Autor Hummerich, Holger
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2012 | Zeitschriftenartikel
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. u.a. (2012)
Human Molecular Genetics, 21(8) pp. 1897-1906. DOI: https://doi.org/10.1093/hmg/ddr607
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2015 | Zeitschriftenartikel
Rare structural genetic variation in human prion diseases
Lukic, A.; Uphill, J.; Brown, C. A.; Beck, J.; Poulter, M.; Campbell, T. & Adamson, G. u.a. (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 | Zeitschriftenartikel
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. u.a. (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 | Zeitschriftenartikel |
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. u.a. (2016)
BMC Medical Genetics, 17 art. 28. DOI: https://doi.org/10.1186/s12881-016-0278-2
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2020 | Zeitschriftenartikel
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. u.a. (2020)
The Lancet Neurology, 19(10) pp. 840-848. DOI: https://doi.org/10.1016/S1474-4422(20)30273-8
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