Skip directly to search Skip directly to A to Z list Skip directly to navigation Skip directly to page options Skip directly to site content

Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Dec 4, 2023. (Total: 223640Documents)
   dataset        GWAS Only
Filtered By:

Previous    

Records 1 - 6 (of 6 Records)

Query Trace: Kuru and PRNP[original query]
Increased susceptibility to Kuru of carriers of the PRNP 129 methionine/methionine genotype.
The Journal of infectious diseases 2001 Jan 183 (2): 192-196.
Lee H S, Brown P, Cervenáková L, Garruto R M, Alpers M P, Gajdusek D C, Goldfarb L
Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study. GWAS Catalog
The Lancet. Neurology 2009 Jan 8 (1): 57-66.
Mead Simon, Poulter Mark, Uphill James, Beck John, Whitfield Jerome, Webb Thomas E F, Campbell Tracy, Adamson Gary, Deriziotis Pelagia, Tabrizi Sarah J, Hummerich Holger, Verzilli Claudio, Alpers Michael P, Whittaker John C, Collinge Jo
Genetic susceptibility, evolution and the kuru epidemic.
Philosophical transactions of the Royal Society of London. Series B, Biological sciences 2008 Nov 363 (1510): 3741-6.
Mead Simon, Whitfield Jerome, Poulter Mark, Shah Paresh, Uphill James, Beck Jonathan, Campbell Tracy, Al-Dujaily Huda, Hummerich Holger, Alpers Michael P, Collinge Jo
Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP. GWAS Catalog
Human molecular genetics 2012 Apr 21 (8): 1897-906.
Mead Simon, Uphill James, Beck John, Poulter Mark, Campbell Tracy, Lowe Jessica, Adamson Gary, Hummerich Holger, Klopp Norman, Rückert Ina-Maria, Wichmann H-Erich, Azazi Dhoyazan, Plagnol Vincent, Pako Wandagi H, Whitfield Jerome, Alpers Michael P, Whittaker John, Balding David J, Zerr Inga, Kretzschmar Hans, Collinge Jo
RARB and STMN2 polymorphisms are not associated with sporadic Creutzfeldt-Jakob disease (CJD) in the Korean population.
Molecular biology reports 2014 41 (4): 2389-95.
Jeong Byung-Hoon, Kim Hae-Jung, Lee Kyung-Hee, Carp Richard I, Kim Yong-S
Rare structural genetic variation in human prion diseases.
Neurobiology of aging 2015 May 36 (5): 2004.e1-8.
Lukic Ana, Uphill James, Brown Craig A, Beck John, Poulter Mark, Campbell Tracy, Adamson Gary, Hummerich Holger, Whitfield Jerome, Ponto Claudia, Zerr Inga, Lloyd Sarah E, Collinge John, Mead Sim
TOP