Eilís Hannon
- Molecular Biology top 2%
- Genetics top 1%
- Physiology top 5%
- Pediatrics, Perinatology and Child Health top 2%
- Psychiatry and Mental health top 2%
- Co-authors
- Jonathan MillLeonard C. SchalkwykKatie LunnonJoe BurrageNicholas J. BrayDavid J. LlewellynElina HyppönenElżbieta Kuźma
- Topics
- Epigenetics and DNA Methylation (68 papers)Genetic Syndromes and Imprinting (28 papers)Genetic Associations and Epidemiology (23 papers)
- Cited by
- Biological PsychiatryGeneticsAging
- Partner nations
- United KingdomUnited StatesAustralia
In The Last Decade
Eilís Hannon
93 papers receiving 4.2k citations
Hit Papers
Peers
Comparison fields: 5 of 135
- Molecular Biology 2.7k
- Genetics 1.3k
- Physiology 616
- Pediatrics, Perinatology and Child Health 533
- Psychiatry and Mental health 512
Countries citing papers authored by Eilís Hannon
This map shows the geographic impact of Eilís Hannon'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 Eilís Hannon with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Eilís Hannon more than expected).
Fields of papers citing papers by Eilís Hannon
This network shows the impact of papers produced by Eilís Hannon. 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 Eilís Hannon. The network helps show where Eilís Hannon may publish in the future.
Co-authorship network of co-authors of Eilís Hannon
This figure shows the co-authorship network connecting the top 25 collaborators of Eilís Hannon. A scholar is included among the top collaborators of Eilís Hannon based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Eilís Hannon. Eilís Hannon is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 1 | |
| 2 | 1 | |
| 3 | 3 | |
| 4 | 18 | |
| 5 | 7 | |
| 6 | 15 | |
| 7 | 60 | |
| 8 | 8 | |
| 9 | 14 | |
| 10 | 32 | |
| 11 | 7 | |
| 12 | 81 | |
| 13 | 14 | |
| 14 | 110 | |
| 15 | 59 | |
| 16 | 27 | |
| 17 | 180 | |
| 18 | 84 | |
| 19 | 117 | |
| 20 | 67 |
About Eilís Hannon
Eilís Hannon is a scholar working on Genetics, Biological Psychiatry and Molecular Biology, having authored 99 papers that have together received 4.2k indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (68 papers), Genetic Syndromes and Imprinting (28 papers) and Genetic Associations and Epidemiology (23 papers). The work is most often cited by research in Biological Psychiatry (255 citations), Genetics (1.3k citations) and Aging (79 citations). Eilís Hannon has collaborated with scholars based in United Kingdom, United States and Australia. Frequent co-authors include Jonathan Mill, Leonard C. Schalkwyk, Katie Lunnon, Joe Burrage, Nicholas J. Bray, David J. Llewellyn, Elina Hyppönen, Elżbieta Kuźma, Ilianna Lourida and Thomas J. Littlejohns. Their work appears in journals such as JAMA, Nature Communications and Nature Neuroscience.
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.