Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 31 Records) |
| Query Trace: Stroke and TAG[original query] |
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| IL-6 gene variation is associated with IL-6 and C-reactive protein levels but not cardiovascular outcomes in the Cardiovascular Health Study. Human genetics 2007 Dec 122 (5): 485-94. Walston Jeremy D, Fallin M Daniele, Cushman Mary, Lange Leslie, Psaty Bruce, Jenny Nancy, Browner Warren, Tracy Russell, Durda Peter, Reiner Al |
| Cholesterol ester transfer protein, interleukin-8, peroxisome proliferator activator receptor alpha, and Toll-like receptor 4 genetic variations and risk of incident nonfatal myocardial infarction and ischemic stroke. The American journal of cardiology 2008 Jun 101 (12): 1683-8. Enquobahrie DA, Smith NL, Bis JC, Carty CL, Rice KM, Lumley T, Hindorff LA, Lemaitre RN, Williams MA, Siscovick DS, Heckbert SR, Psaty BM |
| Common variation in cytochrome P450 epoxygenase genes and the risk of incident nonfatal myocardial infarction and ischemic stroke. Pharmacogenetics and genomics 2008 Jun 18 (6): 535-43. Marciante Kristin D, Totah Rheem A, Heckbert Susan R, Smith Nicholas L, Lemaitre Rozenn N, Lumley Thomas, Rice Kenneth M, Hindorff Lucia A, Bis Joshua C, Hartman Brittany, Psaty Bruce |
| No association of PLIN polymorphisms with hemorrhagic and ischemic stroke. Stroke; a journal of cerebral circulation 2008 Feb 39 (2): 470-2. Song Weihua, Chen Jingzhou, Sun Kai, Yu Hui, Hui Rut |
| Gene variation of the transient receptor potential cation channel, subfamily M, member 7 (TRPM7), and risk of incident ischemic stroke: prospective, nested, case-control study. Stroke; a journal of cerebral circulation 2009 Sep 40 (9): 2965-8. Romero José R, Ridker Paul M, Zee Robert Y |
| Tissue factor gene polymorphisms and haplotypes and the risk of ischemic vascular events: four studies and a meta-analysis. Journal of thrombosis and haemostasis : JTH 2009 Jul . de Gaetano M, Quacquaruccio G, Pezzini A, Latella MC, Di Castelnuovo A, Del Zotto E, Padovan A, Lichy C, Grond-Ginsbach C, Gattone M, Giannuzzi P, Novak N, Dorn J, Trevisan M, Donati MB, Iacoviello L |
| Identification of CELSR1 as a susceptibility gene for ischemic stroke in Japanese individuals by a genome-wide association study. Atherosclerosis 2009 Nov 207 (1): 144-9. Yamada Yoshiji, Fuku Noriyuki, Tanaka Masashi, Aoyagi Yukitoshi, Sawabe Motoji, Metoki Norifumi, Yoshida Hidemi, Satoh Kei, Kato Kimihiko, Watanabe Sachiro, Nozawa Yoshinori, Hasegawa Aki, Kojima Tosh |
| Common genetic variation in DDAH2 is associated with intracerebral haemorrhage in a Chinese population: a multi-centre case-control study in China. Clinical science (London, England : 1979) 2009 Oct 117 (7): 273-9. Bai Yongyi, Chen Jingzhou, Sun Kai, Xin Ying, Liu Junhao, Hui Rut |
| Lack of association between variations of PDE4D and ischemic stroke in the Japanese population. Stroke; a journal of cerebral circulation 2009 Apr 40 (4): 1245-51. Matsushita Tomonaga, Kubo Michiaki, Yonemoto Koji, Ninomiya Toshiharu, Ashikawa Kyota, Liang Bailing, Hata Jun, Doi Yasufumi, Kitazono Takanari, Ibayashi Setsuro, Iida Mitsuo, Kiyohara Yutaka, Nakamura Yusu |
| Apolipoprotein B levels, APOB alleles, and risk of ischemic cardiovascular disease in the general population, a review. Atherosclerosis 2009 Sep 206 (1): 17-30. Benn Marian |
| Genetic variants in eleven telomere-associated genes and the risk of incident cardio/cerebrovascular disease: The Women's Genome Health Study. Clinica chimica acta; international journal of clinical chemistry 2011 Jan 412 (1-2): 199-202. Zee Robert Y L, Ridker Paul M, Chasman Daniel |
| Liver X receptor a gene polymorphisms and variable cardiovascular outcomes in patients treated with antihypertensive therapy: results from the INVEST-GENES study. Pharmacogenetics and genomics 2011 Jun 21 (6): 333-40. Price Elvin Tyrone, Pacanowski Michael A, Martin Michael A, Cooper-DeHoff Rhonda M, Pepine Carl J, Zineh Issam, Johnson Julie |
| The transforming growth factor-ß receptor genes and the risk of intracranial aneurysms. International journal of stroke : official journal of the International Stroke Society 2012 Dec 7 (8): 645-8. Ruigrok Ynte M, Baas Annette F, Medic Jelena, Wijmenga Cisca, Rinkel Gabriel J |
