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

SNPs in SNCA, MCCC1, DLG2, GBF1 and MBNL2 are associated with Parkinson's disease in southern Chinese population.

Journal of cellular and molecular medicine - 1 Aug 2020

Zhao Aonan, Li Yuanyuan, Niu Mengyue, Li Guanglu, Luo Ningdi, Zhou Liche, Kang Wenyan, Liu Jun

Abstract excerpt

Numerous single nucleotide polymorphisms (SNPs), which have been identified as susceptibility factors for Parkinson's disease (PD) as per genome-wide association studies, have not been fully characterized for PD patients in China. This study aimed to replicate the relationship between 12 novel SNPs of 12 genes and PD risk in southern Chinese population. Twelve SNPs of 12 genes were detected in 231 PD patients and...

Read the complete abstract on PubMed

Topics

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

Share to alpha-Synuclein
Share to Carbon-Carbon Ligases

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Guanine Nucleotide Exchange Factors

Share to Guanylate Kinases

Share to Parkinson Disease

Share to Population Surveillance

Share to RNA-Binding Proteins

Share to Tumor Suppressor Proteins

Source

Open in PubMed Open full text

Identifiers

PMID: 32652860
DOI: 10.1111/jcmm.15508
PMCID: PMC7412680

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

SNPs in SNCA, MCCC1, DLG2, GBF1 and MBNL2 are associated with Parkinson's disease in southern Chinese population.PMID 32652860Read ↗

Genome-wide association study using whole-genome sequencing identifies risk loci for Parkinson’s disease in Chinese populationSemantic proximity Read ↗

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

Association analysis and polygenic risk score evaluation of 38 GWAS-identified Loci in a Chinese population with Parkinson's disease.Semantic proximity Read ↗

A Pooling Genome-Wide Association Study Combining a Pathway Analysis for Typical Sporadic Parkinson's Disease in the Han Population of Chinese Mainland.Semantic proximity Read ↗

The genetic spectrum of a cohort of patients clinically diagnosed as Parkinson’s disease in mainland ChinaSemantic proximity Read ↗

Target gene capture sequencing in Chinese population of sporadic Parkinson disease.Semantic proximity Read ↗

The association between LIN28A gene rare variants and Parkinson's disease in Chinese population.Semantic proximity Read ↗

Gene4PD: a comprehensive genetic database of Parkinson's diseaseSemantic proximity Read ↗

Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease.Semantic proximity Read ↗

Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease.Semantic proximity Read ↗

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

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

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