# Mario Sabatelli

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/mario-sabatelli/

## Facts

| Field | Value |
| --- | --- |
| Citations | 16,367 |
| Field | Amyotrophic Lateral Sclerosis Research |
| h-index | 53 |
| i10-index | 172 |
| Last Known Institution | Università Cattolica del Sacro Cuore |
| OpenAlex ID | https://openalex.org/A5022524234 |
| ORCID iD | https://orcid.org/0000-0001-6635-4985 |
| Works | 346 |

## Researcher papers

- [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/)
- [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/)
- [Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis](https://scholariq.org/papers/mutations-in-the-matrin-3-gene-cause-familial-amyotrophic-lateral-sclerosis/)
- [A Genome-Wide Association Study of Myasthenia Gravis](https://scholariq.org/papers/a-genome-wide-association-study-of-myasthenia-gravis/)
- [Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72](https://scholariq.org/papers/clinical-characteristics-of-patients-with-familial-amyotrophic-lateral-sclerosis/)
- [Two Italian kindreds with familial amyotrophic lateral sclerosis due to FUS mutation](https://scholariq.org/papers/two-italian-kindreds-with-familial-amyotrophic-lateral-sclerosis-due-to-fus/)
- [Identification of genetic risk loci and prioritization of genes and pathways for myasthenia gravis: a genome-wide association study](https://scholariq.org/papers/identification-of-genetic-risk-loci-and-prioritization-of-genes-and-pathways-for/)
- [Genetic counselling in ALS: facts, uncertainties and clinical suggestions](https://scholariq.org/papers/genetic-counselling-in-als-facts-uncertainties-and-clinical-suggestions/)

## Researcher topics

- [Amyotrophic Lateral Sclerosis Research](https://scholariq.org/topics/amyotrophic-lateral-sclerosis-research/)
- [Peripheral Neuropathies and Disorders](https://scholariq.org/topics/peripheral-neuropathies-and-disorders/)
- [Neurogenetic and Muscular Disorders Research](https://scholariq.org/topics/neurogenetic-and-muscular-disorders-research/)
- [Hereditary Neurological Disorders](https://scholariq.org/topics/hereditary-neurological-disorders/)
- [Amyloidosis: Diagnosis, Treatment, Outcomes](https://scholariq.org/topics/amyloidosis-diagnosis-treatment-outcomes/)

## Researcher university

- [Università Cattolica del Sacro Cuore](https://scholariq.org/institutions/universita-cattolica-del-sacro-cuore/)

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