Charlotte G. Cole

18.3k total citations · 3 hit papers
33 papers, 5.0k citations indexed

About

Charlotte G. Cole is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Charlotte G. Cole has authored 33 papers receiving a total of 5.0k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 13 papers in Genetics and 9 papers in Cancer Research. Recurrent topics in Charlotte G. Cole's work include Cancer Genomics and Diagnostics (9 papers), Genomics and Rare Diseases (7 papers) and Muscle Physiology and Disorders (5 papers). Charlotte G. Cole is often cited by papers focused on Cancer Genomics and Diagnostics (9 papers), Genomics and Rare Diseases (7 papers) and Muscle Physiology and Disorders (5 papers). Charlotte G. Cole collaborates with scholars based in United Kingdom, United States and Italy. Charlotte G. Cole's co-authors include Simon Forbes, Sally Bamford, Sari Ward, Zbysław Sońdka, Nidhi Bindal, Chai Yin Kok, Mingming Jia, David Beare, Peter J. Campbell and Tisham De and has published in prestigious journals such as Nucleic Acids Research, Nature reviews. Cancer and Cancer Research.

In The Last Decade

Charlotte G. Cole

32 papers receiving 4.9k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

COSMIC: exploring the world's knowledge of somatic mutations in human cancer

2014 1.7k citations Simon Forbes, David Beare et al. Nucleic Acids Research profile →
COSMIC: somatic cancer genetics at high-resolution

2016 1.3k citations Simon Forbes, David Beare et al. Nucleic Acids Research profile →
The COSMIC Cancer Gene Census: describing genetic dysfunction across all human cancers

2018 875 citations Zbysław Sońdka, Sally Bamford et al. Nature reviews. Cancer profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Charlotte G. Cole United Kingdom	18	3.5k	1.9k	1.0k	850	697	33	5.0k
David Beare United Kingdom	21	4.2k 1.2×	2.2k 1.2×	1.3k 1.3×	963 1.1×	813 1.2×	38	6.1k
Elisabeth Dawson United Kingdom	17	2.8k 0.8×	1.4k 0.8×	1.1k 1.0×	971 1.1×	599 0.9×	35	4.4k
Jon W. Teague United Kingdom	15	3.1k 0.9×	1.7k 0.9×	1.2k 1.2×	782 0.9×	698 1.0×	24	4.5k
Cyriac Kandoth United States	14	3.4k 1.0×	2.3k 1.2×	1.4k 1.4×	636 0.7×	784 1.1×	27	5.3k
Mingming Jia China	12	3.7k 1.1×	2.1k 1.1×	1.5k 1.5×	840 1.0×	896 1.3×	19	5.6k
Steven E. Schumacher United States	14	3.0k 0.9×	2.2k 1.2×	1.1k 1.1×	761 0.9×	1.1k 1.6×	16	4.8k
Sari Ward United Kingdom	5	2.7k 0.8×	1.6k 0.9×	888 0.9×	591 0.7×	595 0.9×	9	3.9k
Maija Wolf Finland	28	2.4k 0.7×	1.1k 0.6×	739 0.7×	832 1.0×	647 0.9×	45	3.6k
Kerry Fenwick United Kingdom	38	2.8k 0.8×	1.9k 1.0×	2.2k 2.1×	850 1.0×	1.1k 1.5×	60	4.9k
Mark D.M. Leiserson United States	15	3.1k 0.9×	1.8k 1.0×	1.2k 1.2×	534 0.6×	630 0.9×	33	4.6k

Countries citing papers authored by Charlotte G. Cole

Since Specialization

Citations

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

Fields of papers citing papers by Charlotte G. Cole

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Charlotte G. Cole. 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 Charlotte G. Cole. The network helps show where Charlotte G. Cole may publish in the future.

Co-authorship network of co-authors of Charlotte G. Cole

This figure shows the co-authorship network connecting the top 25 collaborators of Charlotte G. Cole. A scholar is included among the top collaborators of Charlotte G. Cole 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 Charlotte G. Cole. Charlotte G. Cole 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

Sońdka, Zbysław, Sally Bamford, Charlotte G. Cole, et al.. (2018). The COSMIC Cancer Gene Census: describing genetic dysfunction across all human cancers. Nature reviews. Cancer. 18(11). 696–705. 875 indexed citations breakdown →

Forbes, Simon, David Beare, Harry Boutselakis, et al.. (2016). COSMIC: somatic cancer genetics at high-resolution. Nucleic Acids Research. 45(D1). D777–D783. 1291 indexed citations breakdown →

