Human Genome Epidemiology Literature Finder
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Records 1 - 10 (of 10 Records) |
| Query Trace: Disease and THBS1[original query] |
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| Evidence for substantial effect modification by gender in a large-scale genetic association study of the metabolic syndrome among coronary heart disease patients. Human genetics 2003 Dec 114 (1): 87-98. McCarthy Jeanette J, Meyer Joanne, Moliterno David J, Newby L Kristin, Rogers William J, Topol Eric J, |
| Polymorphisms in hypoxia inducible factor 1 and the initial clinical presentation of coronary disease. American heart journal 2007 Dec 154 (6): 1035-42. Hlatky Mark A, Quertermous Thomas, Boothroyd Derek B, Priest James R, Glassford Alec J, Myers Richard M, Fortmann Stephen P, Iribarren Carlos, Tabor Holly K, Assimes Themistocles L, Tibshirani Robert J, Go Alan |
| Polymorphisms associated with in vitro aspirin resistance are not associated with clinical outcomes in patients with coronary artery disease who report regular aspirin use. American heart journal 2011 Jul 162 (1): 166-72.e1. Voora Deepak, Horton John, Shah Svati H, Shaw Linda K, Newby L Krist |
| Association between variations in coagulation system genes and carotid plaque. Journal of the neurological sciences 2012 Dec 323 (1-2): 93-8. Della-Morte David, Beecham Ashley, Dong Chuanhui, Wang Liyong, McClendon Mark S, Gardener Hannah, Blanton Susan H, Sacco Ralph L, Rundek Tatja |
| Polymorphisms in host genes encoding NOSII, C-reactive protein, and adhesion molecules thrombospondin and E-selectin are risk factors for Plasmodium falciparum malaria in India. European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology 2015 Oct 34 (10): 2029-39. Kanchan K, Pati S S, Mohanty S, Mishra S K, Sharma S K, Awasthi S, , Venkatesh V, Habib |
| Association between single nucleotide polymorphisms in thrombospondins genes and coronary artery disease: A meta-analysis. Thrombosis research 2015 Jul 136 (1): 45-51. Zhang Xiao-Jie, Wei Chun-Yan, Li Wen-Bo, Zhang Ling-Li, Zhou Ying, Wang Zhi-Hao, Tang Meng-Xiong, Zhang Wei, Zhang Yun, Zhong Mi |
| Genome-wide copy number analysis reveals candidate gene loci that confer susceptibility to high-grade prostate cancer. Urologic oncology 2017 09 35 (9): 545.e1-545.e11. Poniah Prevathe, Mohd Zain Shamsul, Abdul Razack Azad Hassan, Kuppusamy Shanggar, Karuppayah Shankar, Sian Eng Hooi, Mohamed Zahur |
| Long-range genomic regulators of THBS1 and LTBP4 modify disease severity in duchenne muscular dystrophy.
Annals of neurology 2018 Jul . Weiss Robert B, Vieland Veronica J, Dunn Diane M, Kaminoh Yuuki, Flanigan Kevin M, |
| Evaluating Genetic Modifiers of Duchenne Muscular Dystrophy Disease Progression Using Modeling and MRI. Neurology 2022 10 99 (21): e2406-e2416. Barnard Alison M, Hammers David W, Triplett William T, Kim Sarah, Forbes Sean C, Willcocks Rebecca J, Daniels Michael J, Senesac Claudia R, Lott Donovan J, Arpan Ishu, Rooney William D, Wang Richard T, Nelson Stanley F, Sweeney H Lee, Vandenborne Krista, Walter Glenn |
| [Predictive significance of genetic analysis of the development of dry eye disease of different origin]. Vestnik oftalmologii 2024 1 139 (6): 13-18. T N Safonova, G V Zaitseva, V I Loginov, A M Burdenn |
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