Elly I. Lewerissa

Nijmegen, GE 6500HB, Netherlands

Last Updated: 09/26/2026

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Found 10 publications

Integrative transcriptomics and electrophysiological profiling of hiPSC-derived neurons identifies novel druggable pathways in Koolen-de Vries Syndrome.

Integrative transcriptomics and electrophysiological profiling of hiPSC-derived neurons identifies novel druggable pathways in Koolen-de Vries Syndrome.

Journal: Molecular psychiatry

Published: November 27, 2024

CACNA1A haploinsufficiency leads to reduced synaptic function and increased intrinsic excitability.

CACNA1A haploinsufficiency leads to reduced synaptic function and increased intrinsic excitability.

Journal: Brain : a journal of neurology

Published: February 16, 2024

Epigenetic regulation of autophagy-related genes: Implications for neurodevelopmental disorders.

Epigenetic regulation of autophagy-related genes: Implications for neurodevelopmental disorders.

Journal: Autophagy

Published: September 07, 2023

SCN1A-deficient excitatory neuronal networks display mutation-specific phenotypes.

SCN1A-deficient excitatory neuronal networks display mutation-specific phenotypes.

Journal: Brain : a journal of neurology

Published: January 18, 2023

ANK2 loss-of-function variants are associated with epilepsy, and lead to impaired axon initial segment plasticity and hyperactive network activity in hiPSC-derived neuronal networks.

ANK2 loss-of-function variants are associated with epilepsy, and lead to impaired axon initial segment plasticity and hyperactive network activity in hiPSC-derived neuronal networks.

Journal: Human molecular genetics

Published: October 14, 2022

Neuronal network activity and connectivity are impaired in a conditional knockout mouse model with PCDH19 mosaic expression.

Neuronal network activity and connectivity are impaired in a conditional knockout mouse model with PCDH19 mosaic expression.

Journal: Molecular psychiatry

Published: March 22, 2022

Loss-of-function variants in the schizophrenia risk gene SETD1A alter neuronal network activity in human neurons through the cAMP/PKA pathway.

Loss-of-function variants in the schizophrenia risk gene SETD1A alter neuronal network activity in human neurons through the cAMP/PKA pathway.

Journal: Cell reports

Published: September 27, 2021

Imbalanced autophagy causes synaptic deficits in a human model for neurodevelopmental disorders.

Imbalanced autophagy causes synaptic deficits in a human model for neurodevelopmental disorders.

Journal: Autophagy

Published: July 21, 2021

The epilepsy-associated protein PCDH19 undergoes NMDA receptor-dependent proteolytic cleavage and regulates the expression of immediate-early genes.

The epilepsy-associated protein PCDH19 undergoes NMDA receptor-dependent proteolytic cleavage and regulates the expression of immediate-early genes.

Journal: Cell reports

Published: March 27, 2021

Histone Methylation by the Kleefstra Syndrome Protein EHMT1 Mediates Homeostatic Synaptic Scaling.

Histone Methylation by the Kleefstra Syndrome Protein EHMT1 Mediates Homeostatic Synaptic Scaling.

Journal: Neuron

Published: May 26, 2015

Showing 1-10 of 10

Last Updated: 09/26/2026