A Curtis
Impact in
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- Neuroscience and Neuropharmacology Research
- Genetic Neurodegenerative Diseases
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- Genetics and Neurodevelopmental Disorders
Papers in
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- 14-3-3 protein interactions 1
- Mitochondrial Function and Pathology 1
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- Hereditary Neurological Disorders 2
- Co-authors
- V. Spencer (2 shared papers)R M Gardiner (1 shared paper)Sarah Hutchings (1 shared paper)Michelle Rees (1 shared paper)Frances Elmslie (1 shared paper)Smaragda Kamakari (2 shared papers)John Burn (2 shared papers)Susan Lindsay (2 shared papers)
- Journals
- Genomics (1 paper)Neurology (1 paper)Journal of Medical Genetics (1 paper)Nucleic Acids Research (1 paper)Human Genetics (1 paper)
- Partner nations
- United KingdomSweden
In The Last Decade
A Curtis
7 papers receiving 201 citations
Peers
Comparison fields: 5 of 36
- Cellular and Molecular Neuroscience 80
- Genetics 63
- Molecular Biology 129
- Neurology 22
- Cognitive Neuroscience 30
Countries citing papers authored by A Curtis
This map shows the geographic impact of A 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 A Curtis with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites A Curtis more than expected).
Fields of papers citing papers by A Curtis
This network shows the impact of papers produced by A 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 A Curtis. The network helps show where A Curtis may publish in the future.
Co-authors
The 25 scholars most cited alongside A 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
| # | Work | ||
|---|---|---|---|
| 1 | 1996 | 68 | |
| 2 | 1993 | 39 | |
| 3 | A large, dominant pedigree of atrioventricular septal defect (AVSD): exclusion from the Down syndrome critical region on chromosome 21. | 1993 | 38 |
| 4 | 1998 | 34 | |
| 5 | 1992 | 22 | |
| 6 | 1996 | 10 | |
| 7 | 1991 | 1 |
About A Curtis
A Curtis is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Neurology, Clinical Psychology and Atomic and Molecular Physics, and Optics, having authored 7 papers that have together received 212 indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (2 papers), Autism Spectrum Disorder Research (1 paper), Genetics and Neurodevelopmental Disorders (1 paper), Amyotrophic Lateral Sclerosis Research (1 paper), Family and Disability Support Research (1 paper), Superconducting Materials and Applications (1 paper), 14-3-3 protein interactions (1 paper) and Mitochondrial Function and Pathology (1 paper). The work is most often cited by research in Cellular and Molecular Neuroscience (80 citations), Genetics (63 citations), Molecular Biology (129 citations), Neurology (22 citations) and Cognitive Neuroscience (30 citations). A Curtis has collaborated with scholars based in United Kingdom and Sweden. Frequent co-authors include V. Spencer, R M Gardiner, Sarah Hutchings, Michelle Rees, Frances Elmslie, Smaragda Kamakari, John Burn, Susan Lindsay, A. Stephenson and L. D. Allan. Their work appears in journals such as Genomics, Neurology, Journal of Medical Genetics, Nucleic Acids Research 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.