McDonagh, Ellen M.
European Bioinformatics Institute · Open Targets
5 papers on CoChatORCID 0000-0001-5806-6174
Most cited papers
- Verified
Mutational signature in colorectal cancer caused by genotoxic pks+ E. coli
Pleguezuelos-Manzano, C., Puschhof, J., Rosendahl Huber, A., van Hoeck, A., Wood, H. M., Nomburg, J., Gurjao, C., Manders, F., Dalmasso, G., Stege, P. B., et al. (2020) · Nature
Genetic factors in colorectal cancerCancer Genomics and Diagnostics
Cited by 1,208
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PanelApp crowdsources expert knowledge to establish consensus diagnostic gene panels
Martin, A. R., Williams, E., Foulger, R. E., Leigh, S., Daugherty, L. C., Niblock, O., Leong, I. U. S., Smith, K. R., Gerasimenko, O., Haraldsdottir, E., et al. (2019) · Nature Genetics
Genomics and Rare DiseasesBiomedical Text Mining and Ontologies
Cited by 559
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The next-generation Open Targets Platform: reimagined, redesigned, rebuilt
Ochoa, D., Hercules, A., Carmona, M., Suveges, D., Baker, J., Malangone, C., Lopez, I., Miranda, A., Cruz-Castillo, C., Fumis, L., et al. (2023) · Nucleic Acids Research
Computational Drug Discovery MethodsBiomedical Text Mining and Ontologies
Cited by 432
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Whole genome sequencing for the diagnosis of neurological repeat expansion disorders in the UK: a retrospective diagnostic accuracy and prospective clinical validation study
Ibañez, K., Polke, J., Hagelstrom, R. T., Dolzhenko, E., Pasko, D., Thomas, E. R. A., Daugherty, L. C., Kasperaviciute, D., Smith, K. R., McDonagh, E. M., et al. (2022) · The Lancet Neurology
Genetic Neurodegenerative DiseasesGenomics and Rare Diseases
Cited by 187
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PharmGKB summary: very important pharmacogene information for N-acetyltransferase 2
McDonagh, E. M., Boukouvala, S., Aklillu, E., Hein, D. W., Altman, R. B., & Klein, T. E. (2014) · Pharmacogenetics and Genomics
Pharmacogenetics and Drug MetabolismGenetic Associations and Epidemiology
Cited by 146
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