Human Genome Epidemiology Literature Finder
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Records 1 - 23 (of 23 Records) |
| Query Trace: Disease and EPHX2[original query] |
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| Genetic polymorphisms of microsomal and soluble epoxide hydrolase and the risk of Parkinson's disease. Pharmacogenetics 2001 Nov 11 (8): 703-8. Farin F M, Janssen P, Quigley S, Abbott D, Hassett C, Smith-Weller T, Franklin G M, Swanson P D, Longstreth W T, Omiecinski C J, Checkoway |
| Genetic variation in soluble epoxide hydrolase (EPHX2) and risk of coronary heart disease: The Atherosclerosis Risk in Communities (ARIC) study. Human molecular genetics 2006 May 15 (10): 1640-9. Lee Craig R, North Kari E, Bray Molly S, Fornage Myriam, Seubert John M, Newman John W, Hammock Bruce D, Couper David J, Heiss Gerardo, Zeldin Darryl |
| Genetic analysis of the soluble epoxide hydrolase gene, EPHX2, in subclinical cardiovascular disease in the Diabetes Heart Study. Diabetes & vascular disease research 2008 Jun 5 (2): 128-34. Burdon Kathryn P, Lehtinen Allison B, Langefeld Carl D, Carr J Jeffrey, Rich Stephen S, Freedman Barry I, Herrington David, Bowden Donald |
| Genetic variation in soluble epoxide hydrolase (EPHX2) is associated with an increased risk of ischemic stroke in white Europeans. Stroke; a journal of cerebral circulation 2008 May 39 (5): 1593-6. Gschwendtner Andreas, Ripke Stephan, Freilinger Tobias, Lichtner Peter, Müller-Myhsok Bertram, Wichmann H-Erich, Meitinger Thomas, Dichgans Mart |
| Genetically reduced soluble epoxide hydrolase activity and risk of stroke and other cardiovascular disease. Stroke; a journal of cerebral circulation 2010 Jan 41 (1): 27-33. Lee Julie, Dahl Morten, Grande Peer, Tybjaerg-Hansen Anne, Nordestgaard Børge |
| Variation in the human soluble epoxide hydrolase gene and risk of restenosis after percutaneous coronary intervention. BMC cardiovascular disorders 2009 9 (1): 48. Kullmann Silke, Binner Priska, Rackebrandt Kirsten, Huge Andreas, Haltern Georg, Lankisch Mark, Füth Reiner, von Hodenberg Eberhard, Bestehorn Hans-Peter, Scheffold Thom |
| Homozygosity for the EPHX2 K55R polymorphism increases the long-term risk of ischemic stroke in men: a study in Swedes. Pharmacogenetics and genomics 2010 Feb 20 (2): 94-103. Fava Cristiano, Montagnana Martina, Danese Elisa, Almgren Peter, Hedblad Bo, Engström Gunnar, Berglund Göran, Minuz Pietro, Melander Ol |
| Association between polymorphisms of CYP2J2 and EPHX2 genes and risk of coronary artery disease. Pharmacogenetics and genomics 2011 Aug 21 (8): 489-94. Xu Yujun, Ding Hu, Peng Jia, Cui Guanglin, Liu Lei, Cianflone Katherine, Wang Dao W |
| Role of soluble epoxide hydrolase in age-related vascular cognitive decline. Prostaglandins & other lipid mediators 2014 Oct 113-115 30-7. Nelson Jonathan W, Young Jennifer M, Borkar Rohan N, Woltjer Randy L, Quinn Joseph F, Silbert Lisa C, Grafe Marjorie R, Alkayed Nabil |
| CYP2C8 rs17110453 and EPHX2 rs751141 two-locus interaction increases susceptibility to ischemic stroke. Gene 2015 Jul 565 (1): 85-9. Yi Xingyang, Zhang Biao, Wang Chun, Liao Duanxiu, Lin Jing, Chi Lif |
| Association of gain-of-function EPHX2 polymorphism Lys55Arg with acute kidney injury following cardiac surgery. PloS one 2017 12 (5): e0175292. Shuey Megan M, Billings Frederic T, Wei Shouzou, Milne Ginger L, Nian Hui, Yu Chang, Brown Nancy |
| Association between the EPHX2 p.Lys55Arg polymorphism and prognosis following an acute coronary syndrome. Prostaglandins & other lipid mediators 2018 Aug 138 15-22. Oni-Orisan Akinyemi, Cresci Sharon, Jones Philip G, Theken Katherine N, Spertus John A, Lee Craig |
| Eicosanoids via CYP450 and cardiovascular disease: Hints from genetic and nutrition studies. Prostaglandins & other lipid mediators 2018 10 139 41-47. Fava Cristiano, Bonafini Sa |
| Identification of Metabolism-Associated Prostate Cancer Subtypes and Construction of a Prognostic Risk Model. Frontiers in oncology 2020 12 10 598801. Zhang Yanlong, Zhang Ruiqiao, Liang Fangzhi, Zhang Liyun, Liang Xuez |
| Genetic polymorphisms in neuroendocrine disorder-related candidate genes associated with pre-pregnancy obesity in gestational diabetes mellitus patients by using a stratification approach. Annals of translational medicine 2020 11 8 (17): 1060. Lee Kai Wei, Ching Siew Mooi, Devaraj Navin Kumar, Hoo Fan K |
| The Human Genetic Variants CYP2J2 rs2280275 and EPHX2 rs751141 and Risk of Diabetic Nephropathy in Egyptian Type 2 Diabetic Patients. The application of clinical genetics 2020 13 165-178. Habieb Mona S, Dawood Ashraf A, Emara Mahmoud M, Elhelbawy Mohammad G, Elhelbawy Nesreen |
A large-scale genome-wide association study meta-analysis of cannabis use disorder.
