Yerbol Z. Kurmangaliyev

Isocall is a scalable method for joint transcript identification from long-read RNA-seq data, showing high precision and handling large datasets efficiently.

The paper identifies sex-specific gene expression and synaptic connections in Drosophila circadian neurons, revealing molecular mechanisms underlying sexual dimorphism in circadian behavior.

The paper examines sex-biased gene expression in Drosophila sexual circuits using single-cell transcriptomics, finding limited and cell-type-specific expression with species-specific divergence and shared gene programs.

The paper identifies non-canonical circadian oscillators in Drosophila neurons that exhibit molecular rhythms despite lacking core clock genes.

The paper identifies LC17 neurons and their electrical synapses as critical for visual approach behavior in fruit flies.

The paper investigates how Kenyon cells in insect mushroom bodies form combinatorial connections with olfactory projection neurons through spatial and molecular mechanisms.

The paper identifies molecular gradients in Drosophila neurons that regulate synaptic connectivity for visuomotor transformation.

The paper identifies a single transcription factor isoform, broad-z4, as a terminal selector that controls neuronal identity in Drosophila by switching the identity of two visual projection neurons.

The paper identifies synaptic specificity determinants by integrating connectomes and transcriptomes in Drosophila.

This study uses multi-omics analysis to show that sarcospan overexpression in mdx mice compensates for dystrophin deficiency by altering cytoskeleton-matrix interactions and mechanotransduction pathways.

The paper shows that sequential axon arrival and physical occupancy determine the integration of visual projection neurons onto the dendrites of the giant fiber in Drosophila.

The paper shows that the Ecdysone pathway regulates timing of transcription factor expression, which in turn controls cell-type specific wiring programs in fly neurons.

The paper identifies modular transcriptional programs that independently control dendritic and axonal connectivity in Drosophila T4/T5 neurons.