Human Genome Epidemiology Literature Finder
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Records 1 - 13 (of 13 Records) |
| Query Trace: Disease and GUCY1A3[original query] |
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Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
Nature 2011 Oct 478 (7367): 7367. Ehret GB, Munroe PB, Rice KM, Bochud M, Johnson AD, Chasman DI, Smith AV, Tobin MD, Verwoert GC, Hwang SJ, Pihur V, Vollenweider P, O'Reilly PF, Amin N, Bragg-Gresham JL, Teumer A, Glazer NL, Launer L, Zhao JH, Aulchenko Y, Heath S, Sõber S, Parsa A, Luan J, Arora P, Dehghan A, Zhang F, Lucas G, Hicks AA, Jackson AU, Peden JF, Tanaka T, Wild SH, Rudan I, Igl W, Milaneschi Y, Parker AN, Fava C, Chambers JC, Fox ER, Kumari M, Go MJ, van der Harst P, Kao WH, Sjögren M, Vinay DG, Alexander M, Tabara Y, Shaw-Hawkins S, Whincup PH, Liu Y, Shi G, Kuusisto J, Tayo B, Seielstad M, Sim X, Nguyen KD, Lehtimäki T, Matullo G, Wu Y, Gaunt TR, Onland-Moret NC, Cooper MN, Platou CG, Org E, Hardy R, Dahgam S, Palmen J, Vitart V, Braund PS, Kuznetsova T, Uiterwaal CS, Adeyemo A, Palmas W, Campbell H, Ludwig B, Tomaszewski M, Tzoulaki I, Palmer ND, Aspelund T, Garcia M, Chang YP, O'Connell JR, Steinle NI, Grobbee DE, Arking DE, Kardia SL, Morrison AC, Hernandez D, Najjar S, McArdle WL, Hadley D, Brown MJ, Connell JM, Hingorani AD, Day IN, Lawlor DA, Beilby JP, Lawrence RW, Clarke R, Hopewell JC, Ongen H, Dreisbach AW, Li Y, Young JH, Bis JC, Kähönen M, Viikari J, Adair LS, Lee NR, Chen MH, Olden M, Pattaro C, Bolton JA, Köttgen A, Bergmann S, Mooser V, Chaturvedi N, Frayling TM, Islam M, Jafar TH, Erdmann J, Kulkarni SR, Bornstein SR, Grässler J, Groop L, Voight BF, Kettunen J, Howard P, Taylor A, Guarrera S, Ricceri F, Emilsson V, Plump A, Barroso I, Khaw KT, Weder AB, Hunt SC, Sun YV, Bergman RN, Collins FS, Bonnycastle LL, Scott LJ, Stringham HM, Peltonen L, Perola M, Vartiainen E, Brand SM, Staessen JA, Wang TJ, Burton PR, Soler Artigas M, Dong Y, Snieder H, Wang X, Zhu H, Lohman KK, Rudock ME, Heckbert SR, Smith NL, Wiggins KL, Doumatey A, Shriner D, Veldre G, Viigimaa M, Kinra S, Prabhakaran D, Tripathy V, Langefeld CD, Rosengren A, Thelle DS, Corsi AM, Singleton A, Forrester T, Hilton G, McKenzie CA, Salako T, Iwai N, Kita Y, Ogihara T, Ohkubo T, Okamura T, Ueshima H, Umemura S, Eyheramendy S, Meitinger T, Wichmann HE, Cho YS, Kim HL, Lee JY, Scott J, Sehmi JS, Zhang W, Hedblad B, Nilsson P, Smith GD, Wong A, Narisu N, Stan?