Tracey Flint
Impact in
- Genetics top 2%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Neurogenetic and Muscular Disorders Research
- Genetic Associations and Epidemiology
- Molecular Biology top 10%
- Muscle Physiology and Disorders
Papers in
- Genetics 23
- Genetics and Neurodevelopmental Disorders 15
- Genomic variations and chromosomal abnormalities 8
- Genetic Associations and Epidemiology 5
- Genomics and Rare Diseases 4
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- Muscle Physiology and Disorders 8
- RNA modifications and cancer 4
- Co-authors
- Ole Mors (17 shared papers)H. Ewald (14 shared papers)Kay E. Davies (10 shared papers)Andreas Speer (4 shared papers)K. E. Davies (4 shared papers)Torben A. Kruse (4 shared papers)S. M. Forrest (4 shared papers)A. Roche (4 shared papers)
- Journals
- Psychiatric Genetics (6 papers)Genomics (5 papers)Journal of Medical Genetics (4 papers)American Journal of Medical Genetics Part B Neuropsychiatric Genetics (3 papers)Human Genetics (2 papers)
- Partner nations
- DenmarkUnited KingdomUnited States
In The Last Decade
Tracey Flint
43 papers receiving 1.4k citations
Peers
Comparison fields: 5 of 86
- Genetics 728
- Molecular Biology 863
- Genetics 123
- Cognitive Neuroscience 228
- Biological Psychiatry 24
Countries citing papers authored by Tracey Flint
This map shows the geographic impact of Tracey Flint'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 Tracey Flint with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Tracey Flint more than expected).
Fields of papers citing papers by Tracey Flint
This network shows the impact of papers produced by Tracey Flint. 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 Tracey Flint. The network helps show where Tracey Flint may publish in the future.
Co-authors
The 25 scholars most cited alongside Tracey Flint, 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 44 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1991 | 286 | |
| 2 | 1988 | 147 | |
| 3 | 1995 | 127 | |
| 4 | 2002 | 95 | |
| 5 | 1991 | 93 | |
| 6 | 1988 | 49 | |
| 7 | 1987 | 41 | |
| 8 | 1995 | 41 | |
| 9 | 1991 | 39 | |
| 10 | 2011 | 39 | |
| 11 | 1990 | 39 | |
| 12 | 1989 | 37 | |
| 13 | 1991 | 34 | |
| 14 | 2002 | 29 | |
| 15 | 1992 | 28 | |
| 16 | 1990 | 28 | |
| 17 | 2013 | 28 | |
| 18 | 2003 | 28 | |
| 19 | 1991 | 23 | |
| 20 | 2006 | 21 |
About Tracey Flint
Tracey Flint is a scholar working on Genetics, Molecular Biology, Cellular and Molecular Neuroscience, Cognitive Neuroscience and Immunology, having authored 44 papers that have together received 1.4k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (15 papers), Genomic variations and chromosomal abnormalities (8 papers), Muscle Physiology and Disorders (8 papers), Genetic Associations and Epidemiology (5 papers), Genetic Neurodegenerative Diseases (4 papers), Genomics and Rare Diseases (4 papers), Autism Spectrum Disorder Research (4 papers) and RNA modifications and cancer (4 papers). The work is most often cited by research in Genetics (728 citations), Molecular Biology (863 citations), Genetics (123 citations), Cognitive Neuroscience (228 citations) and Biological Psychiatry (24 citations). Tracey Flint has collaborated with scholars based in Denmark, United Kingdom and United States. Frequent co-authors include Ole Mors, H. Ewald, Kay E. Davies, Andreas Speer, K. E. Davies, Torben A. Kruse, S. M. Forrest, A. Roche, Yutaka Nakahori and Mark C. Hirst. Their work appears in journals such as Psychiatric Genetics, Genomics, Journal of Medical Genetics, American Journal of Medical Genetics Part B Neuropsychiatric Genetics and Human Genetics.
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.