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Géza Berecki

6PUBLICATIONS

37CO-AUTHORS

Other European languagesNeonatologyGene expression (incl. microarray and other genome-wide approaches)Medical devices

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Publications (6)

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|Feb 05, 2026

Mechanisms of SCN2A loss of function do not predict presence or phenotype of epilepsy.

Marsha Tan, Beatrice Southby Goad, Meagan Allen

|Apr 22, 2025

Antisense oligonucleotide treatment in a preterm infant with early-onset SCN2A developmental and epileptic encephalopathy.

Matias Wagner, Géza Berecki, Walid Fazeli

|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 <i>grime</i> 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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Frequent Collaborators

1 joint publications

Arie O Verkerk

1 joint publications

Gregory J Baillie

1 joint publications

Irina Vetter

1 joint publications

Teun P de Boer

1 joint publications

Jeroen Bakkers

1 joint publications

Kelly A Smith

1 joint publications

Isabella Overmars

1 joint publications

Samuel F Berkovic

1 joint publications

Matias Wagner

1 joint publications

Andreas W Flemmer

Frequent Collaborators

1 joint publications

Arie O Verkerk

1 joint publications

Gregory J Baillie

1 joint publications

Irina Vetter

1 joint publications

Teun P de Boer

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