Changhoon Kim

The paper sequenced 3,135 Japanese individuals to identify genetic variants and construct a reference haplotype, highlighting the need for diverse population inclusion in genetic catalogs.

The paper uses whole-genome sequencing to analyze indigenous ancestry in Uruguayans, identifying Amerindian genetic heritage and estimating admixture timing.

The paper reports the de novo assembly and annotation of the soybean cultivar Hwangkeum, revealing genetic variants and structural features compared to the Williams 82 reference genome.

This study identifies novel genetic loci for coronary artery disease in Japanese and transethnic populations and develops a polygenic risk score that outperforms population-specific scores.

The paper introduces a whole-genome reference panel of 1,781 Northeast Asians, showing improved imputation accuracy for rare and low-frequency variants compared to existing panels.

The paper compares the human reference genome GRCh38 with a high contiguity ethnic genome AK1 to identify missing sequences and their implications for human genetics.

The paper identifies a batch effect in 1000 Genomes Project data causing spurious mutation calls and affecting GWAS results, suggesting legacy data may need to be retired or upgraded.