Catherine E. Cottrell
Impact in
- Cancer Research top 5%
- Cancer Genomics and Diagnostics
- Genetics top 10%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Glioma Diagnosis and Treatment
Papers in
-
- RNA modifications and cancer 6
- Genetics 22
- Genomics and Rare Diseases 14
- Glioma Diagnosis and Treatment 11
- Genomic variations and chromosomal abnormalities 6
- Co-authors
- Eric J. Duncavage (7 shared papers)Christina M. Lockwood (5 shared papers)John D. Pfeifer (8 shared papers)Ian S. Hagemann (5 shared papers)Jonathan W. Heusel (6 shared papers)Andrew J. Bredemeyer (3 shared papers)Haley Abel (4 shared papers)Samantha N. McNulty (5 shared papers)
- Journals
- Molecular Case Studies (8 papers)Journal of Molecular Diagnostics (6 papers)Inorganic Chemistry (3 papers)Genes Chromosomes and Cancer (3 papers)European Journal of Medical Genetics (2 papers)
- Partner nations
- United StatesCanadaGermany
In The Last Decade
Catherine E. Cottrell
62 papers receiving 1.0k citations
Peers
Comparison fields: 5 of 89
- Cancer Research 389
- Genetics 295
- Pathology and Forensic Medicine 175
- Pulmonary and Respiratory Medicine 316
- Genetics 99
Countries citing papers authored by Catherine E. Cottrell
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
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.
All Works
Showing the 20 most-cited of 69 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2014 | 172 | |
| 2 | 2018 | 66 | |
| 3 | 2015 | 56 | |
| 4 | 2011 | 46 | |
| 5 | 2014 | 46 | |
| 6 | 2013 | 39 | |
| 7 | 2017 | 34 | |
| 8 | 2022 | 31 | |
| 9 | 2015 | 29 | |
| 10 | 2016 | 29 | |
| 11 | 2015 | 27 | |
| 12 | 2011 | 26 | |
| 13 | 2016 | 25 | |
| 14 | 2018 | 24 | |
| 15 | 2017 | 23 | |
| 16 | 2019 | 23 | |
| 17 | 2018 | 23 | |
| 18 | 2020 | 19 | |
| 19 | 1972 | 19 | |
| 20 | 1972 | 18 |
About Catherine E. Cottrell
Catherine E. Cottrell is a scholar working on Molecular Biology, Genetics, Cancer Research, Genetics and Pulmonary and Respiratory Medicine, having authored 69 papers that have together received 1.1k indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (18 papers), Genomics and Rare Diseases (14 papers), Glioma Diagnosis and Treatment (11 papers), Vascular Malformations and Hemangiomas (7 papers), RNA modifications and cancer (6 papers), Genomic variations and chromosomal abnormalities (6 papers), Lung Cancer Treatments and Mutations (6 papers) and Sarcoma Diagnosis and Treatment (5 papers). The work is most often cited by research in Cancer Research (389 citations), Genetics (295 citations), Pathology and Forensic Medicine (175 citations), Pulmonary and Respiratory Medicine (316 citations) and Genetics (99 citations). Catherine E. Cottrell has collaborated with scholars based in United States, Canada and Germany. Frequent co-authors include Eric J. Duncavage, Christina M. Lockwood, John D. Pfeifer, Ian S. Hagemann, Jonathan W. Heusel, Andrew J. Bredemeyer, Haley Abel, Samantha N. McNulty, Ramaswamy Govindan and Rakesh Nagarajan. Their work appears in journals such as Molecular Case Studies, Journal of Molecular Diagnostics, Inorganic Chemistry, Genes Chromosomes and Cancer and European Journal of Medical 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.