Jackie Boyle
Impact in
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- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
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- RNA modifications and cancer
- RNA Research and Splicing
- RNA regulation and disease
Papers in
- Genetics 12
- BRCA gene mutations in cancer 6
- Genetics and Neurodevelopmental Disorders 5
- Genomics and Rare Diseases 4
- Genomic variations and chromosomal abnormalities 3
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- Prenatal Screening and Diagnostics 4
- Ethics and Legal Issues in Pediatric Healthcare 3
- Co-authors
- Gillian Turner (4 shared papers)Jozef Gécz (4 shared papers)Ainsley J. Newson (5 shared papers)Louise Christie (5 shared papers)Hilde Van Esch (2 shared papers)Marijke Bauters (1 shared paper)Jean‐Pierre Fryns (1 shared paper)Bruce Bennetts (2 shared papers)
- Journals
- Twin Research and Human Genetics (5 papers)European Journal of Human Genetics (3 papers)Frontiers in Psychiatry (1 paper)International Journal of Environmental Research and Public Health (1 paper)European Journal of Medical Genetics (1 paper)
- Partner nations
- AustraliaUnited KingdomUnited States
In The Last Decade
Jackie Boyle
16 papers receiving 192 citations
Peers
Comparison fields: 5 of 52
- Genetics 88
- Molecular Biology 106
- Clinical Biochemistry 9
- Cognitive Neuroscience 25
- Cell Biology 20
Countries citing papers authored by Jackie Boyle
This map shows the geographic impact of Jackie Boyle'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 Jackie Boyle with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jackie Boyle more than expected).
Fields of papers citing papers by Jackie Boyle
This network shows the impact of papers produced by Jackie Boyle. 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 Jackie Boyle. The network helps show where Jackie Boyle may publish in the future.
Co-authors
The 25 scholars most cited alongside Jackie Boyle, 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 | 2015 | 40 | |
| 2 | 2007 | 37 | |
| 3 | 2009 | 30 | |
| 4 | 2013 | 25 | |
| 5 | 2020 | 14 | |
| 6 | 2023 | 11 | |
| 7 | 2018 | 10 | |
| 8 | 2016 | 8 | |
| 9 | 2007 | 5 | |
| 10 | 2018 | 4 | |
| 11 | 2021 | 4 | |
| 12 | 2020 | 2 | |
| 13 | 2024 | 2 | |
| 14 | 2020 | 2 | |
| 15 | 2023 | 1 | |
| 16 | 2024 | 1 | |
| 17 | 2023 | 0 | |
| 18 | 2021 | 0 |
About Jackie Boyle
Jackie Boyle is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Public Health, Environmental and Occupational Health and Pathology and Forensic Medicine, having authored 18 papers that have together received 196 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (6 papers), Genetics and Neurodevelopmental Disorders (5 papers), Prenatal Screening and Diagnostics (4 papers), Genomics and Rare Diseases (4 papers), Ethics and Legal Issues in Pediatric Healthcare (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Genetic factors in colorectal cancer (2 papers) and Autism Spectrum Disorder Research (2 papers). The work is most often cited by research in Genetics (88 citations), Molecular Biology (106 citations), Clinical Biochemistry (9 citations), Cognitive Neuroscience (25 citations) and Cell Biology (20 citations). Jackie Boyle has collaborated with scholars based in Australia, United Kingdom and United States. Frequent co-authors include Gillian Turner, Jozef Gécz, Ainsley J. Newson, Louise Christie, Hilde Van Esch, Marijke Bauters, Jean‐Pierre Fryns, Bruce Bennetts, Karen Govaerts and Veronica Wiley. Their work appears in journals such as Twin Research and Human Genetics, European Journal of Human Genetics, Frontiers in Psychiatry, International Journal of Environmental Research and Public Health 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.