Catherine E. Cottrell

2.4k citations
80 papers · 1.8k · h-index 24

Impact in

    • Cancer Genomics and Diagnostics
  • Genetics top 5%
    • Genomics and Rare Diseases
    • Glioma Diagnosis and Treatment
    • Genomic variations and chromosomal abnormalities

Papers in

    • Genomics and Rare Diseases 23
    • Glioma Diagnosis and Treatment 11
    • Genomic variations and chromosomal abnormalities 6
    • Genetic and rare skin diseases. 4
    • Cancer Genomics and Diagnostics 17

Catherine E. Cottrell

75 papers receiving 1.7k citations

Peers

Catherine E. Cottrell
Comparison fields: 5 of 76
  • Cancer Research 346
  • Genetics 426
  • Genetics 105
  • Pulmonary and Respiratory Medicine 292
  • Public Health, Environmental and Occupational Health 218
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Citations per field
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Citations per year

Countries citing papers authored by Catherine E. Cottrell

Since Specialization
Citations

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

Fields of papers citing papers by Catherine E. Cottrell

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Catherine E. Cottrell, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Catherine E. Cottrell Line = papers co-authored together Catherine E. Cottrell links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 80 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2012211
2 2014198
3 2013158
4 201577
5 201877
6 201457
7 201754
8 201152
9 201346
10 202240
11 202239
12 201737
13 202135
14 201634
15 201532
16 201530
17 201930
18 202230
19 201129
20 201827

About Catherine E. Cottrell

Catherine E. Cottrell is a scholar working on Genetics, Cancer Research, Genetics, Pulmonary and Respiratory Medicine and Molecular Biology, having authored 80 papers that have together received 1.8k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (23 papers), Cancer Genomics and Diagnostics (17 papers), Glioma Diagnosis and Treatment (11 papers), Vascular Malformations and Hemangiomas (8 papers), Sarcoma Diagnosis and Treatment (7 papers), Genomic variations and chromosomal abnormalities (6 papers), Lung Cancer Treatments and Mutations (4 papers) and Genetic and rare skin diseases. (4 papers). The work is most often cited by research in Cancer Research (346 citations), Genetics (426 citations), Genetics (105 citations), Pulmonary and Respiratory Medicine (292 citations) and Public Health, Environmental and Occupational Health (218 citations). Catherine E. Cottrell has collaborated with scholars based in United States, Germany and Canada. Frequent co-authors include Christina M. Lockwood, Ian S. Hagemann, John D. Pfeifer, Eric James Duncavage, Andrew J. Bredemeyer, Haley Abel, Ramaswamy Govindan, Rakesh Nagarajan, Jonathan W. Heusel and Hussam Al‐Kateb. Their work appears in journals such as Journal of Molecular Diagnostics, Genes Chromosomes and Cancer, The American Journal of Surgical Pathology, Neuro-Oncology Advances and Clinical Genetics.

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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