Human Genome Epidemiology Literature Finder
|
Records 1 - 30 (of 38 Records) |
| Query Trace: Coronary artery disease and Cdkn2b[original query] |
|---|
| 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 |
| 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 |
| Genetic variation and coronary atherosclerosis in patients with systemic lupus erythematosus. Lupus 2014 Aug 23 (9): 876-80. Chung C P, Solus J F, Oeser A, Li C, Raggi P, Smith J R, Stein C |
| Association of six genetic variants with myocardial infarction. International journal of molecular medicine 2015 May 35 (5): 1451-9. Matsuoka Reiko, Abe Shintaro, Tokoro Fumitaka, Arai Masazumi, Noda Toshiyuki, Watanabe Sachiro, Horibe Hideki, Fujimaki Tetsuo, Oguri Mitsutoshi, Kato Kimihiko, Minatoguchi Shinya, Yamada Yoshi |
| 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 |
| Association of the rs10757274 SNP with coronary artery disease in a small group of a Pakistani population. Anatolian journal of cardiology 2015 Jan . Nawaz Syed Kashif, Noreen Aasma, Rani Asima, Yousaf Memoona, Arshad Muhamm |
| 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 |
| Intronic Polymorphisms in the CDKN2B-AS1 Gene Are Strongly Associated with the Risk of Myocardial Infarction and Coronary Artery Disease in the Saudi Population. International journal of molecular sciences 2016 17 (3): . AbdulAzeez Sayed, Al-Nafie Awatif N, Al-Shehri Abdullah, Borgio J Francis, Baranova Ekaterina V, Al-Madan Mohammed S, Al-Ali Rudaynah A, Al-Muhanna Fahad, Al-Ali Abdullah, Al-Mansori Mohammed, Ibrahim Mohammed Fakhry, Asselbergs Folkert W, Keating Brendan, Koeleman Bobby P C, Al-Ali Amein |
| Analysis of Two CDKN2B-AS Polymorphisms in Relation to Coronary Artery Disease Patients in North of Iran. International journal of molecular and cellular medicine 2017 6 (1): 31-37. Mafi Golchin Maryam, Ghaderian Sayyed Mohammad Hossein, Akhavan-Niaki Haleh, Jalalian Rozita, Heidari Laleh, Salami Seyed Alire |
| 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 |
| 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 |
| The role of CDKN2B in cardiovascular risk in ethnic Saudi Arabs: A validation study. Gene 2018 Jun . AlRasheed Maha M, Hefnawy MennatAllah M, Elsherif Nourhan N, Alhawassi Tariq M, Abanmy Norah O, AlRasheed Nora M, Alqahtani Fulwah Y, Aleanizy Fadilah S, Muiya Paul, Al-Boudari Olayan M, Dzimiri Ndu |
| Association of a Chromosome Locus 9p21.3 CDKN2B-AS1 Variant rs4977574 with Hypertension: The TAMRISK Study. Genetic testing and molecular biomarkers 2018 May 22 (5): 327-330. Kunnas Tarja, Piesanen Jaakko, Nikkari Seppo |
| Evaluation of the role of CDKN2B gene in type 2 diabetes mellitus and hypertension in ethnic Saudi Arabs. Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society 2018 Dec 26 (8): 1199-1203. AlRasheed Maha Mesh |
| The association between the chromosome 9p21 CDKN2B-AS1 gene variants and the lipid metabolism: A pre-diagnostic biomarker for coronary artery disease. Anatolian journal of cardiology 2019 Jan 21 (1): 31-38. Temel ?ehime Gülsün, Ergören Mahmut Çerk |
| Phenotypic Refinement of Heart Failure in a National Biobank Facilitates Genetic Discovery. Circulation 2018 Nov . Aragam Krishna G, Chaffin Mark, Levinson Rebecca T, McDermott Gregory, Choi Seung-Hoan, Shoemaker M Benjamin, Haas Mary E, Weng Lu-Chen, Lindsay Mark E, Smith J Gustav, Newton-Cheh Christopher, Roden Dan M, London Barry, Wells Quinn S, Ellinor Patrick T, Kathiresan Sekar, Lubitz Steven A, |
| CDKN2B gene expression is affected by 9p21.3 rs10757278 in CAD patients, six months after the MI. Clinical biochemistry 2019 Aug . Zivoti? Ivan, Djuri? Tamara, Stankovi? Aleksandra, Milasinovic Dejan, Stankovic Goran, Dekleva Milica, Markovi? Nikoli? Natasa, Alavanti? Dragan, Zivkovi? Ma |
| Genome-wide association study of coronary artery calcification in asymptomatic Korean populations. PloS one 2019 14 (3): e0214370. Choi Su-Yeon, Shin Eunsoon, Choe Eun Kyung, Park Boram, Lee Heesun, Park Hyo Eun, Lee Jong-Eun, Choi Seung |
| Association of the PSRC1 rs599839 Variant with Coronary Artery Disease in a Mexican Population. Medicina (Kaunas, Lithuania) 2020 8 56 (9): . Rodríguez-Arellano Martha Eunice, Solares-Tlapechco Jacqueline, Costa-Urrutia Paula, Cárdenas-Hernández Helios, Vallejo-Gómez Marajael, Granados Julio, Salas-Padilla Serg |
| Associations Between Common Polymorphisms of CDKN2B-AS and Susceptibility to ASCVD. Angiology 2020 Jul 3319720941387. Huang Yupeng, Jin Hongyan, Yang Guoka |
Genome-wide association study on coronary artery disease in type 1 diabetes suggests beta-defensin 127 as a risk locus.
