David Lewis‐Smith

2.7k total citations
18 papers, 288 citations indexed

About

David Lewis‐Smith is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, David Lewis‐Smith has authored 18 papers receiving a total of 288 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 9 papers in Genetics and 4 papers in Neurology. Recurrent topics in David Lewis‐Smith's work include Genomics and Rare Diseases (6 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Biomedical Text Mining and Ontologies (3 papers). David Lewis‐Smith is often cited by papers focused on Genomics and Rare Diseases (6 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Biomedical Text Mining and Ontologies (3 papers). David Lewis‐Smith collaborates with scholars based in United Kingdom, United States and Luxembourg. David Lewis‐Smith's co-authors include Rita Horváth, Patrick F. Chinnery, Jennifer Duff, Angela Pyle, Helen Griffin, Rhys H. Thomas, Ingo Helbig, Anne‐Marie Childs, Patrick Yu‐Wai‐Man and Kimberli J. Kamer and has published in prestigious journals such as Brain, Neurology and The American Journal of Human Genetics.

In The Last Decade

David Lewis‐Smith

17 papers receiving 287 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
David Lewis‐Smith United Kingdom 11 195 80 54 50 38 18 288
Clara DM van Karnebeek Canada 7 190 1.0× 105 1.3× 49 0.9× 40 0.8× 78 2.1× 7 349
Yasuhiro Suzuki Japan 8 122 0.6× 58 0.7× 42 0.8× 98 2.0× 54 1.4× 16 259
Martino Montomoli Italy 8 166 0.9× 91 1.1× 39 0.7× 75 1.5× 87 2.3× 11 299
Fatima Jaffer United Kingdom 6 138 0.7× 67 0.8× 86 1.6× 47 0.9× 22 0.6× 12 264
Zhongdong Lin China 10 133 0.7× 84 1.1× 30 0.6× 53 1.1× 16 0.4× 23 321
Marina Michelson Israel 8 138 0.7× 62 0.8× 56 1.0× 28 0.6× 45 1.2× 19 239
Giacomo Garone Italy 10 106 0.5× 117 1.5× 57 1.1× 47 0.9× 26 0.7× 26 270
Maura Ruzhnikov United States 9 96 0.5× 73 0.9× 23 0.4× 48 1.0× 29 0.8× 21 213
Emmanuelle Lagrue France 8 110 0.6× 79 1.0× 64 1.2× 23 0.5× 12 0.3× 20 229

Countries citing papers authored by David Lewis‐Smith

Since Specialization
Citations

This map shows the geographic impact of David 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 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 Lewis‐Smith more than expected).

Fields of papers citing papers by David Lewis‐Smith

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by David 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 Lewis‐Smith. The network helps show where David Lewis‐Smith may publish in the future.

Co-authorship network of co-authors of David Lewis‐Smith

This figure shows the co-authorship network connecting the top 25 collaborators of David Lewis‐Smith. A scholar is included among the top collaborators of David Lewis‐Smith based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with David Lewis‐Smith. David Lewis‐Smith is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

18 of 18 papers shown
1.
Lewis‐Smith, David, Hany El‐Naggar, Kieron J. Sweeney, et al.. (2025). Driving after vagus nerve stimulation therapy: Is it possible?. Epilepsia Open. 10(6). 2018–2024.
2.
3.
Galer, Peter D., David Lewis‐Smith, Shridhar Parthasarathy, et al.. (2023). Enriching representation learning using 53 million patient notes through human phenotype ontology embedding. Artificial Intelligence in Medicine. 139. 102523–102523. 10 indexed citations
4.
McLeod, Faye, et al.. (2022). Altered synaptic connectivity in an in vitro human model of STXBP1 encephalopathy. Brain. 146(3). 850–857. 14 indexed citations
5.
Lewis‐Smith, David, Stephan R. Jaiser, & Rhys H. Thomas. (2022). Autoimmune musicogenic bilateral temporal lobe epilepsy. Epileptic Disorders. 24(5). 961–964. 1 indexed citations
6.
Fowkes, Ross, et al.. (2022). A review of the clinical spectrum of BRAT1 disorders and case of developmental and epileptic encephalopathy surviving into adulthood. Epilepsy & Behavior Reports. 19. 100549–100549. 5 indexed citations
7.
Lewis‐Smith, David, et al.. (2022). Late-onset cluster seizures and intellectual disability associated with a novel truncation variant in SMC1A. Epilepsy & Behavior Reports. 19. 100556–100556. 3 indexed citations
8.
Lewis‐Smith, David, Shridhar Parthasarathy, Julie Xian, et al.. (2022). Computational analysis of neurodevelopmental phenotypes: Harmonization empowers clinical discovery. Human Mutation. 43(11). 1642–1658. 11 indexed citations
9.
Lewis‐Smith, David, Shiva Ganesan, Peter D. Galer, et al.. (2021). Phenotypic homogeneity in childhood epilepsies evolves in gene-specific patterns across 3251 patient-years of clinical data. European Journal of Human Genetics. 29(11). 1690–1700. 8 indexed citations
10.
Crawford, Katherine, Julie Xian, Katherine L. Helbig, et al.. (2021). Computational analysis of 10,860 phenotypic annotations in individuals with SCN2A-related disorders. Genetics in Medicine. 23(7). 1263–1272. 32 indexed citations
11.
Lewis‐Smith, David, Peter D. Galer, Ganna Balagura, et al.. (2021). Modeling seizures in the Human Phenotype Ontology according to contemporary ILAE concepts makes big phenotypic data tractable. Epilepsia. 62(6). 1293–1305. 13 indexed citations
12.
Ganesan, Shiva, David Lewis‐Smith, Manuela Pendziwiat, et al.. (2020). Semantic Similarity Analysis Reveals Robust Gene-Disease Relationships in Developmental and Epileptic Encephalopathies. The American Journal of Human Genetics. 107(4). 683–697. 22 indexed citations
13.
Lewis‐Smith, David, Noham Wolpe, Boyd Ghosh, & James B. Rowe. (2020). Alien limb in the corticobasal syndrome: phenomenological characteristics and relationship to apraxia. Journal of Neurology. 267(4). 1147–1157. 11 indexed citations
14.
Ledingham, David, et al.. (2016). THE NEWCASTLE EXPERIENCE OF ANTI-MOG ASSOCIATED DISEASE. Journal of Neurology Neurosurgery & Psychiatry. 87(12). e1.49–e1. 10 indexed citations
15.
Lewis‐Smith, David, Kimberli J. Kamer, Helen Griffin, et al.. (2016). Homozygous deletion in MICU1 presenting with fatigue and lethargy in childhood. Neurology Genetics. 2(2). e59–e59. 79 indexed citations
16.
Bánsági, Boglárka, David Lewis‐Smith, Endre Pál, et al.. (2016). Phenotypic convergence of Menkes and Wilson disease. Neurology Genetics. 2(6). e119–e119. 13 indexed citations
17.
Lewis‐Smith, David, Jennifer Duff, Angela Pyle, et al.. (2016). Novel HSPB1 mutation causes both motor neuronopathy and distal myopathy. Neurology Genetics. 2(6). e110–e110. 18 indexed citations
18.
Horváth, Rita, David Lewis‐Smith, Konstantinos Douroudis, et al.. (2015). SCP2 mutations and neurodegeneration with brain iron accumulation. Neurology. 85(21). 1909–1911. 36 indexed citations

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.

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