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    显示项目51-86 / 86. (共2页)
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    日期题名關聯
    2019-08 Genomewide sex-by-snp interaction scan identifies adgrv1 for the sex differences of opioid dependence in african american and supporting evidence in relations with treatment side effects in the asian population European Neuropsychopharmacology. 2019 Aug;29(Suppl. 4):S1183-S1184.
    2019-07 Haplotypes constructed by Whole exome sequencing to map and identify a novel disease-causing RP2 gene variant from a recessive X linked Retinities Pigmentosa family European Journal of Human Genetics. 2019 Jul;27(Suppl. 1):66-67.
    2019-07 IGF1 gene is associated with triglyceride levels in subjects with family history of hypertension from the SAPPHIRe and TWB projects European Journal of Human Genetics. 2019 Jul;27:163.
    2019-07 In vitro functional analysis of a novel RP2 alleles European Journal of Human Genetics. 2019 Jul;27:68.
    2019-05-01 A multi-omics data simulator for complex disease studies and its application to evaluate multi-omics data analysis methods for disease classification GigaScience. 2019 May 1;8(5):Article number giz045.
    2019-03 Genetic loci determining total immunoglobulin E levels from birth through adulthood Allergy. 2019 Mar;74(3):621-625.
    2018-10 GRK5 is associated with the regulation of methadone dosage in heroin dependence International Journal of Neuropsychopharmacology. 2018 Oct;21(10):910-917.
    2018-06 IGF1 gene is associated with triglyceride levels in subjects with family history of hypertension from the SAPPHIRe and TWB projects International Journal of Medical Sciences. 2018 Jun;15(10):1035-1042.
    2018-01 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. 2018 Jan;8:Article number 228.
    2017-11-16 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. 2017 Nov 16;12(11):Article number e0187639.
    2017-10-05 Single marker family-based association analysis conditional on parental information Methods in Molecular Biology. 2017 Oct 5;1666(Chapter 19):391-407.
    2017-09-04 Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease Nature Genetics. 2017 Sep 04;49(10):1450-1457.
    2017-08-08 Genome-wide copy number variation analysis identified deletions in SFMBT1 associated with fasting plasma glucose in a Han Chinese population BMC Genomics. 2017 Aug 8;18:Article number 591.
    2017-07 Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms Nature Genetics. 2017 Jul;49(7):1113-1119.
    2017-04-04 Obesity disproportionately impacts lung volumes, airflow and exhaled nitric oxide in children PLoS ONE. 2017 Apr 4;12(4):Article number e0174691.
    2016-12-15 Fine-mapping of lipid regions in global populations discovers ethnic-specific signals and refines previously identified lipid loci Human Molecular Genetics. 2016 Dec 15;25(24):5500-5512.
    2016-10-18 A combined association test for rare variants using family and case-control data BMC Proceedings. 2016 Oct 18;10(Suppl. 7):Article number 33.
    2016-10 Apoptosis pathway CASP10 gene associated with methadone dose and interacted with GRK5 European Neuropsychopharmacology. 2016 Oct;26(Suppl. 2):S693-S694.
    2016-09-13 Pathway analysis incorporating protein-protein interaction networks identified candidate pathways for the seven common diseases PLoS ONE. 2016 Sep 13;11(9):Article number e0162910.
    2016-09-12 The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals Nature Genetics. 2016 Sep 12;48(10):1171-1184.
    2016-08-02 Cost-effectiveness analysis of different genetic testing strategies for lynch syndrome in Taiwan PLoS ONE. 2016 Aug 2;11(8):Article number e0160599.
    2016-07-08 GCORE-sib: An efficient gene-gene interaction tool for genome-wide association studies based on discordant sib pairs BMC Bioinformatics. 2016 Jul 8;17:Article number 273.
    2016-06 An efficient gene-gene interaction test for genome-wide association studies in trio families Bioinformatics. 2016 Jun;32(12):1848-1855.
    2016-06 GESDB: A platform of simulation resources for genetic epidemiology studies Database. 2016 Jun;2016:Article number baw082.
    2016-06 FamPipe: An automatic analysis pipeline for analyzing sequencing data in families for disease studies PLoS Computational Biology. 2016 Jun;12(6):Article number e1004980.
    2016-02 SeqSIMLA2_exact: Simulate multiple disease sites in large pedigrees with given disease status for diseases with low prevalence Bioinformatics. 2016 Feb;32(4):557-562.
    2015-08-18 Effect of common genetic variants of growth arrest-specific 6 gene on insulin resistance, obesity and type 2 diabetes in an Asian population PLoS ONE. 2015 Aug 18;10(8):Article number e0135681.
    2015-05-15 A multi-SNP association test for complex diseases incorporating an optimal P-value threshold algorithm in nuclear families BMC Genomics. 2015 May 15;16:Article number 381.
    2015-01 SeqSIMLA2: Simulating correlated quantitative traits accounting for shared environmental effects in user-specified pedigree structure Genetic Epidemiology. 2015 Jan;39(1):20-24.
    2014-09-22 Family-based association test using both common and rare variants and accounting for directions of effects for sequencing data PLoS ONE. 2014 Sep 22;9(9):Article number e107800.
    2014-06-17 Identification of rare variants for hypertension with incorporation of linkage information BMC Proceedings. 2014 Jun 17;8(Suppl. 1):Article number S109.
    2014-04 The association of genetic polymorphisms in the kappa-opioid receptor 1 gene with body weight, alcohol use, and withdrawal symptoms in patients with methadone maintenance Journal of Clinical Psychopharmacology. 2014 Apr;34(2):205-211.
    2013-09-04 Pathway-PDT: A flexible pathway analysis tool for nuclear families BMC Bioinformatics. 2013 Sep 4;14:Article number 267.
    2013-06-20 SeqSIMLA: A sequence and phenotype simulation tool for complex disease studies BMC Bioinformatics. 2013 Jun 20;14:Article number 199.
    2013-04 PUPPI: A pathway analysis method using protein-protein interaction network for case-control data 2013 IEEE Symposium on Computational Intelligence in Bioinformatics and Computational Biology (CIBCB). 2013 Apr:238-241.
    2012-05 A two-stage random forest-based pathway analysis method PLoS ONE. 2012 May;7(5):Article number e36662.

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