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Article

Lack of replication of association between GIGYF2 variants and Parkinson disease.

Human molecular genetics - 15 Jan 2009

Bras Jose, Simón-Sánchez Javier, Federoff Monica, Morgadinho Ana, Januario Cristina, Ribeiro Maria, Cunha Luis, Oliveira Catarina, Singleton Andrew B

Abstract excerpt

Mutations in GIGYF2 have recently been described as causative of Parkinson's disease in Europeans. In an attempt to replicate these results in independent populations, we sequenced the entire coding region of GIGYF2 in a large series of Portuguese and North American samples. We report the finding...

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Source

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Identifiers

PMID: 18923002
DOI: 10.1093/hmg/ddn340
PMCID: PMC2638775

Genes

GIGYF2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-18923002-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

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Lack of replication of association between GIGYF2 variants and Parkinson disease.PMID 18923002Read ↗

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GIGYF2 has no major role in Parkinson genetic etiology in a Belgian population.Semantic proximity Read ↗

Mutational screening and zebrafish functional analysis of GIGYF2 as a Parkinson-disease gene.Semantic proximity Read ↗

The GIGYF2 variants are not associated with Parkinson's disease in the mainland Chinese population.Semantic proximity Read ↗

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