David St Clair
Impact in
- Biological Psychiatry top 5%
- Genetics top 2%
- Genetic Associations and Epidemiology
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
Papers in
- Genetics 24
- Genetic Associations and Epidemiology 18
- Genomics and Rare Diseases 8
- Genetics and Neurodevelopmental Disorders 7
- Genomic variations and chromosomal abnormalities 6
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- 14-3-3 protein interactions 3
- Congenital heart defects research 3
- Epigenetics and DNA Methylation 3
- Co-authors
- Douglas Blackwood (3 shared papers)Walter Muir (1 shared paper)A D Carothers (1 shared paper)G. Spowart (1 shared paper)ChristineM. Gosden (1 shared paper)Harold J. Evans (1 shared paper)Augustine Kong (3 shared papers)Kāri Stefánsson (3 shared papers)
- Journals
- Molecular Psychiatry (6 papers)Schizophrenia Research (5 papers)The British Journal of Psychiatry (3 papers)Psychiatric Genetics (3 papers)The American Journal of Human Genetics (3 papers)
- Partner nations
- United KingdomChinaUnited States
In The Last Decade
David St Clair
50 papers receiving 2.6k citations
David St Clair's Hit Papers
Peers
Comparison fields: 5 of 129
- Biological Psychiatry 98
- Genetics 1.0k
- Developmental Neuroscience 117
- Cellular and Molecular Neuroscience 468
- Psychiatry and Mental health 276
Countries citing papers authored by David St Clair
This map shows the geographic impact of David St Clair'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 St Clair with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites David St Clair more than expected).
Fields of papers citing papers by David St Clair
This network shows the impact of papers produced by David St Clair. 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 St Clair. The network helps show where David St Clair may publish in the future.
Co-authors
The 25 scholars most cited alongside David St Clair, 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 52 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Association within a family of a balanced autosomal translocation with major mental illness Hit paper breakdown → | 1990 | 558 |
| 2 | 2003 | 430 | |
| 3 | 2005 | 182 | |
| 4 | 2012 | 168 | |
| 5 | 2010 | 118 | |
| 6 | 2000 | 81 | |
| 7 | 2009 | 66 | |
| 8 | 2007 | 62 | |
| 9 | 1989 | 57 | |
| 10 | 2006 | 53 | |
| 11 | 2005 | 50 | |
| 12 | 2011 | 50 | |
| 13 | 2001 | 49 | |
| 14 | 2009 | 47 | |
| 15 | 2012 | 46 | |
| 16 | 2001 | 44 | |
| 17 | 2002 | 39 | |
| 18 | 2011 | 38 | |
| 19 | 2008 | 36 | |
| 20 | 2005 | 35 |
About David St Clair
David St Clair is a scholar working on Genetics, Molecular Biology, Cellular and Molecular Neuroscience, Cognitive Neuroscience and Psychiatry and Mental health, having authored 52 papers that have together received 2.6k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (18 papers), Genomics and Rare Diseases (8 papers), Genetics and Neurodevelopmental Disorders (7 papers), Genomic variations and chromosomal abnormalities (6 papers), 14-3-3 protein interactions (3 papers), Congenital heart defects research (3 papers), HER2/EGFR in Cancer Research (3 papers) and Epigenetics and DNA Methylation (3 papers). The work is most often cited by research in Biological Psychiatry (98 citations), Genetics (1.0k citations), Developmental Neuroscience (117 citations), Cellular and Molecular Neuroscience (468 citations) and Psychiatry and Mental health (276 citations). David St Clair has collaborated with scholars based in United Kingdom, China and United States. Frequent co-authors include Douglas Blackwood, Walter Muir, A D Carothers, G. Spowart, ChristineM. Gosden, Harold J. Evans, Augustine Kong, Kāri Stefánsson, Gerome Breen and Jeffrey R. Gulcher. Their work appears in journals such as Molecular Psychiatry, Schizophrenia Research, The British Journal of Psychiatry, Psychiatric Genetics and The American Journal of 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.