(Q37316511)

English

Variants in triggering receptor expressed on myeloid cells 2 are associated with both behavioral variant frontotemporal lobar degeneration and Alzheimer's disease

scientific article published on 09 April 2013

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scholarly article

1 reference

Europe PubMed Central

19 August 2017

Variants in triggering receptor expressed on myeloid cells 2 are associated with both behavioral variant frontotemporal lobar degeneration and Alzheimer's disease (English)

1 reference

Europe PubMed Central

19 August 2017

Alzheimer's disease

0 references

frontotemporal lobar degeneration

1 reference

based on heuristic

inferred from title

13

object named as

Eric M Reiman

1 reference

Europe PubMed Central

19 August 2017

Kenneth S. Kosik

12

object named as

Kenneth S Kosik

1 reference

Europe PubMed Central

19 August 2017

Francisco Lopera

2

object named as

Francisco Lopera

1 reference

Europe PubMed Central

19 August 2017

author name string

Margarita Giraldo

1

1 reference

Europe PubMed Central

19 August 2017

Ashley L Siniard

3

1 reference

Europe PubMed Central

19 August 2017

Jason J Corneveaux

4

1 reference

Europe PubMed Central

19 August 2017

Isabelle Schrauwen

5

1 reference

Europe PubMed Central

19 August 2017

Julian Carvajal

6

1 reference

Europe PubMed Central

19 August 2017

Claudia Muñoz

7

1 reference

Europe PubMed Central

19 August 2017

Manuel Ramirez-Restrepo

8

1 reference

Europe PubMed Central

19 August 2017

Chris Gaiteri

9

1 reference

Europe PubMed Central

19 August 2017

Amanda J Myers

10

1 reference

Europe PubMed Central

19 August 2017

Richard J Caselli

11

1 reference

Europe PubMed Central

19 August 2017

Matthew J Huentelman

14

1 reference

Europe PubMed Central

19 August 2017

publication date

9 April 2013

1 reference

Europe PubMed Central

19 August 2017

Neurobiology of Aging

1 reference

Europe PubMed Central

19 August 2017

34

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Europe PubMed Central

19 August 2017

2077.e11-8

1 reference

Europe PubMed Central

19 August 2017

8

1 reference

Europe PubMed Central

19 August 2017

Using exome sequencing to reveal mutations in TREM2 presenting as a frontotemporal dementia-like syndrome without bone involvement

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3830921

6 September 2017

TREM2 Variants in Alzheimer's Disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3830921

6 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3830921

6 September 2017

TREM2 and β-catenin regulate bone homeostasis by controlling the rate of osteoclastogenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3830921

6 September 2017

Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3830921

6 September 2017

The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3830921

6 September 2017

Association of CR1, CLU and PICALM with Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individuals

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3830921

6 September 2017

Genotype imputation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3830921

6 September 2017

The Sequence Alignment/Map format and SAMtools

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3830921

6 September 2017

Fast and accurate short read alignment with Burrows-Wheeler transform

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3830921

6 September 2017

Genetic control of human brain transcript expression in Alzheimer disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3830921

6 September 2017

Amyloid deposition begins in the striatum of presenilin-1 mutation carriers from two unrelated pedigrees

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3830921

6 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3830921

6 September 2017

Nasu-Hakola disease (polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy--PLOSL): a dementia associated with bone cystic lesions. From clinical to genetic and molecular aspects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3830921

6 September 2017

TREMs in the immune system and beyond

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3830921

6 September 2017

Mutations in two genes encoding different subunits of a receptor signaling complex result in an identical disease phenotype

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3830921

6 September 2017

Clinical and pathological diagnosis of frontotemporal dementia: report of the Work Group on Frontotemporal Dementia and Pick's Disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3830921

6 September 2017

A DAP12-mediated pathway regulates expression of CC chemokine receptor 7 and maturation of human dendritic cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3830921

6 September 2017

Cutting edge: inflammatory responses can be triggered by TREM-1, a novel receptor expressed on neutrophils and monocytes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3830921

6 September 2017

Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3830921

6 September 2017

Staging of Alzheimer's disease-related neurofibrillary changes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3830921

14 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3830921

26 June 2018

A genetic cluster of early onset Parkinson's disease in a Colombian population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3830921

26 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3830921

2 September 2018

Nasu-Hakola disease with a splicing mutation of TREM2 in a Japanese family.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3830921

2 September 2018

Mutations in TREM2 lead to pure early-onset dementia without bone cysts.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3830921

2 September 2018

The National Alzheimer's Coordinating Center (NACC) Database: an Alzheimer disease database.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3830921

2 September 2018

A survey of genetic human cortical gene expression

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3830921

3 December 2018

Genetic demography of Antioquia (Colombia) and the Central Valley of Costa Rica

1 reference

https://pubmed.ncbi.nlm.nih.gov/23582655

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Single-day apolipoprotein E genotyping

1 reference

https://pubmed.ncbi.nlm.nih.gov/23582655

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Use of isolated inbred human populations for identification of disease genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/23582655

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1016/J.NEUROBIOLAGING.2013.02.016

1 reference

Europe PubMed Central

19 August 2017

release_laerormwq5b4zb5jiptsb4z3wm

1 reference

https://api.fatcat.wiki/v0/release/laerormwq5b4zb5jiptsb4z3wm

24 November 2022

based on heuristic

mapped directly with Wikidata item

1 reference

Europe PubMed Central

19 August 2017

1 reference

Europe PubMed Central

19 August 2017

ResearchGate publication ID

0 references

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