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Ren-Hua Chung, Ph.D. - Publications

Affiliations: 
2006 North Carolina State University, Raleigh, NC 
Area:
Biostatistics Biology, Bioinformatics Biology, Genetics
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27 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Fang CP, Liu TH, Chung RH, Tsou HH, Kuo HW, Wang SC, Liu CC, Liu SC, Chen ACH, Liu YL. Genetic variants in NECTIN4 encoding an adhesion molecule are associated with continued opioid use. Plos One. 15: e0234549. PMID 32555608 DOI: 10.1371/Journal.Pone.0234549  0.34
2020 Fang CP, Wang SC, Tsou HH, Chung RH, Hsu YT, Liu SC, Kuo HW, Liu TH, Chen ACH, Liu YL. Genetic polymorphisms in the opioid receptor delta 1 (OPRD1) gene are associated with methadone dose in methadone maintenance treatment for heroin dependence. Journal of Human Genetics. PMID 31907389 DOI: 10.1038/S10038-019-0718-X  0.373
2020 Fang C, Liu T, Chung R, Tsou H, Kuo H, Wang S, Liu C, Liu SC, Chen ACH, Liu Y. SNPs in the NECTIN4 gene loci in the MMT study. Plos One. DOI: 10.1371/Journal.Pone.0234549.S004  0.359
2019 Chung RH, Kang CY. A multi-omics data simulator for complex disease studies and its application to evaluate multi-omics data analysis methods for disease classification. Gigascience. 8. PMID 31029063 DOI: 10.1093/Gigascience/Giz045  0.324
2018 Wang SC, Chung RH, Kuo HW, Liu TH, Fang CP, Liu SC, Liu CC, Tsou HH, Chen ACH, Liu YL. GRK5 is associated with the regulation of methadone dosage in heroin dependence. The International Journal of Neuropsychopharmacology. PMID 30060048 DOI: 10.1093/Ijnp/Pyy066  0.311
2018 Wang WC, Chiu YF, Chung RH, Hwu CM, Lee IT, Lee CH, Chang YC, Hung KY, Quertermous T, Chen YI, Hsiung CA. Gene Is Associated With Triglyceride Levels In Subjects With Family History Of Hypertension From The SAPPHIRe And TWB Projects. International Journal of Medical Sciences. 15: 1035-1042. PMID 30013445 DOI: 10.7150/Ijms.25742  0.309
2017 Chung RH, Kang CY. A Powerful Gene-Based Test Accommodating Common and Low-Frequency Variants to Detect Both Main Effects and Gene-Gene Interaction Effects in Case-Control Studies. Frontiers in Genetics. 8: 228. PMID 29358944 DOI: 10.3389/Fgene.2017.00228  0.395
2017 Liu TH, Chung RH, Wang SC, Fang CP, Tsou HH, Shih CL, Kuo HW, Wang Y, Liu YL. Missense mutation at CLDN8 associated with a high plasma interferon gamma-inducible protein 10 level in methadone-maintained patients with urine test positive for morphine. Plos One. 12: e0187639. PMID 29145422 DOI: 10.1371/Journal.Pone.0187639  0.359
2017 Zhao W, Rasheed A, Tikkanen E, Lee JJ, Butterworth AS, Howson JMM, Assimes TL, Chowdhury R, Orho-Melander M, Damrauer S, Small A, Asma S, Imamura M, Yamauch T, Chambers JC, ... ... Chung RH, et al. Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease. Nature Genetics. PMID 28869590 DOI: 10.1038/Ng.3943  0.361
2017 Chung RH, Chiu YF, Hung YJ, Lee WJ, Wu KD, Chen HL, Lin MW, Chen YI, Quertermous T, Hsiung CA. Genome-wide copy number variation analysis identified deletions in SFMBT1 associated with fasting plasma glucose in a Han Chinese population. Bmc Genomics. 18: 591. PMID 28789618 DOI: 10.1186/S12864-017-3975-0  0.316
2017 Howson JMM, Zhao W, Barnes DR, Ho WK, Young R, Paul DS, Waite LL, Freitag DF, Fauman EB, Salfati EL, Sun BB, Eicher JD, Johnson AD, Sheu WHH, Nielsen SF, ... ... Chung RH, et al. Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms. Nature Genetics. PMID 28530674 DOI: 10.1038/Ng.3874  0.395
2016 Lin PL, Tsai WY, Chung RH. A combined association test for rare variants using family and case-control data. Bmc Proceedings. 10: 215-219. PMID 27980639 DOI: 10.1186/S12919-016-0033-X  0.365
