Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 63 Records) |
Query Trace: TRIB1[original query] |
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Monozygotic twins with NASH cirrhosis: cumulative effect of multiple single nucleotide polymorphisms? Annals of hepatology 0 15 (2): 277-82. Grove Jane I, Austin Mark, Tibble Jeremy, Aithal Guruprasad P, Verma Sumi |
Meta-analysis of lipid-traits in Hispanics identifies novel loci, population-specific effects, and tissue-specific enrichment of eQTLs.
Scientific reports 2016 Jan 6 19429. Below Jennifer E, Parra Esteban J, Gamazon Eric R, Torres Jason, Krithika S, Candille Sophie, Lu Yingchang, Manichakul Ani, Peralta-Romero Jesus, Duan Qing, Li Yun, Morris Andrew P, Gottesman Omri, Bottinger Erwin, Wang Xin-Qun, Taylor Kent D, Ida Chen Y-D, Rotter Jerome I, Rich Stephen S, Loos Ruth J F, Tang Hua, Cox Nancy J, Cruz Miguel, Hanis Craig L, Valladares-Salgado Ad |
A microsatellite repeat in PCA3 long non-coding RNA is associated with prostate cancer risk and aggressiveness. Scientific reports 2017 Dec 7 (1): 16862. Lai John, Moya Leire, An Jiyuan, Hoffman Andrea, Srinivasan Srilakshmi, Panchadsaram Janaththani, Walpole Carina, Perry-Keene Joanna L, Chambers Suzanne, , Lehman Melanie L, Nelson Colleen C, Clements Judith A, Batra Jyots |
Identification of seven novel loci associated with amino acid levels using single-variant and gene-based tests in 8545 Finnish men from the METSIM study.
Human molecular genetics 2018 2 27 (9): 1664-1674. Teslovich Tanya M, Kim Daniel Seung, Yin Xianyong, Stancáková Alena, Jackson Anne U, Wielscher Matthias, Naj Adam, Perry John R B, Huyghe Jeroen R, Stringham Heather M, Davis James P, Raulerson Chelsea K, Welch Ryan P, Fuchsberger Christian, Locke Adam E, Sim Xueling, Chines Peter S, Narisu Narisu, Kangas Antti J, Soininen Pasi, , Ala-Korpela Mika, Gudnason Vilmundur, Musani Solomon K, Jarvelin Marjo-Riitta, Schellenberg Gerard D, Speliotes Elizabeth K, Kuusisto Johanna, Collins Francis S, Boehnke Michael, Laakso Markku, Mohlke Karen |
Intensive genetic analysis for Chinese patients with very high triglyceride levels: Relations of mutations to triglyceride levels and acute pancreatitis. EBioMedicine 2018 Dec 38 171-177. Jin Jing-Lu, Sun Di, Cao Ye-Xuan, Zhang Hui-Wen, Guo Yuan-Lin, Wu Na-Qiong, Zhu Cheng-Gang, Gao Ying, Dong Qiu-Ting, Liu Geng, Dong Qian, Li Jian-J |
Association Analysis of a Microsatellite Repeat in the TRIB1 Gene With Prostate Cancer Risk, Aggressiveness and Survival. Frontiers in genetics 2018 10 9 428. Moya Leire, Lai John, Hoffman Andrea, Srinivasan Srilakshmi, Panchadsaram Janaththani, Chambers Suzanne, Clements Judith A, Batra Jyotsna, |
TRIB1 rs17321515 gene polymorphism increases the risk of coronary heart disease in general population and non-alcoholic fatty liver disease patients in Chinese Han population. Lipids in health and disease 2019 Aug 18 (1): 165. Liu Qun, Liu Shou-Sheng, Zhao Zhen-Zhen, Zhao Ben-Tian, Du Shui-Xian, Jin Wen-Wen, Xin Yong-Ni |
Associations for BCO2, PCSK9, and TR1B1 Polymorphism and Lifestyle Factors with Ischemic Stroke: A Nested Case-Control Study. Yonsei medical journal 2019 Jul 60 (7): 659-666. Zhao Tian Yu, Li Zheng, Lei Song, Huang Liu, Yang L |
RAD51B (rs8017304 and rs2588809), TRIB1 (rs6987702, rs4351379, and rs4351376), COL8A1 (rs13095226), and COL10A1 (rs1064583) Gene Variants with Predisposition to Age-Related Macular Degeneration. Disease markers 2019 2019 5631083. Vilkeviciute Alvita, Kriauciuniene Loresa, Chaleckis Romanas, Deltuva Vytenis Pranas, Liutkeviciene Ra |
TRIB1 rs17321515 and rs2954029 gene polymorphisms increase the risk of non-alcoholic fatty liver disease in Chinese Han population. Lipids in health and disease 2019 Mar 18 (1): 61. Liu Qun, Xue Feng, Meng Jing, Liu Shou-Sheng, Chen Li-Zhen, Gao Hui, Geng Ning, Jin Wen-Wen, Xin Yong-Ning, Xuan Shi-Yi |
