Ummi Ciptasari
Nijmegen, GE 6500HB, Netherlands
Last Updated: 09/26/2026
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Found 8 publications
CACNA1A haploinsufficiency leads to reduced synaptic function and increased intrinsic excitability.
Journal: Brain : a journal of neurology
Published: February 16, 2024
A human in vitro neuronal model for studying homeostatic plasticity at the network level.
Journal: Stem cell reports
Published: April 19, 2023
Multiscale modeling uncovers 7q11.23 copy number variation-dependent changes in ribosomal biogenesis and neuronal maturation and excitability.
Journal: The Journal of clinical investigation
Published: February 03, 2023
The OTUD7A-Ankyrin pathway: a newly identified disease mechanism for the 15q13.3 microdeletion disorder.
Journal: Molecular psychiatry
Published: January 20, 2023
An in silico and in vitro human neuronal network model reveals cellular mechanisms beyond NaV1.1 underlying Dravet syndrome.
Journal: Stem cell reports
Published: January 10, 2023
Defective metabolic programming impairs early neuronal morphogenesis in neural cultures and an organoid model of Leigh syndrome.
Journal: Nature communications
Published: October 01, 2020
The phenomenal epigenome in neurodevelopmental disorders.
Journal: Human molecular genetics
Published: July 08, 2020
Showing 1-8 of 8
Last Updated: 09/26/2026