Author Mead, Simon
-
2010 | Journal Article |
Genetic Evidence Implicates the Immune System and Cholesterol Metabolism in the Aetiology of Alzheimer's Disease
Jones, L.; Holmans, P. A.; Hamshere, M. L.; Harold, D.; Moskvina, V.; Ivanov, D. & Pocklington, A. et al. (2010)
PLoS ONE, 5(11) art. e13950. DOI: https://doi.org/10.1371/journal.pone.0013950
Details DOI PMID PMC
-
2012 | Journal Article
Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP
Mead, S.; Uphill, J.; Beck, J.; Poulter, M.; Campbell, T.; Lowe, J. & Adamson, G. et al. (2012)
Human Molecular Genetics, 21(8) pp. 1897-1906. DOI: https://doi.org/10.1093/hmg/ddr607
Details DOI PMID PMC WoS
-
2014 | Journal Article
R47H TREM2 variant increases risk of typical early-onset Alzheimer's disease but not of prion or frontotemporal dementia
Slattery, C. F.; Beck, J. A.; Harper, L.; Adamson, G.; Abdi, Z.; Uphill, J. & Campbell, T. et al. (2014)
Alzheimer s & Dementia, 10(6) pp. 602-608. DOI: https://doi.org/10.1016/j.jalz.2014.05.1751
Details DOI PMID PMC WoS
-
2014 | Journal Article
Ascertainment Bias Causes False Signal of Anticipation in Genetic Prion Disease
Minikel, E. V.; Zerr, I.; Collins, S. J.; Ponto, C.; Boyd, A.; Klug, G. M. J. A. & Karch, A. et al. (2014)
The American Journal of Human Genetics, 95(4) pp. 371-382. DOI: https://doi.org/10.1016/j.ajhg.2014.09.003
Details DOI PMID PMC WoS
-
2015 | Journal Article
Rare structural genetic variation in human prion diseases
Lukic, A.; Uphill, J.; Brown, C. A.; Beck, J.; Poulter, M.; Campbell, T. & Adamson, G. et al. (2015)
Neurobiology of Aging, 36(5) pp. 2004-U20. DOI: https://doi.org/10.1016/j.neurobiolaging.2015.01.011
Details DOI WoS
-
2015 | Journal Article
Inherited mtDNA variations are not strong risk factors in human prion disease
Hudson, G.; Uphill, J.; Hummerich, H.; Blevins, J.; Gambetti, P.; Zerr, I. & Collinge, J. et al. (2015)
Neurobiology of Aging, 36(10) art. 2908.e1. DOI: https://doi.org/10.1016/j.neurobiolaging.2015.07.005
Details DOI PMID PMC WoS
-
2016 | Journal Article |
Variants of PLCXD3 are not associated with variant or sporadic Creutzfeldt-Jakob disease in a large international study
Balendra, R.; Uphill, J.; Collinson, C.; Druyeh, R.; Adamson, G.; Hummerich, H. & Zerr, I. et al. (2016)
BMC Medical Genetics, 17 art. 28. DOI: https://doi.org/10.1186/s12881-016-0278-2
Details DOI PMID PMC WoS
-
2019 | Journal Article
Age at onset in genetic prion disease and the design of preventive clinical trials
Minikel, E. V.; Vallabh, S. M.; Orseth, M. C.; Brandel, J.-P.; Haïk, S.; Laplanche, J.-L. & Zerr, I. et al. (2019)
Neurology, 93(2) pp. e125-e134. DOI: https://doi.org/10.1212/WNL.0000000000007745
Details DOI
-
2020 | Journal Article
Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association study
Jones, E.; Hummerich, H.; Viré, E.; Uphill, J.; Dimitriadis, A.; Speedy, H. & Campbell, T. et al. (2020)
The Lancet Neurology, 19(10) pp. 840-848. DOI: https://doi.org/10.1016/S1474-4422(20)30273-8
Details DOI
-
2021 | Journal Article | Research Paper
Biomarkers and diagnostic guidelines for sporadic Creutzfeldt-Jakob disease
Hermann, P.; Appleby, B.; Brandel, J.-P.; Caughey, B.; Collins, S.; Geschwind, M. D. & Green, A. et al. (2021)
The Lancet. Neurology, 20(3) pp. 235-246. DOI: https://doi.org/10.1016/S1474-4422(20)30477-4
Details DOI PMID PMC