# Rocco Liguori

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/rocco-liguori/

## Facts

| Field | Value |
| --- | --- |
| Citations | 16,090 |
| Field | Neurological disorders and treatments |
| h-index | 66 |
| i10-index | 286 |
| Last Known Institution | Institute of Neurological Sciences |
| OpenAlex ID | https://openalex.org/A5068622580 |
| ORCID iD | 0000-0002-1815-1013 |
| Works | 614 |

## Researcher papers

- [OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes](https://scholariq.org/papers/opa1-mutations-induce-mitochondrial-dna-instability-and-optic-atrophy-plus/)
- [Sympathetic skin response](https://scholariq.org/papers/sympathetic-skin-response/)
- [Morvan's syndrome: peripheral and central nervous system and cardiac involvement with antibodies to voltage-gated potassium channels](https://scholariq.org/papers/morvan-s-syndrome-peripheral-and-central-nervous-system-and-cardiac-involvement/)
- [Melanopsin retinal ganglion cell loss in <scp>A</scp>lzheimer disease](https://scholariq.org/papers/melanopsin-retinal-ganglion-cell-loss-in-scp-a-scp-lzheimer-disease/)
- [Skin nerve α-synuclein deposits](https://scholariq.org/papers/skin-nerve-synuclein-deposits/)
- [Efficient mitochondrial biogenesis drives incomplete penetrance in Leber’s hereditary optic neuropathy](https://scholariq.org/papers/efficient-mitochondrial-biogenesis-drives-incomplete-penetrance-in-leber-s/)
- [Skin α-Synuclein Aggregation Seeding Activity as a Novel Biomarker for Parkinson Disease](https://scholariq.org/papers/skin-synuclein-aggregation-seeding-activity-as-a-novel-biomarker-for-parkinson/)
- [Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability](https://scholariq.org/papers/clinical-genetic-and-expression-studies-of-mutations-in-the-potassium-channel/)
- [Idebenone treatment in Leber's hereditary optic neuropathy](https://scholariq.org/papers/idebenone-treatment-in-leber-s-hereditary-optic-neuropathy/)
- [Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder](https://scholariq.org/papers/mutations-in-slc25a46-encoding-a-ugo1-like-protein-cause-an-optic-atrophy/)
- [Nocturnal Sleep Dynamics Identify Narcolepsy Type 1](https://scholariq.org/papers/nocturnal-sleep-dynamics-identify-narcolepsy-type-1/)
- [Antibodies Against Hypocretin Receptor 2 Are Rare in Narcolepsy](https://scholariq.org/papers/antibodies-against-hypocretin-receptor-2-are-rare-in-narcolepsy/)

## Researcher topics

- [Neurological disorders and treatments](https://scholariq.org/topics/neurological-disorders-and-treatments/)
- [Parkinson's Disease Mechanisms and Treatments](https://scholariq.org/topics/parkinson-s-disease-mechanisms-and-treatments/)
- [Mitochondrial Function and Pathology](https://scholariq.org/topics/mitochondrial-function-and-pathology/)
- [Genetic Neurodegenerative Diseases](https://scholariq.org/topics/genetic-neurodegenerative-diseases/)
- [Amyotrophic Lateral Sclerosis Research](https://scholariq.org/topics/amyotrophic-lateral-sclerosis-research/)

## Researcher university

- [Institute of Neurological Sciences](https://scholariq.org/institutions/institute-of-neurological-sciences/)

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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.