Minsoo Kim

The paper identifies extensive isoform diversity in the developing human neocortex and links it to neuropsychiatric disorder risk mechanisms.

The paper constructs a cross-ancestry, cell-type-informed gene regulatory atlas of the developing human brain, identifying genetic regulation and linking it to neuropsychiatric disorders.

GeneticsMakie.jl provides a fast, scalable, and customizable visualization tool for locus-level genetic and genomic data, enabling integration of multiple annotations and association results.

The paper introduces a new statistical method for multivariate variance components models to analyze brain isoform expression and identifies novel psychiatric disease mechanisms.

This paper introduces isoTWAS, a method that improves discovery of genetic risk mechanisms for neuropsychiatric disorders by analyzing isoform-level transcriptome-wide associations.

This paper conducts a multi-ancestry GWAS meta-analysis of suicide attempt, identifying 12 genome-wide significant loci and finding shared genetic risks with ADHD, smoking, and risk tolerance.

A genome-wide association study of 69,369 schizophrenia cases and 236,642 controls identifies 270 risk loci, prioritizes 130 genes, and links common and rare risk variants to neuronal synaptic biology.

This study identifies genetic loci associated with suicide attempts and shows shared genetic architecture with psychiatric disorders and non-psychiatric risk factors.

The paper investigates the role of the complement system and C4A in schizophrenia by analyzing gene co-expression networks and finds that synaptic pathways, not the complement system, are linked to schizophrenia risk.