Armstrong, Ruth
Royal Free London NHS Foundation Trust · University of Cambridge · Cancer Research UK · National Institute for Health and Care Research · Cancer Research UK Cambridge Center · NIHR Cambridge Biomedical Research Centre · University College London
2 papers on CoChatORCID 0000-0002-7958-2829
Most cited papers
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Whole-genome sequencing of patients with rare diseases in a national health system
Turro, E., Astle, W. J., Megy, K., Gräf, S., Greene, D., Shamardina, O., Allen, H. L., Sanchis-Juan, A., Frontini, M., Thys, C., et al. (2020) · Nature
Genomics and Rare DiseasesGenetic Associations and Epidemiology
Cited by 554
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KAT6A Syndrome: genotype–phenotype correlation in 76 patients with pathogenic KAT6A variants
Kennedy, J., Goudie, D., Blair, E., Chandler, K., Joss, S., McKay, V., Green, A., Armstrong, R., Lees, M., Kamien, B., et al. (2019) · Genetics in Medicine
Genomics and Rare DiseasesGenetics and Neurodevelopmental Disorders
Cited by 107
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