Danielle Gleason
Impact in
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- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
Papers in
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- Connexins and lens biology 1
- Advanced biosensing and bioanalysis techniques 1
- Chromatin Remodeling and Cancer 1
- Genetics 3
- Genetics and Neurodevelopmental Disorders 2
- Co-authors
- Christopher A. Walsh (6 shared papers)Robert Hill (3 shared papers)Adria Bodell (2 shared papers)Brenda J. Barry (4 shared papers)Ganeshwaran H. Mochida (3 shared papers)A. James Barkovich (3 shared papers)Bernard S. Chang (3 shared papers)Vijay Ganesh (2 shared papers)
- Journals
- The American Journal of Human Genetics (2 papers)Human Mutation (1 paper)Nature Genetics (1 paper)Liver Transplantation (1 paper)Annals of Neurology (1 paper)
- Partner nations
- United StatesUnited KingdomSaudi Arabia
In The Last Decade
Danielle Gleason
7 papers receiving 485 citations
Peers
Comparison fields: 5 of 73
- Genetics 156
- Neurology 42
- Cell Biology 79
- Molecular Biology 319
- Cellular and Molecular Neuroscience 71
Countries citing papers authored by Danielle Gleason
This map shows the geographic impact of Danielle Gleason'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 Danielle Gleason with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Danielle Gleason more than expected).
Fields of papers citing papers by Danielle Gleason
This network shows the impact of papers produced by Danielle Gleason. 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 Danielle Gleason. The network helps show where Danielle Gleason may publish in the future.
Co-authors
The 25 scholars most cited alongside Danielle Gleason, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2010 | 213 | |
| 2 | 2009 | 107 | |
| 3 | 2010 | 64 | |
| 4 | 2008 | 49 | |
| 5 | 2009 | 27 | |
| 6 | 2010 | 14 | |
| 7 | 2020 | 13 |
About Danielle Gleason
Danielle Gleason is a scholar working on Molecular Biology, Genetics, Neurology, Surgery and Genetics, having authored 7 papers that have together received 487 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (2 papers), Neurological diseases and metabolism (1 paper), Hereditary Neurological Disorders (1 paper), Connexins and lens biology (1 paper), Advanced biosensing and bioanalysis techniques (1 paper), Chromatin Remodeling and Cancer (1 paper), Opioid Use Disorder Treatment (1 paper) and Barrier Structure and Function Studies (1 paper). The work is most often cited by research in Genetics (156 citations), Neurology (42 citations), Cell Biology (79 citations), Molecular Biology (319 citations) and Cellular and Molecular Neuroscience (71 citations). Danielle Gleason has collaborated with scholars based in United States, United Kingdom and Saudi Arabia. Frequent co-authors include Christopher A. Walsh, Robert Hill, Adria Bodell, Brenda J. Barry, Ganeshwaran H. Mochida, A. James Barkovich, Bernard S. Chang, Vijay Ganesh, Lina Basel‐Vanagaite and John J. Reynolds. Their work appears in journals such as The American Journal of Human Genetics, Human Mutation, Nature Genetics, Liver Transplantation and Annals of Neurology.
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.