Jack Reilly
Impact in
- Genetics top 10%
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
-
- Epigenetics and DNA Methylation
- RNA modifications and cancer
- Cancer-related gene regulation
Papers in
- Genetics 10
- Genomics and Rare Diseases 5
- Genetics and Neurodevelopmental Disorders 4
- Genomic variations and chromosomal abnormalities 3
- Genetic Syndromes and Imprinting 3
-
- Epigenetics and DNA Methylation 10
- RNA modifications and cancer 3
- Genomics and Chromatin Dynamics 2
- Co-authors
- C.A. Thomas (5 shared papers)Steven S. Smith (2 shared papers)Brian Irving Carr (1 shared paper)Arthur D. Riggs (1 shared paper)Carl D. Winberg (1 shared paper)Bekim Sadiković (5 shared papers)Jennifer Kerkhof (5 shared papers)Peter Ainsworth (3 shared papers)
- Journals
- Genetics in Medicine (3 papers)The American Journal of Human Genetics (2 papers)Journal of Molecular Diagnostics (2 papers)Frontiers in Genetics (1 paper)Neuromuscular Disorders (1 paper)
- Partner nations
- United StatesCanadaFrance
In The Last Decade
Jack Reilly
24 papers receiving 652 citations
Peers
Comparison fields: 5 of 74
- Genetics 286
- Molecular Biology 409
- Cancer Research 69
- Genetics 49
- 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
Showing the 20 most-cited of 24 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1984 | 135 | |
| 2 | 2021 | 116 | |
| 3 | 2017 | 108 | |
| 4 | 1980 | 61 | |
| 5 | 2022 | 55 | |
| 6 | 2016 | 47 | |
| 7 | 2022 | 24 | |
| 8 | 1982 | 23 | |
| 9 | 1980 | 20 | |
| 10 | 1982 | 16 | |
| 11 | 1982 | 14 | |
| 12 | 2022 | 11 | |
| 13 | 2024 | 7 | |
| 14 | 2023 | 7 | |
| 15 | 2024 | 6 | |
| 16 | 1983 | 6 | |
| 17 | 2022 | 5 | |
| 18 | 2024 | 4 | |
| 19 | 1979 | 3 | |
| 20 | 2020 | 3 |
About Jack Reilly
Jack Reilly is a scholar working on Genetics, Molecular Biology, Cancer Research, Insect Science and Infectious Diseases, having authored 24 papers that have together received 678 indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (10 papers), Genomics and Rare Diseases (5 papers), Genetics and Neurodevelopmental Disorders (4 papers), Genomic variations and chromosomal abnormalities (3 papers), RNA modifications and cancer (3 papers), Genetic Syndromes and Imprinting (3 papers), Cancer Genomics and Diagnostics (2 papers) and Genomics and Chromatin Dynamics (2 papers). The work is most often cited by research in Genetics (286 citations), Molecular Biology (409 citations), Cancer Research (69 citations), Genetics (49 citations) and Clinical Biochemistry (24 citations). Jack Reilly has collaborated with scholars based in United States, Canada and France. Frequent co-authors include C.A. Thomas, Steven S. Smith, Brian Irving Carr, Arthur D. Riggs, Carl D. Winberg, Bekim Sadiković, Jennifer Kerkhof, Peter Ainsworth, Laila Cigana Schenkel and Alan Stuart. Their work appears in journals such as Genetics in Medicine, The American Journal of Human Genetics, Journal of Molecular Diagnostics, Frontiers in Genetics and Neuromuscular Disorders.
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.