J M Varley

2.1k total citations
33 papers, 1.6k citations indexed

About

J M Varley is a scholar working on Molecular Biology, Oncology and Cancer Research. According to data from OpenAlex, J M Varley has authored 33 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 19 papers in Oncology and 8 papers in Cancer Research. Recurrent topics in J M Varley's work include Cancer-related Molecular Pathways (15 papers), Cancer Genomics and Diagnostics (7 papers) and Hedgehog Signaling Pathway Studies (5 papers). J M Varley is often cited by papers focused on Cancer-related Molecular Pathways (15 papers), Cancer Genomics and Diagnostics (7 papers) and Hedgehog Signaling Pathway Studies (5 papers). J M Varley collaborates with scholars based in United Kingdom, United States and Australia. J M Varley's co-authors include Jillian M. Birch, D. Gareth Evans, Anna Kelsey, Louise James, Mary Thorncroft, Gail McGown, RA Walker, K. Tricker, WJ Gullick and Erika L.D. Mitchell and has published in prestigious journals such as Journal of Molecular Biology, Oncogene and Human Molecular Genetics.

In The Last Decade

J M Varley

33 papers receiving 1.5k citations

Peers

J M Varley

ONCOL

GENET

PFM

Christian‐Jacques Larsen France

G L Shen-Ong United States

Frank Hong United States

A. Thomas Look United States

W. F. Benedict United States

Arjan Buijs Netherlands

Tomohiko Taki Japan

Helena Kempski United Kingdom

Peter Scully United States

Yuesheng Jin Sweden

Christian‐Jacques Larsen France

J M Varley

1.6k ×1.8

819 ×1.1

ONCOL

268 ×0.8

297 ×0.9

GENET

207 ×0.9

PFM

Citations per year, relative to J M Varley J M Varley (= 1×) peers Christian‐Jacques Larsen

Countries citing papers authored by J M Varley

Since Specialization

Citations

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

Fields of papers citing papers by J M Varley

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of J M Varley

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

All Works

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20 of 20 papers shown

Warren, C, Louise James, R. T. Ramsden, et al.. (2003). Identification of recurrent regions of chromosome loss and gain in vestibular schwannomas using comparative genomic hybridisation. Journal of Medical Genetics. 40(11). 802–806. 57 indexed citations

Spreadborough, A.R., et al.. (2002). Delayed Chromosome Changes in Gamma-Irradiated Normal and Li-Fraumeni Fibroblasts. Radiation Research. 157(2). 158–165. 16 indexed citations

Varley, J M, Claire Attwooll, Gail McGown, et al.. (2001). Characterization of germline TP53 splicing mutations and their genetic and functional analysis. Oncogene. 20(21). 2647–2654. 46 indexed citations

Spreadborough, A.R., et al.. (2001). The relationship between radiation-induced G1 arrest and chromosome aberrations in Li-Fraumeni fibroblasts with or without germline TP53 mutations. British Journal of Cancer. 85(2). 293–296. 15 indexed citations

Harris, Martin, John D. Coyne, Muhammad Usman Tariq, et al.. (2000). Extraskeletal Myxoid Chondrosarcoma With Neuroendocrine Differentiation. The American Journal of Surgical Pathology. 24(7). 1020–1026. 55 indexed citations

James, Louise, et al.. (2000). Genomic alterations associated with loss of heterozygosity for TP53 in Li-Fraumeni syndrome fibroblasts. British Journal of Cancer. 83(4). 467–472. 17 indexed citations

McGown, Gail, et al.. (1999). Exclusion of the genes CDKN2 and PTEN as causative gene defects in Li–Fraumeni syndrome. British Journal of Cancer. 80(1-2). 9–10. 15 indexed citations

Varley, J M, Gail McGown, Mary Thorncroft, et al.. (1998). A novel TP53 splicing mutation in a Li-Fraumeni syndrome family: a patient with Wilms' tumour is not a mutation carrier. British Journal of Cancer. 78(8). 1081–1083. 17 indexed citations

Varley, J M, Peter Chapman, Gail McGown, et al.. (1998). Genetic and functional studies of a germline TP53 splicing mutation in a Li–Fraumeni-like family. Oncogene. 16(25). 3291–3298. 41 indexed citations

10.

James, Louise, Erika L.D. Mitchell, Lia P. Menasce, & J M Varley. (1997). Comparative genomic hybridisation of ductal carcinoma in situ of the breast: identification of regions of DNA amplification and deletion in common with invasive breast carcinoma. Oncogene. 14(9). 1059–1065. 88 indexed citations

11.

Hey, Y., et al.. (1997). Assignment of C0X6A1 to 6p21 and a pseudogene (C0X6A1P) to 1p31.1 by in situ hybridization and somatic cell hybrids. Cytogenetic and Genome Research. 77(3-4). 167–168. 15 indexed citations

12.

Lomax, Martine E., D M Barnes, R Gilchrist, et al.. (1997). Two functional assays employed to detect an unusual mutation in the oligomerisation domain of p53 in a Li-Fraumeni like family. Oncogene. 14(15). 1869–1874. 54 indexed citations

13.

Varley, J M, D. Gareth Evans, & Jillian M. Birch. (1997). Li-Fraumeni syndrome – a molecular and clinical review. British Journal of Cancer. 76(1). 1–14. 248 indexed citations

14.

Mitchell, Erika L.D., et al.. (1995). Determination of the gene order of the three loci CD2, NGFB, and NRAS at human chromosome band 1p13 and refinement of their localisation at the subband level by fluorescence in situ hybridisation. Cytogenetic and Genome Research. 70(3-4). 183–185. 16 indexed citations

15.

Stack, Michael E, David Jones, Daniel S. Liscia, et al.. (1995). Detailed mapping and loss of heterozygosity analysis suggests a suppressor locus involved in sporadic breast cancer within a distal region of chromosome band 17p13.3. Human Molecular Genetics. 4(11). 2047–2055. 45 indexed citations

16.

Helps, Nicholas R., Susan Adams, William J. Brammar, & J M Varley. (1995). The drosophila melanogaster homologue of the human BBC1 gene is highly expressed during embryogenesis. Gene. 162(2). 245–248. 18 indexed citations

17.

Walker, R A, et al.. (1992). Differential expression of translation-associated genes in benign and malignant human breast tumours. British Journal of Cancer. 65(1). 65–71. 28 indexed citations

18.

Varley, J M, et al.. (1990). Identification and Characterization of a Gene that Controls Colony Morphology and Auto-Aggregation in Escherichia Coli K12. Journal of General Microbiology. 136(3). 455–462. 43 indexed citations

19.

Elvin, Paul, et al.. (1990). A sequence previously identified as metastasis-related encodes an acidic ribosomal phosphoprotein, P2. British Journal of Cancer. 61(1). 83–88. 33 indexed citations

20.

Walker, RA, WJ Gullick, & J M Varley. (1989). An evaluation of immunoreactivity for c-erbB-2 protein as a marker of poor short-term prognosis in breast cancer. British Journal of Cancer. 60(3). 426–429. 88 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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