Human Genome Epidemiology Literature Finder
Heart, Lung, Blood and Sleep Disorders
Records 1 - 25 (of 25 Records) |
Query Trace: Heart And Vascular Diseases [original query] |
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Genome-wide Association Studies of Retinal Vessel Tortuosity Identify Numerous Novel Loci Revealing Genes and Pathways Associated With Ocular and Cardiometabolic Diseases.
Ophthalmology science 2023 5 3 (3): 100288. Tomasoni Mattia, Beyeler Michael Johannes, Vela Sofia Ortin, Mounier Ninon, Porcu Eleonora, Corre Tanguy, Krefl Daniel, Button Alexander Luke, Abouzeid Hana, Lazaros Konstantinidis, Bochud Murielle, Schlingemann Reinier, Bergin Ciara, Bergmann Sv |
Lack of association between polymorphisms of catalase, copper-zinc superoxide dismutase (SOD), extracellular SOD and endothelial nitric oxide synthase genes and macroangiopathy in patients with type 2 diabetes mellitus. Journal of internal medicine 2001 May 249 (5): 451-9. Ukkola O, Erkkilä P H, Savolainen M J, Kesäniemi Y |
Tyrosine phosphatase 1B and leptin receptor genes and their interaction in type 2 diabetes. Journal of internal medicine 2004 Jul 256 (1): 48-55. Santaniemi M, Ukkola O, Kesäniemi Y |
Association of LMNA 1908C/T polymorphism with cerebral vascular disease and diabetic nephropathy in Japanese men with type 2 diabetes. Clinical endocrinology 2005 Sep 63 (3): 317-22. Liang H, Murase Y, Katuta Y, Asano A, Kobayashi J, Mabuchi H |
VKORC1 haplotypes are associated with arterial vascular diseases (stroke, coronary heart disease, and aortic dissection). Circulation 2006 Mar 113 (12): 1615-21. Wang Yibo, Zhang Weili, Zhang Yuhui, Yang Yuejin, Sun Lizhong, Hu Shengshou, Chen Jilin, Zhang Channa, Zheng Yi, Zhen Yisong, Sun Kai, Fu Chunyan, Yang Tao, Wang Jianwei, Sun Jing, Wu Haiying, Glasgow Wayne C, Hui Rut |
Decreased frequencies of ABCA1 polymorphisms R219K and V771M in Hungarian patients with cerebrovascular and cardiovascular diseases. Cerebrovascular diseases (Basel, Switzerland) 2006 21 (4): 254-9. Andrikovics Hajnalka, Pongrácz Endre, Kalina Ethkos, Szilvási Anikó, Aslanidis Charalampos, Schmitz Gerd, Tordai Atti |
Association of OAZ1 gene polymorphisms with subclinical and clinical vascular events. Arteriosclerosis, thrombosis, and vascular biology 2007 Oct 27 (10): 2120-6. Dumont Julie, Zureik Mahmoud, Bauters Christophe, Grupposo Marie-Catherine, Cottel Dominique, Montaye Michèle, Hamon Martial, Ducimetière Pierre, Amouyel Philippe, Brousseau Thier |
Common polymorphisms in CYP2C9, subclinical atherosclerosis and risk of ischemic vascular disease in 52,000 individuals. The pharmacogenomics journal 2009 Oct 9 (5): 327-32. Kaur-Knudsen D, Bojesen S E, Nordestgaard B |