2016 Lin PL, Yu YW, Chung RH. Pathway Analysis Incorporating Protein-Protein Interaction Networks Identified Candidate Pathways for the Seven Common Diseases. Plos One. 11: e0162910. PMID 27622767 DOI: 10.1371/Journal.Pone.0162910  0.379
2016 Sung PY, Wang YT, Hsiung CA, Chung RH. GCORE-sib: An efficient gene-gene interaction tool for genome-wide association studies based on discordant sib pairs. Bmc Bioinformatics. 17: 273. PMID 27391654 DOI: 10.1186/S12859-016-1145-Z  0.404
2016 Chung RH, Tsai WY, Kang CY, Yao PJ, Tsai HJ, Chen CH. FamPipe: An Automatic Analysis Pipeline for Analyzing Sequencing Data in Families for Disease Studies. Plos Computational Biology. 12: e1004980. PMID 27272119 DOI: 10.1371/Journal.Pcbi.1004980  0.354
2016 Sung PY, Wang YT, Yu YW, Chung RH. An efficient gene-gene interaction test for genome-wide association studies in trio families. Bioinformatics (Oxford, England). PMID 26873927 DOI: 10.1093/Bioinformatics/Btw077  0.392
2015 Yao PJ, Chung RH. SeqSIMLA2_exact: Simulate multiple disease sites in large pedigrees with given disease status for diseases with low prevalence. Bioinformatics (Oxford, England). PMID 26515824 DOI: 10.1093/Bioinformatics/Btv626  0.33
2015 Wang YT, Sung PY, Lin PL, Yu YW, Chung RH. A multi-SNP association test for complex diseases incorporating an optimal P-value threshold algorithm in nuclear families. Bmc Genomics. 16: 381. PMID 25975968 DOI: 10.1186/S12864-015-1620-3  0.428
2015 Chung RH, Tsai WY, Hsieh CH, Hung KY, Hsiung CA, Hauser ER. SeqSIMLA2: simulating correlated quantitative traits accounting for shared environmental effects in user-specified pedigree structure. Genetic Epidemiology. 39: 20-4. PMID 25250827 DOI: 10.1002/Gepi.21850  0.317
2014 Wang SC, Tsou HH, Chung RH, Chang YS, Fang CP, Chen CH, Ho IK, Kuo HW, Liu SC, Shih YH, Wu HY, Huang BH, Lin KM, Chen AC, Hsiao CF, et al. The association of genetic polymorphisms in the κ-opioid receptor 1 gene with body weight, alcohol use, and withdrawal symptoms in patients with methadone maintenance. Journal of Clinical Psychopharmacology. 34: 205-11. PMID 24525640 DOI: 10.1097/Jcp.0000000000000082  0.344
2013 Park YS, Schmidt M, Martin ER, Pericak-Vance MA, Chung RH. Pathway-PDT: a flexible pathway analysis tool for nuclear families. Bmc Bioinformatics. 14: 267. PMID 24006871 DOI: 10.1186/1471-2105-14-267  0.346
2013 Chung RH, Shih CC. SeqSIMLA: a sequence and phenotype simulation tool for complex disease studies. Bmc Bioinformatics. 14: 199. PMID 23782512 DOI: 10.1186/1471-2105-14-199  0.375
2012 Chung RH, Chen YE. A two-stage random forest-based pathway analysis method Plos One. 7. PMID 22586488 DOI: 10.1371/Journal.Pone.0036662  0.361
2012 Thomas V, Liu Z, Srinivasan SK, Chung R, Martin E, Levine EA, Freimanis RI, Hu JJ. Abstract 2613: Racial/Ethnic specific polygenic models of breast cancer risk Cancer Research. 72: 2613-2613. DOI: 10.1158/1538-7445.Am2012-2613  0.305
2009 Chung R, Edwards T, Scott W, Almonte C, Burt A, Powell E, Beecham G, Konidari I, Pericak-Vance M, Haines J, Zuchner S, Wang G, Wang L, Vance J, Martin E. P1.126 Developing a risk model for Parkinson disease Parkinsonism & Related Disorders. 15: S61. DOI: 10.1016/S1353-8020(09)70248-2  0.429
2008 Chung RH, Schmidt S, Martin ER, Hauser ER. Ordered-subset analysis (OSA) for family-based association mapping of complex traits. Genetic Epidemiology. 32: 627-37. PMID 18473393 DOI: 10.1002/Gepi.20340  0.38
2005 Martin ER, Bronson PG, Li YJ, Wall N, Chung RH, Schmechel DE, Small G, Xu PT, Bartlett J, Schnetz-Boutaud N, Haines JL, Gilbert JR, Pericak-Vance MA. Interaction between the alpha-T catenin gene (VR22) and APOE in Alzheimer's disease. Journal of Medical Genetics. 42: 787-92. PMID 16199552 DOI: 10.1136/Jmg.2004.029553  0.314
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