Sally Cottrell

735 total citations
7 papers, 174 citations indexed

About

Sally Cottrell is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Oncology. According to data from OpenAlex, Sally Cottrell has authored 7 papers receiving a total of 174 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 4 papers in Pathology and Forensic Medicine and 3 papers in Oncology. Recurrent topics in Sally Cottrell's work include Genetic factors in colorectal cancer (4 papers), Cancer Genomics and Diagnostics (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Sally Cottrell is often cited by papers focused on Genetic factors in colorectal cancer (4 papers), Cancer Genomics and Diagnostics (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Sally Cottrell collaborates with scholars based in United Kingdom, Mexico and Germany. Sally Cottrell's co-authors include William D. Foulkes, John Trowsdale, Gordon J. Allan, Walter F. Bodmer, Glen Brice, Rohan Taylor, Steve Jeffery, Sahar Mansour, D. Timothy Bishop and Kristiana Gordon and has published in prestigious journals such as The American Journal of Human Genetics, European Journal of Cancer and Genomics.

In The Last Decade

Sally Cottrell

7 papers receiving 168 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sally Cottrell United Kingdom	6	97	78	68	35	31	7	174
Hiromi O. Shiwaku Japan	5	89 0.9×	106 1.4×	146 2.1×	32 0.9×	30 1.0×	7	248
F. Michiels France	5	120 1.2×	28 0.4×	153 2.3×	19 0.5×	67 2.2×	7	327
Nikhil R. Bhagwat United States	7	71 0.7×	42 0.5×	276 4.1×	33 0.9×	29 0.9×	8	340
N. Lannoy Belgium	10	61 0.6×	66 0.8×	144 2.1×	42 1.2×	75 2.4×	20	303
Daria Carmela Loconte Italy	7	26 0.3×	38 0.5×	101 1.5×	35 1.0×	39 1.3×	13	201
Elsa C. Bik Netherlands	5	91 0.9×	179 2.3×	83 1.2×	33 0.9×	69 2.2×	6	270
George A. R. Wiggins New Zealand	8	64 0.7×	24 0.3×	166 2.4×	23 0.7×	35 1.1×	17	260
Vincent Yeung United States	5	98 1.0×	27 0.3×	206 3.0×	20 0.6×	10 0.3×	14	275
Wiebke Antonopoulos Germany	8	81 0.8×	24 0.3×	107 1.6×	20 0.6×	10 0.3×	11	206
Erica McCoy United States	4	122 1.3×	17 0.2×	257 3.8×	53 1.5×	60 1.9×	4	345

Countries citing papers authored by Sally Cottrell

Since Specialization

Citations

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

Fields of papers citing papers by Sally Cottrell

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sally Cottrell

This figure shows the co-authorship network connecting the top 25 collaborators of Sally Cottrell. A scholar is included among the top collaborators of Sally 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 Sally Cottrell. Sally 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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7 of 7 papers shown

1.

Gordon, Kristiana, Fiona Connell, Glen Brice, et al.. (2012). FLT4/VEGFR3and Milroy Disease: Novel Mutations, a Review of Published Variants and Database Update. Human Mutation. 34(1). 23–31. 54 indexed citations

2.

Buiting, Karin, Bärbel Dittrich, Bernd Dworniczak, et al.. (1999). A 28-kb Deletion Spanning D15S63 (PW71) in Five Families: A Rare Neutral Variant?. The American Journal of Human Genetics. 65(6). 1588–1594. 7 indexed citations

3.

Whitelaw, S, Sally Cottrell, Victoria A. Murday, et al.. (1996). Genetic mapping of hereditary mixed polyposis syndrome to chromosome 6q.. PubMed. 58(4). 770–6. 46 indexed citations

4.

Hall, N. R., Graham R. Taylor, P J Finan, et al.. (1994). Intron splice acceptor site sequence variation in the hereditary non-polyposis colorectal cancer gene hMSH2. European Journal of Cancer. 30(10). 1550–1552. 12 indexed citations

5.

Allan, Gordon J., Sally Cottrell, John Trowsdale, & William D. Foulkes. (1994). Loss of heterozygosity on chromosome 5 in sporadic ovarian carcinoma is a late event and is not associated with mutations in APC at 5q21-22. Human Mutation. 3(3). 283–291. 34 indexed citations

6.

Cottrell, Sally, Huw Thomas, T. Alwyn Jones, et al.. (1993). A Long-Range Restriction Map of Human Chromosome 5q21-q23. Genomics. 17(1). 15–24. 5 indexed citations

7.

Williams, Sarah V., T. Alwyn Jones, Sally Cottrell, et al.. (1991). Fine Mapping of Probes in the Adenomatous Polyposis Coli Region of Chromosome 5 by In Situ Hybridization. Genes Chromosomes and Cancer. 3(5). 382–389. 16 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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