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

Genetic association study between STK39 and CCDC62/HIP1R and Parkinson's disease.

PloS one - 1 Jan 2013

Li Nan-Nan, Tan Eng-King, Chang Xue-Li, Mao Xue-Ye, Zhang Jin-Hong, Zhao Dong-Mei, Liao Qiao, Yu Wen-Juan, Peng Rong

Abstract excerpt

BACKGROUND: The first large-scale meta-analysis of published genome-wide association studies (GWAS) in Parkinson's disease (PD) identified 5 new genetic loci (ACMSD, STK39, MCCC1/LAMP3, SYT11, and CCDC62/HIP1R). Very recently, a large-scale replication and heterogeneity study also reported that S...

Read the complete abstract on PubMed

Topics

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

Share to Adaptor Proteins, Signal Transducing
Share to Asian People
Share to China

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Association Studies

Share to Microfilament Proteins

Share to Parkinson Disease

Share to Protein Serine-Threonine Kinases

Share to Vesicular Transport Proteins

Source

Open in PubMed Open full text

Identifiers

PMID: 24312176
DOI: 10.1371/journal.pone.0079211
PMCID: PMC3842305

Genes

CCDC62
STK39
ACMSD
LAMP3
MAF
MCCC1
SYT11

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-24312176-2026-09-04.2. 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

Genetic association study between STK39 and CCDC62/HIP1R and Parkinson's disease.PMID 24312176Read ↗

Association analysis of STK39, MCCC1/LAMP3 and sporadic PD in the Chinese Han population.Semantic proximity Read ↗

MCCC1/LAMP3 reduces risk of sporadic Parkinson's disease in Han Chinese.Semantic proximity Read ↗

Supportive evidence for 11 loci from genome-wide association studies in Parkinson's disease.Semantic proximity Read ↗

Association of three candidate genetic variants in RAB7L1/NUCKS1, MCCC1 and STK39 with sporadic Parkinson's disease in Han Chinese.Semantic proximity Read ↗

The single nucleotide polymorphism Rs12817488 is associated with Parkinson's disease in the Chinese population.Semantic proximity Read ↗

Analysis of genome-wide association study-linked loci in Parkinson's disease of Mainland China.Semantic proximity Read ↗

Association of GCH1 and MIR4697, but not SIPA1L2 and VPS13C polymorphisms, with Parkinson's disease in Taiwan.Semantic proximity Read ↗

Identification of Risk Loci for Parkinson Disease in Asians and Comparison of Risk Between Asians and Europeans: A Genome-Wide Association Study.Semantic proximity Read ↗

The role of genetics in Parkinson's disease: a large cohort study in Chinese mainland population.Semantic proximity Read ↗

Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.Semantic proximity Read ↗

Association of four new candidate genetic variants with Parkinson's disease in a Han Chinese population.Semantic proximity Read ↗

Polymorphism in MIR4697 but not VPS13C, GCH1, or SIPA1L2 is associated with risk of Parkinson's disease in a Han Chinese population.Semantic proximity Read ↗

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