Marshall, Andrew

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

Corneal Confocal Microscopy Identifies Small-Fiber Neuropathy in Subjects With Impaired Glucose Tolerance Who Develop Type 2 Diabetes

Azmi, S., Ferdousi, M., Petropoulos, I. N., Ponirakis, G., Alam, U., Fadavi, H., Asghar, O., Marshall, A., Atkinson, A. J., Jones, W., et al. (2015) · Diabetes Care

Pain Mechanisms and TreatmentsOcular Surface and Contact Lens

Cited by 148

An ultrafast system for signaling mechanical pain in human skin

Nagi, S. S., Marshall, A. G., Makdani, A., Jarocka, E., Liljencrantz, J., Ridderström, M., Shaikh, S., O’Neill, F., Saade, D., Donkervoort, S., et al. (2019) · Science Advances

Pain Mechanisms and TreatmentsIon Channels and Receptors

Cited by 140

Spinal signalling of C-fiber mediated pleasant touch in humans

Marshall, A. G., Sharma, M. L., Marley, K., Olausson, H., & McGlone, F. P. (2019) · eLife

Tactile and Sensory InteractionsPain Mechanisms and Treatments

Cited by 73

De Novo Truncating Mutations in WASF1 Cause Intellectual Disability with Seizures

Ito, Y., Carss, K. J., Duarte, S. T., Hartley, T., Keren, B., Kurian, M. A., Marey, I., Charles, P., Mendonça, C., Nava, C., et al. (2018) · The American Journal of Human Genetics

Genetics and Neurodevelopmental DisordersGenomics and Rare Diseases

Cited by 41