M. Seabright

6.7k total citations · 2 hit papers
29 papers, 5.6k citations indexed

About

M. Seabright is a scholar working on Genetics, Plant Science and Molecular Biology. According to data from OpenAlex, M. Seabright has authored 29 papers receiving a total of 5.6k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 11 papers in Plant Science and 8 papers in Molecular Biology. Recurrent topics in M. Seabright's work include Genomic variations and chromosomal abnormalities (13 papers), Chromosomal and Genetic Variations (11 papers) and Prenatal Screening and Diagnostics (6 papers). M. Seabright is often cited by papers focused on Genomic variations and chromosomal abnormalities (13 papers), Chromosomal and Genetic Variations (11 papers) and Prenatal Screening and Diagnostics (6 papers). M. Seabright collaborates with scholars based in United Kingdom, United States and Italy. M. Seabright's 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 and has published in prestigious journals such as Nature, The Lancet and Archives of Disease in Childhood.

In The Last Decade

M. Seabright

29 papers receiving 5.1k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

A RAPID BANDING TECHNIQUE FOR HUMAN CHROMOSOMES

1971 4.4k citations M. Seabright The Lancet profile →
The use of proteolytic enzymes for the mapping of structural rearrangements in the chromosomes of man

1972 393 citations M. Seabright Chromosoma profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
M. Seabright United Kingdom	16	2.7k	2.2k	1.7k	695	645	29	5.6k
L. Zech Sweden	32	2.0k 0.7×	2.3k 1.1×	1.2k 0.7×	906 1.3×	418 0.6×	105	5.5k
David A. Hungerford United States	23	2.2k 0.8×	2.6k 1.2×	1.2k 0.7×	1.1k 1.5×	560 0.9×	52	6.5k
J.L. Hamerton Canada	33	2.8k 1.0×	2.0k 0.9×	1.3k 0.8×	414 0.6×	1.0k 1.6×	134	5.3k
Stanley M. Gartler United States	42	3.3k 1.2×	4.7k 2.1×	751 0.4×	412 0.6×	504 0.8×	133	6.8k
Maimon M. Cohen United States	45	4.0k 1.5×	3.3k 1.5×	725 0.4×	275 0.4×	899 1.4×	212	8.0k
T. Caspersson Sweden	26	1.6k 0.6×	2.0k 0.9×	1.0k 0.6×	340 0.5×	360 0.6×	59	4.1k
Stephen T. Reeders United States	37	2.9k 1.1×	2.9k 1.3×	849 0.5×	468 0.7×	412 0.6×	83	5.7k
D.G. Harnden United Kingdom	33	1.6k 0.6×	2.5k 1.1×	434 0.3×	400 0.6×	454 0.7×	90	4.8k
James German United States	42	1.8k 0.7×	5.7k 2.6×	1.1k 0.7×	442 0.6×	568 0.9×	113	7.9k
Verne M. Chapman United States	49	4.1k 1.5×	5.7k 2.6×	996 0.6×	198 0.3×	659 1.0×	165	8.3k

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 of co-authors of M. Seabright

This figure shows the co-authorship network connecting the top 25 collaborators of M. Seabright. A scholar is included among the top collaborators of M. Seabright based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with M. Seabright. M. Seabright is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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

20 of 20 papers shown

1.

Fitchett, M, et al.. (1987). Chromosome abnormalities involving band 13q14 in hematologic malignancies. Cancer Genetics and Cytogenetics. 24(1). 143–150. 80 indexed citations

2.

Dennis, N R, et al.. (1986). Chromosome abnormalities in pupils attending ESN/M schools.. Archives of Disease in Childhood. 61(3). 223–226. 19 indexed citations

3.

Madan, K., M. Seabright, R H Lindenbaum, & Martin Bobrow. (1984). Paracentric inversions in man.. Journal of Medical Genetics. 21(6). 407–412. 39 indexed citations

4.

Mufti, G J, Terry J. Hamblin, & M. Seabright. (1982). Acute transformation of a myeloproliferative state in sideroblastic anaemia with abnormal karyotype.. Journal of Medical Genetics. 19(6). 478–478. 6 indexed citations

5.

Seabright, M., N. Gregson, & M.E. Johnson. (1980). A familial polymorphic variant of chromosome 5.. Journal of Medical Genetics. 17(6). 444–446. 4 indexed citations

6.

Seabright, M., N. Gregson, M.M. Aronson, A.E. Greene, & L.L. Coriell. (1979). Recombinant chromosome 13 with a duplication of the short arm. Cytogenetic and Genome Research. 23(4). 281–281. 2 indexed citations

7.

Seabright, M.. (1979). The Eukaryotic Chromosome. Journal of Medical Genetics. 16(3). 244–244. 46 indexed citations

8.

Seabright, M., et al.. (1979). Silver staining of nucleolar organizer regions in the domestic cat, <i>Felis catus</i>. Cytogenetic and Genome Research. 24(4). 245–247. 4 indexed citations

9.

Seabright, M., et al.. (1978). Rearrangements involving four chromosomes in a child with congenital abnormalities. Cytogenetic and Genome Research. 20(1-6). 150–154. 15 indexed citations

10.

Seabright, M., et al.. (1978). Cytogenetic Findings in 108 Cases of Chronic Myeloid Leukemia. Clinical Genetics. 14(5). 308–309. 12 indexed citations

11.

Seabright, M., et al.. (1978). A further case of a 22;22 Robertsonian translocation associated with recurrent abortions. Human Genetics. 41(3). 359–361. 13 indexed citations

12.

Seabright, M., et al.. (1977). Two cases of trisomy 21 and one XXY case with atypical clinical features. Human Genetics. 38(2). 239–244. 2 indexed citations

13.

Seabright, M., et al.. (1976). Trisomy 9 associated with an enlarged 9qh segment in a liveborn. Human Genetics. 34(3). 323–325. 30 indexed citations

14.

Seabright, M., Robert C. Miller, A.E. Greene, & L.L. Coriell. (1975). A (4;21) translocation, unbalanced, 46 chromosomes. Cytogenetic and Genome Research. 14(2). 152–153. 1 indexed citations

15.

Cooke, Patricia, M. Seabright, & Margaret Wheeler. (1975). The differential distribution of X-ray induced chromosome lesions in trypsin-banded preparations from human subjects. Human Genetics. 28(3). 221–231. 34 indexed citations

16.

Seabright, M., Patricia Cooke, & Margaret Wheeler. (1975). Variation in trypsin banding at different stages of contraction in human chromosomes and the definition, by measurement, of the ?average? karyotype. Human Genetics. 29(1). 35–40. 5 indexed citations

17.

Seabright, M., et al.. (1975). A family with an inherited translocation involving the no. 4/no. 21 chromosomes.. Journal of Medical Genetics. 12(4). 408–411. 13 indexed citations

18.

Seabright, M.. (1973). High resolution studies on the pattern of induced exchanges in the human karyotype. Chromosoma. 40(4). 333–346. 111 indexed citations

19.

Seabright, M.. (1972). HUMAN CHROMOSOME BANDING. The Lancet. 299(7757). 967–967. 21 indexed citations

20.

Seabright, M.. (1971). A RAPID BANDING TECHNIQUE FOR HUMAN CHROMOSOMES. The Lancet. 298(7731). 971–972. 4422 indexed citations breakdown →

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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