Milos Pjanic

This study uses single-cell RNA sequencing to track the maturation of human choroid plexus organoids and identifies a stage-dependent window of developmental plasticity.

This study performs a single-nucleus transcriptome-wide association study to identify gene-trait associations in brain disorders, revealing cell-type-specific genetic regulation and ancestry-specific patterns.

The paper constructs a single-nucleus atlas of genetic regulation in the human brain, identifying cell-type-specific regulatory effects and disease-associated genes.

The paper profiles human myeloid cells across aging and Alzheimer's disease, identifies AD-associated changes, and links GPNMB to neuroprotection via TREM2.

The paper constructs a single-cell transcriptomic atlas of the human dorsolateral prefrontal cortex across neurodegenerative and neuropsychiatric diseases, revealing shared and distinct molecular mechanisms.

This study creates a single-nucleus transcriptomic atlas of the human DLPFC across the lifespan, revealing three transcriptomic phases and ten age-related trajectories linked to neurodevelopmental and neurodegenerative disease risk.

The paper processes single-nuclei multi-omics data from 388 human brains to identify regulatory elements and build cell-type networks, revealing changes in aging and neuropsychiatric disorders.

The paper maps QTLs for TCF21 binding, chromatin accessibility, and chromosomal looping in coronary artery smooth muscle cells and links them to CAD GWAS loci.

The paper investigates the role of AHR in atherosclerosis by showing it suppresses chondrogenic fate of modulated smooth muscle cells in lesions.

The paper identifies noncoding RNAs as key mediators linking coronary artery disease GWAS variants to causal genes.

The paper identifies five genes modulating coronary artery disease risk through smooth muscle cells by integrating eQTL and GWAS data with transcriptomic and epigenomic analyses.

ChIPSeqFPro processes ChIP-Seq and ATAC-Seq data from fastq files to bigwig files through quality control, mapping, peak calling, and visualization steps.