S Cottrell

960 total citations
14 papers, 604 citations indexed

About

S Cottrell is a scholar working on Pathology and Forensic Medicine, Genetics and Oncology. According to data from OpenAlex, S Cottrell has authored 14 papers receiving a total of 604 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Pathology and Forensic Medicine, 6 papers in Genetics and 5 papers in Oncology. Recurrent topics in S Cottrell's work include Genetic factors in colorectal cancer (7 papers), Genetic Syndromes and Imprinting (4 papers) and Colorectal Cancer Treatments and Studies (4 papers). S Cottrell is often cited by papers focused on Genetic factors in colorectal cancer (7 papers), Genetic Syndromes and Imprinting (4 papers) and Colorectal Cancer Treatments and Studies (4 papers). S Cottrell collaborates with scholars based in United Kingdom, United States and Italy. S Cottrell's co-authors include Walter F. Bodmer, D C Bicknell, L Kaklamanis, S V Hodgson, Christina Lich, Angela Barnicoat, Karin Buiting, Bernhard Horsthemke, R K S Phillips and Karen Nugent and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Lancet and Gastroenterology.

In The Last Decade

S Cottrell

14 papers receiving 583 citations

Peers

S Cottrell

PFM

ONCOL

GENET

Joan Shaw United Kingdom

Andreas Laner Germany

Nanna Claij Netherlands

Slavomir Dzieciatkowski United States

Rosa Arribas Spain

Masaaki Nagatake Japan

Helena Zientek Poland

Elke Holinski‐Feder Germany

B. Ponder United Kingdom

Margreethe van Vliet Netherlands

Joan Shaw United Kingdom

S Cottrell

275 ×0.7

PFM

178 ×0.7

ONCOL

218 ×1.0

83 ×0.5

GENET

109 ×0.8

Citations per year, relative to S Cottrell S Cottrell (= 1×) peers Joan Shaw

Countries citing papers authored by S Cottrell

Since Specialization

Citations

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

Fields of papers citing papers by S Cottrell

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of S Cottrell

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

All Works

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14 of 14 papers shown

Secnik, Kristina, et al.. (2006). PDB20 BLOOD GLUCOSE MONITORING RECOMMENDATIONS AND PRACTICES IN PATIENTS WITH TYPE 2 DIABETES: A SURVEY OF HEALTH CARE PROFESSIONALSAND PATIENTS IN THE UK. Value in Health. 9(3). A37–A37. 4 indexed citations

Thompson, Dorothy, A Kriss, S Cottrell, & David Taylor. (1999). Visual evoked potential evidence of albino-like chiasmal misrouting in a patient with Angelman syndrome with no ocular features of albinism. Developmental Medicine & Child Neurology. 41(9). 633–638. 10 indexed citations

Buiting, Karin, Christina Lich, S Cottrell, Angela Barnicoat, & Bernhard Horsthemke. (1999). A 5-kb imprinting center deletion in a family with Angelman syndrome reduces the shortest region of deletion overlap to 880 bp. Human Genetics. 105(6). 665–666. 79 indexed citations

Thompson, Dorothy, A Kriss, S Cottrell, & David Taylor. (1999). Visual evoked potential evidence of albino‐like chiasmal misrouting in a patient with Angelman syndrome with no ocular features of albinism. Developmental Medicine & Child Neurology. 41(9). 633–638. 2 indexed citations

Whitelaw, S, I. Tomlinson, H. J. W. Thomas, et al.. (1997). Clinical and molecular features of the hereditary mixed polyposis syndrome. Gastroenterology. 112(2). 327–334. 100 indexed citations

Chan, Christopher T., Tristan R. McKay, S Cottrell, et al.. (1997). Counselling dilemmas associated with the molecular characterisation of two Angelman syndrome families.. Journal of Medical Genetics. 34(8). 651–655. 5 indexed citations

Nugent, Karen, et al.. (1994). Phenotypic expression in familial adenomatous polyposis: partial prediction by mutation analysis.. Gut. 35(11). 1622–1623. 95 indexed citations

Hodgson, S V, Aman S. Coonar, P.J.V. Hanson, et al.. (1993). Two cases of 5q deletions in patients with familial adenomatous polyposis: possible link with Caroli's disease.. Journal of Medical Genetics. 30(5). 369–375. 48 indexed citations

Cottrell, S, Walter F. Bodmer, D C Bicknell, & L Kaklamanis. (1992). Molecular analysis of APC mutations in familial adenomatous polyposis and sporadic colon carcinomas. The Lancet. 340(8820). 626–630. 191 indexed citations

10.

Cottrell, S & Walter F. Bodmer. (1992). Two Mspl polymorphisms within the APC gene. Human Molecular Genetics. 1(5). 352–352. 17 indexed citations

11.

Hampton, Garret M., S Cottrell, Kevin Howe, et al.. (1992). Yeast artificial chromosomes for the molecular analysis of the familial polyposis APC gene region.. Proceedings of the National Academy of Sciences. 89(17). 8249–8253. 5 indexed citations

12.

Hampton, G. M., S Cottrell, Anthony P. Monaco, et al.. (1991). PHYSICAL MAPPING OF THE APC REGION. The American Journal of Human Genetics. 49. 390–390. 2 indexed citations

13.

Bodmer, Walter F., et al.. (1989). Genetic analysis of colorectal cancer.. PubMed. 20. 49–59. 10 indexed citations

14.

Varesco, Liliana, H. J. W. Thomas, S Cottrell, et al.. (1989). CpG island clones from a deletion encompassing the gene for adenomatous polyposis coli.. Proceedings of the National Academy of Sciences. 86(24). 10118–10122. 36 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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