子类别 圖書 [1/2] 會議論文/會議摘要 [12/12] 期刊論文 [72/72] 邻近社群 MARK LAWRENCE WAHLQVIST(2008-2012) [138/140] 吳易謙 [54/55] 吳秀英 [10/10] 廖本揚 [39/39] 廖玉潔 [63/65] 張新儀 [245/268] 李孟智 [51/54] 李蘭 [28/28] 林培生 [25/25] 林煜軒 [47/47] 林肇堂 [35/35] 梁賡義 [15/15] 江博煌 [72/78] 溫啟邦(2001-2010) [177/188] 潘文涵 [110/115] 熊昭 [369/379] 莊淑鈞 [43/44] 莊紹源 [162/168] 蔡慧如 [162/165] 蔡憶文(1999-2010) [34/34] 蕭金福 [188/197] 藍祚運(2003-2011) [22/23] 許志成 [385/393] 邱亞文(2005-2013) [63/99] 邱弘毅 [49/49] 邱燕楓 [82/82] 郭耿南(2003-2010) [89/105] 鄒小蕙 [101/105] 陳主智 [61/61] 陳慶餘(2006-2010) [70/70] 陳美惠 [32/32] 陳豐奇 [53/55] 陳麗光 [106/106] 黃國晉 [15/15] 丘政民(2000-2004) [8/8] 其他 [238/244] 劉仁沛(1998-2002) [64/65] 姚姿君(1999-2002) [3/3] 戴東原(2003-2005) [21/22] 李明亮(2003-2007) [6/6] 林仲彥(1999-2005) [31/33] 林錦瑜(2002-2003) [5/5] 涂醒哲(2003-2004) [4/4] 石曜堂(1999-2006) [20/24] 蔡碧紋(2004-2006) [3/4] 陳淑媛(2001-2004) [3/3] 社群统计 近3年内发表的文件:34(39.53%) 含全文笔数:85(98.84%) 文件下载次数统计 下载大于0次:85(100.00%) 下载大于100次:63(74.12%) 全文下载总次数:21393(0.40%) 最后更新时间: 2024-11-28 15:50 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... Alcohol drinking may modify the ass... A linear relationship of ankle-brac... Understanding and alleviating infor... Machine learning models for predict... Pulse pressure is associated with d...

跳至: (选择年份) 2024 2023 2022 2021 2020 2019 2018 2017 2016 2015 2014 2013 2012 2011 2010 2009 2008 2007 2006 2005 2004 2003 2002 2001 2000 1999 1998 1997 1996 1995 1994 1993 1992 1991 1990 1985 1980 1975 1970 1960 1950 (选择月份) January February March April May June July August September October November December 或输入年份:

由新到旧排序 由最旧的开始

显示项目51-86 / 86. (共2页) << < 1 2  每页显示[10|25|50]项目

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.

显示项目51-86 / 86. (共2页) << < 1 2  每页显示[10|25|50]项目