|A transforming KIF5B and RET gene fusion in lung adenocarcinoma revealed from whole-genome and transcriptome sequencing|
YS Ju, WC Lee, JY Shin, S Lee, T Bleazard, JK Won, YT Kim, JI Kim, ...
Genome research 22 (3), 436-445, 2012
|A highly annotated whole-genome sequence of a Korean individual|
JI Kim, YS Ju, H Park, S Kim, S Lee, JH Yi, J Mudge, NA Miller, D Hong, ...
nature 460 (7258), 1011-1015, 2009
|Comprehensive analysis of the transcriptional and mutational landscape of follicular and papillary thyroid cancers|
SK Yoo, S Lee, S Kim, HG Jee, BA Kim, H Cho, YS Song, SW Cho, ...
PLoS genetics 12 (8), e1006239, 2016
|Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencing|
H Park, JI Kim, YS Ju, O Gokcumen, RE Mills, S Kim, S Lee, D Suh, ...
Nature genetics 42 (5), 400-405, 2010
|Extensive genomic and transcriptional diversity identified through massively parallel DNA and RNA sequencing of eighteen Korean individuals|
YS Ju, JI Kim, S Kim, D Hong, H Park, JY Shin, S Lee, WC Lee, S Kim, ...
Nature genetics 43 (8), 745-752, 2011
|Genetic alterations of JAK/STAT cascade and histone modification in extranodal NK/T-cell lymphoma nasal type|
S Lee, HY Park, SY Kang, SJ Kim, J Hwang, S Lee, SH Kwak, KS Park, ...
Oncotarget 6 (19), 17764, 2015
|An epigenomic roadmap to induced pluripotency reveals DNA methylation as a reprogramming modulator|
DS Lee, JY Shin, PD Tonge, MC Puri, S Lee, H Park, WC Lee, ...
Nature communications 5 (1), 5619, 2014
|Genetic diagnosis of Duchenne and Becker muscular dystrophy using next-generation sequencing technology: comprehensive mutational search in a single platform|
BC Lim, S Lee, JY Shin, JI Kim, H Hwang, KJ Kim, YS Hwang, JS Seo, ...
Journal of medical genetics 48 (11), 731-736, 2011
|Deep resequencing of 131 Crohn's disease associated genes in pooled DNA confirmed three reported variants and identified eight novel variants|
SN Hong, C Park, SJ Park, CK Lee, BD Ye, YS Kim, S Lee, J Chae, JI Kim, ...
Gut 65 (5), 788-796, 2016
|Comprehensive genomic analyses associate UGT8 variants with musical ability in a Mongolian population|
H Park, S Lee, HJ Kim, YS Ju, JY Shin, D Hong, M von Grotthuss, DS Lee, ...
Journal of medical genetics 49 (12), 747-752, 2012
|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
|Tissue response to poly (l-lactic acid)-based blend with phospholipid polymer for biodegradable cardiovascular stents|
HI Kim, K Ishihara, S Lee, JH Seo, HY Kim, D Suh, MU Kim, T Konno, ...
Biomaterials 32 (9), 2241-2247, 2011
|Noninvasive prenatal diagnosis of duchenne muscular dystrophy: comprehensive genetic diagnosis in carrier, proband, and fetus|
SK Yoo, BC Lim, J Byeun, H Hwang, KJ Kim, YS Hwang, JH Lee, JS Park, ...
Clinical chemistry 61 (6), 829-837, 2015
|Whole-exome and transcriptome sequencing of refractory diffuse large B-cell lymphoma|
HY Park, SB Lee, HY Yoo, SJ Kim, WS Kim, JI Kim, YH Ko
Oncotarget 7 (52), 86433, 2016
|Transcriptome analyses of chronic traumatic encephalopathy show alterations in protein phosphatase expression associated with tauopathy|
JS Seo, S Lee, JY Shin, YJ Hwang, H Cho, SK Yoo, Y Kim, S Lim, YK Kim, ...
Experimental & molecular medicine 49 (5), e333-e333, 2017
|Nonsynonymous variants in PAX4 and GLP1R are associated with type 2 diabetes in an East Asian population|
SH Kwak, J Chae, S Lee, S Choi, BK Koo, JW Yoon, JH Park, B Cho, ...
Diabetes 67 (9), 1892-1902, 2018
|Reference-unbiased copy number variant analysis using CGH microarrays|
YS Ju, D Hong, S Kim, SS Park, S Kim, S Lee, H Park, JI Kim, JS Seo
Nucleic acids research 38 (20), e190-e190, 2010
|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
|Combined linkage and association analyses identify a novel locus for obesity near PROX1 in Asians|
HJ Kim, YJ Yoo, YS Ju, S Lee, S Cho, J Sung, JI Kim, JS Seo
Obesity 21 (11), 2405-2412, 2013
|Targeted resequencing of candidate genes reveals novel variants associated with severe Behçet’s uveitis|
SJ Kim, S Lee, C Park, JS Seo, JI Kim, HG Yu
Experimental & molecular medicine 45 (10), e49-e49, 2013