Katrin Linda

Nijmegen, GE, Netherlands

Last Updated: 09/26/2026

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Found 16 publications

Astrocytes contribute to olanzapine-mediated reversal of Kleefstra Syndrome-associated neurodevelopmental regression.

Astrocytes contribute to olanzapine-mediated reversal of Kleefstra Syndrome-associated neurodevelopmental regression.

Journal: The Journal of clinical investigation

Published: June 30, 2026

Navigating Human Astrocyte Differentiation: Direct and Rapid One-Step Differentiation of Induced Pluripotent Stem Cells to Functional Astrocytes Supporting Neuronal Network Development.

Navigating Human Astrocyte Differentiation: Direct and Rapid One-Step Differentiation of Induced Pluripotent Stem Cells to Functional Astrocytes Supporting Neuronal Network Development.

Journal: Glia

Published: October 31, 2025

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

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

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

Human neuronal networks on micro-electrode arrays are a highly robust tool to study disease-specific genotype-phenotype correlations in vitro.

Human neuronal networks on micro-electrode arrays are a highly robust tool to study disease-specific genotype-phenotype correlations in vitro.

Journal: Stem cell reports

Published: January 12, 2021

Biallelic variants in TMEM222 cause a new autosomal recessive neurodevelopmental disorder.

Biallelic variants in TMEM222 cause a new autosomal recessive neurodevelopmental disorder.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: June 19, 2020

Cadherin-13 is a critical regulator of GABAergic modulation in human stem-cell-derived neuronal networks.

Cadherin-13 is a critical regulator of GABAergic modulation in human stem-cell-derived neuronal networks.

Journal: Molecular psychiatry

Published: May 07, 2020

m.3243A > G-Induced Mitochondrial Dysfunction Impairs Human Neuronal Development and Reduces Neuronal Network Activity and Synchronicity.

m.3243A > G-Induced Mitochondrial Dysfunction Impairs Human Neuronal Development and Reduces Neuronal Network Activity and Synchronicity.

Journal: Cell reports

Published: July 08, 2019

Distinct Pathogenic Genes Causing Intellectual Disability and Autism Exhibit a Common Neuronal Network Hyperactivity Phenotype.

Distinct Pathogenic Genes Causing Intellectual Disability and Autism Exhibit a Common Neuronal Network Hyperactivity Phenotype.

Journal: Cell reports

Published: April 12, 2019

Neuronal network dysfunction in a model for Kleefstra syndrome mediated by enhanced NMDAR signaling.

Neuronal network dysfunction in a model for Kleefstra syndrome mediated by enhanced NMDAR signaling.

Journal: Nature communications

Published: January 22, 2019

The promise of induced pluripotent stem cells for neurodevelopmental disorders.

The promise of induced pluripotent stem cells for neurodevelopmental disorders.

Journal: Progress in neuro-psychopharmacology & biological psychiatry

Published: July 17, 2017

Showing 1-12 of 16

Last Updated: 09/26/2026