Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 30 Records) |
Query Trace: Coronary Artery Disease and CDKN2A[original query] |
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Chromosome 9p21 SNPs Associated with Multiple Disease Phenotypes Correlate with ANRIL Expression. PLoS genetics 2010 Apr 6 (4): e1000899. Cunnington Michael S, Santibanez Koref Mauro, Mayosi Bongani M, Burn John, Keavney Berna |
ANRIL expression is associated with atherosclerosis risk at chromosome 9p21. Arteriosclerosis, thrombosis, and vascular biology 2010 1 30 (3): 620-7. Holdt Lesca M, Beutner Frank, Scholz Markus, Gielen Stephan, Gäbel Gábor, Bergert Hendrik, Schuler Gerhard, Thiery Joachim, Teupser Dani |
Genome-wide association study of coronary artery disease in the Japanese.
European journal of human genetics : EJHG 2012 Mar 20 (3): 333-40. Takeuchi Fumihiko, Yokota Mitsuhiro, Yamamoto Ken, Nakashima Eitaro, Katsuya Tomohiro, Asano Hiroyuki, Isono Masato, Nabika Toru, Sugiyama Takao, Fujioka Akihiro, Awata Nobuhisa, Ohnaka Keizo, Nakatochi Masahiro, Kitajima Hidetoshi, Rakugi Hiromi, Nakamura Jiro, Ohkubo Takayoshi, Imai Yutaka, Shimamoto Kazuaki, Yamori Yukio, Yamaguchi Shuhei, Kobayashi Shotai, Takayanagi Ryoichi, Ogihara Toshio, Kato Norihi |
The chromosome 9p21.3 coronary heart disease risk allele is associated with altered gene expression in normal heart and vascular tissues. PloS one 2012 7 (6): e39574. Pilbrow Anna P, Folkersen Lasse, Pearson John F, Brown Chris M, McNoe Les, Wang Nancy M, Sweet Wendy E, Tang W H Wilson, Black Michael A, Troughton Richard W, Richards A Mark, Franco-Cereceda Anders, Gabrielsen Anders, Eriksson Per, Moravec Christine S, Cameron Vicky |
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 |
Functional analyses of coronary artery disease associated variation on chromosome 9p21 in vascular smooth muscle cells. Human molecular genetics 2012 Sep 21 (18): 4021-9. Motterle Anna, Pu Xiangyuan, Wood Harriet, Xiao Qingzhong, Gor Shivani, Ng Fu Liang, Chan Kenneth, Cross Frank, Shohreh Beski, Poston Robin N, Tucker Arthur T, Caulfield Mark J, Ye S |
A replication study of GWAS-derived lipid genes in Asian Indians: the chromosomal region 11q23.3 harbors loci contributing to triglycerides. PloS one 2012 7 (5): e37056. Braun Timothy R, Been Latonya F, Singhal Akhil, Worsham Jacob, Ralhan Sarju, Wander Gurpreet S, Chambers John C, Kooner Jaspal S, Aston Christopher E, Sanghera Dharambir |
Bayesian refinement of association signals for 14 loci in 3 common diseases. Nature genetics 2012 Dec 44 (12): 1294-301. , Maller Julian B, McVean Gilean, Byrnes Jake, Vukcevic Damjan, Palin Kimmo, Su Zhan, Howson Joanna M M, Auton Adam, Myers Simon, Morris Andrew, Pirinen Matti, Brown Matthew A, Burton Paul R, Caulfield Mark J, Compston Alastair, Farrall Martin, Hall Alistair S, Hattersley Andrew T, Hill Adrian V S, Mathew Christopher G, Pembrey Marcus, Satsangi Jack, Stratton Michael R, Worthington Jane, Craddock Nick, Hurles Matthew, Ouwehand Willem, Parkes Miles, Rahman Nazneen, Duncanson Audrey, Todd John A, Kwiatkowski Dominic P, Samani Nilesh J, Gough Stephen C L, McCarthy Mark I, Deloukas Panagiotis, Donnelly Pet |
