# Using Exome Sequencing to Reveal Mutations in TREM2 Presenting as a Frontotemporal Dementia–like Syndrome Without Bone Involvement

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/using-exome-sequencing-to-reveal-mutations-in-trem2-presenting-as-a/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Rita Guerreiro,Ebba Lohmann,José Brás,J. Raphael Gibbs,Jonathan D. Rohrer,Nicole Gurunlian,Burcu Dursun,Başar Bılgıç,Haşmet Hanağası,Hakan Gürvıt,Murat Emre,Andrew Singleton,John Hardy |
| Citations | 389 |
| DOI | 10.1001/jamaneurol.2013.579 |
| Fields | Neuroscience |
| Open Access | true |
| OA Status | green |
| OA URL | https://www.ncbi.nlm.nih.gov/pmc/articles/4001789 |
| OpenAlex ID | https://openalex.org/W1984557585 |
| PMID | 23318515 |
| Type | article |
| Year | 2013 |

## Paper authors

- [Hakan Gürvıt](https://scholariq.org/researchers/hakan-gurv-t/)

## Paper journal

- [JAMA Neurology](https://scholariq.org/journals/jama-neurology/)

## Paper primary topic

- [Neuroinflammation and Neurodegeneration Mechanisms](https://scholariq.org/topics/neuroinflammation-and-neurodegeneration-mechanisms/)

## Paper topics

- [Neuroinflammation and Neurodegeneration Mechanisms](https://scholariq.org/topics/neuroinflammation-and-neurodegeneration-mechanisms/)
- [Neurological Disease Mechanisms and Treatments](https://scholariq.org/topics/neurological-disease-mechanisms-and-treatments/)
- [Barrier Structure and Function Studies](https://scholariq.org/topics/barrier-structure-and-function-studies/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.