TRIB1 and TRPS1 variants, G?×?G and G?×?E interactions on serum lipid levels, the risk of coronary heart disease and ischemic stroke. Scientific reports 2019 Feb 9 (1): 2376. Zhang Qing-Hui, Yin Rui-Xing, Chen Wu-Xian, Cao Xiao-Li, Wu Jin-Zh |
Genetic polymorphisms associated with nonalcoholic fatty liver disease in Uyghur population: a case-control study and meta-analysis. Lipids in health and disease 2019 Jan 18 (1): 14. Cai Wen, Weng Di-Hua, Yan Ping, Lin Yu-Ting, Dong Zheng-Hui, Mailamuguli , Yao H |
Do TRIB1 and IL-9 Gene Polymorphisms Impact the Development and Manifestation of Pituitary Adenoma? In vivo (Athens, Greece) 0 34 (5): 2499-2505. Mickevicius Tomas, Vilkeviciute Alvita, Glebauskiene Brigita, Kriauciuniene Loresa, Liutkeviciene Ra |
Validating a non-invasive, ALT-based non-alcoholic fatty liver phenotype in the million veteran program. PloS one 2020 15 (8): e0237430. Serper Marina, Vujkovic Marijana, Kaplan David E, Carr Rotonya M, Lee Kyung Min, Shao Qing, Miller Donald R, Reaven Peter D, Phillips Lawrence S, O'Donnell Christopher J, Meigs James B, Wilson Peter W F, Vickers-Smith Rachel, Kranzler Henry R, Justice Amy C, Gaziano John M, Muralidhar Sumitra, Pyarajan Saiju, DuVall Scott L, Assimes Themistocles L, Lee Jennifer S, Tsao Philip S, Rader Daniel J, Damrauer Scott M, Lynch Julie A, Saleheen Danish, Voight Benjamin F, Chang Kyong-Mi, |
Interaction between Coffee Drinking and TRIB1 rs17321515 Single Nucleotide Polymorphism on Coronary Heart Disease in a Taiwanese Population. Nutrients 2020 May 12 (5): . Liu Yin-Tso, Tantoh Disline Manli, Wang Lee, Nfor Oswald Ndi, Hsu Shu-Yi, Ho Chien-Chang, Lung Chia-Chi, Chang Horng-Rong, Liaw Yung- |
Bile acids profile, histopathological indices and genetic variants for non-alcoholic fatty liver disease progression. Metabolism: clinical and experimental 2020 Dec 154457. Nimer Nisreen, Choucair Ibrahim, Wang Zeneng, Nemet Ina, Li Lin, Gukasyan Janet, Weeks Taylor L, Alkhouri Naim, Zein Nizar, Tang W H Wilson, Fischbach Michael A, Brown J Mark, Allayee Hooman, Dasarathy Srinivasan, Gogonea Valentin, Hazen Stanley |
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Nature metabolism 2020 10 2 (10): 1135-1148. Folkersen Lasse, Gustafsson Stefan, Wang Qin, Hansen Daniel Hvidberg, Hedman Åsa K, Schork Andrew, Page Karen, Zhernakova Daria V, Wu Yang, Peters James, Eriksson Niclas, Bergen Sarah E, Boutin Thibaud S, Bretherick Andrew D, Enroth Stefan, Kalnapenkis Anette, Gådin Jesper R, Suur Bianca E, Chen Yan, Matic Ljubica, Gale Jeremy D, Lee Julie, Zhang Weidong, Quazi Amira, Ala-Korpela Mika, Choi Seung Hoan, Claringbould Annique, Danesh John, Davey Smith George, de Masi Federico, Elmståhl Sölve, Engström Gunnar, Fauman Eric, Fernandez Celine, Franke Lude, Franks Paul W, Giedraitis Vilmantas, Haley Chris, Hamsten Anders, Ingason Andres, Johansson Åsa, Joshi Peter K, Lind Lars, Lindgren Cecilia M, Lubitz Steven, Palmer Tom, Macdonald-Dunlop Erin, Magnusson Martin, Melander Olle, Michaelsson Karl, Morris Andrew P, Mägi Reedik, Nagle Michael W, Nilsson Peter M, Nilsson Jan, Orho-Melander Marju, Polasek Ozren, Prins Bram, Pålsson Erik, Qi Ting, Sjögren Marketa, Sundström Johan, Surendran Praveen, Võsa Urmo, Werge Thomas, Wernersson Rasmus, Westra Harm-Jan, Yang Jian, Zhernakova Alexandra, Ärnlöv Johan, Fu Jingyuan, Smith J Gustav, Esko Tõnu, Hayward Caroline, Gyllensten Ulf, Landen Mikael, Siegbahn Agneta, Wilson James F, Wallentin Lars, Butterworth Adam S, Holmes Michael V, Ingelsson Erik, Mälarstig Ande |
Association of Genetic Risk Score With NAFLD in An Ethnically Diverse Cohort. Hepatology communications 2021 Jun . Wang Jun, Conti David V, Bogumil David, Sheng Xin, Noureddin Mazen, Wilkens Lynne R, Le Marchand Loic, Rosen Hugo R, Haiman Christopher A, Setiawan Veronica Wen |
Genome-Wide Association Study of NAFLD Using Electronic Health Records.
