(Q36472325)

14 August 2017

Association study of TREM2 polymorphism rs75932628 with leucoaraiosis or Parkinson's disease in the Han Chinese population (English)

1 reference

14 August 2017

1 reference

Zhiming Li

1

1 reference

14 August 2017

Li Zhong

2

1 reference

14 August 2017

Long Gu

3

1 reference

14 August 2017

Wenqing Huang

4

1 reference

14 August 2017

Xinzhen Shi

5

1 reference

14 August 2017

Xilin Zhang

6

1 reference

14 August 2017

Xingkai An

7

1 reference

14 August 2017

Qing Lin

8

1 reference

14 August 2017

Chi-Meng Tzeng

9

1 reference

14 August 2017

12 January 2016

1 reference

14 August 2017

1 reference

14 August 2017

6

1 reference

14 August 2017

1

1 reference

14 August 2017

e009499

1 reference

More evidence for association of a rare TREM2 mutation (R47H) with Alzheimer's disease risk.

14 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4716257

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4716257

P268S in NOD2 associates with susceptibility to Parkinson's disease in Chinese population

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4716257

TREM2 is associated with the risk of Alzheimer's disease in Spanish population

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4716257

TREM2 Variants in Alzheimer's Disease

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4716257

Variant of TREM2 Associated with the Risk of Alzheimer's Disease

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4716257

White matter lesions in Parkinson disease

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4716257

The genetic causes of basal ganglia calcification, dementia, and bone cysts: DAP12 and TREM2.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4716257

TREMs in the immune system and beyond

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4716257

A role for TREM2 ligands in the phagocytosis of apoptotic neuronal cells by microglia

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4716257

Lack of genetic association between TREM2 and late-onset Alzheimer's disease in a Japanese population.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4716257

Triggering receptor expressed on myeloid cells 2 variant is rare in late-onset Alzheimer's disease in Han Chinese individuals

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4716257

Investigating the role of rare heterozygous TREM2 variants in Alzheimer's disease and frontotemporal dementia.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4716257

TREM2 R47H variant as a risk factor for early-onset Alzheimer's disease.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4716257

TREM2 and Neurodegenerative Disease

21 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26758262

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Triggering receptor expressed on myeloid cells 2 variants are rare in Parkinson's disease in a Han Chinese cohort

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26758262

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/BMJOPEN-2015-009499

1 reference

release_cfu7eixxzncmbi2ylpskkfwbaq

14 August 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/cfu7eixxzncmbi2ylpskkfwbaq

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference

14 August 2017

PubMed publication ID

26758262

1 reference