Association between 9p21.3 genomic markers and coronary artery disease in East Asians: a meta-analysis involving 9,813 cases and 10,710 controls. Molecular biology reports 2013 Jan 40 (1): 337-43. Guo Jin, Li Wei, Wu Zhenqiang, Cheng Xiaoru, Wang Yang, Chen T |
Large scale association analysis identifies three susceptibility loci for coronary artery disease. PloS one 2011 6 (12): e29427. Saade Stephanie, Cazier Jean-Baptiste, Ghassibe-Sabbagh Michella, Youhanna Sonia, Badro Danielle A, Kamatani Yoichiro, Hager Jörg, Yeretzian Joumana S, El-Khazen Georges, Haber Marc, Salloum Angelique K, Douaihy Bouchra, Othman Raed, Shasha Nabil, Kabbani Samer, Bayeh Hamid El, Chammas Elie, Farrall Martin, Gauguier Dominique, Platt Daniel E, Zalloua Pierre A, |
Phenome-wide association study (PheWAS) for detection of pleiotropy within the Population Architecture using Genomics and Epidemiology (PAGE) Network. PLoS genetics 2013 Jan 9 (1): 1. Pendergrass SA, Brown-Gentry K, Dudek S, Frase A, Torstenson ES, Goodloe R, Ambite JL, Avery CL, Buyske S, B?žková P, Deelman E, Fesinmeyer MD, Haiman CA, Heiss G, Hindorff LA, Hsu CN, Jackson RD, Kooperberg C, Le Marchand L, Lin Y, Matise TC, Monroe KR, Moreland L, Park SL, Reiner A, Wallace R, Wilkens LR, Crawford DC, Ritchie MD |
A genome-wide association study of a coronary artery disease risk variant.
Journal of human genetics 2013 Jan . Lee JY, Lee BS, Shin DJ, Woo Park K, Shin YA, Joong Kim K, Heo L, Young Lee J, Kyoung Kim Y, Jin Kim Y, Bum Hong C, Lee SH, Yoon D, Jung Ku H, Oh IY, Kim BJ, Lee J, Park SJ, Kim J, Kawk HK, Lee JE, Park HK, Lee JE, Nam HY, Park HY, Shin C, Yokota M, Asano H, Nakatochi M, Matsubara T, Kitajima H, Yamamoto K, Kim HL, Han BG, Cho MC, Jang Y, Kim HS, Euy Park J, Lee JY |
Genetic susceptibility for ischemic infarction and arteriolosclerosis based on neuropathologic evaluations. Cerebrovascular diseases (Basel, Switzerland) 2013 36 (3): 181-8. Chou S H-Y, Shulman J M, Keenan B T, Secor E A, Buchman A S, Schneider J, Bennett D A, De Jager P |
Resequencing and clinical associations of the 9p21.3 region: a comprehensive investigation in the Framingham heart study. Circulation 2013 Jan . Johnson AD, Hwang SJ, Voorman A, Morrison A, Peloso GM, Hu YH, Thanassoulis G, Newton-Cheh C, Rogers IS, Hoffman U, Freedman JE, Fox CS, Psaty BM, Boerwinkle E, Cupples LA, O'Donnell CJ |
Disease-associated polymorphisms in 9p21 are not associated with extreme longevity. Geriatrics & gerontology international 2015 Jun 15 (6): 797-803. Congrains Ada, Kamide Kei, Hirose Nobuyoshi, Arai Yasumichi, Oguro Ryousuke, Nakama Chikako, Imaizumi Yuki, Kawai Tatsuo, Kusunoki Hiroshi, Yamamoto Hiroko, Onishi-Takeya Miyuki, Takeya Yasushi, Yamamoto Koichi, Sugimoto Ken, Akasaka Hiroshi, Saitoh Shigeyuki, Miura Tetsuji, Awata Nobuhisa, Kato Norihiro, Katsuya Tomohiro, Ikebe Kazunori, Gondo Yasuyuki, Rakugi Hiro |
Associations between the CDKN2A/B, ADTRP and PDGFD polymorphisms and the development of coronary atherosclerosis in Japanese patients. Journal of atherosclerosis and thrombosis 2014 21 (7): 680-90. Dechamethakun Sariya, Ikeda Shinobu, Arai Tomio, Sato Noriko, Sawabe Motoji, Muramatsu Masaa |