Analysis of multigenerational families with thoracic aortic aneurysms and dissections due to TGFBR1 or TGFBR2 mutations. Journal of medical genetics 2009 Jun . Tran-Fadulu VT, Pannu H, Kim DH, Vick GW, Lonsford CM, Lafont AL, Boccalandro C, Smart S, Peterson KL, Zenger-Hain J, Willing MC, Coselli J, Lemaire SA, Ahn C, Byers PH, Milewicz DM |
Variant on 9p21 strongly associates with coronary heart disease, but lacks association with common stroke. European journal of human genetics : EJHG 2009 Mar . Lemmens R, Abboud S, Robberecht W, Vanhees L, Pandolfo M, Thijs V, Goris A |
Frequencies of four ATP-binding cassette transporter G8 polymorphisms in patients with ischemic vascular diseases. Genetic testing and molecular biomarkers 2010 Oct 14 (5): 667-72. Szilvási Anikó, Andrikovics Hajnalka, Pongrácz Endre, Kalina Akos, Komlósi Zsolt, Klein Izabella, Tordai Atti |
Association study of polymorphisms in the receptor for advanced glycation end-products (RAGE) gene with susceptibility and prognosis of heart failure. Gene 2012 Nov 510 (1): 7-13. Cohen Carolina Rodrigues, Diel Vanessa Backes Nascimento, La Porta Vanessa Laubert, Rohde Luís Eduardo, Biolo Andréia, Clausell Nadine, Dos Santos Kátia Gonçalv |
Implication of VEGFR2 in systemic lupus erythematosus: a combined genetic and structural biological approach. Clinical and experimental rheumatology 2012 Oct . Vazgiourakis VM, Zervou MI, Eliopoulos E, Sharma S, Sidiropoulos P, Franek BS, Myrthianou E, Melissourgaki M, Niewold TB, Boumpas DT, Goulielmos GN |
Genetic loci for retinal arteriolar microcirculation.
PloS one 2013 8 (6): e65804. Sim Xueling, Jensen Richard A, Ikram M Kamran, Cotch Mary Frances, Li Xiaohui, MacGregor Stuart, Xie Jing, Smith Albert Vernon, Boerwinkle Eric, Mitchell Paul, Klein Ronald, Klein Barbara E K, Glazer Nicole L, Lumley Thomas, McKnight Barbara, Psaty Bruce M, de Jong Paulus T V M, Hofman Albert, Rivadeneira Fernando, Uitterlinden Andre G, van Duijn Cornelia M, Aspelund Thor, Eiriksdottir Gudny, Harris Tamara B, Jonasson Fridbert, Launer Lenore J, , Attia John, Baird Paul N, Harrap Stephen, Holliday Elizabeth G, Inouye Michael, Rochtchina Elena, Scott Rodney J, Viswanathan Ananth, , Li Guo, Smith Nicholas L, Wiggins Kerri L, Kuo Jane Z, Taylor Kent D, Hewitt Alex W, Martin Nicholas G, Montgomery Grant W, Sun Cong, Young Terri L, Mackey David A, van Zuydam Natalie R, Doney Alex S F, Palmer Colin N A, Morris Andrew D, Rotter Jerome I, Tai E Shyong, Gudnason Vilmundur, Vingerling Johannes R, Siscovick David S, Wang Jie Jin, Wong Tien |
Genetic variation associated with circulating monocyte count in the eMERGE Network.