Cardiovascular research 2021 Jan 117 (2): 600-612. Antikainen Anni A V, Sandholm Niina, Trégouët David-Alexandre, Charmet Romain, McKnight Amy Jayne, Ahluwalia Tarunveer S, Syreeni Anna, Valo Erkka, Forsblom Carol, Gordin Daniel, Harjutsalo Valma, Hadjadj Samy, Maxwell Alexander P, Rossing Peter, Groop Per-Henr |
| 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 |
| Multiethnic Genome-Wide Association Study of Subclinical Atherosclerosis in Individuals With Type 2 Diabetes.
Circulation. Genomic and precision medicine 2021 7 14 (4): e003258. Lu Yingchang, Dimitrov Latchezar, Chen Shyh-Huei, Bielak Lawrence F, Bis Joshua C, Feitosa Mary F, Lu Lingyi, Kavousi Maryam, Raffield Laura M, Smith Albert V, Wang Lihua, Weiss Stefan, Yao Jie, Zhu Jiaxi, Gudmundsson Elias F, Gudmundsdottir Valborg, Bos Daniel, Ghanbari Mohsen, Ikram M Arfan, Hwang Shih-Jen, Taylor Kent D, Budoff Matthew J, Gíslason Gauti K, O'Donnell Christopher J, An Ping, Franceschini Nora, Freedman Barry I, Fu Yi-Ping, Guo Xiuqing, Heiss Gerardo, Kardia Sharon L R, Wilson James G, Langefeld Carl D, Schminke Ulf, Uitterlinden André G, Lange Leslie A, Peyser Patricia A, Gudnason Vilmundur G, Psaty Bruce M, Rotter Jerome I, Bowden Donald W, Ng Maggie C |
| A Study of Associations Between rs9349379 (PHACTR1), rs2891168 (CDKN2B-AS), rs11838776 (COL4A2) and rs4880 (SOD2) Polymorphic Variants and Coronary Artery Disease in Iranian Population. Biochemical genetics 2021 Jun . Yari Abolfazl, Saleh-Gohari Nasrollah, Mirzaee Moghaddameh, Hashemi Fatemeh, Saeidi Kolso |
| 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, |
| Association of Myocardial Infarction with CDKN2B Antisense RNA 1 (CDKN2B-AS1) rs1333049 Polymorphism in Slovenian Subjects with Type 2 Diabetes Mellitus. Genes 2022 3 13 (3): . Tibaut Miha, Naji Franjo, Petrovi? Dani |
| CDKN2B-AS (rs2891168), SOD2 (rs4880), and PON1 (rs662) polymorphisms and susceptibility to coronary artery disease and type 2 diabetes mellitus in Iranian patients: A case-control study. Health science reports 2023 11 6 (11): e1717. Abolfazl Yari, Zahra M Karam, Seyed M E Meybodi, Marzieh L Sargazi, Kolsoum Saei |
| 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 |
| Deletion of the Murine Ortholog of the Human 9p21.3 Locus Leads to Insulin Resistance and Obesity in Hypercholesterolemic Mice. Cells 2024 6 13 (11): . Sanna Kettunen, Tuisku Suoranta, Sadegh Beikverdi, Minja Heikkilä, Anna Slita, Iida Räty, Elias Ylä-Herttuala, Katariina Öörni, Anna-Kaisa Ruotsalainen, Seppo Ylä-Herttua |
- Page last reviewed:Feb 1, 2024
- Content source: