Alastair Compston
Affiliations: | University of Cambridge, Cambridge, England, United Kingdom |
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"Alastair Compston"Mean distance: 16.29 (cluster 17)
Children
Sign in to add traineeMichael S. Zandi | grad student | Cambridge | |
Mojtaba Zarei | post-doc | 1999-2001 | Cambridge |
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Publications
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Compston A. (2020) Review: Multiple sclerosis in the digital age: 'seeing through a glass darkly'. Journal of Neurology, Neurosurgery, and Psychiatry |
Ban M, Liao W, Baker A, et al. (2020) Transcript specific regulation of expression influences susceptibility to multiple sclerosis. European Journal of Human Genetics : Ejhg |
Lehmann HC, Compston A, Hartung HP. (2018) 150th anniversary of clinical description of multiple sclerosis: Leopold Ordenstein's legacy. Neurology. 90: 1011-1016 |
Compston A. (2014) Update on disease modifying therapies in MS. Multiple Sclerosis and Related Disorders. 3: 767 |
Goris A, van Setten J, Diekstra F, et al. (2014) No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis. Human Molecular Genetics. 23: 1916-22 |
Ban M, Caillier S, Mero IL, et al. (2013) No evidence of association between mutant alleles of the CYP27B1 gene and multiple sclerosis. Annals of Neurology. 73: 430-2 |
Connick P, Kolappan M, Crawley C, et al. (2012) Autologous mesenchymal stem cells for the treatment of secondary progressive multiple sclerosis: an open-label phase 2a proof-of-concept study. The Lancet. Neurology. 11: 150-6 |
Patsopoulos NA, et al. (2011) Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci. Annals of Neurology. 70: 897-912 |
Sawcer S, et al. (2011) Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. Nature. 476: 214-9 |
Zuvich RL, Bush WS, McCauley JL, et al. (2011) Interrogating the complex role of chromosome 16p13.13 in multiple sclerosis susceptibility: independent genetic signals in the CIITA-CLEC16A-SOCS1 gene complex. Human Molecular Genetics. 20: 3517-24 |