Ghayda Mirzaa

27PUBLICATIONS
235CO-AUTHORS
NeurogeneticsGene expression (incl. microarray and other genome-wide approaches)Neurology and neuromuscular diseasesCell and nuclear divisionMedical infection agents (incl. prions)
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Publications (27)

|Apr 02, 2026
Correction: Comprehensive analysis of CNOT3-related neurodevelopmental disorders: phenotypic and genotypic characterization.

Camille Engel, Michaela Rendek, Jessica Assoumani

|Jan 28, 2026
Predictive value of seizure onset for gross motor dysfunction in individuals with pathogenic GABRB2 and GABRB3 variants.

Sebastian Ortiz, Leonardo Affronte, Chiara Bagliani

|Dec 06, 2025
Early neurological symptoms and epilepsy outcomes in individuals with the recurrent GABRG2 p.(Ala106Thr) gain-of-function variant: Structural and phenotypic insights.

Sebastian Ortiz, Chiara Bagliani, Susan X N Lin

|Nov 25, 2025
Missense variants in DPYSL5 associated with neurodevelopmental disorders and brain malformations cause impaired neuronal maturation in vitro.

Florence Desprez, Solène Remize, Liberty François-Moutal

|Nov 10, 2025
Pathogenic variants in SMARCA1 cause an X-linked neurodevelopmental disorder modulated by NURF complex composition.

Ghayda M Mirzaa, Keqin Yan, Raissa Relator

|Jul 19, 2025
Phase 1 study of ABI-009 (nab-rapamycin) for surgically refractory epilepsy (RaSuRE).

Koko Hall, Russell Saneto, Stephanie Randle

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Frequent Collaborators

4 joint publications

Juliette Piard

4 joint publications

William Dobyns

3 joint publications

Elena Gardella

3 joint publications

Renzo Guerrini