Pei-shan Hou
No. 155, Sec. 2, Linong St
Beitou, TPQ 11221, Taiwan
Beitou, TPQ 11221, Taiwan
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 24 publications
Generation of an induced pluripotent stem cell line (KCGMHi001-A) from a patient with CEP85L related posterior predominant lissencephaly (LIS10).
Journal: Stem cell research
Published: February 19, 2026
Opportunities and challenges in studying non-coding RNAs using neural organoid models.
Journal: Frontiers in molecular neuroscience
Published: February 02, 2026
Distinct contributions of calmodulin-encoding genes to the migration and development of neocortical layer 4 neurons.
Journal: Biochemical and biophysical research communications
Published: August 05, 2025
CEP170 as a novel molecular link between centrosomal function and cerebral cortical development.
Journal: Journal of biomedical science
Published: July 17, 2025
TRPML2 channel modulation by PI(3,5)P₂ and small-molecule agonists controls endosomal vesicle dynamics.
Journal: Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie
Published: May 22, 2025
Deep-layer neurons compensate for the loss of layer 4 sensory recipient cells in the developing neocortex.
Journal: Neuroscience letters
Published: April 14, 2025
Comparative Analysis of Temperature-Dependent Endocytic Regulation of Notch Signaling in Chick and Mouse Neural Progenitors.
Journal: Cells, tissues, organs
Published: March 09, 2025
Epilepsy-associated FOXJ3 variants link a transcriptional program of the PTEN-mTOR pathway to neuronal specification and cortical lamination.
Journal: Nature communications
Published: January 24, 2025
Mapping Genetic Associations With Functional Brain Area Alterations in Schizophrenia and Implications for Cortical Development.
Journal: Brain and behavior
Published: November 11, 2024
Local cortical structure pattern and genetic links in schizophrenia: An MRI and CRISPR/Cas9 study.
Journal: Progress in neuro-psychopharmacology & biological psychiatry
Published: September 19, 2024
Functional defects in FOXG1 variants predict the severity of brain anomalies in FOXG1 syndrome.
Journal: Molecular psychiatry
Published: March 13, 2024
Novel lissencephaly-associated NDEL1 variant reveals distinct roles of NDE1 and NDEL1 in nucleokinesis and human cortical malformations.
Journal: Acta neuropathologica
Published: October 23, 2023
Last Updated: 09/26/2026