邻近类别 圖書 [1/2] 會議論文/會議摘要 [12/12] 类别统计 近3年内发表的文件:29(40.28%) 含全文笔数:72(100.00%) 文件下载次数统计 下载大于0次:72(100.00%) 下载大于100次:53(73.61%) 全文下载总次数:18655(86.47%) 最后更新时间: 2024-12-01 10:54 上传排行 数据加载中..... 下载排行 数据加载中..... 最近上传 Association of bone turnover marker... Latent space representation of elec... Rare variant contribution to the he... Clustering-based risk stratificatio... Using large language model (LLM) to... Understanding and alleviating infor... Machine learning models for predict... Pulse pressure is associated with d... Whole genome association study of t... Machine learning models for blood p...

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日期	题名	關聯
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.
2016-09-13	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.
2014-04	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.
2012-05	A two-stage random forest-based pathway analysis method	PLoS ONE. 2012 May;7(5):Article number e36662.

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