áková A, Raffel LJ, Yao J, Kathiresan S, O'Donnell CJ, Schwartz SM, Ikram MA, Longstreth WT, Mosley TH, Seshadri S, Shrine NR, Wain LV, Morken MA, Swift AJ, Laitinen J, Prokopenko I, Zitting P, Cooper JA, Humphries SE, Danesh J, Rasheed A, Goel A, Hamsten A, Watkins H, Bakker SJ, van Gilst WH, Janipalli CS, Mani KR, Yajnik CS, Hofman A, Mattace-Raso FU, Oostra BA, Demirkan A, Isaacs A, Rivadeneira F, Lakatta EG, Orru M, Scuteri A, Ala-Korpela M, Kangas AJ, Lyytikäinen LP, Soininen P, Tukiainen T, Würtz P, Ong RT, Dörr M, Kroemer HK, Völker U, Völzke H, Galan P, Hercberg S, Lathrop M, Zelenika D, Deloukas P, Mangino M, Spector TD, Zhai G, Meschia JF, Nalls MA, Sharma P, Terzic J, Kumar MV, Denniff M, Zukowska-Szczechowska E, Wagenknecht LE, Fowkes FG, Charchar FJ, Schwarz PE, Hayward C, Guo X, Rotimi C, Bots ML, Brand E, Samani NJ, Polasek O, Talmud PJ, Nyberg F, Kuh D, Laan M, Hveem K, Palmer LJ, van der Schouw YT, Casas JP, Mohlke KL, Vineis P, Raitakari O, Ganesh SK, Wong TY, Tai ES, Cooper RS, Laakso M, Rao DC, Harris TB, Morris RW, Dominiczak AF, Kivimaki M, Marmot MG, Miki T, Saleheen D, Chandak GR, Coresh J, Navis G, Salomaa V, Han BG, Zhu X, Kooner JS, Melander O, Ridker PM, Bandinelli S, Gyllensten UB, Wright AF, Wilson JF, Ferrucci L, Farrall M, Tuomilehto J, Pramstaller PP, Elosua R, Soranzo N, Sijbrands EJ, Altshuler D, Loos RJ, Shuldiner AR, Gieger C, Meneton P, Uitterlinden AG, Wareham NJ, Gudnason V, Rotter JI, Rettig R, Uda M, Strachan DP, Witteman JC, Hartikainen AL, Beckmann JS, Boerwinkle E, Vasan RS, Boehnke M, Larson MG, Järvelin MR, Psaty BM, Abecasis GR, Chakravarti A, Elliott P, van Duijn CM, Newton-Cheh C, Levy D, Caulfield MJ, Johnson T |
| Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease.
Nature genetics 2012 Aug 44 (8): 890-4. Lu Xiangfeng, Wang Laiyuan, Chen Shufeng, He Lin, Yang Xueli, Shi Yongyong, Cheng Jing, Zhang Liang, Gu C Charles, Huang Jianfeng, Wu Tangchun, Ma Yitong, Li Jianxin, Cao Jie, Chen Jichun, Ge Dongliang, Fan Zhongjie, Li Ying, Zhao Liancheng, Li Hongfan, Zhou Xiaoyang, Chen Lanying, Liu Donghua, Chen Jingping, Duan Xiufang, Hao Yongchen, Wang Ligui, Lu Fanghong, Liu Zhendong, Yao Cailiang, Shen Chong, Pu Xiaodong, Yu Lin, Fang Xianghua, Xu Lihua, Mu Jianjun, Wu Xianping, Zheng Runping, Wu Naqiong, Zhao Qi, Li Yun, Liu Xiaoli, Wang Mengqin, Yu Dahai, Hu Dongsheng, Ji Xu, Guo Dongshuang, Sun Dongling, Wang Qianqian, Yang Ying, Liu Fangchao, Mao Qunxia, Liang Xiaohua, Ji Jingfeng, Chen Panpan, Mo Xingbo, Li Dianjiang, Chai Guoping, Tang Yida, Li Xiangdong, Du Zhenhan, Liu Xuehui, Dou Chenlong, Yang Zili, Meng Qingjie, Wang Dong, Wang Renping, Yang Jun, Schunkert Heribert, Samani Nilesh J, Kathiresan Sekar, Reilly Muredach P, Erdmann Jeanette, , Peng Xiaozhong, Wu Xigui, Liu Depei, Yang Yuejin, Chen Runsheng, Qiang Boqin, Gu Dongfe |
| Genome-wide association study in Chinese identifies novel loci for blood pressure and hypertension.