Hepatology communications 2021 Sep . Fairfield Cameron J, Drake Thomas M, Pius Riinu, Bretherick Andrew D, Campbell Archie, Clark David W, Fallowfield Jonathan A, Hayward Caroline, Henderson Neil C, Joshi Peter K, Mills Nicholas L, Porteous David J, Ramachandran Prakash, Semple Robert K, Shaw Catherine A, Sudlow Cathie L M, Timmers Paul R H J, Wilson James F, Wigmore Stephen J, Harrison Ewen M, Spiliopoulou Athi |
Rare variant analysis in eczema identifies exonic variants in DUSP1, NOTCH4 and SLC9A4.
Nature communications 2021 11 12 (1): 6618. Grosche Sarah, Marenholz Ingo, Esparza-Gordillo Jorge, Arnau-Soler Aleix, Pairo-Castineira Erola, Rüschendorf Franz, Ahluwalia Tarunveer S, Almqvist Catarina, Arnold Andreas, , Baurecht Hansjörg, Bisgaard Hans, Bønnelykke Klaus, Brown Sara J, Bustamante Mariona, Curtin John A, Custovic Adnan, Dharmage Shyamali C, Esplugues Ana, Falchi Mario, Fernandez-Orth Dietmar, Ferreira Manuel A R, Franke Andre, Gerdes Sascha, Gieger Christian, Hakonarson Hakon, Holt Patrick G, Homuth Georg, Hubner Norbert, Hysi Pirro G, Jarvelin Marjo-Riitta, Karlsson Robert, Koppelman Gerard H, Lau Susanne, Lutz Manuel, Magnusson Patrik K E, Marks Guy B, Müller-Nurasyid Martina, Nöthen Markus M, Paternoster Lavinia, Pennell Craig E, Peters Annette, Rawlik Konrad, Robertson Colin F, Rodriguez Elke, Sebert Sylvain, Simpson Angela, Sleiman Patrick M A, Standl Marie, Stölzl Dora, Strauch Konstantin, Szwajda Agnieszka, Tenesa Albert, Thompson Philip J, Ullemar Vilhelmina, Visconti Alessia, Vonk Judith M, Wang Carol A, Weidinger Stephan, Wielscher Matthias, Worth Catherine L, Xu Chen-Jian, Lee Young- |
A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation.
