V. Choi

Identification of the rare compound heterozygous variants in the NEB gene in a Korean family with intellectual disability, epilepsy and early-childhood-onset generalized muscle weakness

Hyun-Seok Jin, Seon-Yong Jeong, Kyung Kim, 2014, Journal of Human Genetics.

Identification of a rare homozygous c.790C>T variation in the TFB2M gene in Korean patients with autism spectrum disorder.

Jinhyuk Lee, Jeonghyung Kim, Seon-Yong Jeong, 2018, Biochemical and biophysical research communications.

Low Frequency of MKRN3 Mutations in Central Precocious Puberty Among Korean Girls

Hyun-Seok Jin, H-S Jin, Hae-sang Lee, 2015, Hormone and Metabolic Research.

Association of the I264T Variant in the Sulfide Quinone Reductase-Like (SQRDL) Gene with Osteoporosis in Korean Postmenopausal Women

Hyun-Seok Jin, Hyun-Seok Jin, Bo-Young Kim, 2015, PloS one.