C. McKeown

1.4k total citations
16 papers, 930 citations indexed

About

C. McKeown is a scholar working on Pathology and Forensic Medicine, Molecular Biology and Surgery. According to data from OpenAlex, C. McKeown has authored 16 papers receiving a total of 930 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Pathology and Forensic Medicine, 5 papers in Molecular Biology and 4 papers in Surgery. Recurrent topics in C. McKeown's work include Genetic factors in colorectal cancer (6 papers), Colorectal Cancer Treatments and Studies (3 papers) and RNA regulation and disease (2 papers). C. McKeown is often cited by papers focused on Genetic factors in colorectal cancer (6 papers), Colorectal Cancer Treatments and Studies (3 papers) and RNA regulation and disease (2 papers). C. McKeown collaborates with scholars based in United Kingdom, United States and India. C. McKeown's co-authors include Fiona MacDonald, Dion Morton, Yvonne Wallis, D. Gareth Evans, Janusz Jankowski, D. S. A. Sanders, Shane McKee, Trevor Cole, Eamonn R. Maher and M. Helen Rajpar and has published in prestigious journals such as Nature, Human Molecular Genetics and British journal of surgery.

In The Last Decade

C. McKeown

16 papers receiving 892 citations

Peers

C. McKeown

PFM

GENET

SURGE

ONCOL

Jonathan P. Park United States

Wim J.M. Van de Ven Belgium

Lana N. Pho United States

Anneke Y. van der Veen Netherlands

Siavash Ghazvini United States

Kees J. Vissers Netherlands

Graham W. Neill United Kingdom

Anna‐Maria Björkqvist Finland

Ulrike Reich Germany

Kumi Nakazaki Japan

Jonathan P. Park United States

C. McKeown

462 ×0.9

203 ×0.6

PFM

267 ×1.1

GENET

88 ×0.5

SURGE

177 ×1.0

ONCOL

Citations per year, relative to C. McKeown C. McKeown (= 1×) peers Jonathan P. Park

Countries citing papers authored by C. McKeown

Since Specialization

Citations

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

Fields of papers citing papers by C. McKeown

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by C. McKeown. 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 C. McKeown. The network helps show where C. McKeown may publish in the future.

Co-authorship network of co-authors of C. McKeown

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

All Works

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16 of 16 papers shown

McKeown, C., U. Thaker, W. D. Cubitt, & Viola Novelli. (2003). Retrospective screening for hepatitis C in a tertiary paediatric referral centre.. PubMed. 6(1). 40–3. 3 indexed citations

Brunetti‐Pierri, Nicola, George F. Gray, C. McKeown, et al.. (2002). X‐linked recessive chondrodysplasia punctata: Spectrum of arylsulfatase E gene mutations and expanded clinical variability. American Journal of Medical Genetics Part A. 117A(2). 164–168. 32 indexed citations

Richards, Frances M., Shane McKee, M. Helen Rajpar, et al.. (1999). Germline E-cadherin Gene (CDH1) Mutations Predispose to Familial Gastric Cancer and Colorectal Cancer. Human Molecular Genetics. 8(4). 607–610. 251 indexed citations

Churchman, Michael, Egle Avizienyte, C. McKeown, et al.. (1999). Germline mutations of the LKB1 (STK11) gene in Peutz-Jeghers patients. Journal of Medical Genetics. 36(5). 365–368. 46 indexed citations

Wallis, Yvonne, Dion Morton, C. McKeown, & Fiona MacDonald. (1999). Molecular analysis of the APC gene in 205 families: extended genotype-phenotype correlations in FAP and evidence for the role of APC amino acid changes in colorectal cancer predisposition. Journal of Medical Genetics. 36(1). 14–20. 133 indexed citations

Morton, Dion, Fiona MacDonald, G Barker, et al.. (1993). Screening practice for familial adenomatous polyposis: the potential for regional registers. British journal of surgery. 80(2). 255–258. 25 indexed citations

Levinsky, R J, Christine Kinnon, Adam Finn, et al.. (1993). Mapping of the X linked form of hyper IgM syndrome (HIGM1). Journal of Medical Genetics. 30(3). 202–205. 15 indexed citations

Feighery, Conleth, Adam Finn, C. McKeown, et al.. (1992). Mapping of the x-linked form of hyper-IgM syndrome (HIGM1) to Xq26 by close linkage to HPRT. Genomics. 14(2). 551–553. 47 indexed citations

Morton, Dion, Fiona MacDonald, John P. Neoptolemos, et al.. (1992). The use of DNA from paraffin wax preserved tissue for predictive diagnosis in familial adenomatous polyposis.. Journal of Medical Genetics. 29(8). 571–573. 6 indexed citations

10.

Morton, Dion, Jonathan Gibson, Fiona MacDonald, et al.. (1992). Role of congenital hypertrophy of the retinal pigment epithelium in the predictive diagnosis of familial adenomatous polyposis. British journal of surgery. 79(7). 689–693. 31 indexed citations

11.

Patton, M A, et al.. (1991). Floating-Harbor syndrome.. Journal of Medical Genetics. 28(3). 201–204. 32 indexed citations

12.

McKeown, C., et al.. (1988). An autosomal dominant multiple pterygium syndrome.. Journal of Medical Genetics. 25(2). 96–103. 28 indexed citations

13.

Wright, Alan F., S.S. Bhattacharya, John Clayton, et al.. (1987). Linkage relationships between X-linked retinitis pigmentosa and nine short-arm markers: exclusion of the disease locus from Xp21 and localization to between DXS7 and DXS14.. PubMed. 41(4). 635–44. 38 indexed citations

14.

McKeown, C., et al.. (1987). Wolf-Hirschhorn locus is distal to D4S10 on short arm of chromosome 4.. Journal of Medical Genetics. 24(7). 410–412. 22 indexed citations

15.

Clayton, John, Alan F. Wright, Marcelle Jay, et al.. (1986). Genetic linkage between X-linked retinitis pigmentosa and DNA probe DXS7 {L1.28}: further linkage data, heterogeneity testing, and risk estimation. Human Genetics. 74(2). 168–171. 18 indexed citations

16.

Bhattacharya, Siladitya, Alan F. Wright, John Clayton, et al.. (1984). Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28. Nature. 309(5965). 253–255. 203 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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