# Jacques Motté

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/jacques-motte/

## Facts

| Field | Value |
| --- | --- |
| Citations | 4,284 |
| Field | Epilepsy research and treatment |
| h-index | 33 |
| i10-index | 46 |
| OpenAlex ID | https://openalex.org/A5110524815 |
| Works | 59 |

## Researcher papers

- [A Novel CNS Gene Required for Neuronal Migration and Involved in X-Linked Subcortical Laminar Heterotopia and Lissencephaly Syndrome](https://scholariq.org/papers/a-novel-cns-gene-required-for-neuronal-migration-and-involved-in-x-linked/)
- [GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction](https://scholariq.org/papers/grin2a-mutations-in-acquired-epileptic-aphasia-and-related-childhood-focal/)
- [Levodopa-responsive dystonia](https://scholariq.org/papers/levodopa-responsive-dystonia/)
- [The three stages of epilepsy in patients with <i>CDKL5</i> mutations](https://scholariq.org/papers/the-three-stages-of-epilepsy-in-patients-with-i-cdkl5-i-mutations/)
- [Epileptic encephalopathies of the Landau‐Kleffner and continuous spike and waves during slow‐wave sleep types: Genomic dissection makes the link with autism](https://scholariq.org/papers/epileptic-encephalopathies-of-the-landau-kleffner-and-continuous-spike-and-waves/)
- [Mutational, functional, and expression studies of the<i>TCF4</i>gene in Pitt-Hopkins syndrome](https://scholariq.org/papers/mutational-functional-and-expression-studies-of-the-i-tcf4-i-gene-in-pitt/)
- [The 2q37-deletion syndrome: an update of the clinical spectrum including overweight, brachydactyly and behavioural features in 14 new patients](https://scholariq.org/papers/the-2q37-deletion-syndrome-an-update-of-the-clinical-spectrum-including/)
- [Linkage of Benign Familial Infantile Convulsions to Chromosome 16p12-q12 Suggests Allelism to the Infantile Convulsions and Choreoathetosis Syndrome](https://scholariq.org/papers/linkage-of-benign-familial-infantile-convulsions-to-chromosome-16p12-q12/)
- [Benign hereditary chorea: phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in the<i>TITF1/NKX2-1</i>gene](https://scholariq.org/papers/benign-hereditary-chorea-phenotype-prognosis-therapeutic-outcome-and-long-term/)
- [Mapping of neuronal networks underlying generalized seizures induced by increasing doses of pentylenetetrazol in the immature and adult rat: a c-Fos immunohistochemical study](https://scholariq.org/papers/mapping-of-neuronal-networks-underlying-generalized-seizures-induced-by/)
- [Idiopathic Hypersomnia: A Report of Three Adolescent-Onset Cases in a Two-Generation Family](https://scholariq.org/papers/idiopathic-hypersomnia-a-report-of-three-adolescent-onset-cases-in-a-two/)

## Researcher topics

- [Epilepsy research and treatment](https://scholariq.org/topics/epilepsy-research-and-treatment/)
- [Neuroscience and Neuropharmacology Research](https://scholariq.org/topics/neuroscience-and-neuropharmacology-research/)
- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)
- [Neonatal and fetal brain pathology](https://scholariq.org/topics/neonatal-and-fetal-brain-pathology/)
- [Viral Infections and Immunology Research](https://scholariq.org/topics/viral-infections-and-immunology-research/)

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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.