M. Seabright

6.7k citations
29 papers · 5.6k indexed · 2 hit papers · h-index 16
  • Genetics top 0.5%
    • Genomic variations and chromosomal abnormalities 13
    • Chronic Lymphocytic Leukemia Research 2
    • Genetics and Neurodevelopmental Disorders 2
  • Hematology top 1%
  • Genetics top 2%
    • Genomic variations and chromosomal abnormalities 13
    • Chronic Lymphocytic Leukemia Research 2
    • Genetics and Neurodevelopmental Disorders 2
    • Chromosomal and Genetic Variations 11
    • Prenatal Screening and Diagnostics 6
    • Fetal and Pediatric Neurological Disorders 3
    • Genomics and Chromatin Dynamics 4
    • DNA and Nucleic Acid Chemistry 3

M. Seabright

29 papers receiving 5.1k citations

Hit Papers

The use of proteolytic enzymes for the mapping of structu...393197120261989200710002.0k3.0k4.0k

Peers

M. Seabright
Comparison fields: 5 of 132
  • Genetics 2.7k
  • Hematology 695
  • Genetics 502
  • Plant Science 1.7k
  • Developmental Biology 76
Replace J.L. Hamerton with:
J.L. Hamerton Canada
David A. Hungerford United States
Doris H. Wurster‐Hill United States
L. Zech Sweden
John S. Waye Canada
A. T. Sumner United Kingdom
Maimon M. Cohen United States
Jorge J. Yunis United States
Stephen T. Reeders United States
Ram S. Verma United States
M. Seabright relative to J.L. Hamerton Canada J.L. Hamerton's profile →
Citations per field
00.5×1.5×1.8×
J.L. Hamerton · 1×
Citations per year

Countries citing papers authored by M. Seabright

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network

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.

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

All Works

20 of 20 papers shown
#Work
1 198780
2 198619
3 198439
4 19826
5 19804
6 19792
7 197946
8 19794
9 197815
10 197812
11 197813
12 19772
13 197630
14 19751
15 197534
16 19755
17 197513
18 1973111
19 197221
20
A RAPID BANDING TECHNIQUE FOR HUMAN CHROMOSOMESbreakdown →
19714422

About M. Seabright

M. Seabright is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Plant Science, Genetics and Hematology, 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), DNA and Nucleic Acid Chemistry (3 papers), Fetal and Pediatric Neurological Disorders (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 Italy. 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.

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