David Garrick
Impact in
- Genetics top 1%
- Genetics and Neurodevelopmental Disorders
- Molecular Biology top 2%
- Epigenetics and DNA Methylation
- Genomics and Chromatin Dynamics
- RNA modifications and cancer
- CRISPR and Genetic Engineering
- RNA Research and Splicing
- Cancer-related gene regulation
Papers in
-
- Genomics and Chromatin Dynamics 18
- Epigenetics and DNA Methylation 15
- Cancer-related gene regulation 4
- Genetics 13
- Genetics and Neurodevelopmental Disorders 9
- Hemoglobinopathies and Related Disorders 8
- Co-authors
- Douglas R. Higgs (23 shared papers)Emma Whitelaw (5 shared papers)David I. K. Martin (3 shared papers)Steven Fiering (2 shared papers)Richard J. Gibbons (15 shared papers)Helena Ayyub (11 shared papers)W. G. Wood (6 shared papers)J A Sharpe (2 shared papers)
- Journals
- Nature Genetics (4 papers)Leukemia (3 papers)Proceedings of the National Academy of Sciences (3 papers)Journal of Clinical Investigation (2 papers)Epigenetics & Chromatin (2 papers)
- Partner nations
- United KingdomFranceAustralia
In The Last Decade
David Garrick
54 papers receiving 3.6k citations
Hit Papers
Peers
Comparison fields: 5 of 129
- Genetics 1.2k
- Molecular Biology 2.9k
- Cancer Research 376
- Genetics 259
- Immunology 370
Countries citing papers authored by David Garrick
This map shows the geographic impact of David Garrick'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 David Garrick with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites David Garrick more than expected).
Fields of papers citing papers by David Garrick
This network shows the impact of papers produced by David Garrick. 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 David Garrick. The network helps show where David Garrick may publish in the future.
Co-authors
The 25 scholars most cited alongside David Garrick, 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 61 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Repeat-induced gene silencing in mammals Hit paper breakdown → | 1998 | 759 |
| 2 | 2003 | 415 | |
| 3 | 2000 | 374 | |
| 4 | 2012 | 194 | |
| 5 | 2011 | 176 | |
| 6 | 2005 | 159 | |
| 7 | 2011 | 155 | |
| 8 | 2005 | 150 | |
| 9 | 1995 | 139 | |
| 10 | 2006 | 122 | |
| 11 | 2017 | 105 | |
| 12 | 2003 | 97 | |
| 13 | 2016 | 77 | |
| 14 | 2009 | 74 | |
| 15 | 2011 | 65 | |
| 16 | 1999 | 51 | |
| 17 | 2011 | 47 | |
| 18 | 2003 | 45 | |
| 19 | 2008 | 45 | |
| 20 | 1996 | 41 |
About David Garrick
David Garrick is a scholar working on Molecular Biology, Genetics, Hematology, Genetics and Pediatrics, Perinatology and Child Health, having authored 61 papers that have together received 3.7k indexed citations. Recurring topics across this work include Genomics and Chromatin Dynamics (18 papers), Epigenetics and DNA Methylation (15 papers), Genetics and Neurodevelopmental Disorders (9 papers), Hemoglobinopathies and Related Disorders (8 papers), Cancer-related molecular mechanisms research (4 papers), Cancer-related gene regulation (4 papers), Shakespeare, Adaptation, and Literary Criticism (3 papers) and Acute Myeloid Leukemia Research (3 papers). The work is most often cited by research in Genetics (1.2k citations), Molecular Biology (2.9k citations), Cancer Research (376 citations), Genetics (259 citations) and Immunology (370 citations). David Garrick has collaborated with scholars based in United Kingdom, France and Australia. Frequent co-authors include Douglas R. Higgs, Emma Whitelaw, David I. K. Martin, Steven Fiering, Richard J. Gibbons, Helena Ayyub, W. G. Wood, J A Sharpe, Cristina Tufarelli and Tarra L. McDowell. Their work appears in journals such as Nature Genetics, Leukemia, Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and Epigenetics & Chromatin.
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.