Author Collinge, John

• 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 
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• 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 
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• 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 
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• 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 
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• 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 
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• 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 
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