christine Gosden, Marjorie Newton	1986	26
18	Isochromosome for long arm of Y chromosome in patient with Turner's syndrome and sex chromosome mosaicism (45,X-46,XYqi). Journal of Medical Genetics ·M.A. Ferguson‐Smith, E. Boyd, M Ferguson-Smith, Jessica C. Pritchard, A F Yusuf, Brian A. Gray	1969	26
19	Trends in prenatal diagnosis of Down syndrome and other autosomal trisomies in Scotland 1990 to 1994, with associated cytogenetic and epidemiological findings Genetic Epidemiology ·A D Carothers, E. Boyd, Gordon Lowther, Peter Ellis, D A Couzin, M.J.W. Faed, A. Robb	1999	25
20	Familial Wolf-Hirschhorn syndrome resulting from a cryptic translocation: a clinical and molecular study. Journal of Medical Genetics ·Evan Reid, Norma Morrison, L Barron, E. Boyd, Alexander Cooke, D W Fielding, John Tolmie	1996	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 1.3k 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.

Explore authors with similar magnitude of impact

E. Boyd

Impact in

Papers in i

In The Last Decade

E. Boyd

Peers

Countries citing papers authored by E. Boyd

Fields of papers citing papers by E. Boyd

All Works

About E. Boyd

Explore authors with similar magnitude of impact

Papers in