Brown, Jeremy M
University of Cambridge
2 papers on CoChatORCID 0000-0002-1929-5844
Most cited papers
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Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia
Skibinski, G., Parkinson, N. J., Brown, J. M., Chakrabarti, L., Lloyd, S. L., Hummerich, H., Nielsen, J. E., Hodges, J. R., Spillantini, M. G., Thusgaard, T., et al. (2005) · Nature Genetics
Alzheimer's disease research and treatmentsAmyotrophic Lateral Sclerosis Research
Cited by 822
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Large C9orf72 Hexanucleotide Repeat Expansions Are Seen in Multiple Neurodegenerative Syndromes and Are More Frequent Than Expected in the UK Population
Beck, J., Poulter, M., Hensman, D., Rohrer, J. D., Mahoney, C. J., Adamson, G., Campbell, T., Uphill, J., Borg, A., Fratta, P., et al. (2013) · The American Journal of Human Genetics
Amyotrophic Lateral Sclerosis ResearchGenetic Neurodegenerative Diseases
Cited by 345
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