Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Lack of association between the LRRK2 A419V variant and Asian Parkinson's disease.

Annals of the Academy of Medicine, Singapore - 1 May 2013

Gopalai Aroma Agape, Lim Shen Yang, Aziz Zariah Abdul, Lim Soo Kun, Tan Li Ping, Chong Yip Boon, Tan Chong Tin, Puvanarajah Santhi, Viswanathan Shanti, Kuppusamy Rishikesan, Tan Ai Huey, Lim Thien Thien, Eow Gaik Bee, Norlinah Mohamed Ibrahim, Li Hui Hua, Zhao Yi, Ahmad-Annuar Azlina

Abstract excerpt

INTRODUCTION: The G2385R and R1628P LRRK2 gene variants have been associated with an increased risk of Parkinson's disease (PD) in the Asian population. Recently, a new LRRK2 gene variant, A419V, was reported to be a third risk variant for PD in Asian patients. Our objective was to investigate th...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Alanine
Share to Cytosine

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Leucine-Rich Repeat Serine-Threonine Protein Kinase-2

Share to Malaysia

Share to Parkinson Disease

Share to Singapore

Share to Thymine

Share to Valine

Source

Identifiers

PMID: 23771111

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-23771111-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

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

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Lack of association between the LRRK2 A419V variant and Asian Parkinson's disease.PMID 23771111Read ↗

LRRK2 A419V is not associated with Parkinson's disease in different Chinese populations.Semantic proximity Read ↗

LRRK2 A419V variant is a risk factor for Parkinson's disease in Asian population.Semantic proximity Read ↗

The G2019S LRRK2 mutation is uncommon in an Asian cohort of Parkinson's disease patients.Semantic proximity Read ↗

Genetic analysis of LRRK2 A419V variant in ethnic Chinese.Semantic proximity Read ↗

<i>LRRK2</i> p.G2385R and p.R1628P Variants in a Multi-Ethnic Asian Parkinson’s Cohort: Epidemiology and Clinical InsightsSemantic proximity Read ↗

The association between the LRRK2 G2385R variant and the risk of Parkinson's disease: a meta-analysis based on 23 case-control studies.Semantic proximity Read ↗

Analysis of LRRK2 Gly2385Arg genetic variant in non-Chinese Asians.Semantic proximity Read ↗

Evaluation of the Role of LRRK2 Gene in Parkinson’s Disease in an East Indian CohortSemantic proximity Read ↗

Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study.Semantic proximity Read ↗

Clinical and functional evidence for the pathogenicity of the LRRK2 p.Arg1067Gln variantSemantic proximity Read ↗

The association between the LRRK2 R1628P variant and the risk of Parkinson's disease in Asian: a meta-analysis.Semantic proximity Read ↗

LRRK2 Gly2385Arg variant is a risk factor of Parkinson's disease among Han-Chinese from mainland China.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.