Showing results (41-50 of 52) with videos related to
Sort By:
Pageof 6
The American Journal of Cardiology|August 31, 2021
Frequency and Significance of Right Bundle Branch Block and Subclinical Coronary Atherosclerosis in Asymptomatic IndividualsHyeji Lee, Young-Jee Jeon, Byung Ju Kang, et al.Briefings in Bioinformatics|July 5, 2024
CWAS-Plus: estimating category-wide association of rare noncoding variation from whole-genome sequencing data with cell-type-specific functional dataYujin Kim, Minwoo Jeong, In Gyeong Koh, et al.Medrxiv : the Preprint Server for Health Sciences|May 3, 2024
CWAS-Plus: Estimating category-wide association of rare noncoding variation from whole-genome sequencing data with cell-type-specific functional dataYujin Kim, Minwoo Jeong, In Gyeong Koh, et al.Journal of Medicinal Chemistry|April 14, 2022
Effect of Structural Fine-Tuning on Chelate Stability and Liver Uptake of Anionic MRI Contrast AgentsAh Rum Baek, Hee-Kyung Kim, Soyeon Kim, et al.Epidemiology and Health|July 26, 2024
Association between smoking status and subclinical coronary atherosclerosis in asymptomatic Korean individualsHyeji Lee, Jinhee Ha, Kyung Sun Park, et al.The American Journal of Cardiology|July 30, 2023
Differential Impact of Degree of Hypertension on Subclinical Coronary Atherosclerosis in Asymptomatic Subjects With and Without Diabetes MellitusHyun Woo Park, Sangyong Jo, Kyung Sun Park, et al.Journal of Thoracic Disease|November 4, 2020
Active tuberculosis risk associated with malignancies: an 18-year retrospective cohort study in KoreaJaekyung Cheon, Changyoung Kim, Eun Ji Park, et al.Human Genomics|January 6, 2025
Uncovering potential causal genes for undiagnosed congenital anomalies using an in-house pipeline for trio-based whole-genome sequencingJeong-Min Kim, Hye-Won Cho, Dong Mun Shin, et al.Genome Medicine|August 21, 2025
Evaluation of familial phenotype deviation to measure the impact of de novo mutations in autismSoo-Whee Kim, Hyeji Lee, Da Yea Song, et al.Genome Biology|March 24, 2026
Co-occurrence of rare variants implicates gene pairs in cytoskeletal pathways and is associated with increased severity in autism spectrum disorderHyeji Lee, Kahee Ko, Seoyeon Kim, et al.Pageof 6