Jack Reilly
Impact in
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- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
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- Cancer Genomics and Diagnostics
Papers in
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- Epigenetics and DNA Methylation 4
- RNA modifications and cancer 2
- Insect Resistance and Genetics 2
- Protein Degradation and Inhibitors 1
- Genetics 6
- Genomics and Rare Diseases 4
- Genomic variations and chromosomal abnormalities 4
- Co-authors
- C.A. Thomas (4 shared papers)Brian I. Carr (1 shared paper)Arthur D. Riggs (1 shared paper)Steven S. Smith (1 shared paper)Carl D. Winberg (1 shared paper)Jennifer Kerkhof (5 shared papers)Bekim Sadiković (5 shared papers)Laila C. Schenkel (3 shared papers)
- Journals
- Journal of Molecular Diagnostics (2 papers)Nature (1 paper)Carcinogenesis (1 paper)FEBS Letters (1 paper)Frontiers in Genetics (1 paper)
- Partner nations
- United StatesCanada
In The Last Decade
Jack Reilly
14 papers receiving 377 citations
Peers
Comparison fields: 5 of 65
- Genetics 131
- Cancer Research 64
- Genetics 43
- Molecular Biology 260
- Clinical Biochemistry 24
Countries citing papers authored by Jack Reilly
This map shows the geographic impact of Jack Reilly'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 Jack Reilly with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jack Reilly more than expected).
Fields of papers citing papers by Jack Reilly
This network shows the impact of papers produced by Jack Reilly. 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 Jack Reilly. The network helps show where Jack Reilly may publish in the future.
Co-authors
The 25 scholars most cited alongside Jack Reilly, 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 | 1984 | 117 | |
| 2 | 2017 | 94 | |
| 3 | 1980 | 58 | |
| 4 | 2016 | 43 | |
| 5 | 1982 | 19 | |
| 6 | 1980 | 17 | |
| 7 | 1982 | 14 | |
| 8 | 1982 | 13 | |
| 9 | 1983 | 6 | |
| 10 | 1979 | 3 | |
| 11 | 2022 | 3 | |
| 12 | 2021 | 2 | |
| 13 | 2020 | 2 | |
| 14 | 1980 | 2 |
About Jack Reilly
Jack Reilly is a scholar working on Molecular Biology, Genetics, Cancer Research, Infectious Diseases and Insect Science, having authored 14 papers that have together received 393 indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (4 papers), Genomics and Rare Diseases (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Cancer Genomics and Diagnostics (2 papers), RNA modifications and cancer (2 papers), Insect Resistance and Genetics (2 papers), Protein Degradation and Inhibitors (1 paper) and Genetic factors in colorectal cancer (1 paper). The work is most often cited by research in Genetics (131 citations), Cancer Research (64 citations), Genetics (43 citations), Molecular Biology (260 citations) and Clinical Biochemistry (24 citations). Jack Reilly has collaborated with scholars based in United States and Canada. Frequent co-authors include C.A. Thomas, Brian I. Carr, Arthur D. Riggs, Steven S. Smith, Carl D. Winberg, Jennifer Kerkhof, Bekim Sadiković, Laila C. Schenkel, Joan H.M. Knoll and Alan Stuart. Their work appears in journals such as Journal of Molecular Diagnostics, Nature, Carcinogenesis, FEBS Letters and Frontiers in 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.