M.V. Bell

1.3k total citations
15 papers, 1.1k citations indexed

About

M.V. Bell is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, M.V. Bell has authored 15 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 9 papers in Genetics and 2 papers in Surgery. Recurrent topics in M.V. Bell's work include Genetics and Neurodevelopmental Disorders (9 papers), Glycosylation and Glycoproteins Research (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). M.V. Bell is often cited by papers focused on Genetics and Neurodevelopmental Disorders (9 papers), Glycosylation and Glycoproteins Research (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). M.V. Bell collaborates with scholars based in United Kingdom, United States and India. M.V. Bell's co-authors include David G. Jackson, J I Bell, Gavin Screaton, Adrian R. Krainer, Magdalena Plebanski, Javier F. Cáceres, Akila Mayeda, Mark Patterson, Ruth N. MacKinnon and Mark C. Hirst and has published in prestigious journals such as Science, Cell and Nucleic Acids Research.

In The Last Decade

M.V. Bell

15 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
M.V. Bell United Kingdom	13	790	482	192	164	96	15	1.1k
Ellen Magenis United States	18	694 0.9×	815 1.7×	59 0.3×	44 0.3×	101 1.1×	31	1.4k
David C. Ward United States	15	805 1.0×	267 0.6×	67 0.3×	51 0.3×	120 1.3×	19	1.3k
Deborah Shears United Kingdom	10	611 0.8×	532 1.1×	130 0.7×	37 0.2×	69 0.7×	22	957
David B. Everman United States	20	657 0.8×	466 1.0×	84 0.4×	49 0.3×	51 0.5×	39	1.1k
Nandita Quaderi Italy	12	655 0.8×	387 0.8×	86 0.4×	88 0.5×	58 0.6×	18	849
Kristel De Boulle Belgium	15	1.2k 1.5×	1.2k 2.6×	198 1.0×	575 3.5×	220 2.3×	22	1.9k
Fiona Blanco‐Kelly Spain	23	1.3k 1.6×	358 0.7×	121 0.6×	33 0.2×	132 1.4×	70	1.6k
Maria Guida Boavida Portugal	15	697 0.9×	233 0.5×	148 0.8×	25 0.2×	86 0.9×	37	1.1k
Louise J. Campbell United Kingdom	17	1.4k 1.7×	430 0.9×	114 0.6×	103 0.6×	219 2.3×	33	1.7k

Countries citing papers authored by M.V. Bell

Since Specialization

Citations

This map shows the geographic impact of M.V. Bell'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.V. Bell with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M.V. Bell more than expected).

Fields of papers citing papers by M.V. Bell

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M.V. Bell. 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.V. Bell. The network helps show where M.V. Bell may publish in the future.

Co-authorship network of co-authors of M.V. Bell

This figure shows the co-authorship network connecting the top 25 collaborators of M.V. Bell. A scholar is included among the top collaborators of M.V. Bell 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.V. Bell. M.V. Bell is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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15 of 15 papers shown

Zarn, Jürg A., David G. Jackson, M.V. Bell, et al.. (1995). The small cell lung cancer antigen cluster-4 and the leukocyte antigen CD24 are allelic isoforms of the same gene (CD24) on chromosome band 6q21. Cytogenetic and Genome Research. 70(1-2). 119–125. 26 indexed citations

Screaton, Gavin, Javier F. Cáceres, Akila Mayeda, et al.. (1995). Identification and characterization of three members of the human SR family of pre-mRNA splicing factors.. The EMBO Journal. 14(17). 4336–4349. 254 indexed citations

Screaton, Gavin, M.V. Bell, J I Bell, & David G. Jackson. (1993). The identification of a new alternative exon with highly restricted tissue expression in transcripts encoding the mouse Pgp-1 (CD44) homing receptor. Comparison of all 10 variable exons between mouse, human, and rat. Journal of Biological Chemistry. 268(17). 12235–12238. 207 indexed citations

Bell, M.V., Mark C. Hirst, Yutaka Nakahori, et al.. (1991). Physical mapping across the fragile X: Hypermethylation and clinical expression of the fragile X syndrome. Cell. 64(4). 861–866. 287 indexed citations

Hirst, Mark C., M.V. Bell, Ruth N. MacKinnon, et al.. (1991). Mapping of a cerebellar degeneration related protein and DXS304 around the fragile site. American Journal of Medical Genetics. 38(2-3). 354–356. 7 indexed citations

Hirst, Mark C., Katrina Rack, Yutaka Nakahori, et al.. (1991). A YAC contig across the fragile X site defines the region of fragility. Nucleic Acids Research. 19(12). 3283–3288. 35 indexed citations

Hirst, Mark C., A. Roche, Tracey Flint, et al.. (1991). Linear order of new and established DNA markers around the fragile site at Xq27.3. Genomics. 10(1). 243–249. 23 indexed citations

Glass, Ian A., Lindsay A. Pirrit, Elizabeth M. White, et al.. (1991). Linkage analysis in the fragile X syndrome using multiple distal Xq polymorphic DNA markers. American Journal of Medical Genetics. 38(2-3). 298–304. 2 indexed citations

MacKinnon, Ruth N., Mark C. Hirst, M.V. Bell, et al.. (1990). Microdissection of the fragile X region.. PubMed. 47(2). 181–6. 32 indexed citations

10.

Bell, M.V., Mark Patterson, Huw Dorkins, & Kay E. Davies. (1989). Physical mapping of DXS134 close to the DXS52 locus. Human Genetics. 82(1). 27–30. 13 indexed citations

11.

Bell, M.V., et al.. (1989). MASA syndrome: further clinical delineation and chromosomal localisation. Human Genetics. 82(4). 367–70. 55 indexed citations

12.

Suthers, G K, David F. Callen, V.J. Hyland, et al.. (1989). A New DNA Marker Tightly Linked to the Fragile X Locus ( FRAXA ). Science. 246(4935). 1298–1300. 54 indexed citations

13.

Patterson, Mark, M.V. Bell, J.F. Bloomfield, et al.. (1989). Genetic and physical mapping of a novel region close to the fragile X site on the human X chromosome. Genomics. 4(4). 570–578. 37 indexed citations

14.

Bell, M.V., J.F. Bloomfield, Michael J. McKinley, et al.. (1989). Physical linkage of a GABAA receptor subunit gene to the DXS374 locus in human Xq28.. PubMed. 45(6). 883–8. 35 indexed citations

15.

Davies, K. E., Mark Patterson, Susan Kenwrick, et al.. (1988). Fine mapping of glycerol kinase deficiency and congenital adrenal hypoplasia within Xp21 on the short arm of the human X chromosome. American Journal of Medical Genetics. 29(3). 557–564. 21 indexed citations

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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