Denise Perry
Impact in
- Genetics top 10%
- Genomics and Rare Diseases
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 12
- Genomics and Rare Diseases 7
- Genomic variations and chromosomal abnormalities 6
- BRCA gene mutations in cancer 3
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 1
- Genetics and Neurodevelopmental Disorders 1
- Co-authors
- Douglas L. Kelley (1 shared paper)Roxanne Parrott (1 shared paper)Judee K. Burgoon (1 shared paper)Joseph B. Walther (1 shared paper)Beth A. Le Poire (1 shared paper)Ashley N. Tomlinson (2 shared papers)Barbara A. Bernhardt (2 shared papers)Myra I. Roche (2 shared papers)
- Journals
- Molecular Case Studies (1 paper)Alzheimer s & Dementia Translational Research & Clinical Interventions (1 paper)Journal of Empirical Research on Human Research Ethics (1 paper)Journal of Social and Personal Relationships (1 paper)Annals of Human Genetics (1 paper)
- Partner nations
- United StatesBelgiumDemocratic Republic of the Congo
In The Last Decade
Denise Perry
17 papers receiving 525 citations
Peers
Comparison fields: 5 of 80
- Genetics 230
- Medical Terminology 1
- Information Systems and Management 29
- Public Health, Environmental and Occupational Health 106
- Communication 20
Countries citing papers authored by Denise Perry
This map shows the geographic impact of Denise Perry'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 Denise Perry with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Denise Perry more than expected).
Fields of papers citing papers by Denise Perry
This network shows the impact of papers produced by Denise Perry. 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 Denise Perry. The network helps show where Denise Perry may publish in the future.
Co-authors
The 25 scholars most cited alongside Denise Perry, 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 | 1989 | 135 | |
| 2 | 2015 | 106 | |
| 3 | 2015 | 79 | |
| 4 | 2015 | 43 | |
| 5 | 2018 | 41 | |
| 6 | 2016 | 39 | |
| 7 | 2017 | 33 | |
| 8 | 2020 | 25 | |
| 9 | 2018 | 11 | |
| 10 | 2020 | 9 | |
| 11 | 2018 | 7 | |
| 12 | 2023 | 4 | |
| 13 | 2023 | 2 | |
| 14 | 2021 | 2 | |
| 15 | 2022 | 2 | |
| 16 | 2024 | 1 | |
| 17 | 2022 | 1 | |
| 18 | 2025 | 0 | |
| 19 | ADT Nurses Can Help Ease Bed Constraints, Patient Volumes. | 2017 | 0 |
About Denise Perry
Denise Perry is a scholar working on Genetics, Molecular Biology, General Health Professions, Public Health, Environmental and Occupational Health and Surgery, having authored 19 papers that have together received 540 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (7 papers), Genomic variations and chromosomal abnormalities (6 papers), BRCA gene mutations in cancer (3 papers), Ethics in Clinical Research (3 papers), Ethics in medical practice (2 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (1 paper), Attachment and Relationship Dynamics (1 paper) and Genetics and Neurodevelopmental Disorders (1 paper). The work is most often cited by research in Genetics (230 citations), Medical Terminology (1 citation), Information Systems and Management (29 citations), Public Health, Environmental and Occupational Health (106 citations) and Communication (20 citations). Denise Perry has collaborated with scholars based in United States, Belgium and Democratic Republic of the Congo. Frequent co-authors include Douglas L. Kelley, Roxanne Parrott, Judee K. Burgoon, Joseph B. Walther, Beth A. Le Poire, Ashley N. Tomlinson, Barbara A. Bernhardt, Myra I. Roche, Debra Skinner and Sarah Scollon. Their work appears in journals such as Molecular Case Studies, Alzheimer s & Dementia Translational Research & Clinical Interventions, Journal of Empirical Research on Human Research Ethics, Journal of Social and Personal Relationships and Annals of Human 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.