# Andrea Calvo

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/andrea-calvo/

## Facts

| Field | Value |
| --- | --- |
| Citations | 21,256 |
| Field | Amyotrophic Lateral Sclerosis Research |
| h-index | 74 |
| i10-index | 212 |
| Last Known Institution | Amyotrophic Lateral Sclerosis Association |
| OpenAlex ID | https://openalex.org/A5049549975 |
| ORCID iD | 0000-0002-5122-7243 |
| Works | 463 |

## Researcher papers

Showing 12 of 25.

- [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/)
- [Comparison of tocilizumab monotherapy versus methotrexate monotherapy in patients with moderate to severe rheumatoid arthritis: the AMBITION study](https://scholariq.org/papers/comparison-of-tocilizumab-monotherapy-versus-methotrexate-monotherapy-in/)
- [Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis](https://scholariq.org/papers/genome-wide-association-analyses-identify-new-risk-variants-and-the-genetic/)
- [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/)
- [Prognosis for patients with amyotrophic lateral sclerosis: development and validation of a personalised prediction model](https://scholariq.org/papers/prognosis-for-patients-with-amyotrophic-lateral-sclerosis-development-and/)
- [Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture](https://scholariq.org/papers/genome-sequencing-analysis-identifies-new-loci-associated-with-lewy-body/)
- [Projected increase in amyotrophic lateral sclerosis from 2015 to 2040](https://scholariq.org/papers/projected-increase-in-amyotrophic-lateral-sclerosis-from-2015-to-2040/)
- [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/)
- [NEK1 variants confer susceptibility to amyotrophic lateral sclerosis](https://scholariq.org/papers/nek1-variants-confer-susceptibility-to-amyotrophic-lateral-sclerosis/)
- [<i>SQSTM1</i> mutations in frontotemporal lobar degeneration and amyotrophic lateral sclerosis](https://scholariq.org/papers/i-sqstm1-i-mutations-in-frontotemporal-lobar-degeneration-and-amyotrophic/)

## 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

- [Amyotrophic Lateral Sclerosis Association](https://scholariq.org/institutions/amyotrophic-lateral-sclerosis-association/)

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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.