The lancet. Psychiatry 2020 Oct . Johnson Emma C, Demontis Ditte, Thorgeirsson Thorgeir E, Walters Raymond K, Polimanti Renato, Hatoum Alexander S, Sanchez-Roige Sandra, Paul Sarah E, Wendt Frank R, Clarke Toni-Kim, Lai Dongbing, Reginsson Gunnar W, Zhou Hang, He June, Baranger David A A, Gudbjartsson Daniel F, Wedow Robbee, Adkins Daniel E, Adkins Amy E, Alexander Jeffry, Bacanu Silviu-Alin, Bigdeli Tim B, Boden Joseph, Brown Sandra A, Bucholz Kathleen K, Bybjerg-Grauholm Jonas, Corley Robin P, Degenhardt Louisa, Dick Danielle M, Domingue Benjamin W, Fox Louis, Goate Alison M, Gordon Scott D, Hack Laura M, Hancock Dana B, Hartz Sarah M, Hickie Ian B, Hougaard David M, Krauter Kenneth, Lind Penelope A, McClintick Jeanette N, McQueen Matthew B, Meyers Jacquelyn L, Montgomery Grant W, Mors Ole, Mortensen Preben B, Nordentoft Merete, Pearson John F, Peterson Roseann E, Reynolds Maureen D, Rice John P, Runarsdottir Valgerdur, Saccone Nancy L, Sherva Richard, Silberg Judy L, Tarter Ralph E, Tyrfingsson Thorarinn, Wall Tamara L, Webb Bradley T, Werge Thomas, Wetherill Leah, Wright Margaret J, Zellers Stephanie, Adams Mark J, Bierut Laura J, Boardman Jason D, Copeland William E, Farrer Lindsay A, Foroud Tatiana M, Gillespie Nathan A, Grucza Richard A, Harris Kathleen Mullan, Heath Andrew C, Hesselbrock Victor, Hewitt John K, Hopfer Christian J, Horwood John, Iacono William G, Johnson Eric O, Kendler Kenneth S, Kennedy Martin A, Kranzler Henry R, Madden Pamela A F, Maes Hermine H, Maher Brion S, Martin Nicholas G, McGue Matthew, McIntosh Andrew M, Medland Sarah E, Nelson Elliot C, Porjesz Bernice, Riley Brien P, Stallings Michael C, Vanyukov Michael M, Vrieze Scott, , Davis Lea K, Bogdan Ryan, Gelernter Joel, Edenberg Howard J, Stefansson Kari, Børglum Anders D, Agrawal Arpa |
| Oxidative Stress Genes in Diabetes Mellitus Type 2: Association with Diabetic Kidney Disease. Oxidative medicine and cellular longevity 2021 2021 2531062. Roumeliotis Athanasios, Roumeliotis Stefanos, Tsetsos Fotis, Georgitsi Marianthi, Georgianos Panagiotis I, Stamou Aikaterini, Vasilakou Anna, Kotsa Kalliopi, Tsekmekidou Xanthippi, Paschou Peristera, Panagoutsos Stylianos, Liakopoulos Vassili |
| Genetics Variants in the Epoxygenase Pathway of Arachidonic Metabolism Are Associated with Eicosanoids Levels and the Risk of Diabetic Nephropathy. Journal of clinical medicine 2021 Sep 10 (17): . Mota-Zamorano Sonia, Robles Nicolás R, González Luz M, Valdivielso José M, Lopez-Gomez Juan, Cancho Bárbara, García-Pino Guadalupe, Gervasini Guiller |
| Association of rs11780592 Polymorphism in the Human Soluble Epoxide Hydrolase Gene (EPHX2) with Oxidized LDL and Mortality in Patients with Diabetic Chronic Kidney Disease. Oxidative medicine and cellular longevity 2021 2021 8817502. Roumeliotis Stefanos, Roumeliotis Athanasios, Stamou Aikaterini, Panagoutsos Stylianos, Manolopoulos Vangelis G, Tsetsos Fotis, Georgitsi Marianthi, Liakopoulos Vassili |
| Discovering Genotype Variants in an Infant with VACTERL through Clinical Exome Sequencing: A Support for Personalized Risk Assessment and Disease Prevention. Pediatric reports 2021 1 13 (1): 45-56. Pelizzo Gloria, Chiricosta Luigi, Mazzon Emanuela, Zuccotti Gian Vincenzo, Avanzini Maria Antonietta, Croce Stefania, Lima Mario, Bramanti Placido, Calcaterra Valer |
| A hypothesis-driven study to comprehensively investigate the association between genetic polymorphisms in EPHX2 gene and cardiovascular diseases: Findings from the UK Biobank. Gene 2022 Feb 822 146340. Zhu Xiaoming, Li Yuxin, Yu Tingting, Li Sen, Chen Mul |
| Wide-spread enhancer effect of SNP rs2279590 on regulating epoxide hydrolase-2 and protein tyrosine kinase 2-beta gene expression. Gene 2022 12 854 147096. Padhy Biswajit, Kapuganti Ramani Shyam, Hayat Bushra, Mohanty Pranjya Paramita, Alone Debasmita Pank |
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