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

doi:10.1016/j.neulet.2015.12.029

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

Community

Back to search

Article

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

Neuroscience letters - 26 Jan 2016

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

Abstract excerpt

Parkinson's disease (PD) is the second most common neurodegenerative disorder after Alzheimer's disease and is characterized by the degeneration of dopaminergic neurons in substantia nigra. Recently, rs75932628 (p.R47H) of the triggering receptor expressed on myeloid cells 2 gene (TREM2) was identified to be associated with PD in American, Spanish, Irish, and Polish population. To explore whether TREM2 variants...

Read the complete abstract on PubMed

Topics

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

Share to Aged

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Asian People

Share to Case-Control Studies

Share to Genetic Association Studies

Share to Membrane Glycoproteins

Share to Parkinson Disease

Share to Polymorphism, Single Nucleotide

Share to Receptors, Immunologic

Source

Open in PubMed

Identifiers

PMID: 26704436
DOI: 10.1016/j.neulet.2015.12.029

Genes

TREM2

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 TREM2 variants in Chinese Han patients with sporadic Parkinson's disease.PMID 26704436Read ↗

Triggering receptor expressed on myeloid cells 2 variants are rare in Parkinson's disease in a Han Chinese cohort.Semantic proximity Read ↗

Assessment of TREM2 rs75932628 association with Parkinson's disease and multiple system atrophy in a Chinese population.Semantic proximity Read ↗

Targeting TREM2 for Parkinson's Disease: Where to Go?Semantic proximity Read ↗

TREM2 rare variant p.R47H is not associated with Parkinson's disease.Semantic proximity Read ↗

Association study of TREM2 polymorphism rs75932628 with leucoaraiosis or Parkinson's disease in the Han Chinese population.Semantic proximity Read ↗

Assessment of TREM2 rs75932628 association with amyotrophic lateral sclerosis in a Chinese population.Semantic proximity Read ↗

Analysis of Cerebrospinal Fluid Soluble TREM2 and Polymorphisms in Sporadic Parkinson's Disease in a Chinese Population.Semantic proximity Read ↗

Convergent Genetic and Expression Datasets Highlight TREM2 in Parkinson's Disease Susceptibility.Semantic proximity Read ↗

The role of TREM2 R47H as a risk factor for Alzheimer's disease, frontotemporal lobar degeneration, amyotrophic lateral sclerosis, and Parkinson's disease.Semantic proximity Read ↗

Differential role of triggering receptors expressed on myeloid cells 2 R47H in 3 neurodegenerative diseases based on a systematic review and meta-analysis.Semantic proximity Read ↗

TREM2 in neurodegeneration: evidence for association of the p.R47H variant with frontotemporal dementia and Parkinson's disease.Semantic proximity Read ↗

TREM2 R47H variant and risk of essential tremor: a cross-sectional international multicenter study.Semantic proximity Read ↗

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