Human molecular genetics 2013 Jan . Crosslin DR, McDavid A, Weston N, Zheng X, Hart E, de Andrade M, Kullo IJ, McCarty CA, Doheny KF, Pugh E, Kho A, Hayes MG, Ritchie MD, Saip A, Crawford DC, Crane PK, Newton K, Carrell DS, Gallego CJ, Nalls MA, Li R, Mirel DB, Crenshaw A, Couper DJ, Tanaka T, van Rooij FJ, Chen MH, Smith AV, Zakai NA, Yango Q, Garcia M, Liu Y, Lumley T, Folsom AR, Reiner AP, Felix JF, Dehghan A, Wilson JG, Bis JC, Fox CS, Glazer NL, Cupples LA, Coresh J, Eiriksdottir G, Gudnason V, Bandinelli S, Frayling TM, Chakravarti A, van Duijn CM, Melzer D, Levy D, Boerwinkle E, Singleton AB, Hernandez DG, Longo DL, Witteman JC, Psaty BM, Ferrucci L, Harris TB, O'Donnell CJ, Ganesh SK, Larson EB, Carlson CS, Jarvik GP |
RNF213 rare variants in an ethnically diverse population with Moyamoya disease. Stroke; a journal of cerebral circulation 2014 Nov 45 (11): 3200-7. Cecchi Alana C, Guo Dongchuan, Ren Zhao, Flynn Kelly, Santos-Cortez Regie Lyn P, Leal Suzanne M, Wang Gao T, Regalado Ellen S, Steinberg Gary K, Shendure Jay, Bamshad Michael J, , Grotta James C, Nickerson Deborah A, Pannu Hariyadarshi, Milewicz Dianna |
Endothelial nitric oxide synthase polymorphism and prognosis in systolic heart failure patients. Nitric oxide : biology and chemistry / official journal of the Nitric Oxide Society 2015 May 47 91-6. Azzam Naiel, Zafrir Barak, Fares Fuad, Smith Yoav, Salman Nabeeh, Nevzorov Roman, Amir Off |
Lack of an association between matrix metalloproteinase polymorphisms and coronary heart disease in a Han Chinese population. Genetics and molecular research : GMR 2015 14 (4): 12254-61. Wang C M, Ye H D, Li Y R, Hong Q X, Tang L L, Zhou A N, Xu M Q, Duan S |
Lack of association between oxidative stress-related gene polymorphisms and chronic migraine in an Italian population. Expert review of neurotherapeutics 2015 Feb 15 (2): 215-25. Gentile Giovanna, Negro Andrea, D'Alonzo Lidia, Aimati Laura, Simmaco Maurizio, Martelletti Paolo, Borro Mari |
IL6R haplotype rs4845625*T/rs4537545*C is a risk factor for simultaneously high CRP, LDL and ApoB levels. Genes and immunity 2017 Aug . Arguinano A A, Naderi E, Ndiaye N C, Stathopoulou M, Dadé S, Alizadeh B, Visvikis-Siest |
Poor outcomes in carriers of the RNF213 variant (p.Arg4810Lys) with pulmonary arterial hypertension. The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation 2019 9 39 (2): 103-112. Hiraide Takahiro, Kataoka Masaharu, Suzuki Hisato, Aimi Yuki, Chiba Tomohiro, Isobe Sarasa, Katsumata Yoshinori, Goto Shinichi, Kanekura Kohsuke, Yamada Yoshitake, Moriyama Hidenori, Kitakata Hiroki, Endo Jin, Yuasa Shinsuke, Arai Yasumichi, Hirose Nobuyoshi, Satoh Toru, Hakamata Yoji, Sano Motoaki, Gamou Shinobu, Kosaki Kenjiro, Fukuda Keiic |
Vitamin D and cause-specific vascular disease and mortality: a Mendelian randomisation study involving 99,012 Chinese and 106,911 European adults. BMC medicine 2019 Aug 17 (1): 160. Huang Tao, Afzal Shoaib, Yu Canqing, Guo Yu, Bian Zheng, Yang Ling, Millwood Iona Y, Walters Robin G, Chen Yiping, Chen Ningyu, Gao Ruqin, Chen Junshi, Clarke Robert, Chen Zhengming, Ellervik Christina, Nordestgaard Børge G, Lv Jun, Li Liming, |
MTHFR and risk of stroke and heart disease in a low-folate population: a prospective study of 156?000 Chinese adults. International journal of epidemiology 2023 10 . Derrick A Bennett, Sarah Parish, Iona Y Millwood, Yu Guo, Yiping Chen, Iain Turnbull, Ling Yang, Jun Lv, Canqing Yu, George Davey Smith, Yongjun Wang, Yilong Wang, Richard Peto, Rory Collins, Robin G Walters, Liming Li, Zhengming Chen, Robert Clarke, |
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