Parkinson, Nick
Roslin Institute · Cambridge University Hospitals NHS Foundation Trust · University of Edinburgh
3 papers on CoChatORCID 0000-0001-6336-5654
Most cited papers
- Verified
ALS phenotypes with mutations in CHMP2B (charged multivesicular body protein 2B)
Parkinson, N., Ince, P. G., Smith, M. O., Highley, R., Skibinski, G., Andersen, P. M., Morrison, K. E., Pall, H. S., Hardiman, O., Collinge, J., et al. (2006) · Neurology
Amyotrophic Lateral Sclerosis ResearchHereditary Neurological Disorders
Cited by 395
- Verified
GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19
Pairo-Castineira, E., Rawlik, K., Bretherick, A. D., Qi, T., Wu, Y., Nassiri, I., McConkey, G. A., Zechner, M., Klaric, L., Griffiths, F., et al. (2023) · Nature
Genetic Associations and EpidemiologyCOVID-19 Clinical Research Studies
Cited by 225
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Progressive neuronal inclusion formation and axonal degeneration in CHMP2B mutant transgenic mice
Ghazi-Noori, S., Froud, K. E., Mizielinska, S., Powell, C., Smidak, M., Fernandez de Marco, M., O’Malley, C., Farmer, M., Parkinson, N., Fisher, E. M. C., et al. (2012) · Brain
Alzheimer's disease research and treatmentsAmyotrophic Lateral Sclerosis Research
Cited by 115
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