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Genome Medicine|August 7, 2025
Contribution of rare coding variants to microcephaly in individuals with neurodevelopmental disordersJihoon G Yoon, Hyunsoo Jang, Seungbok Lee, et al.Nature Genetics|July 5, 2011
Extensive genomic and transcriptional diversity identified through massively parallel DNA and RNA sequencing of eighteen Korean individualsYoung Seok Ju, Jong-Il Kim, Sheehyun Kim, et al.Nature Communications|December 11, 2014
An epigenomic roadmap to induced pluripotency reveals DNA methylation as a reprogramming modulatorDong-Sung Lee, Jong-Yeon Shin, Peter D Tonge, et al.Experimental & Molecular Medicine|May 20, 2017
Transcriptome analyses of chronic traumatic encephalopathy show alterations in protein phosphatase expression associated with tauopathyJeong-Sun Seo, Seungbok Lee, Jong-Yeon Shin, et al.Nature Genetics|April 6, 2010
Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencingHansoo Park, Jong-Il Kim, Young Seok Ju, et al.Orphanet Journal of Rare Diseases|October 8, 2022
The Korean undiagnosed diseases program phase I: expansion of the nationwide network and the development of long-term infrastructureSoo Yeon Kim, Seungbok Lee, Hyewon Woo, et al.Nature|July 10, 2009
A highly annotated whole-genome sequence of a Korean individualJong-Il Kim, Young Seok Ju, Hansoo Park, et al.Pageof 13