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Article

Do polymorphisms in the familial Parkinsonism genes contribute to risk for sporadic Parkinson's disease?

Movement disorders : official journal of the Movement Disorder Society - 30 Apr 2009

Sutherland Greg T, Halliday Glenda M, Silburn Peter A, Mastaglia Frank L, Rowe Dominic B, Boyle Richard S, O'Sullivan John D, Ly Tina, Wilton Steve D, Mellick George D

Abstract excerpt

Recent whole genome association studies provided little evidence that polymorphisms at the familial Parkinsonism loci influence the risk for Parkinson's disease (PD). However, these studies are not designed to detect the types of subtle effects that common variants may impose. Here, we use an alt...

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Source

Identifiers

PMID: 19224617
DOI: 10.1002/mds.22214

Genes

HTRA2
MAPT
PINK1
PRKN
SNCA
UCHL1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-19224617-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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