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 analysis of MC1R variants in Chinese Han patients with sporadic Parkinson's disease.

Neuroscience letters - 12 Jan 2016

He Sihan, Tan Ting, Song Zhi, Yuan Lamei, Deng Xiong, Ni Bin, Chen Yong, Deng Hao

Abstract excerpt

Parkinson's disease (PD, OMIM 168600) is a neurodegenerative disorder featured by degeneration of melanin-positive dopaminergic neurons. Epidemiologic studies have suggested that PD and malignant melanoma (MM) might share common genetic components. Recently, the p.R160W variant in the melanocortin 1 receptor gene (MC1R, OMIM 155555), a risk factor for MM, has been identified to be associated with PD in Spanish...

Read the complete abstract on PubMed

Topics

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

Share to Aged
Share to Asian People
Share to Case-Control Studies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Association Studies

Share to Genetic Variation

Share to Haplotypes

Share to Parkinson Disease

Share to Receptor, Melanocortin, Type 1

Source

Identifiers

PMID: 26628245
DOI: 10.1016/j.neulet.2015.11.034

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genetic analysis of MC1R variants in Chinese Han patients with sporadic Parkinson's disease.PMID 26628245Read ↗

MC1R variants in Chinese Han patients with sporadic Parkinson's disease.Semantic proximity Read ↗

The MC1R melanoma risk variant p.R160W is associated with Parkinson disease.Semantic proximity Read ↗

The role of the melanoma gene MC1R in Parkinson disease and REM sleep behavior disorder.Semantic proximity Read ↗

SLC6A3 rs28363170 and rs3836790 variants in Han Chinese patients with sporadic Parkinson's disease.Semantic proximity Read ↗

Genetic analysis of TREM2 variants in Chinese Han patients with sporadic Parkinson's disease.Semantic proximity Read ↗

The melanocortin 1 receptor (Mc1r) variants do not account for the co-occurrence of Parkinson's disease and malignant melanoma.Semantic proximity Read ↗

Association study between two novel single nucleotide polymorphisms and sporadic Parkinson's disease in Chinese Han population.Semantic proximity Read ↗

Genetic analysis of SLC41A1 in Chinese Parkinson's disease patients.Semantic proximity Read ↗

Systematic Genetic Analysis of the SMPD1 Gene in Chinese Patients with Parkinson's Disease.Semantic proximity Read ↗

An association analysis of the R1628P and G2385R polymorphisms of the LRRK2 gene in multiple system atrophy in a Chinese population.Semantic proximity Read ↗

Genetic analysis of the TMEM230 gene in Chinese Han patients with Parkinson's disease.Semantic proximity Read ↗

Association of GLP-1 receptor gene polymorphisms with sporadic Parkinson's disease in Chinese Han population.Semantic proximity Read ↗

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