| Whole-exome sequencing identifies mutations of KIF22 in spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type BJ Min, N Kim, T Chung, OH Kim, G Nishimura, CY Chung, HR Song, ... The American Journal of Human Genetics 89 (6), 760-766, 2011 | 66 | 2011 |
| A novel mutation of TMPRSS3 related to milder auditory phenotype in Korean postlingual deafness: a possible future implication for a personalized auditory … J Chung, SM Park, SO Chang, T Chung, KY Lee, AR Kim, JH Park, V Kim, ... Journal of molecular medicine 92, 651-663, 2014 | 52 | 2014 |
| FARS2 mutation and epilepsy: possible link with early-onset epileptic encephalopathy JS Cho, SH Kim, HY Kim, T Chung, D Kim, S Jang, SB Lee, SK Yoo, ... Epilepsy Research 129, 118-124, 2017 | 30 | 2017 |
| Destabilization and Mislocalization of POU 3 F 4 by C‐Terminal Frameshift Truncation and Extension Mutation BY Choi, DH Kim, T Chung, M Chang, EH Kim, AR Kim, J Seok, ... Human mutation 34 (2), 309-316, 2013 | 30 | 2013 |
| Prediction of binding property of RNA-binding proteins using multi-sized filters and multi-modal deep convolutional neural network T Chung, D Kim PloS one 14 (4), e0216257, 2019 | 12 | 2019 |
| SH3 domain-peptide binding energy calculations based on structural ensemble and multiple peptide templates S Hong, T Chung, D Kim PloS one 5 (9), e12654, 2010 | 4 | 2010 |
