Human Genome Epidemiology Literature Finder
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Records 1 - 19 (of 19 Records) |
| Query Trace: Diabetes Mellitus and PCSK9[original query] |
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| The PCSK9 gene E670G polymorphism affects low-density lipoprotein cholesterol levels but is not a risk factor for coronary artery disease in ethnic Chinese in Taiwan. Clinical chemistry and laboratory medicine : CCLM / FESCC 2009 47 (2): 154-8. Hsu Lung-An, Teng Ming-Sheng, Ko Yu-Lin, Chang Chi-Jen, Wu Semon, Wang Chun-Li, Hu Chiao-Fe |
| 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 |
| Variations of the proprotein convertase subtilisin/kexin type 9 gene in coronary artery disease. The Journal of international medical research 2019 Apr 300060519839519. Chiang Shih-Min, Yang Yi-Sun, Yang Shun-Fa, Tsai Chin-Feng, Ueng Kwo-Chn |
| 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 |
| Genetic Assessment of Potential Long-Term On-Target Side Effects of PCSK9 (Proprotein Convertase Subtilisin/Kexin Type 9) Inhibitors. Circulation. Genomic and precision medicine 2019 1 12 (1): e002196. Nelson Christopher P, Lai Florence Y, Nath Mintu, Ye Shu, Webb Thomas R, Schunkert Heribert, Samani Nilesh |
Genome-wide association study for circulating fibroblast growth factor 21 and 23.
Scientific reports 2020 Sep 10 (1): 14578. Chuang Gwo-Tsann, Liu Pi-Hua, Chyan Tsui-Wei, Huang Chen-Hao, Huang Yu-Yao, Lin Chia-Hung, Lin Jou-Wei, Hsu Chih-Neng, Tsai Ru-Yi, Hsieh Meng-Lun, Lee Hsiao-Lin, Yang Wei-Shun, Robinson-Cohen Cassianne, Hsiung Chia-Ni, Shen Chen-Yang, Chang Yi-Che |
| PCSK9 Protein and rs562556 Polymorphism Are Associated With Arterial Plaques in Healthy Middle-Aged Population: The STANISLAS Cohort. Journal of the American Heart Association 2020 Apr 9 (7): e014758. Ferreira João Pedro, Xhaard Constance, Lamiral Zohra, Borges-Canha Marta, Neves João Sérgio, Dandine-Roulland Claire, LeFloch Edith, Deleuze Jean-François, Bacq-Daian Delphine, Bozec Erwan, Girerd Nicolas, Boivin Jean-Marc, Zannad Faiez, Rossignol Patri |
| Genetic associations between serum low LDL-cholesterol levels and variants in LDLR, APOB, PCSK9 and LDLRAP1 in African populations. PloS one 2020 15 (2): e0229098. Hayat Mahtaab, Kerr Robyn, Bentley Amy R, Rotimi Charles N, Raal Frederick J, Ramsay Michè |
| Clinical Application of a Novel Genetic Risk Score for Ischemic Stroke in Patients With Cardiometabolic Disease. Circulation 2020 11 143 (5): 470-478. Marston Nicholas A, Patel Parth N, Kamanu Frederick K, Nordio Francesco, Melloni Giorgio M, Roselli Carolina, Gurmu Yared, Weng Lu-Chen, Bonaca Marc P, Giugliano Robert P, Scirica Benjamin M, O'Donoghue Michelle L, Cannon Christopher P, Anderson Christopher D, Bhatt Deepak L, Gabriel Steg Philippe, Cohen Marc, Storey Robert F, Sever Peter, Keech Anthony C, Raz Itamar, Mosenzon Ofri, Antman Elliott M, Braunwald Eugene, Ellinor Patrick T, Lubitz Steven A, Sabatine Marc S, Ruff Christian |
| PCSK9 E670G (rs505151) Variant and Coronary Artery Disease Risk Among Diabetics. Genetic testing and molecular biomarkers 2021 9 25 (9): 615-623. Mohamed Samy H, Hassaan Mohamed M M, Ibrahim Basma A, Sabbah Norhan |
| Susceptibility of ApoB and PCSK9 Genetic Polymorphisms to Diabetic Kidney Disease Among Chinese Diabetic Patients. Frontiers in medicine 2021 8 659188. Ma Liang, Wang Shaoting, Zhao Hailing, Yu Meijie, Deng Xiangling, Jiang Yongwei, Cao Yongtong, Li Ping, Niu Wenqu |
| 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 |
| Common and Rare PCSK9 Variants Associated with Low-Density Lipoprotein Cholesterol Levels and the Risk of Diabetes Mellitus: A Mendelian Randomization Study.
International journal of molecular sciences 2022 9 23 (18): . Hsu Lung-An, Teng Ming-Sheng, Wu Semon, Chou Hsin-Hua, Ko Yu-L |
| Genetic Testing Enables the Diagnosis of Familial Hypercholesterolemia Underdiagnosed by Clinical Criteria: Analysis of Japanese Early-Onset Coronary Artery Disease Patients. Cardiology research and practice 2023 5 2023 2236422. Hiroshi Miyama, Yoshinori Katsumata, Mizuki Momoi, Genki Ichihara, Taishi Fujisawa, Jin Endo, Takashi Kawakami, Masaharu Kataoka, Shinsuke Yuasa, Motoaki Sano, Kazuki Sato, Keiichi Fuku |
| 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 |
| Association of genetic variants related to combined lipid-lowering and antihypertensive therapies with risk of cardiovascular disease: 2?×?2 factorial Mendelian randomization analyses. BMC medicine 2024 5 22 (1): 201. Ying Li, Hongwei Liu, Chong Shen, Jianxin Li, Fangchao Liu, Keyong Huang, Dongfeng Gu, Yun Li, Xiangfeng |
| Effect of the PCSK9 R46L genetic variant on plasma insulin and glucose levels, risk of diabetes mellitus and cardiovascular disease: A meta-analysis. Nutrition, metabolism, and cardiovascular diseases : NMCD 2024 5 . Sen Liu, Jindong Wan, Dan Wang, Yi Yang, Jie Fang, Tao Luo, Dengpan Liang, Jun Hu, Jixin Hou, Peijian Wa |
| Association of lipid-lowering drugs with the risk of type 2 diabetes and its complications: a mendelian randomized study. Diabetology & metabolic syndrome 2024 10 16 (1): 240. Yue-Yang Zhang, Bing-Xue Chen, Qin W |
- Page last reviewed:Feb 1, 2024
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