Danielle McKenna
Impact in
- Pharmacology top 10%
- Inflammatory mediators and NSAID effects
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- Osteoarthritis Treatment and Mechanisms
Papers in
- Genetics 10
- BRCA gene mutations in cancer 8
- Genomics and Rare Diseases 2
- Genomic variations and chromosomal abnormalities 2
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- Genetic factors in colorectal cancer 7
- Co-authors
- Jessica M. Long (9 shared papers)Susan M. Domchek (11 shared papers)Kara N. Maxwell (7 shared papers)Katherine L. Nathanson (9 shared papers)Payal D. Shah (5 shared papers)Angela R. Bradbury (5 shared papers)Jacquelyn Powers (6 shared papers)Bryson W. Katona (7 shared papers)
- Journals
- Familial Cancer (2 papers)JCO Precision Oncology (2 papers)Cancer Prevention Research (1 paper)Journal of Clinical Oncology (1 paper)JCO Clinical Cancer Informatics (1 paper)
- Partner nations
- United StatesUnited KingdomNorway
In The Last Decade
Danielle McKenna
13 papers receiving 271 citations
Peers
Comparison fields: 5 of 62
- Pharmacology 143
- Rheumatology 68
- Cancer Research 45
- Genetics 70
- Pathology and Forensic Medicine 34
Countries citing papers authored by Danielle McKenna
This map shows the geographic impact of Danielle McKenna'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 Danielle McKenna with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Danielle McKenna more than expected).
Fields of papers citing papers by Danielle McKenna
This network shows the impact of papers produced by Danielle McKenna. 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 Danielle McKenna. The network helps show where Danielle McKenna may publish in the future.
Co-authors
The 25 scholars most cited alongside Danielle McKenna, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2001 | 160 | |
| 2 | 2019 | 30 | |
| 3 | 2019 | 20 | |
| 4 | 2018 | 19 | |
| 5 | 2018 | 14 | |
| 6 | 2018 | 14 | |
| 7 | 2020 | 12 | |
| 8 | 2024 | 5 | |
| 9 | 2023 | 3 | |
| 10 | 2023 | 1 | |
| 11 | 2010 | 1 | |
| 12 | 2021 | 1 | |
| 13 | 2022 | 1 | |
| 14 | 2023 | 0 | |
| 15 | 2024 | 0 | |
| 16 | 2022 | 0 | |
| 17 | 2018 | 0 |
About Danielle McKenna
Danielle McKenna is a scholar working on Genetics, Pathology and Forensic Medicine, Oncology, Cancer Research and Surgery, having authored 17 papers that have together received 281 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (8 papers), Genetic factors in colorectal cancer (7 papers), Cancer Genomics and Diagnostics (5 papers), Cancer-related Molecular Pathways (3 papers), Colorectal Cancer Screening and Detection (3 papers), Ethics in Clinical Research (2 papers), Genomics and Rare Diseases (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). The work is most often cited by research in Pharmacology (143 citations), Rheumatology (68 citations), Cancer Research (45 citations), Genetics (70 citations) and Pathology and Forensic Medicine (34 citations). Danielle McKenna has collaborated with scholars based in United States, United Kingdom and Norway. Frequent co-authors include Jessica M. Long, Susan M. Domchek, Kara N. Maxwell, Katherine L. Nathanson, Payal D. Shah, Angela R. Bradbury, Jacquelyn Powers, Bryson W. Katona, Jennifer J.D. Morrissette and Anil K. Rustgi. Their work appears in journals such as Familial Cancer, JCO Precision Oncology, Cancer Prevention Research, Journal of Clinical Oncology and JCO Clinical Cancer Informatics.
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.