David Curtis
Impact in
- Genetics top 0.2%
- Genetic Associations and Epidemiology
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genetic Mapping and Diversity in Plants and Animals
- Genomics and Rare Diseases
- Biological Psychiatry top 2%
Papers in
- Genetics 133
- Genetic Associations and Epidemiology 88
- Genetics and Neurodevelopmental Disorders 36
- Genomics and Rare Diseases 29
- Genomic variations and chromosomal abnormalities 24
- Genetic Mapping and Diversity in Plants and Animals 12
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- Epigenetics and DNA Methylation 14
- Co-authors
- Pak C. Sham (19 shared papers)Andrew McQuillin (38 shared papers)Hugh Gurling (32 shared papers)Jing Hua Zhao (2 shared papers)Hugh Gurling (25 shared papers)Hannes Pétursson (29 shared papers)Gursharan Kalsi (27 shared papers)Robin Sherrington (18 shared papers)
- Journals
- Annals of Human Genetics (40 papers)Psychiatric Genetics (30 papers)American Journal of Medical Genetics Part B Neuropsychiatric Genetics (8 papers)Human Heredity (8 papers)The British Journal of Psychiatry (8 papers)
- Partner nations
- United KingdomUnited StatesIceland
In The Last Decade
David Curtis
242 papers receiving 7.3k citations
David Curtis's Hit Papers
Peers
Comparison fields: 5 of 179
- Genetics 3.1k
- Biological Psychiatry 199
- Psychiatry and Mental health 1.0k
- Cellular and Molecular Neuroscience 1.0k
- Gastroenterology 233
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 252 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Monte Carlo tests for associations between disease and alleles at highly polymorphic loci Hit paper breakdown → | 1995 | 809 |
| 2 | An extended transmission/disequilibrium test (TDT) for multi‐allele marker loci Hit paper breakdown → | 1995 | 510 |
| 3 | 1999 | 357 | |
| 4 | 2001 | 299 | |
| 5 | 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 | 174 |
| 6 | 1995 | 163 | |
| 7 | 1997 | 154 | |
| 8 | 1997 | 151 | |
| 9 | 2003 | 126 | |
| 10 | 2008 | 102 | |
| 11 | 1997 | 89 | |
| 12 | 1997 | 85 | |
| 13 | 1995 | 83 | |
| 14 | 2018 | 81 | |
| 15 | 2002 | 80 | |
| 16 | Model-free linkage analysis using likelihoods. | 1995 | 79 |
| 17 | 2005 | 77 | |
| 18 | Mutations of the KIT (mast/stem cell growth factor receptor) proto-oncogene account for a continuous range of phenotypes in human piebaldism. | 1992 | 76 |
| 19 | Linkage analysis of idiopathic generalized epilepsy (IGE) and marker loci on chromosome 6p in families of patients with juvenile myoclonic epilepsy: no evidence for an epilepsy locus in the HLA region. | 1993 | 76 |
| 20 | 1992 | 74 |
About David Curtis
David Curtis is a scholar working on Genetics, Molecular Biology, Psychiatry and Mental health, Cellular and Molecular Neuroscience and Clinical Psychology, having authored 252 papers that have together received 7.7k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (88 papers), Genetics and Neurodevelopmental Disorders (36 papers), Genomics and Rare Diseases (29 papers), Genomic variations and chromosomal abnormalities (24 papers), Epigenetics and DNA Methylation (14 papers), Bipolar Disorder and Treatment (14 papers), Autism Spectrum Disorder Research (12 papers) and Genetic Mapping and Diversity in Plants and Animals (12 papers). The work is most often cited by research in Genetics (3.1k citations), Biological Psychiatry (199 citations), Psychiatry and Mental health (1.0k citations), Cellular and Molecular Neuroscience (1.0k citations) and Gastroenterology (233 citations). David Curtis has collaborated with scholars based in United Kingdom, United States and Iceland. Frequent co-authors include Pak C. Sham, Andrew McQuillin, Hugh Gurling, Jing Hua Zhao, Hugh Gurling, Hannes Pétursson, Gursharan Kalsi, Robin Sherrington, Bernard V. North and Jon Brynjolfsson. Their work appears in journals such as Annals of Human Genetics, Psychiatric Genetics, American Journal of Medical Genetics Part B Neuropsychiatric Genetics, Human Heredity and The British Journal of Psychiatry.
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.