Forbes, Simon, David Beare, Prasad Gunasekaran, et al.. (2014). COSMIC: exploring the world's knowledge of somatic mutations in human cancer. Nucleic Acids Research. 43(D1). D805–D811. 1693 indexed citations breakdown →

Bindal, Nidhi, Simon Forbes, David Beare, et al.. (2011). COSMIC: the catalogue of somatic mutations in cancer. Genome biology. 12(S1). 81 indexed citations

Shepherd, Rebecca, Simon Forbes, David Beare, et al.. (2011). Data mining using the Catalogue of Somatic Mutations in Cancer BioMart. Database. 2011(0). bar018–bar018. 35 indexed citations

Forbes, Simon, Nidhi Bindal, Sally Bamford, et al.. (2010). Abstract 93: COSMIC: The catalogue of somatic mutations in cancer receives full genome variant annotations. Cancer Research. 70(8_Supplement). 93–93. 1 indexed citations

Forbes, Simon, Nidhi Bindal, Sally Bamford, et al.. (2009). COSMIC (the Catalogue of Somatic Mutations in Cancer): a resource to investigate acquired mutations in human cancer. Nucleic Acids Research. 38(suppl_1). D652–D657. 417 indexed citations

Dunham, Ian, Charlotte G. Cole, Joan Shaw, et al.. (2004). Novel microsatellite markers and single nucleotide polymorphisms refine the tylosis with oesophageal cancer ( TOC ) minimal region on 17q25 to 42.5�kb: sequencing does not identify the causative gene. Human Genetics. 114(6). 534–540. 27 indexed citations

Collins, John, Carol A. Edwards, Matthew P. Davis, et al.. (2004). A genome annotation-driven approach to cloning the human ORFeome. Genome biology. 5(10). R84–R84. 32 indexed citations

10.

Coffey, Alison J., Simon G. Gregory, & Charlotte G. Cole. (2003). Alu-PCR Fingerprinting of YACs. Humana Press eBooks. 97–114.

11.

Cole, Charlotte G., John Collins, & Ian Dunham. (2003). YAC Library Screening I: Preparation of Hybridization Filters and PCR Pools. Humana Press eBooks. 23–32. 1 indexed citations

12.

Collins, John, Charlotte G. Cole, Luc J Smink, et al.. (2002). Reevaluating Human Gene Annotation: A Second-Generation Analysis of Chromosome 22. Genome Research. 13(1). 27–36. 60 indexed citations

13.

Cole, Charlotte G., et al.. (1998). Fine-Mapping, Genomic Organization, and Transcript Analysis of the Human Ubiquitin-Conjugating Enzyme Gene UBE2L3. Genomics. 51(1). 124–127. 18 indexed citations

14.

Forbes, Simon, Michael P. Richardson, Alison J. Coffey, et al.. (1996). Refined Mapping and YAC Contig Construction of the X-Linked Cleft Palate and Ankyloglossia Locus (CPX) Including the Proximal X–Y Homology Breakpoint within Xq21.3. Genomics. 31(1). 36–43. 26 indexed citations

15.

Hafezparast, Majid, Charlotte G. Cole, Gagandeep Kaur, R. S. Athwal, & Penny A. Jeggo. (1994). An extended panel of hamster-human hybrids for chromosome 2q. Somatic Cell and Molecular Genetics. 20(6). 541–548. 3 indexed citations

16.

Cole, Charlotte G., Ketan Patel, Janet Shipley, et al.. (1992). Identification of region-specific yeast artificial chromosomes using pools of Alu element-mediated polymerase chain reaction probes labeled via linear amplification. Genomics. 14(4). 931–938. 6 indexed citations

17.

Cole, Charlotte G., Ian Dunham, Alison J. Coffey, et al.. (1992). A random STS strategy for construction of YAC contigs spanning defined chromosomal regions. Genomics. 14(2). 256–262. 9 indexed citations

18.

Cole, Charlotte G., Peter N. Goodfellow, Martin Bobrow, & D. R. Bentley. (1991). Generation of novel sequence tagged sites (STSs) from discrete chromosomal regions using Alu-PCR. Genomics. 10(3). 816–826. 55 indexed citations

19.

Hart, K, Stephen Abbs, Martin C. Wapenaar, et al.. (1989). Molecular deletions in the Duchenne/Becker muscular dystrophy gene. Clinical Genetics. 35(4). 251–260. 8 indexed citations

20.

Walker, A.P., K Hart, Charlotte G. Cole, et al.. (1986). Linkage studies in Duchenne and Becker muscular dystrophies.. Journal of Medical Genetics. 23(6). 538–547. 14 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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