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日期	题名	關聯
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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