Human molecular genetics 2015 Feb 24 (3): 865-74. Lu Xiangfeng, Wang Laiyuan, Lin Xu, Huang Jianfeng, Charles Gu C, He Meian, Shen Hongbing, He Jiang, Zhu Jingwen, Li Huaixing, Hixson James E, Wu Tangchun, Dai Juncheng, Lu Ling, Shen Chong, Chen Shufeng, He Lin, Mo Zengnan, Hao Yongchen, Mo Xingbo, Yang Xueli, Li Jianxin, Cao Jie, Chen Jichun, Fan Zhongjie, Li Ying, Zhao Liancheng, Li Hongfan, Lu Fanghong, Yao Cailiang, Yu Lin, Xu Lihua, Mu Jianjun, Wu Xianping, Deng Ying, Hu Dongsheng, Zhang Weidong, Ji Xu, Guo Dongshuang, Guo Zhirong, Zhou Zhengyuan, Yang Zili, Wang Renping, Yang Jun, Zhou Xiaoyang, Yan Weili, Sun Ningling, Gao Pingjin, Gu Dongfe |
| RNF213 as the major susceptibility gene for Chinese patients with moyamoya disease and its clinical relevance. Journal of neurosurgery 2017 Apr 126 (4): 1106-1113. Zhang Qian, Liu Yaping, Zhang Dong, Wang Rong, Zhang Yan, Wang Shuo, Yu Lanbing, Lu Chaoxia, Liu Fang, Zhou Jian, Zhang Xue, Zhao Jizo |
| Disrupted nitric oxide signaling due to GUCY1A3 mutations increases risk for moyamoya disease, achalasia and hypertension. Clinical genetics 2016 Jan . Wallace Stephanie, Guo Dong-Chuan, Regalado Ellen, Mellor-Crummey Lauren, Banshad Michael, Nickerson Deborah A, Dauser Robert, Hanchard Neil, Marom Ronit, Martin Emil, Berka Vladimir, Sharina Iraida, Ganesan Vijeya, Saunders Dawn, Morris Shaine, Milewicz Dianna |
| Phenotypic Consequences of a Genetic Predisposition to Enhanced Nitric Oxide Signaling. Circulation 2017 10 137 (3): 222-232. Emdin Connor A, Khera Amit V, Klarin Derek, Natarajan Pradeep, Zekavat Seyedeh M, Nomura Akihiro, Haas Mary, Aragam Krishna, Ardissino Diego, Wilson James G, Schunkert Heribert, McPherson Ruth, Watkins Hugh, Elosua Roberto, Bown Matthew J, Samani Nilesh J, Baber Usman, Erdmann Jeanette, Gormley Padhraig, Palotie Aarno, Stitziel Nathan O, Gupta Namrata, Danesh John, Saleheen Danish, Gabriel Stacey, Kathiresan Sek |
| Whole exome sequencing identifies MRVI1 as a susceptibility gene for moyamoya syndrome in neurofibromatosis type 1. PloS one 2018 13 (7): e0200446. Santoro Claudia, Giugliano Teresa, Kraemer Markus, Torella Annalaura, Schwitalla Jan Claudius, Cirillo Mario, Melis Daniela, Berlit Peter, Nigro Vincenzo, Perrotta Silverio, Piluso Giul |
| Genetic variation at the coronary artery disease risk locus GUCY1A3 modifies cardiovascular disease prevention effects of aspirin. European heart journal 2019 Jun . Hall Kathryn T, Kessler Thorsten, Buring Julie E, Passow Dani, Sesso Howard D, Zee Robert Y L, Ridker Paul M, Chasman Daniel I, Schunkert Heribe |
| Genome-wide association study of psoriasis in an Egyptian population.
Experimental dermatology 2019 Mar . Bejaoui Yosra, Witte Mareike, Abdelhady Mohamed, Eldarouti Mohammad, Abdallah Nermeen M A, Elghzaly Ashraf Antar, Tawhid Ziyad, Gaballah Mohammad Ali, Busch Hauke, Munz Matthias, Wendorff Mareike, Ellinghaus Eva, Franke Andre, Ibrahim Saleh |
| Association of the coronary artery disease risk gene GUCY1A3 with ischaemic events after coronary intervention. Cardiovascular research 2019 Feb . Kessler Thorsten, Wolf Bernhard, Eriksson Niclas, Kofink Daniel, Mahmoodi Bakhtawar K, Rai Himanshu, Tragante Vinicius, Åkerblom Axel, Becker Richard C, Bernlochner Isabell, Bopp Roman, James Stefan, Katus Hugo A, Mayer Katharina, Munz Matthias, Nordio Francesco, O'Donoghue Michelle L, Sager Hendrik B, Sibbing Dirk, Solakov Linda, Storey Robert F, Wobst Jana, Asselbergs Folkert W, Byrne Robert A, Erdmann Jeanette, Koenig Wolfgang, Laugwitz Karl-Ludwig, Ten Berg Jurrien M, Wallentin Lars, Kastrati Adnan, Schunkert Heribe |
| Associations between GUCY1A3 genetic polymorphisms and large artery atherosclerotic stroke risk in Chinese Han population: a case-control study. Lipids in health and disease 2019 Dec 18 (1): 233. Li Jian-Li, Liu Liu-Yu, Jiang Dong-Dong, Jiang Yi-Ying, Zhou Guo-Qiu, Mo Dong-Can, Luo M |
| Higher susceptibility to heme oxidation and lower protein stability of the rare aC517Yß sGC variant associated with moyamoya syndrome. Biochemical pharmacology 2021 Feb 114459. Sharina Iraida, Lezgyieva Karina, Krutsenko Yekaterina, Martin Em |
| The promoter polymorphism rs3918226 of endothelial nitric oxide synthase gene as a novel susceptibility marker for peripheral artery disease. Annals of vascular surgery 2024 7 . Sergey Zhabin, Victor Lazarenko, Iulia Azarova, Elena Klyosova, Daniil Bashkatov, Stanislav Kononov, Maxim Dolgintsev, Mikhail Churnosov, Maria Solodilova, Alexey Polonik |
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