Genetic risk factors for variant Creutzfeldt–Jakob disease: a genome-wide association study-Reference-Cited by-同舟云学术

Genetic risk factors for variant Creutzfeldt–Jakob disease: a genome-wide association study

Published:2009-01 Issue:1 Volume:8 Page:57-66
ISSN:1474-4422
Container-title:The Lancet Neurology
language:en
Short-container-title:The Lancet Neurology

Author:

Mead Simon,Poulter Mark,Uphill James,Beck John,Whitfield Jerome,Webb Thomas EF,Campbell Tracy,Adamson Gary,Deriziotis Pelagia,Tabrizi Sarah J,Hummerich Holger,Verzilli Claudio,Alpers Michael P,Whittaker John C,Collinge John

Publisher

Elsevier BV

Subject

Neurology (clinical)

Reference32 articles.

1. Prion diseases of humans and animals: their causes and molecular basis;Collinge;Annu Rev Neurosci,2001

2. Molecular analysis of prion strain variation and the aetiology of ‘new variant’ CJD;Collinge;Nature,1996

3. Transmissions to mice indicate that ‘new variant’ CJD is caused by the BSE agent;Bruce;Nature,1997

4. The same prion strain causes vCJD and BSE;Hill;Nature,1997

5. Kuru in the 21st century—an acquired human prion disease with very long incubation periods;Collinge;Lancet,2006

Cited by 125 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Lack of prion transmission barrier in human PrP transgenic Drosophila;Journal of Biological Chemistry;2024-09

2. Neuropathologically directed profiling of PRNP somatic and germline variants in sporadic human prion disease;Acta Neuropathologica;2024-07-24

3. Neuropathologically-directed profiling ofPRNPsomatic and germline variants in sporadic human prion disease;2024-06-29

4. Genetic characterization of the prion protein gene in camels (Camelus) with comments on the evolutionary history of prion disease in Cetartiodactyla;PeerJ;2024-06-27

5. Genetic and pathological features encipher the phenotypic heterogeneity of Gerstmann-Sträussler-Scheinker disease;Neurobiology of Disease;2024-06