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

Association between a heme oxygenase-2 genetic variant and risk of Parkinson's disease in Han Chinese.

Neuroscience letters - 6 Mar 2017

Tian Sijia, Yang Xinglong, Zhao Quanzhen, Zheng Jinhua, Huang Hongyan, Chen Yalan, An Ran, Xu Yanming

Abstract excerpt

Studies have reported conflicting results about possible associations between variants in heme oxygenase (HMOX) genes and risk of Parkinson's disease (PD) in Caucasians, and little is known about these associations in Asians. We genotyped the single-nucleotide polymorphisms (SNPs) rs2071746 and rs2071747 in HMOX1 and rs1051308 in HMOX2 in 583 Han Chinese with PD and 627 healthy controls using a customized...

Read the complete abstract on PubMed

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Topics

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

Share to Aged, 80 and over
Share to Asian People
Share to China
Share to Genetic Association Studies
Share to Haplotypes
Share to Heme Oxygenase (Decyclizing)
Share to Parkinson Disease
Share to Young Adult

Source

Identifiers

PMID: 28179208
DOI: 10.1016/j.neulet.2017.02.008

Genes

HMOX1
HMOX2

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

Association between a heme oxygenase-2 genetic variant and risk of Parkinson's disease in Han Chinese.PMID 28179208Read ↗

Association of HMOX-1 rs2071747 with sporadic Parkinson's disease in southern Han Chinese.Semantic proximity Read ↗

An association study between Heme oxygenase-1 genetic variants and Parkinson's diseaseSemantic proximity Read ↗

Genetic Analysis of FBXO2, FBXO6, FBXO12, and FBXO41 Variants in Han Chinese Patients with Sporadic Parkinson's Disease.Semantic proximity Read ↗

Heme Oxygenase 1 and 2 Common Genetic Variants and Risk for Essential Tremor.Semantic proximity Read ↗

Aldehyde dehydrogenase 2 genetic variations may increase susceptibility to Parkinson's disease in Han Chinese population.Semantic proximity Read ↗

A polymorphism located at an ATG transcription start site of the heme oxygenase-2 gene is associated with classical Parkinson's disease.Semantic proximity Read ↗

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

MTHFR C677T variant reduces risk of sporadic Parkinson's disease in ethnic Chinese.Semantic proximity Read ↗

ATP13A2 Gene Variants in Patients with Parkinson's Disease in Xinjiang.Semantic proximity Read ↗

Genetic variants in GAPDH confer susceptibility to sporadic Parkinson's disease in a Chinese Han population.Semantic proximity Read ↗

Superoxide dismutase coding of gene polymorphisms associated with susceptibility to Parkinson’s diseaseSemantic proximity Read ↗

Association of Dopamine Beta-Hydroxylase (DBH) Polymorphisms with Susceptibility to Parkinson's Disease.Semantic proximity Read ↗

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