Juang JJ - Search Results

1

An automated microfluidic DNA microarray platform for genetic variant detection in inherited arrhythmic diseases.

Huang SH , Chang YS , Juang JJ , Chang KW , Tsai MH , Lu TP , Lai LC , Chuang EY , Huang NT . Huang SH , et al. Among authors: juang jj. Analyst. 2018 Mar 12;143(6):1367-1377. doi: 10.1039/c7an01648d. Analyst. 2018. PMID: 29423467

2

Genome-wide methylation profiles in coronary artery ectasia.

Lu TP, Chuang NC, Cheng CY, Hsu CA, Wang YC, Lin YH, Lee JK, Wu CK, Hwang JJ, Lin LY, Yeh SS, Chien KL, Juang JJ. Lu TP, et al. Among authors: juang jj. Clin Sci (Lond). 2017 Apr 1;131(7):583-594. doi: 10.1042/CS20160821. Epub 2017 Jan 31. Clin Sci (Lond). 2017. PMID: 28143891

3

Impact of Ancestral Differences and Reassessment of the Classification of Previously Reported Pathogenic Variants in Patients With Brugada Syndrome in the Genomic Era: A SADS-TW BrS Registry.

Chen CJ, Lu TP, Lin LY, Liu YB, Ho LT, Huang HC, Lai LP, Hwang JJ, Yeh SS, Wu CK, Juang JJ, Antzelevitch C. Chen CJ, et al. Among authors: juang jj. Front Genet. 2019 Jan 4;9:680. doi: 10.3389/fgene.2018.00680. eCollection 2018. Front Genet. 2019. PMID: 30662450 Free PMC article.

4

VariED: the first integrated database of gene annotation and expression profiles for variants related to human diseases.

Lee CY, Chattopadhyay A, Chiang LM, Juang JJ, Lai LC, Tsai MH, Lu TP, Chuang EY. Lee CY, et al. Among authors: juang jj. Database (Oxford). 2019 Jan 1;2019:baz075. doi: 10.1093/database/baz075. Database (Oxford). 2019. PMID: 31317185 Free PMC article.

5

GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death.

Juang JJ, Binda A, Lee SJ, Hwang JJ, Chen WJ, Liu YB, Lin LY, Yu CC, Ho LT, Huang HC, Chen CJ, Lu TP, Lai LC, Yeh SS, Lai LP, Chuang EY, Rivolta I, Antzelevitch C. Juang JJ, et al. EBioMedicine. 2020 Jul;57:102843. doi: 10.1016/j.ebiom.2020.102843. Epub 2020 Jul 7. EBioMedicine. 2020. PMID: 32645615 Free PMC article.

6

Long-term outcomes and left ventricular diastolic function of sarcomere mutation-positive and mutation-negative patients with hypertrophic cardiomyopathy: a prospective cohort study.

Chen CJ, Su MM, Liao YC, Chang FL, Wu CK, Lin LY, Chen YS, Lin YH, Hwang JJ, Yu SL, Kao HL, Chen WJ, Lu TP, Shih CY, Yeh SS, Yang DH, Lai LP, Juang JJ. Chen CJ, et al. Among authors: juang jj. Eur Heart J Cardiovasc Imaging. 2020 Nov 22:jeaa317. doi: 10.1093/ehjci/jeaa317. Online ahead of print. Eur Heart J Cardiovasc Imaging. 2020. PMID: 33221870

7

Rare variants discovery by extensive whole-genome sequencing of the Han Chinese population in Taiwan: Applications to cardiovascular medicine.

Juang JJ, Lu TP, Su MW, Lin CW, Yang JH, Chu HW, Chen CH, Hsiao YW, Lee CY, Chiang LM, Yu QY, Hsiao CK, Chen CJ, Wu PE, Pai CH, Chuang EY, Shen CY. Juang JJ, et al. J Adv Res. 2020 Dec 7;30:147-158. doi: 10.1016/j.jare.2020.12.003. eCollection 2021 May. J Adv Res. 2020. PMID: 34026292 Free PMC article.

8

CNVIntegrate: the first multi-ethnic database for identifying copy number variations associated with cancer.

Chattopadhyay A, Teoh ZH, Wu CY, Juang JJ, Lai LC, Tsai MH, Wu CH, Lu TP, Chuang EY. Chattopadhyay A, et al. Among authors: juang jj. Database (Oxford). 2021 Jul 14;2021:baab044. doi: 10.1093/database/baab044. Database (Oxford). 2021. PMID: 34259866 Free PMC article.

9

Develop and Apply Electrocardiography-Based Risk Score to Identify Community-Based Elderly Individuals at High-Risk of Mortality.

Lu TP, Chattopadhyay A, Lu KC, Chuang JY, Yeh SS, Chang IS, Chen CJ, Wu IC, Hsu CC, Chen TY, Tseng WT, Hsiung CA, Juang JJ. Lu TP, et al. Among authors: juang jj. Front Cardiovasc Med. 2021 Oct 8;8:738061. doi: 10.3389/fcvm.2021.738061. eCollection 2021. Front Cardiovasc Med. 2021. PMID: 34692790 Free PMC article.

10

CLIN_SKAT: an R package to conduct association analysis using functionally relevant variants.

Chattopadhyay A, Shih CY, Hsu YC, Juang JJ, Chuang EY, Lu TP. Chattopadhyay A, et al. Among authors: juang jj. BMC Bioinformatics. 2022 Oct 23;23(1):441. doi: 10.1186/s12859-022-04987-2. BMC Bioinformatics. 2022. PMID: 36274122 Free PMC article.

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