Back to search

Article

A genome-wide association study of young onset Parkinson’s disease in European ancestry

2026-06-04

Abstract excerpt

Young onset Parkinson’s disease may be caused by biallelic mutations in PRKN or other autosomal recessive Parkinson’s disease genes, but the majority of patients do not carry known monogenic variants. Previous studies have found an increased cumulative burden of common genetic risk variants for Parkinson’s disease in young onset patients, but the specific genetic architecture of non-monogenic young onset Parkinso...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work
3fada265-43ec-54a7-88f2-8c3e58958aa8
DOI
10.64898/2026.06.03.26354799
Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest
Interactive article relationship graphSelect a related publication card to move it into the centre and load its closest explainable connections. Solid lines are source-backed structured connections. Dashed lines are semantic discovery signals and are not scientific evidence.
A genome-wide association study of young onset Parkinson’s disease in European ancestryDOI 10.64898/2026.06.03.26354799
Select a neighboring publication to make it the new centre.