Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 37 Records) |
| Query Trace: Myocardial Infarction and PCSK9[original query] |
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| Pooled DNA resequencing of 68 myocardial infarction candidate genes in French canadians. Circulation. Cardiovascular genetics 2012 Oct 5 (5): 547-54. Beaudoin Mélissa, Lo Ken Sin, N'Diaye Amidou, Rivas Manuel A, Dubé Marie-Pierre, Laplante Nathalie, Phillips Michael S, Rioux John D, Tardif Jean-Claude, Lettre Guillau |
| LDL-c-linked SNPs are associated with LDL-c and myocardial infarction despite lipid-lowering therapy in patients with established vascular disease. European journal of clinical investigation 2013 Nov . van de Woestijne AP, van der Graaf Y, de Bakker PI, Asselbergs FW, de Borst GJ, Algra A, Spiering W, Visseren FL |
| 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 |
| PCSK9 R46L Loss-of-Function Mutation Reduces Lipoprotein(a), LDL Cholesterol, and Risk of Aortic Valve Stenosis. The Journal of clinical endocrinology and metabolism 2016 May jc20161206. Langsted Anne, Nordestgaard Børge G, Benn Marianne, Tybjærg-Hansen Anne, Kamstrup Pia |
| Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease. The New England journal of medicine 2016 Mar . Authors are not available |
| PCSK9 variant, long-chain n-3 PUFAs, and risk of nonfatal myocardial infarction in Costa Rican Hispanics. The American journal of clinical nutrition 2017 Mar . Yu Zhi, Huang Tao, Zheng Yan, Wang Tiange, Heianza Yoriko, Sun Dianjianyi, Campos Hannia, Qi |
| Genetic spectrum of low density lipoprotein receptor gene variations in South Indian population. Clinica chimica acta; international journal of clinical chemistry 2017 Dec 478 28-36. ArulJothi K N, Suruthi Abirami B, Devi Arikke |
| Blood lipid-related low-frequency variants in LDLR and PCSK9 are associated with onset age and risk of myocardial infarction in Japanese. Scientific reports 2018 May 8 (1): 8107. Tajima Tomoyuki, Morita Hiroyuki, Ito Kaoru, Yamazaki Tsutomu, Kubo Michiaki, Komuro Issei, Momozawa Yukihi |
| Burden of familial heterozygous hypercholesterolemia in Uzbekistan: Time is muscle. Atherosclerosis 2018 Oct 277 524-529. Shek Aleksandr, Alieva Rano, Kurbanov Ravshanbek, Hoshimov Shavkat, Nizamov Ulugbek, Abdullaeva Guzal, Nagay Aleksan |
| Multilocus Analysis of Genetic Susceptibility to Myocardial Infarction in Russians: Replication Study. Acta naturae 0 9 (4): 74-83. Kukava N G, Titov B V, Osmak G J, Matveeva N A, Kulakova O G, Favorov A V, Shakhnovich R M, Ruda M Ya, Favorova O |
| Risk of Premature Atherosclerotic Disease in Patients With Monogenic Versus Polygenic Familial Hypercholesterolemia. Journal of the American College of Cardiology 2019 7 74 (4): 512-522. Trinder Mark, Li Xuan, DeCastro Maria Liza, Cermakova Luba, Sadananda Singh, Jackson Linda M, Azizi Hawmid, Mancini G B John, Francis Gordon A, Frohlich Jiri, Brunham Liam |
| Effects of familial hypercholesterolemia-associated genes on the phenotype of premature myocardial infarction. Lipids in health and disease 2019 Apr 18 (1): 95. Lee Chongyou, Cui Yuxia, Song Junxian, Li Sufang, Zhang Feng, Wu Manyan, Li Long, Hu Dan, Chen Ho |
| Predicting Benefit From Evolocumab Therapy in Patients With Atherosclerotic Disease Using a Genetic Risk Score: Results From the FOURIER Trial. Circulation 2019 11 141 (8): 616-623. Marston Nicholas A, Kamanu Frederick K, Nordio Francesco, Gurmu Yared, Roselli Carolina, Sever Peter S, Pedersen Terje R, Keech Anthony C, Wang Huei, Lira Pineda Armando, Giugliano Robert P, Lubitz Steven A, Ellinor Patrick T, Sabatine Marc S, Ruff Christian |
| Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9. BMC cardiovascular disorders 2019 Oct 19 (1): 240. Schmidt Amand F, Holmes Michael V, Preiss David, Swerdlow Daniel I, Denaxas Spiros, Fatemifar Ghazaleh, Faraway Rupert, Finan Chris, Valentine Dennis, Fairhurst-Hunter Zammy, Hartwig Fernando Pires, Horta Bernardo Lessa, Hypponen Elina, Power Christine, Moldovan Max, van Iperen Erik, Hovingh Kees, Demuth Ilja, Norman Kristina, Steinhagen-Thiessen Elisabeth, Demuth Juri, Bertram Lars, Lill Christina M, Coassin Stefan, Willeit Johann, Kiechl Stefan, Willeit Karin, Mason Dan, Wright John, Morris Richard, Wanamethee Goya, Whincup Peter, Ben-Shlomo Yoav, McLachlan Stela, Price Jackie F, Kivimaki Mika, Welch Catherine, Sanchez-Galvez Adelaida, Marques-Vidal Pedro, Nicolaides Andrew, Panayiotou Andrie G, Onland-Moret N Charlotte, van der Schouw Yvonne T, Matullo Giuseppe, Fiorito Giovanni, Guarrera Simonetta, Sacerdote Carlotta, Wareham Nicholas J, Langenberg Claudia, Scott Robert A, Luan Jian'an, Bobak Martin, Malyutina Sofia, Paj?k Andrzej, Kubinova Ruzena, Tamosiunas Abdonas, Pikhart Hynek, Grarup Niels, Pedersen Oluf, Hansen Torben, Linneberg Allan, Jess Tine, Cooper Jackie, Humphries Steve E, Brilliant Murray, Kitchner Terrie, Hakonarson Hakon, Carrell David S, McCarty Catherine A, Lester Kirchner H, Larson Eric B, Crosslin David R, de Andrade Mariza, Roden Dan M, Denny Joshua C, Carty Cara, Hancock Stephen, Attia John, Holliday Elizabeth, Scott Rodney, Schofield Peter, O'Donnell Martin, Yusuf Salim, Chong Michael, Pare Guillaume, van der Harst Pim, Said M Abdullah, Eppinga Ruben N, Verweij Niek, Snieder Harold, , Christen Tim, Mook-Kanamori D O, , Gustafsson Stefan, Lind Lars, Ingelsson Erik, Pazoki Raha, Franco Oscar, Hofman Albert, Uitterlinden Andre, Dehghan Abbas, Teumer Alexander, Baumeister Sebastian, Dörr Marcus, Lerch Markus M, Völker Uwe, Völzke Henry, Ward Joey, Pell Jill P, Meade Tom, Christophersen Ingrid E, Maitland-van der Zee Anke H, Baranova Ekaterina V, Young Robin, Ford Ian, Campbell Archie, Padmanabhan Sandosh, Bots Michiel L, Grobbee Diederick E, Froguel Philippe, Thuillier Dorothée, Roussel Ronan, Bonnefond Amélie, Cariou Bertrand, Smart Melissa, Bao Yanchun, Kumari Meena, Mahajan Anubha, Hopewell Jemma C, Seshadri Sudha, , Dale Caroline, Costa Rui Providencia E, Ridker Paul M, Chasman Daniel I, Reiner Alex P, Ritchie Marylyn D, Lange Leslie A, Cornish Alex J, Dobbins Sara E, Hemminki Kari, Kinnersley Ben, Sanson Marc, Labreche Karim, Simon Matthias, Bondy Melissa, Law Philip, Speedy Helen, Allan James, Li Ni, Went Molly, Weinhold Niels, Morgan Gareth, Sonneveld Pieter, Nilsson Björn, Goldschmidt Hartmut, Sud Amit, Engert Andreas, Hansson Markus, Hemingway Harry, Asselbergs Folkert W, Patel Riyaz S, Keating Brendan J, Sattar Naveed, Houlston Richard, Casas Juan P, Hingorani Aroon |
| Prevalence of familial hypercholesterolemia in patients with premature myocardial infarction. Clinical cardiology 2019 1 42 (3): 385-390. Cui Yuxia, Li Sufang, Zhang Feng, Song Junxian, Lee Chongyou, Wu Manyan, Chen Ho |
| Identification of Genetic Variants Associated With Myocardial Infarction in Saudi Arabia. The heart surgery forum 2020 Jul 23 (4): E517-E523. Ai-Ghalayini Kamal W, Salama Mohammed A, Al Mahdi Hadia Bassam, Al-Harthi Sameer, Alhejily Wesam A, Alasnag Mirvat A, Tasbhji Noura O, Al-Quwaie Diana A H, Deloukas Panos, Edris Sher |
| Common gene variants in ASGR1 gene locus associate with reduced cardiovascular risk in absence of pleiotropic effects. Atherosclerosis 2020 Jul 306 15-21. Ali Lubna, Cupido Arjen J, Rijkers Maaike, Hovingh G Kees, Holleboom Adriaan G, Dallinga-Thie Geesje M, Stroes Erik S G, van den Boogert Marjolein A |
| Association of Monogenic vs Polygenic Hypercholesterolemia With Risk of Atherosclerotic Cardiovascular Disease. JAMA cardiology 2020 Feb . Trinder Mark, Francis Gordon A, Brunham Liam |
| Cardiovascular Disease Prevention in Focus: Highlights from the 2019 American Heart Association Scientific Sessions. Current atherosclerosis reports 2020 1 22 (1): 3. Mehta Anurag, Mahtta Dhruv, Gulati Martha, Sperling Laurence S, Blumenthal Roger S, Virani Salim |
