Shapiro, Susan E.
Centre for Human Genetics · National Institute for Health and Care Research · University of Oxford · NIHR Oxford Biomedical Research Centre · Oxford University Hospitals NHS Trust · Wellcome Trust
2 papers on CoChatORCID 0000-0003-0402-0802
Most cited papers
- Verified
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
- Verified
Clinical outcomes resulting from telemedicine interventions: a systematic review
Hersh, W. R., Helfand, M., Wallace, J., Kraemer, D., Patterson, P., Shapiro, S., & Greenlick, M. (2001) · BMC Medical Informatics and Decision Making
Telemedicine and Telehealth ImplementationHealthcare Systems and Technology
Cited by 234
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