David J. Lewis-Smith
Impact in
- Genetics top 5%
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Psychiatry and Mental health top 10%
- Epilepsy research and treatment
Papers in
- Genetics 17
- Genomics and Rare Diseases 13
- Genetics and Neurodevelopmental Disorders 11
- Genomic variations and chromosomal abnormalities 3
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- Neurological diseases and metabolism 2
- Neurological disorders and treatments 2
- Co-authors
- Rhys Huw Thomas (9 shared papers)Rita Horváth (4 shared papers)Patrick Francis Chinnery (4 shared papers)Jennifer Duff (4 shared papers)Angela Pyle (4 shared papers)Ingo Helbig (7 shared papers)Helen R Griffin (3 shared papers)Colin Ellis (5 shared papers)
- Journals
- Neurology (3 papers)Brain (3 papers)Neurology Genetics (3 papers)Epilepsia (2 papers)Epilepsia Open (2 papers)
- Partner nations
- United KingdomUnited StatesItaly
In The Last Decade
David J. Lewis-Smith
31 papers receiving 1.7k citations
David J. Lewis-Smith's Hit Papers
Peers
Comparison fields: 5 of 113
- Genetics 585
- Psychiatry and Mental health 162
- Molecular Biology 735
- Clinical Biochemistry 65
- Health Informatics 12
Countries citing papers authored by David J. Lewis-Smith
This map shows the geographic impact of David J. Lewis-Smith'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 J. Lewis-Smith with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites David J. Lewis-Smith more than expected).
Fields of papers citing papers by David J. Lewis-Smith
This network shows the impact of papers produced by David J. Lewis-Smith. 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 J. Lewis-Smith. The network helps show where David J. Lewis-Smith may publish in the future.
Co-authors
The 25 scholars most cited alongside David J. Lewis-Smith, 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 32 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | The Human Phenotype Ontology in 2021 Hit paper breakdown → | 2020 | 745 |
| 2 | The Human Phenotype Ontology in 2024: phenotypes around the world Hit paper breakdown → | 2023 | 190 |
| 3 | GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture Hit paper breakdown → | 2023 | 124 |
| 4 | 2016 | 85 | |
| 5 | 2021 | 79 | |
| 6 | 2021 | 62 | |
| 7 | 2015 | 40 | |
| 8 | 2021 | 39 | |
| 9 | 2022 | 36 | |
| 10 | 2023 | 32 | |
| 11 | 2024 | 30 | |
| 12 | 2020 | 29 | |
| 13 | 2016 | 25 | |
| 14 | 2022 | 19 | |
| 15 | 2016 | 18 | |
| 16 | 2021 | 17 | |
| 17 | 2020 | 15 | |
| 18 | 2022 | 15 | |
| 19 | 2022 | 15 | |
| 20 | 2020 | 14 |
About David J. Lewis-Smith
David J. Lewis-Smith is a scholar working on Genetics, Neurology, Psychiatry and Mental health, Neurology and Molecular Biology, having authored 32 papers that have together received 1.7k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (13 papers), Genetics and Neurodevelopmental Disorders (11 papers), Biomedical Text Mining and Ontologies (4 papers), Genomic variations and chromosomal abnormalities (3 papers), Epilepsy research and treatment (3 papers), Neurological diseases and metabolism (2 papers), Neurological disorders and treatments (2 papers) and RNA regulation and disease (2 papers). The work is most often cited by research in Genetics (585 citations), Psychiatry and Mental health (162 citations), Molecular Biology (735 citations), Clinical Biochemistry (65 citations) and Health Informatics (12 citations). David J. Lewis-Smith has collaborated with scholars based in United Kingdom, United States and Italy. Frequent co-authors include Rhys Huw Thomas, Rita Horváth, Patrick Francis Chinnery, Jennifer Duff, Angela Pyle, Ingo Helbig, Helen R Griffin, Colin Ellis, Peter D. Galer and Shiva Ganesan. Their work appears in journals such as Neurology, Brain, Neurology Genetics, Epilepsia and Epilepsia Open.
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.