# Nicola Ticozzi

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/nicola-ticozzi/

## Facts

| Field | Value |
| --- | --- |
| Citations | 13,224 |
| Field | Amyotrophic Lateral Sclerosis Research |
| h-index | 51 |
| i10-index | 137 |
| Last Known Institution | University of Milan |
| OpenAlex ID | https://openalex.org/A5047027591 |
| ORCID iD | 0000-0001-5963-7426 |
| Works | 373 |

## Researcher papers

- [Mutations in the <i>FUS/TLS</i> Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis](https://scholariq.org/papers/mutations-in-the-i-fus-tls-i-gene-on-chromosome-16-cause-familial-amyotrophic/)
- [Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways](https://scholariq.org/papers/exome-sequencing-in-amyotrophic-lateral-sclerosis-identifies-risk-genes-and/)
- [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/)
- [Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis](https://scholariq.org/papers/mutations-in-the-profilin-1-gene-cause-familial-amyotrophic-lateral-sclerosis/)
- [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/)
- [Exome-wide Rare Variant Analysis Identifies TUBA4A Mutations Associated with Familial ALS](https://scholariq.org/papers/exome-wide-rare-variant-analysis-identifies-tuba4a-mutations-associated-with/)
- [NEK1 variants confer susceptibility to amyotrophic lateral sclerosis](https://scholariq.org/papers/nek1-variants-confer-susceptibility-to-amyotrophic-lateral-sclerosis/)
- [Mutations in the vesicular trafficking protein annexin A11 are associated with amyotrophic lateral sclerosis](https://scholariq.org/papers/mutations-in-the-vesicular-trafficking-protein-annexin-a11-are-associated-with/)
- [The C9ORF72 expansion mutation is a common cause of ALS+/−FTD in Europe and has a single founder](https://scholariq.org/papers/the-c9orf72-expansion-mutation-is-a-common-cause-of-als-ftd-in-europe-and-has-a/)
- [CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia](https://scholariq.org/papers/ccnf-mutations-in-amyotrophic-lateral-sclerosis-and-frontotemporal-dementia/)
- [EE48 Healthcare Resource Utilization (HCRU), Quality of Life (QoL), and Employment Changes for Early, Middle and Late-Stage People with Amyotrophic Lateral Sclerosis (pALS) in Italy: Results from a Real-World Survey](https://scholariq.org/papers/ee48-healthcare-resource-utilization-hcru-quality-of-life-qol-and-employment/)

## 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/)
- [Parkinson's Disease Mechanisms and Treatments](https://scholariq.org/topics/parkinson-s-disease-mechanisms-and-treatments/)
- [Genetic Neurodegenerative Diseases](https://scholariq.org/topics/genetic-neurodegenerative-diseases/)
- [Neurological diseases and metabolism](https://scholariq.org/topics/neurological-diseases-and-metabolism/)

## Researcher university

- [University of Milan](https://scholariq.org/institutions/university-of-milan/)

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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.