Jen Q. Pan

Genome-wide CRISPR screen in a mouse model of tumor growth and metastasis.

Reduced Sleep Spindles in Schizophrenia: A Treatable Endophenotype That Links Risk Genes to Impaired Cognition?

Functionally Biased D2R Antagonists: Targeting the β-Arrestin Pathway to Improve Antipsychotic Treatment.

Developing High-Throughput Assays to Analyze and Screen Electrophysiological Phenotypes.

Comprehensive comparative analysis of 5'-end RNA-sequencing methods.

Effects of 3D culturing conditions on the transcriptomic profile of stem-cell-derived neurons.

Author Correction: Comprehensive comparative analysis of 5'-end RNA-sequencing methods.

Effects of a patient-derived de novo coding alteration of CACNA1I in mice connect a schizophrenia risk gene with sleep spindle deficits.

Selective inhibition of glycogen synthase kinase 3α corrects pathophysiology in a mouse model of fragile X syndrome.

Neurogranin, Encoded by the Schizophrenia Risk Gene NRGN, Bidirectionally Modulates Synaptic Plasticity via Calmodulin-Dependent Regulation of the Neuronal Phosphoproteome.

Pluripotent stem cell-derived models of neurological diseases reveal early transcriptional heterogeneity.

Novel Fluorescence-Based High-Throughput FLIPR Assay Utilizing Membrane-Tethered Genetic Calcium Sensors to Identify T-Type Calcium Channel Modulators.

AKT inhibition in the central nervous system induces signaling defects resulting in psychiatric symptomatology.

Non-rapid eye movement sleep and wake neurophysiology in schizophrenia.

Mouse mutants in schizophrenia risk genes GRIN2A and AKAP11 show EEG abnormalities in common with schizophrenia patients.

IntelliSleepScorer, a software package with a graphic user interface for automated sleep stage scoring in mice based on a light gradient boosting machine algorithm.

Scanning mutagenesis of the voltage-gated sodium channel Na1.2 using base editing.

A Potential Source of Bias in Group-Level EEG Microstate Analysis.

Brain-region-specific changes in neurons and glia and dysregulation of dopamine signaling in Grin2a mutant mice.

Heterozygous deletion of the autism-associated gene CHD8 impairs synaptic function through widespread changes in gene expression and chromatin compaction.

A spectrum of altered non-rapid eye movement sleep in schizophrenia.

Differential functional consequences of GRIN2A mutations associated with schizophrenia and neurodevelopmental disorders.

Study Protocol: Global Research Initiative on the Neurophysiology of Schizophrenia (GRINS) project.

Electroencephalographic Microstates During Sleep and Wake in Schizophrenia.

A spectrum of altered non-rapid eye movement sleep in schizophrenia.