Géza Berecki

6PUBLICATIONS
37CO-AUTHORS
Other European languagesNeonatologyGene expression (incl. microarray and other genome-wide approaches)Medical devices
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Publications (6)

|Feb 05, 2026
Mechanisms of SCN2A loss of function do not predict presence or phenotype of epilepsy.

Marsha Tan, Beatrice Southby Goad, Meagan Allen

|Jun 28, 2024
Nav1.2 channel mutations preventing fast inactivation lead to SCN2A encephalopathy.

Géza Berecki, Elaine Tao, Katherine B Howell

|May 31, 2022
Functional correlates of clinical phenotype and severity in recurrent SCN2A variants.

Géza Berecki, Katherine B Howell, Jacqueline Heighway

|Feb 18, 2021
The zebrafish grime mutant uncovers an evolutionarily conserved role for Tmem161b in the control of cardiac rhythm.

Charlotte D Koopman, Jessica De Angelis, Swati P Iyer

|Feb 20, 2019
SCN1A gain of function in early infantile encephalopathy.

Géza Berecki, Alexander Bryson, Jan Terhag

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