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Article

Genome-wide study links MTMR7 gene to variant Creutzfeldt-Jakob risk.

Neurobiology of aging - 1 Jul 2012

Sanchez-Juan Pascual, Bishop Matthew T, Aulchenko Yurii S, Brandel Jean-Philippe, Rivadeneira Fernando, Struchalin Maksim, Lambert Jean-Charles, Amouyel Philippe, Combarros Onofre, Sainz Jesus, Carracedo Angel, Uitterlinden Andre G, Hofman Albert, Zerr Inga, Kretzschmar Hans A, Laplanche Jean-Louis, Knight Richard S G, Will Robert G, van Duijn Cornelia M

Abstract excerpt

The aim of our study was to discover genomic variations related to variant Creutzfeldt-Jakob disease (vCJD) susceptibility. A genome-wide association analysis with most vCJD samples available in the world was performed. A series of 93 vCJD UK patients and 1504 UK controls were included in the discovery stage. Our best findings were replicated in an independent population of 22 UK and 20 French vCJD cases. Post...

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Source

Identifiers

PMID: 22137330
DOI: 10.1016/j.neurobiolaging.2011.10.011

Genes

MTMR7
PRNP
ARNT
NPAS2
PLCD3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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