Snehajyoti Chatterjee

This study identifies lysine crotonylation (Kcr) as an epigenetic regulator of long-term memory and glutamatergic neurotransmission, showing its role in gene expression and synaptic function.

This study investigates the molecular effects of PCB exposure on brain function in mice using spatial transcriptomics and identifies disruptions in tight junction proteins and gene expression networks.

This study identifies the transcriptional changes in the retrosplenial cortex during spatial memory consolidation using spatial transcriptomics and shows the role of excitatory neurons in memory formation.

This study identifies sex- and cell type-specific transcriptomic and behavioral effects of 16p11.2 hemideletion in mice, revealing distinct impacts on striatal circuits and locomotor behavior.

NEUROeSTIMator uses deep learning to estimate neuronal activation from single-cell and spatial transcriptomic data, showing robustness across species and brain regions.

The paper shows that GADD34, an Integrated Stress Response effector, is used by neurons to enhance eIF2-dependent translation in response to BDNF stimulation.

This study uses spatial transcriptomics to show that sleep deprivation causes region-specific gene expression changes in the brain, with the hippocampus showing the most significant alterations.

This study uses spatial transcriptomics to identify distinct gene expression signatures in hippocampal subregions during memory consolidation and shows their functional relevance.

This study identifies the gene expression changes in the human brain following electrical stimulation, revealing non-neuronal cell involvement and a conserved gene signature.

The paper identifies ER chaperone genes as effectors of long-term memory and shows their role in mitigating memory deficits in a tau-based ADRD mouse model.

This study identifies 1,146 dysregulated genes in the hippocampus following acute sleep deprivation, revealing distinct transcriptomic changes in RNA splicing, cell adhesion, and synaptic processes.

This study shows that the CBP KIX domain is essential for long-term memory and circadian rhythms by regulating CREB and CLOCK target genes.