James O’Leary
Impact in
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- BRCA gene mutations in cancer
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
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- Ethics in Clinical Research
Papers in
- Genetics 6
- BRCA gene mutations in cancer 6
- Genomics and Rare Diseases 2
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- Prenatal Screening and Diagnostics 3
- Co-authors
- Sharon F. Terry (5 shared papers)Joshua L. Deignan (1 shared paper)Lynn Wein Bush (1 shared paper)David B. Flannery (1 shared paper)Robert G. Best (1 shared paper)Joan Scott (4 shared papers)Karen L. David (1 shared paper)Ingrid A. Holm (1 shared paper)
- Journals
- Genetics in Medicine (2 papers)Progress in community health partnerships (1 paper)Science Translational Medicine (1 paper)American Journal of Medical Genetics Part C Seminars in Medical Genetics (1 paper)Public Health Genomics (1 paper)
- Partner nations
- United StatesHungaryGermany
In The Last Decade
James O’Leary
13 papers receiving 274 citations
Peers
Comparison fields: 5 of 64
- Genetics 148
- Public Health, Environmental and Occupational Health 57
- General Health Professions 36
- Pediatrics, Perinatology and Child Health 25
- Neuropsychology and Physiological Psychology 2
Countries citing papers authored by James O’Leary
This map shows the geographic impact of James O’Leary'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 James O’Leary with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites James O’Leary more than expected).
Fields of papers citing papers by James O’Leary
This network shows the impact of papers produced by James O’Leary. 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 James O’Leary. The network helps show where James O’Leary may publish in the future.
Co-authors
The 25 scholars most cited alongside James O’Leary, 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 | 2018 | 88 | |
| 2 | 2015 | 39 | |
| 3 | 2013 | 31 | |
| 4 | 2008 | 27 | |
| 5 | 2013 | 20 | |
| 6 | 2011 | 19 | |
| 7 | Follow-up services after an emergency department visit for substance abuse. | 2007 | 16 |
| 8 | 2014 | 14 | |
| 9 | 2012 | 8 | |
| 10 | 2011 | 8 | |
| 11 | 2013 | 4 | |
| 12 | 2011 | 4 | |
| 13 | 2011 | 3 |
About James O’Leary
James O’Leary is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Public Health, Environmental and Occupational Health, General Health Professions and Health Information Management, having authored 13 papers that have together received 281 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (6 papers), Prenatal Screening and Diagnostics (3 papers), Genomics and Rare Diseases (2 papers), Family and Disability Support Research (1 paper), Primary Care and Health Outcomes (1 paper), Health and Medical Research Impacts (1 paper), Biosimilars and Bioanalytical Methods (1 paper) and Substance Abuse Treatment and Outcomes (1 paper). The work is most often cited by research in Genetics (148 citations), Public Health, Environmental and Occupational Health (57 citations), General Health Professions (36 citations), Pediatrics, Perinatology and Child Health (25 citations) and Neuropsychology and Physiological Psychology (2 citations). James O’Leary has collaborated with scholars based in United States, Hungary and Germany. Frequent co-authors include Sharon F. Terry, Joshua L. Deignan, Lynn Wein Bush, David B. Flannery, Robert G. Best, Joan Scott, Karen L. David, Ingrid A. Holm, David T. Miller and Jodi D. Hoffman. Their work appears in journals such as Genetics in Medicine, Progress in community health partnerships, Science Translational Medicine, American Journal of Medical Genetics Part C Seminars in Medical Genetics and Public Health Genomics.
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.