| Role of the MMP9 gene in hemorrhagic transformations after tissue-type plasminogen activator treatment in stroke patients. Stroke; a journal of cerebral circulation 2012 May 43 (5): 1398-400. Fernández-Cadenas Israel, Del Río-Espínola Alberto, Carrera Caty, Domingues-Montanari Sophie, Mendióroz Maite, Delgado Pilar, Rosell Anna, Ribó Marc, Giralt Dolors, Quintana Manolo, Castellanos Mar, Obach Victor, Martínez Sergi, Freijo Mari Mar, Jiménez-Conde Jordi, Roquer Jaume, Martí-Fábregas Joan, Molina Carlos A, Alvarez-Sabín José, Montaner Jo |
| The impact of gene polymorphism and high on-treatment platelet reactivity on clinical follow-up: outcomes in patients with acute coronary syndrome after drug-eluting stent implantation. EuroIntervention : journal of EuroPCR in collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology 2013 Jul 9 (3): 316-27. Liang Zhen-Yang, Han Ya-Ling, Zhang Xiao-Lin, Li Yi, Yan Cheng-Hui, Kang Ji |
| Association of SERPINA9 gene variants with carotid artery atherosclerosis: the Atherosclerosis Risk in Communities (ARIC) Carotid MRI Study. International journal of molecular epidemiology and genetics 2013 4 (4): 258-67. Tang Weihong, Morrison Alanna, Wasserman Bruce A, Folsom Aaron R, Sun Wei, Campbell Stephen, Kao W H Linda, Boerwinkle Er |
| Tagging SNPs in the MTHFR gene and risk of ischemic stroke in a Chinese population. International journal of molecular sciences 2014 15 (5): 8931-40. Zhou Bao-Sheng, Bu Guo-Yun, Li Mu, Chang Bin-Ge, Zhou Yi-P |
| TLR4 polymorphism is not associated with biopsy proven giant cell arteritis. Clinical and experimental rheumatology 0 32 (3 Suppl 82): S26-9. Dunstan Emma, Lester Sue, Rischmueller Maureen, Chan Helan, Hewitt Alex W, Hill Catheri |
| Association of the RYR3 gene polymorphisms with atherosclerosis in elderly Japanese population. BMC cardiovascular disorders 2014 14 (1): 6. Zhao Chenxi, Ikeda Shinobu, Arai Tomio, Naka-Mieno Makiko, Sato Noriko, Muramatsu Masaaki, Sawabe Moto |
| DNM3 and genetic modifiers of age of onset in LRRK2 Gly2019Ser parkinsonism: a genome-wide linkage and association study. The Lancet. Neurology 2016 Sep . Trinh Joanne, Gustavsson Emil K, Vilariño-Güell Carles, Bortnick Stephanie, Latourelle Jeanne, McKenzie Marna B, Tu Chelsea Szu, Nosova Ekaterina, Khinda Jaskaran, Milnerwood Austen, Lesage Suzanne, Brice Alexis, Tazir Meriem, Aasly Jan O, Parkkinen Laura, Haytural Hazal, Foroud Tatiana, Myers Richard H, Sassi Samia Ben, Hentati Emna, Nabli Fatma, Farhat Emna, Amouri Rim, Hentati Fayçal, Farrer Matthew |
| Impact of Tag Single Nucleotide Polymorphisms (SNPs) in CCL11 Gene on Risk of Subtypes of Ischemic Stroke in Xinjiang Han Populations. Medical science monitor : international medical journal of experimental and clinical research 2017 Sep 23 4291-4298. Liang Chen, Ni Guihua, Ma Jianhua, Liu Hai, Mao Zhifeng, Sun Honggang, Zhang Xiaoni |
| Association of FOXF2 gene polymorphisms with ischemic stroke in Chinese Han population. Oncotarget 2017 Oct 8 (52): 89867-89875. Shi Chang-He, Tang Mi-Bo, Li Shao-Hua, Wang Zhi-Jie, Liu Xin-Jing, Zhao Lu, Gao Yuan, Li Yu-Sheng, Sun Shi-Lei, Wu Jun, Song Bo, Xu Yu-Mi |
| Variants in the APOB gene was associated with Ischemic Stroke susceptibility in Chinese Han male population. Oncotarget 2018 Jan 9 (2): 2249-2254. Zhou Feng, Guo Tie, Zhou Lv, Zhou Yanhui, Yu D |
| Polymorphism of IL6 receptor gene is associated with ischaemic stroke in patients with metabolic syndrome. Brain research 2019 12 1728 146594. Huang Xiaoya, Ye Qiang, Zhu Zhenguo, Chen Wei, Chen Yanyan, Li Jia, Chen Siyan, Xia Niange, Huang Xiangdong, Ye Zus |
| Association study of genetic variants of the ANGPTL3 gene and susceptibility to ischemic stroke. Neuropsychiatric disease and treatment 2019 15 3015-3020. Gong Qi, Ye Liping, Gui Huiwen, Liu Jing, Li Huanyin, Sun Qi |
| SNPs rs10224002 in PRKAG2 may disturb gene expression and consequently affect hypertension. Molecular biology reports 2019 Jan . Mo Xingbo, Zhang Huan, Zhou Zhengyuan, Zhu Zhengbao, HuangFu Xinfeng, Xu Tan, Wang Aili, Guo Zhirong, Zhang Yongho |
| Susceptible gene polymorphism in patients with three-vessel coronary artery disease. BMC cardiovascular disorders 2020 Apr 20 (1): 172. Liu Ru, Song Lei, Jiang Lin, Tang Xiaofang, Xu Lianjun, Gao Zhan, Zhao Xueyan, Xu Jingjing, Gao Runlin, Yuan Jinqi |
Contribution of Common Genetic Variants to Risk of Early Onset Ischemic Stroke.
