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
-
- Renal and related cancers 3
- Genetics 21
- Genomics and Rare Diseases 15
- Glioma Diagnosis and Treatment 10
- Genomic variations and chromosomal abnormalities 5
- Co-authors
- Christina M. Lockwood (5 shared papers)Ian S. Hagemann (5 shared papers)Eric J. Duncavage (7 shared papers)John D. Pfeifer (8 shared papers)Andrew J. Bredemeyer (4 shared papers)Jonathan W. Heusel (6 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)Genes Chromosomes and Cancer (3 papers)Inorganic Chemistry (3 papers)Neuro-Oncology Advances (2 papers)
- Partner nations
- United StatesCanadaGermany
In The Last Decade
Catherine E. Cottrell
62 papers receiving 1.1k citations
Peers
Comparison fields: 5 of 92
- Cancer Research 308
- Genetics 262
- Genetics 90
- Pulmonary and Respiratory Medicine 264
- Pathology and Forensic Medicine 127
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 71 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2014 | 182 | |
| 2 | 2018 | 69 | |
| 3 | 2015 | 57 | |
| 4 | 2014 | 51 | |
| 5 | 2011 | 50 | |
| 6 | 2013 | 44 | |
| 7 | 2017 | 35 | |
| 8 | 2022 | 34 | |
| 9 | 2015 | 31 | |
| 10 | 2016 | 29 | |
| 11 | 2011 | 28 | |
| 12 | 2015 | 27 | |
| 13 | 2016 | 25 | |
| 14 | 2019 | 24 | |
| 15 | 2018 | 24 | |
| 16 | 2018 | 24 | |
| 17 | 2017 | 23 | |
| 18 | 1972 | 23 | |
| 19 | 2022 | 21 | |
| 20 | 2020 | 20 |
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 71 papers that have together received 1.1k indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (16 papers), Genomics and Rare Diseases (15 papers), Glioma Diagnosis and Treatment (10 papers), Vascular Malformations and Hemangiomas (6 papers), Lung Cancer Treatments and Mutations (6 papers), Sarcoma Diagnosis and Treatment (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Renal and related cancers (3 papers). The work is most often cited by research in Cancer Research (308 citations), Genetics (262 citations), Genetics (90 citations), Pulmonary and Respiratory Medicine (264 citations) and Pathology and Forensic Medicine (127 citations). Catherine E. Cottrell has collaborated with scholars based in United States, Canada and Germany. Frequent co-authors include Christina M. Lockwood, Ian S. Hagemann, Eric J. Duncavage, John D. Pfeifer, Andrew J. Bredemeyer, Jonathan W. Heusel, Haley Abel, Samantha N. McNulty, Ramaswamy Govindan and Rakesh Nagarajan. Their work appears in journals such as Molecular Case Studies, Journal of Molecular Diagnostics, Genes Chromosomes and Cancer, Inorganic Chemistry and Neuro-Oncology Advances.
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.