David Sims
Impact in
- Cancer Research top 2%
- Cancer-related molecular mechanisms research
- Molecular Biology top 2%
- Epigenetics and DNA Methylation
- Genomics and Phylogenetic Studies
- Genomics and Chromatin Dynamics
- Single-cell and spatial transcriptomics
Papers in
-
- Single-cell and spatial transcriptomics 6
- Genomics and Phylogenetic Studies 5
- Genomics and Chromatin Dynamics 4
- Bioinformatics and Genomic Networks 3
- Co-authors
- Chris Paul Ponting (8 shared papers)Andreas Heger (12 shared papers)Ian M. Sudbery (8 shared papers)Nicholas Edward Ilott (8 shared papers)Alan Ashworth (8 shared papers)Christopher J. Lord (8 shared papers)Kerry Fenwick (6 shared papers)Robert J. Klose (2 shared papers)
- Journals
- Nature Communications (7 papers)F1000Research (4 papers)Genome biology (4 papers)The American Journal of Human Genetics (3 papers)Cancer Research (3 papers)
- Partner nations
- United KingdomUnited StatesGermany
In The Last Decade
David Sims
66 papers receiving 5.3k citations
David Sims's Hit Papers
Peers
Comparison fields: 5 of 143
- Cancer Research 549
- Molecular Biology 2.3k
- Cellular and Molecular Neuroscience 441
- Genetics 684
- Oncology 394
Countries citing papers authored by David Sims
This map shows the geographic impact of David Sims'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 Sims with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites David Sims more than expected).
Fields of papers citing papers by David Sims
This network shows the impact of papers produced by David Sims. 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 Sims. The network helps show where David Sims may publish in the future.
Co-authors
The 25 scholars most cited alongside David Sims, 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 68 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Sequencing depth and coverage: key considerations in genomic analyses Hit paper breakdown → | 2014 | 1029 |
| 2 | Fly Cell Atlas: A single-nucleus transcriptomic atlas of the adult fruit fly Hit paper breakdown → | 2022 | 479 |
| 3 | 2012 | 372 | |
| 4 | 2013 | 309 | |
| 5 | 2014 | 271 | |
| 6 | A blood atlas of COVID-19 defines hallmarks of disease severity and specificity Hit paper breakdown → | 2022 | 225 |
| 7 | 2013 | 171 | |
| 8 | 2013 | 134 | |
| 9 | 2015 | 127 | |
| 10 | 2011 | 126 | |
| 11 | 2011 | 108 | |
| 12 | 2018 | 102 | |
| 13 | 2019 | 102 | |
| 14 | 2016 | 98 | |
| 15 | 2019 | 98 | |
| 16 | 2011 | 94 | |
| 17 | 2015 | 87 | |
| 18 | 2014 | 80 | |
| 19 | 2017 | 79 | |
| 20 | 2011 | 78 |
About David Sims
David Sims is a scholar working on Molecular Biology, Cancer Research, Cellular and Molecular Neuroscience, Immunology and Cell Biology, having authored 68 papers that have together received 5.4k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (6 papers), Single-cell and spatial transcriptomics (6 papers), Genomics and Phylogenetic Studies (5 papers), Genomics and Chromatin Dynamics (4 papers), Prostate Cancer Treatment and Research (3 papers), Bioinformatics and Genomic Networks (3 papers), Immune Response and Inflammation (3 papers) and Hereditary Neurological Disorders (3 papers). The work is most often cited by research in Cancer Research (549 citations), Molecular Biology (2.3k citations), Cellular and Molecular Neuroscience (441 citations), Genetics (684 citations) and Oncology (394 citations). David Sims has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Chris Paul Ponting, Andreas Heger, Ian M. Sudbery, Nicholas Edward Ilott, Alan Ashworth, Christopher J. Lord, Kerry Fenwick, Robert J. Klose, Neil P. Blackledge and Hannah K. Long. Their work appears in journals such as Nature Communications, F1000Research, Genome biology, The American Journal of Human Genetics and Cancer Research.
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.