S. Hong

Systematic analysis of inheritance pattern determination in genes that cause rare neurodevelopmental diseases

Jihoon G. Yoon, Jihoon G Yoon, Murim Choi, 2022, Frontiers in Genetics.

Genomic profiling of 553 uncharacterized neurodevelopment patients reveals a high proportion of recessive pathogenic variant carriers in an outbred population

Y. H. Lee, Murim Choi, J. Ko, 2019, Scientific Reports.

Functional annotation of de novo variants from healthy individuals

Jean Lee, Sung Eun Hong, S. Hong, 2019, Genomics & informatics.

Transcriptome-based variant calling and aberrant mRNA discovery enhance diagnostic efficiency for neuromuscular diseases

Jinkuk Kim, Murim Choi, J. Chae, 2022, Journal of Medical Genetics.

Fine-Scale Map of Encyclopedia of DNA Elements Regions in the Korean Population

Y. J. Kim, L. Cardon, B. Weir, 2006, Genetics.