M. Seabright
Impact in
- Genetics top 0.5%
- Genomic variations and chromosomal abnormalities
- Genetic diversity and population structure
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetic Mapping and Diversity in Plants and Animals
- Chronic Lymphocytic Leukemia Research
- Hematology top 1%
- Acute Myeloid Leukemia Research
Papers in
- Genetics 14
- Genomic variations and chromosomal abnormalities 13
- Chronic Lymphocytic Leukemia Research 2
- Genetics and Neurodevelopmental Disorders 2
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- Chromosomal and Genetic Variations 11
- Co-authors
- A. M. Sincock (1 shared paper)R H Lindenbaum (2 shared papers)M Fitchett (2 shared papers)Mike Griffiths (1 shared paper)David Oscier (1 shared paper)Maj Hultén (1 shared paper)Alan McDermott (1 shared paper)Sarah Mould (3 shared papers)
- Journals
- Journal of Medical Genetics (8 papers)Human Genetics (6 papers)Cytogenetic and Genome Research (5 papers)The Lancet (3 papers)Chromosoma (2 papers)
- Partner nations
- United KingdomUnited StatesTunisia
In The Last Decade
M. Seabright
29 papers receiving 5.1k citations
M. Seabright's Hit Papers
Peers
Comparison fields: 5 of 132
- Genetics 2.7k
- Hematology 695
- Genetics 502
- Plant Science 1.7k
- Developmental Biology 76
Countries citing papers authored by M. Seabright
This map shows the geographic impact of M. Seabright'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 M. Seabright with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M. Seabright more than expected).
Fields of papers citing papers by M. Seabright
This network shows the impact of papers produced by M. Seabright. 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 M. Seabright. The network helps show where M. Seabright may publish in the future.
Co-authors
The 25 scholars most cited alongside M. Seabright, 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 29 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | A RAPID BANDING TECHNIQUE FOR HUMAN CHROMOSOMES Hit paper breakdown → | 1971 | 4422 |
| 2 | The use of proteolytic enzymes for the mapping of structural rearrangements in the chromosomes of man Hit paper breakdown → | 1972 | 393 |
| 3 | 1975 | 156 | |
| 4 | 1973 | 111 | |
| 5 | 1987 | 80 | |
| 6 | 1985 | 57 | |
| 7 | 1979 | 46 | |
| 8 | 1984 | 39 | |
| 9 | 1973 | 39 | |
| 10 | 1975 | 34 | |
| 11 | 1976 | 30 | |
| 12 | 1980 | 25 | |
| 13 | 1981 | 24 | |
| 14 | 1978 | 22 | |
| 15 | 1972 | 21 | |
| 16 | 1986 | 19 | |
| 17 | 1978 | 15 | |
| 18 | 1978 | 13 | |
| 19 | 1975 | 13 | |
| 20 | 1984 | 13 |
About M. Seabright
M. Seabright is a scholar working on Genetics, Plant Science, Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics, having authored 29 papers that have together received 5.6k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (13 papers), Chromosomal and Genetic Variations (11 papers), Prenatal Screening and Diagnostics (6 papers), Genomics and Chromatin Dynamics (4 papers), Fetal and Pediatric Neurological Disorders (3 papers), DNA and Nucleic Acid Chemistry (3 papers), Chronic Lymphocytic Leukemia Research (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). The work is most often cited by research in Genetics (2.7k citations), Hematology (695 citations), Genetics (502 citations), Plant Science (1.7k citations) and Developmental Biology (76 citations). M. Seabright has collaborated with scholars based in United Kingdom, United States and Tunisia. Frequent co-authors include A. M. Sincock, R H Lindenbaum, M Fitchett, Mike Griffiths, David Oscier, Maj Hultén, Alan McDermott, Sarah Mould, Patricia Cooke and Margaret Wheeler. Their work appears in journals such as Journal of Medical Genetics, Human Genetics, Cytogenetic and Genome Research, The Lancet and Chromosoma.
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.