Interaction of type 2 diabetes mellitus with chromosome 9p21 rs10757274 polymorphism on the risk of myocardial infarction: a case-control study in Chinese population. BMC cardiovascular disorders 2014 14 170. Zhang Liu-wei, Li Jian-ping, Duan Fang-fang, Liu Zhi-ke, Zhan Si-yan, Hu Yong-hua, Jiang Jie, Zhang Yan, Huo Yong, Chen Da-fa |
Genetic variants associated with myocardial infarction and the risk factors in Chinese population. PloS one 2014 9 (1): e86332. Wang Yongqin, Wang Lefeng, Liu Xin, Zhang Yongzhi, Yu Liping, Zhang Fan, Liu Lisheng, Cai Jun, Yang Xinchun, Wang Xing |
Genetic analysis of the 9p21.3 CAD risk locus in Asian Indians. Thrombosis and haemostasis 2014 May 111 (5): 960-9. Shanker Jayashree, Arvind Prathima, Jambunathan Srikarthika, Nair Jiny, Kakkar Vij |
9p21.3 Coronary Artery Disease Risk Variants Disrupt TEAD Transcription Factor-Dependent Transforming Growth Factor ß Regulation of p16 Expression in Human Aortic Smooth Muscle Cells. Circulation 2015 Oct . Almontashiri Naif A M, Antoine Darlene, Zhou Xun, Vilmundarson Ragnar O, Zhang Sean X, Hao Kennedy N, Chen Hsiao-Huei, Stewart Alexandre F |
Enhanced Megakaryopoiesis and Platelet Activity in Hypercholesterolemic, B6-Ldlr-/-, Cdkn2a-Deficient Mice. Circulation. Cardiovascular genetics 2016 Apr . Wang Wei, Oh Seon, Koester Mark, Abramowicz Sandra, Wang Nan, Tall Alan R, Welch Carrie |
Association Study Between Coronary Artery Disease and rs1333049 Polymorphism at 9p21.3 Locus in Italian Population. Journal of cardiovascular translational research 2017 Jun . Pignataro Piero, Pezone Lucia, Di Gioia Giuseppe, Franco Danilo, Iaccarino Guido, Iolascon Achille, Ciccarelli Michele, Capasso Mar |
Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity.
Nature communications 2017 Oct 8 (1): 910. Joshi Peter K, Pirastu Nicola, Kentistou Katherine A, Fischer Krista, Hofer Edith, Schraut Katharina E, Clark David W, Nutile Teresa, Barnes Catriona L K, Timmers Paul R H J, Shen Xia, Gandin Ilaria, McDaid Aaron F, Hansen Thomas Folkmann, Gordon Scott D, Giulianini Franco, Boutin Thibaud S, Abdellaoui Abdel, Zhao Wei, Medina-Gomez Carolina, Bartz Traci M, Trompet Stella, Lange Leslie A, Raffield Laura, van der Spek Ashley, Galesloot Tessel E, Proitsi Petroula, Yanek Lisa R, Bielak Lawrence F, Payton Antony, Murgia Federico, Concas Maria Pina, Biino Ginevra, Tajuddin Salman M, Seppälä Ilkka, Amin Najaf, Boerwinkle Eric, Børglum Anders D, Campbell Archie, Demerath Ellen W, Demuth Ilja, Faul Jessica D, Ford Ian, Gialluisi Alessandro, Gögele Martin, Graff MariaElisa, Hingorani Aroon, Hottenga Jouke-Jan, Hougaard David M, Hurme Mikko A, Ikram M Arfan, Jylhä Marja, Kuh Diana, Ligthart Lannie, Lill Christina M, Lindenberger Ulman, Lumley Thomas, Mägi Reedik, Marques-Vidal Pedro, Medland Sarah E, Milani Lili, Nagy Reka, Ollier William E R, Peyser Patricia A, Pramstaller Peter P, Ridker Paul M, Rivadeneira Fernando, Ruggiero Daniela, Saba Yasaman, Schmidt Reinhold, Schmidt Helena, Slagboom