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Author Details

Hong Xue
Hong Kong University of Science and Technology
1992
127
30
PMIDPaper TitleJournal TitlePublished Year
34673206GABRB2, a key player in neuropsychiatric disorders and beyond.Gene2022
34530168Copy number variation profile-based genomic typing of premenstrual dysphoric disorder in Chinese.J Genet Genomics2021
33741065Genetic-variant hotspots and hotspot clusters in the human genome facilitating adaptation while increasing instability.Hum Genomics2021
33596747Intrinsic and chemically-induced daughter number variations in cancer cell lines.Cell Cycle2021
32695026Highly Recurrent Copy Number Variations in <i>GABRB2</i> Associated With Schizophrenia and Premenstrual Dysphoric Disorder.Front Psychiatry2020
32005109Genomic subtyping of liver cancers with prognostic application.BMC Cancer2020
32636606Descent of Bacteria and Eukarya From an Archaeal Root of Life.Evol Bioinform Online2020
32929329PARK2 promotes mitochondrial pathway of apoptosis and antimicrotubule drugs chemosensitivity <i>via</i> degradation of phospho-BCL-2.Theranostics2020
30906832AluScanCNV2: An R package for copy number variation calling and cancer risk prediction with next-generation sequencing data.Genes Dis2018
30134973Forward and reverse mutations in stages of cancer development.Hum Genomics2018
30013074Gabrb2-knockout mice displayed schizophrenia-like and comorbid phenotypes with interneuron-astrocyte-microglia dysregulation.Transl Psychiatry2018
28264473Future of the Genetic Code.Life (Basel)2017
28458714Antiaging and Anxiolytic Effects of Combinatory Formulas Based on Four Medicinal Herbs.Evid Based Complement Alternat Med2017
28426226Brain Uptake of Bioactive Flavones in Scutellariae Radix and Its Relationship to Anxiolytic Effect in Mice.Mol Pharm2017
26999216Coevolution Theory of the Genetic Code at Age Forty: Pathway to Translation and Synthetic Life.Life (Basel)2016
26481319Psychiatric genetics in China: achievements and challenges.Mol Psychiatry2016
27663196Variation of global DNA methylation levels with age and in autistic children.Hum Genomics2016
26854351Feature co-localization landscape of the human genome.Sci Rep2016
26200391A novel phosphodiesterase-5 Inhibitor: Yonkenafil modulates neurogenesis, gliosis to improve cognitive function and ameliorates amyloid burden in an APP/PS1 transgenic mice model.Mech Ageing Dev2015
26561861GABRB2 Haplotype Association with Heroin Dependence in Chinese Population.PLoS One2015
26419425SAMSVM: A tool for misalignment filtration of SAM-format sequences with support vector machine.J Bioinform Comput Biol2015
26208496Massive interstitial copy-neutral loss-of-heterozygosity as evidence for cancer being a disease of the DNA-damage response.BMC Med Genomics2015
26207917Glioma Association and Balancing Selection of ZFPM2.PLoS One2015
24197974Quantitative assessment of the associations between DNA repair gene XRCC3 Thr241Met polymorphism and gastric cancer.Tumour Biol2014
26203258Application of Machine Learning to Development of Copy Number Variation-based Prediction of Cancer Risk.Genomics Insights2014
25558350Copy number variation analysis based on AluScan sequences.J Clin Bioinforma2014
24903817Primary study on the lesions and specific proteins in BEAS-2B cells induced with the 2009 A (H1N1) influenza virus.Appl Microbiol Biotechnol2014
24572018Mutations enabling displacement of tryptophan by 4-fluorotryptophan as a canonical amino acid of the genetic code.Genome Biol Evol2014
24402875Genetic association of lipid metabolism related SNPs with myocardial infarction in the Pakistani population.Mol Biol Rep2014
24465431Familial young-onset diabetes, pre-diabetes and cardiovascular disease are associated with genetic variants of DACH1 in Chinese.PLoS One2014
24449341A rapid fluorescence polarization-based method for genotypic detection of drug resistance in Mycobacterium tuberculosis.Appl Microbiol Biotechnol2014
24477584Genetic association of IDE, POU2F1, PON1, IL1α and IL1β with type 2 diabetes in Pakistani population.Mol Biol Rep2014
23638040Social cognitive role of schizophrenia candidate gene GABRB2.PLoS One2013
