Daniel M. Snell
- Molecular Biology
- Genetics
- Cellular and Molecular Neuroscience
- Neurology
- Public Health, Environmental and Occupational Health
- Co-authors
- James M. A. TurnerKaty MalpassKenneth J. SmithJennifer M. PocockDavid A. BechtoldArthur RoachThomas M. PiersWoojin Lee
- Topics
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers)Epigenetics and DNA Methylation (2 papers)Genetic Syndromes and Imprinting (1 paper)
- Journals
- NatureNature CommunicationsBrain
- Partner nations
- United KingdomSwitzerlandSingapore
In The Last Decade
Daniel M. Snell
5 papers receiving 167 citations
Peers
Comparison fields: 5 of 68
- Molecular Biology 64
- Genetics 46
- Cellular and Molecular Neuroscience 30
- Neurology 28
- Public Health, Environmental and Occupational Health 20
Countries citing papers authored by Daniel M. Snell
This map shows the geographic impact of Daniel M. Snell'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 Daniel M. Snell with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Daniel M. Snell more than expected).
Fields of papers citing papers by Daniel M. Snell
This network shows the impact of papers produced by Daniel M. Snell. 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 Daniel M. Snell. The network helps show where Daniel M. Snell may publish in the future.
Co-authorship network of co-authors of Daniel M. Snell
This figure shows the co-authorship network connecting the top 25 collaborators of Daniel M. Snell. A scholar is included among the top collaborators of Daniel M. Snell 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 Daniel M. Snell. Daniel M. Snell is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 0 | |
| 2 | 3 | |
| 3 | 0 | |
| 4 | 9 | |
| 5 | 20 | |
| 6 | 71 | |
| 7 | 65 |
About Daniel M. Snell
Daniel M. Snell is a scholar working on Aging, Developmental Neuroscience and Biophysics, having authored 7 papers that have together received 168 indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers), Epigenetics and DNA Methylation (2 papers) and Genetic Syndromes and Imprinting (1 paper). The work is most often cited by research in Neurology (28 citations), Biological Psychiatry (6 citations) and Developmental Neuroscience (8 citations). Daniel M. Snell has collaborated with scholars based in United Kingdom, Switzerland and Singapore. Frequent co-authors include James M. A. Turner, Katy Malpass, Kenneth J. Smith, Jennifer M. Pocock, David A. Bechtold, Arthur Roach, Thomas M. Piers, Woojin Lee, Jasmin Zohren and Rory J. Maizels. Their work appears in journals such as Nature, Nature Communications and Brain.
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.