P Eline, Smith Blair H, Smith Jennifer A, Sotoodehnia Nona, Steinhagen-Thiessen Elisabeth, van Rooij Frank J A, Verbeek André L, Vermeulen Sita H, Vollenweider Peter, Wang Yunpeng, Werge Thomas, Whitfield John B, Zonderman Alan B, Lehtimäki Terho, Evans Michele K, Pirastu Mario, Fuchsberger Christian, Bertram Lars, Pendleton Neil, Kardia Sharon L R, Ciullo Marina, Becker Diane M, Wong Andrew, Psaty Bruce M, van Duijn Cornelia M, Wilson James G, Jukema J Wouter, Kiemeney Lambertus, Uitterlinden André G, Franceschini Nora, North Kari E, Weir David R, Metspalu Andres, Boomsma Dorret I, Hayward Caroline, Chasman Daniel, Martin Nicholas G, Sattar Naveed, Campbell Harry, Esko T?nu, Kutalik Zoltán, Wilson James |
LncRNA ANRIL Expression and ANRIL Gene Polymorphisms Contribute to the Risk of Ischemic Stroke in the Chinese Han Population. Cellular and molecular neurobiology 2018 Jun . Yang Jialei, Gu Lian, Guo Xiaojing, Huang Jiao, Chen Zhaoxia, Huang Guifeng, Kang Yiwen, Zhang Xiaoting, Long Jianxiong, Su |
GWAS implicated risk variants in different genes contribute additively to increase the risk of coronary artery disease (CAD) in the Pakistani subjects. Lipids in health and disease 2018 Apr 17 (1): 89. Shahid Saleem Ullah, Shabana N A, Rehman Abdul, Humphries Ste |
The SNP rs7865618 of 9p21.3 locus emerges as the most promising marker of coronary artery disease in the southern Indian population. Scientific reports 2020 Dec 10 (1): 21511. Manjula Gorre, Pranavchand Rayabarapu, Kumuda Irgam, Reddy B Sriteja, Reddy Battini Moh |
Association between rs3088440 (G?>?A) polymorphism at 9p21.3 locus with the occurrence and severity of coronary artery disease in an Iranian population. Molecular biology reports 2021 7 48 (8): 5905-5912. Pourgholi Mitra, Abazari Omid, Pourgholi Leyla, Ghasemi-Kasman Maryam, Boroumand Mohammada |
Disease-Associated Risk Variants in ANRIL Are Associated with Tumor-Infiltrating Lymphocyte Presence in Primary Melanomas in the Population-Based GEM Study. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2021 Oct . Davari Danielle R, Orlow Irene, Kanetsky Peter A, Luo Li, Edmiston Sharon N, Conway Kathleen, Parrish Eloise A, Hao Honglin, Busam Klaus J, Sharma Ajay, Kricker Anne, Cust Anne E, Anton-Culver Hoda, Gruber Stephen B, Gallagher Richard P, Zanetti Roberto, Rosso Stefano, Sacchetto Lidia, Dwyer Terence, Ollila David W, Begg Colin B, Berwick Marianne, Thomas Nancy E, |
Effect of 9p21.3 (lncRNA and CDKN2A/2B) variant on lipid profile. Frontiers in cardiovascular medicine 2022 9 9 946289. Wei Baozhu, Liu Yang, Li Hang, Peng Yuanyuan, Luo Z |
Analysis of ANRIL Isoforms and Key Genes in Patients with Severe Coronary Artery Disease. International journal of molecular sciences 2023 11 24 (22): . Francisco Rodríguez-Esparragón, Laura B Torres-Mata, Sara E Cazorla-Rivero, Jaime A Serna Gómez, Jesús M González Martín, Ángeles Cánovas-Molina, José A Medina-Suárez, Ayose N González-Hernández, Lidia Estupiñán-Quintana, María C Bartolomé-Durán, José C Rodríguez-Pérez, Bernardino Clavo Var |
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