Neurology 2022 Aug . Jaworek Thomas, Xu Huichun, Gaynor Brady J, Cole John W, Rannikmae Kristiina, Stanne Tara M, Tomppo Liisa, Abedi Vida, Amouyel Philippe, Armstrong Nicole D, Attia John, Bell Steven, Benavente Oscar R, Boncoraglio Giorgio B, Butterworth Adam, , Carcel-Marquez Jara, Chen Zhengming, Chong Michael, Cruchaga Carlos, Cushman Mary, Danesh John, Debette Stephanie, Duggan David J, Durda Jon Peter, Engstrom Gunnar, Enzinger Chris, Faul Jessica D, Fecteau Natalie S, Fernandez-Cadenas Israel, Gieger Christian, Giese Anne-Katrin, Grewal Raji P, Grittner Ulrike, Havulinna Aki S, Heitsch Laura, Hochberg Marc C, Holliday Elizabeth, Hu Jie, Ilinca Andreea, , Irvin Marguerite R, Jackson Rebecca D, Jacob Mina A, Janssen Raquel Rabionet, Jimenez-Conde Jordi, Johnson Julie A, Kamatani Yoichiro, Kardia Sharon L, Koido Masaru, Kubo Michiaki, Lange Leslie, Lee Jin-Moo, Lemmens Robin, Levi Christopher R, Li Jiang, Li Liming, Lin Kuang, Lopez Haley, Luke Sothear, Maguire Jane, McArdle Patrick F, McDonough Caitrin W, Meschia James F, Metso Tiina, Muller-Nurasyid Martina, O'Connor Timothy D, O'Donnell Martin, Peddareddygari Leema R, Pera Joanna, Perry James A, Peters Annette, Putaala Jukka, Ray Debashree, Rexrode Kathryn, Ribases Marta, Rosand Jonathan, Rothwell Peter M, Rundek Tatjana, Ryan Kathleen A, Sacco Ralph L, Salomaa Veikko, Sanchez-Mora Cristina, Schmidt Reinhold, Sharma Pankaj, Slowik Agnieszka, Smith Jennifer A, Smith Nicholas L, Wassertheil-Smoller Sylvia, Soederholm Martin, Stine O C, Strbian Daniel, Sudlow Cathie L, Tatlisumak Turgut, Terao Chikashi, Thijs Vincent, Torres-Aguila Nuria P, Tregouet David-Alexandre, Tuladhar Anil M, Veldink Jan H, Walters Robin G, Weir David R, Woo Daniel, Worrall Bradford B, Hong Charles C, Ross Owen, Zand Ramin, Leeuw Frank-Erik de, Lindgren Arne G, Pare Guillaume, Anderson Christopher D, Markus Hugh S, Jern Christina, Malik Rainer, Dichgans Martin, Mitchell Braxton D, Kittner Steven J, |
| Association between HMGB1 genetic variants and ischemic stroke susceptibility, onset age, and recurrence risk among Chinese Han individuals. American journal of translational research 2023 6 15 (5): 3326-3341. Luying Qiu, Long Li, Zhiyi He, Fang Liu, Shumin Deng, Yanzhe Wa |
| SNP rs3803264 polymorphisms in THSD1 and abnormally expressed mRNA are associated with hemorrhagic stroke. Frontiers in aging neuroscience 2023 5 15 1144364. Changying Chen, Xincheng Gu, Fangyuan Liu, Congyong Sun, Jialin Mu, Defu Jin, Xuemei Sui, Deqin Geng, Qingqing Li, Yuzhang Jiang, Chong Sh |
- Page last reviewed:Feb 1, 2023
- Page last updated:Sep 25, 2023
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