22113559Applicability of a sensitive duplex real-time PCR assay for identifying B/Yamagata and B/Victoria lineages of influenza virus from clinical specimens.Appl Microbiol Biotechnol2012
23198447[The progress of studies on the relation between circadian rhythm disruption and cancer].Sheng Wu Yi Xue Gong Cheng Xue Za Zhi2012
22206711Epigenetic regulation on GABRB2 isoforms expression: developmental variations and disruptions in psychotic disorders.Schizophr Res2012
22419070A simple method for high-throughput quantification of genome-wide DNA methylation by fluorescence polarization.Epigenetics2012
20404824Imprinting in the schizophrenia candidate gene GABRB2 encoding GABA(A) receptor β(2) subunit.Mol Psychiatry2011
22087792AluScan: a method for genome-wide scanning of sequence and structure variations in the human genome.BMC Genomics2011
22145530Multi-platform gene-expression mining and marker gene analysis.Int J Data Min Bioinform2011
21784794Identifying disease-associated SNP clusters via contiguous outlier detection.Bioinformatics2011
21914441Effects of flavone 6-substitutions on GABAA receptors efficacy.Eur J Pharmacol2011
21569557A hidden two-locus disease association pattern in genome-wide association studies.BMC Bioinformatics2011
21342556The choice of null distributions for detecting gene-gene interactions in genome-wide association studies.BMC Bioinformatics2011
20421687Multitask learning for protein subcellular location prediction.IEEE/ACM Trans Comput Biol Bioinform2011
20067772GABA(A) receptor subtype selectivity underlying anxiolytic effect of 6-hydroxyflavone.Biochem Pharmacol2010
21072167Dopamine D4 receptor gene associated with fairness preference in ultimatum game.PLoS One2010
20817139BOOST: A fast approach to detecting gene-gene interactions in genome-wide case-control studies.Am J Hum Genet2010
20808824Genetic code mutations: the breaking of a three billion year invariance.PLoS One2010
20736343Detecting two-locus associations allowing for interactions in genome-wide association studies.Bioinformatics2010
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Collaborators

Jeffrey Tze-Fei Wong
The Hong Kong University of Science and Technology
Co-authored papers 30
Zhiliang Yu
Co-authored papers 9
Pak C Sham
the University of Hong Kong
Co-authored papers 6
Lin He
Heilongjiang Bayi Agricultural University
Co-authored papers 5
Wai Sang Poon
Prince of Wales Hospital
Co-authored papers 5
Gilberto Ka Kit Leung
The University of Hong Kong
Co-authored papers 4
Stephen Kwok-Wing Tsui
The Chinese University of Hong Kong
Co-authored papers 4
Vishwajit L Nimgaonkar
Co-authored papers 3
Huanming Yang
Experimental Research Center, China Academy of Chinese Medical Sciences
Co-authored papers 3
Yangfan Liu
Co-authored papers 2
Jian-Bing Fan
Nanfang Hospital and Basic Medical College, Southern Medical University
Co-authored papers 2
Jean-Fran??ois Olivier
McGill University Health Center
Co-authored papers 2
Robert W Plumb
Co-authored papers 2
Shao Li
Co-authored papers 2
Ludmila Pawlikowska
Center for Cerebrovascular Research
Co-authored papers 2
David A Hinds
23andMe Inc.
Co-authored papers 2
Suzanne M Leal
Center for Statistical Genetics, Columbia University Medical Center
Co-authored papers 2
Thomas D Willis
Adaptive Biotechnologies
Co-authored papers 2
Li Jin
Fudan University
Co-authored papers 2
Jeffrey Barrett
Wellcome Trust Sanger Institute
Co-authored papers 2
E Clayton
Harvard Medical School, Vanderbilt University, Yale University Yale Law School
Co-authored papers 2
Juliana C N Chan
Co-authored papers 2
Hongbin Zhao
First Hospital of Xingtai
Co-authored papers 2
Fanny Chagnon
McGill University
Co-authored papers 2
Panos Deloukas
William Harvey Research Institute, Queen Mary University of London
Co-authored papers 2
Mark F Leppert
University of Utah
Co-authored papers 2
Chris Clee
Co-authored papers 2
Alexandre Montpetit
McGill University and Genome Quebec Innovation Centre
Co-authored papers 2
John W Belmont
Illumina Inc.
Co-authored papers 2
Ruth Jamieson
Newcastle University
Co-authored papers 2
Release 1.2