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

Alzheimer disease: The involvement of TREM2 R47H variant in Alzheimer disease confirmed, but mechanisms remain elusive.

Nature reviews. Neurology - 1 Jun 2015

Malkki Hemi

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Alzheimer Disease
Share to TREM2 gene
Share to Genetic Predisposition to Disease
Share to Genetic Variation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 25986503
DOI: 10.1038/nrneurol.2015.84

Genes

TREM2

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Alzheimer disease: The involvement of TREM2 R47H variant in Alzheimer disease confirmed, but mechanisms remain elusive.PMID 25986503Read ↗

The role of TREM2 in Alzheimer's disease and other neurodegenerative disorders.Semantic proximity Read ↗

TREMs in Alzheimer's disease: Genetic and clinical investigationsSemantic proximity Read ↗

The role of TREM2 in Alzheimer's disease; evidence from transgenic mouse modelsSemantic proximity Read ↗

Role of TREM2 in Alzheimer's Disease: A Long Road Ahead.Semantic proximity Read ↗

Missense variant in TREML2 protects against Alzheimer's disease.Semantic proximity Read ↗

Variant <i>TREM2</i> as Risk Factor for Alzheimer's DiseaseSemantic proximity Read ↗

TREM2 and Risk of Alzheimer's Disease--Friend or Foe?Semantic proximity Read ↗

TREM2 variants in Alzheimer's disease.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 ↗

Assessing the role of the TREM2 p.R47H variant as a risk factor for Alzheimer's disease and frontotemporal dementia.Semantic proximity Read ↗

Variant TREM2 Signaling in Alzheimer's DiseaseSemantic proximity Read ↗

Trem2 R47H mutation shows mild, but functionally divergent alterations in microglial phenotypes compared to Trem2 deficiency in aged AppNL-F knock-in mice.Semantic proximity Read ↗

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