Hansook K. Chong, Ph.D.

Affiliations: 
2010 Biological Sciences - Ph.D. University of California, Irvine, Irvine, CA 
Area:
Molecular Biology, Bioinformatics Biology
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"Hansook Chong"

Parents

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Timothy F. Osborne grad student 2010 UC Irvine
 (Genome-wide analysis of FXR target genes in mouse liver.)
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Publications

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Richardson ME, Chong H, Mu W, et al. (2018) DNA breakpoint assay reveals a majority of gross duplications occur in tandem reducing VUS classifications in breast cancer predisposition genes. Genetics in Medicine : Official Journal of the American College of Medical Genetics
Chong HK, Wang T, Lu HM, et al. (2014) The validation and clinical implementation of BRCAplus: a comprehensive high-risk breast cancer diagnostic assay. Plos One. 9: e97408
Chong HK, Biesinger J, Seo YK, et al. (2012) Genome-wide analysis of hepatic LRH-1 reveals a promoter binding preference and suggests a role in regulating genes of lipid metabolism in concert with FXR. Bmc Genomics. 13: 51
Jeong YS, Kim D, Lee YS, et al. (2011) Integrated expression profiling and genome-wide analysis of ChREBP targets reveals the dual role for ChREBP in glucose-regulated gene expression. Plos One. 6: e22544
Seo YK, Jeon TI, Chong HK, et al. (2011) Genome-wide localization of SREBP-2 in hepatic chromatin predicts a role in autophagy. Cell Metabolism. 13: 367-75
Lee FY, de Aguiar Vallim TQ, Chong HK, et al. (2010) Activation of the farnesoid X receptor provides protection against acetaminophen-induced hepatic toxicity. Molecular Endocrinology (Baltimore, Md.). 24: 1626-36
Chong HK, Infante AM, Seo YK, et al. (2010) Genome-wide interrogation of hepatic FXR reveals an asymmetric IR-1 motif and synergy with LRH-1. Nucleic Acids Research. 38: 6007-17
Lee FY, de Aguiar Vallim TQ, Chong HK, et al. (2010) Activation of the Farnesoid X-Activated Receptor Provides Protection against Acetaminophen-Induced Hepatic Toxicity The Journal of Clinical Endocrinology & Metabolism. 95: 3563-3563
Seo YK, Chong HK, Infante AM, et al. (2009) Genome-wide analysis of SREBP-1 binding in mouse liver chromatin reveals a preference for promoter proximal binding to a new motif. Proceedings of the National Academy of Sciences of the United States of America. 106: 13765-9
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