# Adriano Chiò

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/adriano-chio/

## Facts

| Field | Value |
| --- | --- |
| Citations | 50,329 |
| Field | Amyotrophic Lateral Sclerosis Research |
| h-index | 106 |
| i10-index | 408 |
| Last Known Institution | Azienda Ospedaliera Citta' della Salute e della Scienza di Torino |
| OpenAlex ID | https://openalex.org/A5090628289 |
| ORCID iD | 0000-0001-9579-5341 |
| Works | 841 |

## Researcher papers

Showing 12 of 35.

- [A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD](https://scholariq.org/papers/a-hexanucleotide-repeat-expansion-in-c9orf72-is-the-cause-of-chromosome-9p21/)
- [State of play in amyotrophic lateral sclerosis genetics](https://scholariq.org/papers/state-of-play-in-amyotrophic-lateral-sclerosis-genetics/)
- [Amyotrophic lateral sclerosis](https://scholariq.org/papers/amyotrophic-lateral-sclerosis-3/)
- [Amyotrophic lateral sclerosis](https://scholariq.org/papers/amyotrophic-lateral-sclerosis-2/)
- [Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study](https://scholariq.org/papers/frequency-of-the-c9orf72-hexanucleotide-repeat-expansion-in-patients-with/)
- [Exome Sequencing Reveals VCP Mutations as a Cause of Familial ALS](https://scholariq.org/papers/exome-sequencing-reveals-vcp-mutations-as-a-cause-of-familial-als/)
- [Prognostic factors in ALS: A critical review](https://scholariq.org/papers/prognostic-factors-in-als-a-critical-review/)
- [EFNS guidelines on the Clinical Management of Amyotrophic Lateral Sclerosis (MALS) – revised report of an EFNS task force](https://scholariq.org/papers/efns-guidelines-on-the-clinical-management-of-amyotrophic-lateral-sclerosis-mals/)
- [Trial of Antisense Oligonucleotide Tofersen for <i>SOD1</i> ALS](https://scholariq.org/papers/trial-of-antisense-oligonucleotide-tofersen-for-i-sod1-i-als/)
- [Global Epidemiology of Amyotrophic Lateral Sclerosis: A Systematic Review of the Published Literature](https://scholariq.org/papers/global-epidemiology-of-amyotrophic-lateral-sclerosis-a-systematic-review-of-the/)
- [Phenotypic heterogeneity of amyotrophic lateral sclerosis: a population based study](https://scholariq.org/papers/phenotypic-heterogeneity-of-amyotrophic-lateral-sclerosis-a-population-based/)
- [Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology](https://scholariq.org/papers/common-and-rare-variant-association-analyses-in-amyotrophic-lateral-sclerosis/)

## Researcher topics

- [Amyotrophic Lateral Sclerosis Research](https://scholariq.org/topics/amyotrophic-lateral-sclerosis-research/)
- [Neurogenetic and Muscular Disorders Research](https://scholariq.org/topics/neurogenetic-and-muscular-disorders-research/)
- [Genetic Neurodegenerative Diseases](https://scholariq.org/topics/genetic-neurodegenerative-diseases/)
- [Parkinson's Disease Mechanisms and Treatments](https://scholariq.org/topics/parkinson-s-disease-mechanisms-and-treatments/)
- [Neurological diseases and metabolism](https://scholariq.org/topics/neurological-diseases-and-metabolism/)

## Researcher university

- [Azienda Ospedaliera Citta' della Salute e della Scienza di Torino](https://scholariq.org/institutions/azienda-ospedaliera-citta-della-salute-e-della-scienza-di-torino/)

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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.