Kwang Joong Kim

发表

A genome-wide association study of a coronary artery disease risk variant

Juyoung Lee, Bok-Ghee Han, Young Jin Kim, 2013, Journal of Human Genetics.

Genome-wide scan of granular corneal dystrophy, type II: confirmation of chromosome 5q31 and identification of new co-segregated loci on chromosome 3q26.3

Jong-Young Lee, Han-Na Kim, Hyung-Lae Kim, 2011, Experimental & Molecular Medicine.

Identification of a genetic locus on chromosome 4q34-35 for type 2 diabetes with overweight

Jong-Young Lee, M. Go, S. Kwak, 2013, Experimental & Molecular Medicine.

Spectrum of rhodopsin mutations in Korean patients with retinitis pigmentosa

Jong-Young Lee, B. Han, Hyung-Lae Kim, 2011, Molecular vision.

Identification and extensive analysis of inverted-duplicated HBV integration in a human hepatocellular carcinoma cell line.

Jong-Young Lee, J. Bok, Chan Park, 2012, BMB reports.

Genetic associations of common deletion polymorphisms in families with Avellino corneal dystrophy.

H. Shin, H. Cheong, Jong-Young Lee, 2009, Biochemical and biophysical research communications.

Microarray-based mutation detection and phenotypic characterization in Korean patients with retinitis pigmentosa

Jong-Young Lee, J. Bok, H. Yu, 2012, Molecular vision.

SNP identification, linkage disequilibrium, and haplotype analysis for a 200-kb genomic region in a Korean population.

Jong-Young Lee, B. Oh, K. Kimm, 2006, Genomics.

Exome sequencing as a tool for short stature gene discovery: analysis of a Korean family with pseudohypoparathyroidism

Y. J. Kim, H. Choi, Bong-Jo Kim, 2014, Genes & Genomics.