| Characterization of familial hypercholesterolemia in Taiwanese ischemic stroke patients. Aging 2021 7 13 (15): 19339-19351. Tung Hsin, Lin Hsueh-Ju, Chen Po-Lin, Lu Tsai-Jung, Jhan Pei-Pei, Chen Jun-Peng, Chen Yi-Ming, Wu Chen-Chin, Lin Yung-Yang, Hsiao Tzu-Hu |
| Lipoprotein(a). Handbook of experimental pharmacology 2021 7 270 201-232. Kronenberg Flori |
| Patients With LDLR and PCSK9 Gene Variants Experienced Higher Incidence of Cardiovascular Outcomes in Heterozygous Familial Hypercholesterolemia. Journal of the American Heart Association 2021 2 10 (4): e018263. Doi Takahito, Hori Mika, Harada-Shiba Mariko, Kataoka Yu, Onozuka Daisuke, Nishimura Kunihiro, Nishikawa Ryo, Tsuda Kosuke, Ogura Masatsune, Son Cheol, Miyamoto Yoshihiro, Noguchi Teruo, Shimokawa Hiroaki, Yasuda Satos |
| Genetic Risk Score to Identify Risk of Venous Thromboembolism in Patients With Cardiometabolic Disease. Circulation. Genomic and precision medicine 2021 1 14 (1): e003006. Marston Nicholas A, Melloni Giorgio E M, Gurmu Yared, Bonaca Marc P, Kamanu Frederick K, Roselli Carolina, Lee Christina, Cavallari Ilaria, Giugliano Robert P, Scirica Benjamin M, Bhatt Deepak L, Steg Philippe Gabriel, Cohen Marc, Storey Robert F, Keech Anthony C, Raz Itamar, Mosenzon Ofri, Braunwald Eugene, Lubitz Steven A, Ellinor Patrick T, Sabatine Marc S, Ruff Christian |
| The Influence of Treatment with PCSK9 Inhibitors and Variants in the CRP (rs1800947), TNFA (rs1800629), and IL6 (rs1800795) Genes on the Corresponding Inflammatory Markers in Patients with Very High Lipoprotein(a) Levels. Journal of cardiovascular development and disease 2022 5 9 (5): . Levstek Tina, Podkrajšek Nik, Rehberger Likozar Andreja, Šebeštjen Miran, Trebušak Podkrajšek Katari |
| The R93C Variant of PCSK9 Reduces the Risk of Premature MI in a Chinese Han Population. Frontiers in genetics 2022 4 13 875269. Yang Lincheng, Pu Tian, Zhang Yan, Yan Hua, Yu Haiyi, Gao W |
| Coronary Artery Disease Risk of Familial Hypercholesterolemia Genetic Variants Independent of Clinically Observed Longitudinal Cholesterol Exposure. Circulation. Genomic and precision medicine 2022 Feb CIRCGEN121003501. Clarke Shoa L, Tcheandjieu Catherine, Hilliard Austin T, Lee Kyung Min, Lynch Julie, Chang Kyong-Mi, Miller Donald, Knowles Joshua W, O'Donnell Christopher, Tsao Philip S, Rader Daniel J, Wilson Peter W, Sun Yan V, Gaziano J Michael, Assimes Themistocles L, |
| E670G PCSK9 polymorphism in HeFH & CAD with diabetes: is the bridge to personalized therapy within reach? Frontiers in clinical diabetes and healthcare 2023 11 4 1277288. Rano Alieva, Aleksandr Shek, Alisher Abdullaev, Khurshid Fozilov, Shovkat Khoshimov, Guzal Abdullaeva, Dariya Zakirova, Rano Kurbanova, Lilia Kan, Andrey K |
| PCSK9 gene variations in the clinical setting of premature cardiovascular disease: A critical appraisal. International journal of cardiology 2024 7 413 132402. Rebeca Lorca, Andrea Aparicio, Luis Gutiérrez, Rut Álvarez-Velasco, Francisco González-Urbistondo, Isaac Pascual, Juan Gómez, Daniel Vazquez-Coto, Claudia Garcia-Lago, Pablo Avanzas, Eliecer Co |
| Effects of genetically proxied lipid-lowering drugs on acute myocardial infarction: a drug-target mendelian randomization study. Lipids in health and disease 2024 6 23 (1): 163. Wendi Xiao, Yueying Li, Zhenhuang Zhuang, Zimin Song, Wenxiu Wang, Ninghao Huang, Xue Dong, Jinzhu Jia, Zhonghua Liu, Yimin Zhao, Lu Qi, Tao Hua |
| Polygenic Risk, Rare Variants, and Family History: Independent and Additive Effects on Coronary Heart Disease. JACC. Advances 2024 6 2 (7): 100567. Seyedmohammad Saadatagah, Mohammadreza Naderian, Ozan Dikilitas, Marwan E Hamed, Hana Bangash, Iftikhar J Kul |
- Page last reviewed:Feb 1, 2024
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