# Michel D. Ferrari

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/michel-d-ferrari/

## Facts

| Field | Value |
| --- | --- |
| Citations | 49,458 |
| Field | Migraine and Headache Studies |
| h-index | 106 |
| i10-index | 461 |
| Last Known Institution | Leiden University Medical Center |
| OpenAlex ID | https://openalex.org/A5039941295 |
| ORCID iD | https://orcid.org/0000-0001-9691-9449 |
| Works | 763 |

## Researcher papers

- [Familial Hemiplegic Migraine and Episodic Ataxia Type-2 Are Caused by Mutations in the Ca2+ Channel Gene CACNL1A4](https://scholariq.org/papers/familial-hemiplegic-migraine-and-episodic-ataxia-type-2-are-caused-by-mutations/)
- [Migraine — Current Understanding and Treatment](https://scholariq.org/papers/migraine-current-understanding-and-treatment/)
- [Oral triptans (serotonin 5-HT1B/1D agonists) in acute migraine treatment: a meta-analysis of 53 trials](https://scholariq.org/papers/oral-triptans-serotonin-5-ht1b-1d-agonists-in-acute-migraine-treatment-a-meta/)
- [Efficacy and tolerability of MK-0974 (telcagepant), a new oral antagonist of calcitonin gene-related peptide receptor, compared with zolmitriptan for acute migraine: a randomised, placebo-controlled, parallel-treatment trial](https://scholariq.org/papers/efficacy-and-tolerability-of-mk-0974-telcagepant-a-new-oral-antagonist-of/)
- [C-terminal truncations in human 3′-5′ DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy](https://scholariq.org/papers/c-terminal-truncations-in-human-3-5-dna-exonuclease-trex1-cause-autosomal/)
- [Fremanezumab versus placebo for migraine prevention in patients with documented failure to up to four migraine preventive medication classes (FOCUS): a randomised, double-blind, placebo-controlled, phase 3b trial](https://scholariq.org/papers/fremanezumab-versus-placebo-for-migraine-prevention-in-patients-with-documented/)
- [De novo mutations in ATP1A3 cause alternating hemiplegia of childhood](https://scholariq.org/papers/de-novo-mutations-in-atp1a3-cause-alternating-hemiplegia-of-childhood/)
- [Recording, analysis, and interpretation of spreading depolarizations in neurointensive care: Review and recommendations of the COSBID research group](https://scholariq.org/papers/recording-analysis-and-interpretation-of-spreading-depolarizations-in/)
- [Structural Brain Changes in Migraine](https://scholariq.org/papers/structural-brain-changes-in-migraine/)

## Researcher topics

- [Migraine and Headache Studies](https://scholariq.org/topics/migraine-and-headache-studies/)
- [Trigeminal Neuralgia and Treatments](https://scholariq.org/topics/trigeminal-neuralgia-and-treatments-2/)
- [Cerebrovascular and genetic disorders](https://scholariq.org/topics/cerebrovascular-and-genetic-disorders/)
- [Neurological Complications and Syndromes](https://scholariq.org/topics/neurological-complications-and-syndromes/)
- [Sympathectomy and Hyperhidrosis Treatments](https://scholariq.org/topics/sympathectomy-and-hyperhidrosis-treatments/)

## Researcher university

- [Leiden University Medical Center](https://scholariq.org/institutions/leiden-university-medical-center/)

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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.