David Curtis
Impact in
- Psychiatry and Mental health top 0.1%
- Schizophrenia research and treatment
- Bipolar Disorder and Treatment
- Genetics top 0.1%
- Genetic Associations and Epidemiology
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
Papers in
-
- Schizophrenia research and treatment 91
- Bipolar Disorder and Treatment 49
- Genetics 140
- Genetic Associations and Epidemiology 125
- Genomics and Rare Diseases 14
- Genomic variations and chromosomal abnormalities 7
- Co-authors
- Pak Chung Sham (31 shared papers)Hugh Gurling (79 shared papers)Bernard V. North (10 shared papers)Jing Hua Zhao (4 shared papers)Andrew McQuillin (41 shared papers)Gursharan Kalsi (43 shared papers)Hannes Pétursson (31 shared papers)Jon Brynjolfsson (30 shared papers)
- Journals
- Annals of Human Genetics (39 papers)Psychiatric Genetics (32 papers)The British Journal of Psychiatry (17 papers)The American Journal of Human Genetics (16 papers)Nature Genetics (11 papers)
- Partner nations
- United KingdomUnited StatesIceland
In The Last Decade
David Curtis
308 papers receiving 25.6k citations
David Curtis's Hit Papers
Peers
Comparison fields: 5 of 177
- Psychiatry and Mental health 9.9k
- Genetics 10.2k
- Biological Psychiatry 304
- Cellular and Molecular Neuroscience 1.6k
- Clinical Psychology 1.5k
Countries citing papers authored by David Curtis
This map shows the geographic impact of David Curtis'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 Curtis with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites David Curtis more than expected).
Fields of papers citing papers by David Curtis
This network shows the impact of papers produced by David Curtis. 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 Curtis. The network helps show where David Curtis may publish in the future.
Co-authors
The 25 scholars most cited alongside David Curtis, 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 318 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs Hit paper breakdown → | 2013 | 1806 |
| 2 | Mapping genomic loci implicates genes and synaptic biology in schizophrenia Hit paper breakdown → | 2022 | 1774 |
| 3 | Analysis of shared heritability in common disorders of the brain Hit paper breakdown → | 2018 | 1477 |
| 4 | Rare chromosomal deletions and duplications increase risk of schizophrenia Hit paper breakdown → | 2008 | 1222 |
| 5 | Genome-wide association study identifies 30 loci associated with bipolar disorder Hit paper breakdown → | 2019 | 1100 |
| 6 | Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder Hit paper breakdown → | 2008 | 1031 |
| 7 | Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders Hit paper breakdown → | 2019 | 992 |
| 8 | Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology Hit paper breakdown → | 2021 | 977 |
| 9 | Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores Hit paper breakdown → | 2015 | 968 |
| 10 | Monte Carlo tests for associations between disease and alleles at highly polymorphic loci Hit paper breakdown → | 1995 | 848 |
| 11 | Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects Hit paper breakdown → | 2016 | 793 |
| 12 | The UK10K project identifies rare variants in health and disease Hit paper breakdown → | 2015 | 790 |
| 13 | Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways Hit paper breakdown → | 2015 | 629 |
| 14 | Rare coding variants in ten genes confer substantial risk for schizophrenia Hit paper breakdown → | 2022 | 581 |
| 15 | 1995 | 545 | |
| 16 | Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases Hit paper breakdown → | 2014 | 436 |
| 17 | Phenotypic characterization of individuals with 30-40 CAG repeats in the Huntington disease (HD) gene reveals HD cases with 36 repeats and apparently normal elderly individuals with 36-39 repeats. | 1996 | 419 |
| 18 | 1999 | 377 | |
| 19 | Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders Hit paper breakdown → | 2016 | 341 |
| 20 | 2001 | 317 |
About David Curtis
David Curtis is a scholar working on Psychiatry and Mental health, Genetics, Clinical Psychology, Gastroenterology and Epidemiology, having authored 318 papers that have together received 26.5k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (125 papers), Schizophrenia research and treatment (91 papers), Bipolar Disorder and Treatment (49 papers), Genomics and Rare Diseases (14 papers), Obsessive-Compulsive Spectrum Disorders (9 papers), Celiac Disease Research and Management (8 papers), Genomic variations and chromosomal abnormalities (7 papers) and Alzheimer's disease research and treatments (6 papers). The work is most often cited by research in Psychiatry and Mental health (9.9k citations), Genetics (10.2k citations), Biological Psychiatry (304 citations), Cellular and Molecular Neuroscience (1.6k citations) and Clinical Psychology (1.5k citations). David Curtis has collaborated with scholars based in United Kingdom, United States and Iceland. Frequent co-authors include Pak Chung Sham, Hugh Gurling, Bernard V. North, Jing Hua Zhao, Andrew McQuillin, Gursharan Kalsi, Hannes Pétursson, Jon Brynjolfsson, P. L. Murphy and Peter Brett. Their work appears in journals such as Annals of Human Genetics, Psychiatric Genetics, The British Journal of Psychiatry, The American Journal of Human Genetics and Nature 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.