Nature genetics 2022 Jun 54 (6): 761-771. Vujkovic Marijana, Ramdas Shweta, Lorenz Kim M, Guo Xiuqing, Darlay Rebecca, Cordell Heather J, He Jing, Gindin Yevgeniy, Chung Chuhan, Myers Robert P, Schneider Carolin V, Park Joseph, Lee Kyung Min, Serper Marina, Carr Rotonya M, Kaplan David E, Haas Mary E, MacLean Matthew T, Witschey Walter R, Zhu Xiang, Tcheandjieu Catherine, Kember Rachel L, Kranzler Henry R, Verma Anurag, Giri Ayush, Klarin Derek M, Sun Yan V, Huang Jie, Huffman Jennifer E, Creasy Kate Townsend, Hand Nicholas J, Liu Ching-Ti, Long Michelle T, Yao Jie, Budoff Matthew, Tan Jingyi, Li Xiaohui, Lin Henry J, Chen Yii-Der Ida, Taylor Kent D, Chang Ruey-Kang, Krauss Ronald M, Vilarinho Silvia, Brancale Joseph, Nielsen Jonas B, Locke Adam E, Jones Marcus B, Verweij Niek, Baras Aris, Reddy K Rajender, Neuschwander-Tetri Brent A, Schwimmer Jeffrey B, Sanyal Arun J, Chalasani Naga, Ryan Kathleen A, Mitchell Braxton D, Gill Dipender, Wells Andrew D, Manduchi Elisabetta, Saiman Yedidya, Mahmud Nadim, Miller Donald R, Reaven Peter D, Phillips Lawrence S, Muralidhar Sumitra, DuVall Scott L, Lee Jennifer S, Assimes Themistocles L, Pyarajan Saiju, Cho Kelly, Edwards Todd L, Damrauer Scott M, Wilson Peter W, Gaziano J Michael, O'Donnell Christopher J, Khera Amit V, Grant Struan F A, Brown Christopher D, Tsao Philip S, Saleheen Danish, Lotta Luca A, Bastarache Lisa, Anstee Quentin M, Daly Ann K, Meigs James B, Rotter Jerome I, Lynch Julie A, , , , , Rader Daniel J, Voight Benjamin F, Chang Kyong- |
Effect of Genetic Polymorphism Including NUP153 and SVEP1 on the Pharmacokinetics and Pharmacodynamics of Ticagrelor in Healthy Chinese Subjects. Clinical drug investigation 2022 May 42 (5): 447-458. Xiang Qian, Liu Zhiyan, Mu Guangyan, Xie Qiufen, Zhang Hanxu, Zhou Shuang, Wang Zining, Guo Ninghong, Huang Jie, Jiang Jie, Li Jian, Yang Guoping, Cui Yim |
Proteomics Analysis of Genetic Liability of Abdominal Aortic Aneurysm Identifies Plasma Neogenin and Kit Ligand: The ARIC Study. Arteriosclerosis, thrombosis, and vascular biology 2022 12 43 (2): 367-378. Steffen Brian T, Pankow James S, Norby Faye L, Lutsey Pamela L, Demmer Ryan T, Guan Weihua, Pankratz Nathan, Li Aixin, Liu Guning, Matsushita Kunihiro, Tin Adrienne, Tang Weiho |
Genome-wide association meta-analysis identifies 17 loci associated with nonalcoholic fatty liver disease. Nature genetics 2023 9 . Yanhua Chen, Xiaomeng Du, Annapurna Kuppa, Mary F Feitosa, Lawrence F Bielak, Jeffrey R O'Connell, Solomon K Musani, Xiuqing Guo, Bratati Kahali, Vincent L Chen, Albert V Smith, Kathleen A Ryan, Gudny Eirksdottir, Matthew A Allison, Donald W Bowden, Matthew J Budoff, John Jeffrey Carr, Yii-Der I Chen, Kent D Taylor, Antonino Oliveri, Adolfo Correa, Breland F Crudup, Sharon L R Kardia, Thomas H Mosley, Jill M Norris, James G Terry, Jerome I Rotter, Lynne E Wagenknecht, Brian D Halligan, Kendra A Young, John E Hokanson, George R Washko, Vilmundur Gudnason, Michael A Province, Patricia A Peyser, Nicholette D Palmer, Elizabeth K Speliot |
Polymorphisms of TRIB1 genes for coronary artery disease and stroke risk: A systematic review and meta-analysis. Gene 2023 7 147613. Jiangang Jiang, Xinmin Chen, Chengwei Li, Xiaoma Du, Huadong Zh |
An adult-based genetic risk score for liver fat associates with liver and plasma lipid traits in children and adolescents. Liver international : official journal of the International Association for the Study of the Liver 2023 5 . Yun Huang, Sara E Stinson, Helene Baek Juel, Morten A V Lund, Louise Aas Holm, Cilius E Fonvig, Trine Nielsen, Niels Grarup, Oluf Pedersen, Michael Christiansen, Elizaveta Chabanova, Henrik S Thomsen, Aleksander Krag, Stefan Stender, Jens-Christian Holm, Torben Hans |
Upregulation of Tribbles decreases body weight and increases sleep duration. Disease models & mechanisms 2023 4 16 (4): . Rebeka Popovic, Yizhou Yu, Nuno Santos Leal, Giorgio Fedele, Samantha H Y Loh, L Miguel Marti |
Effect of TRIB1 Variant on Lipid Profile and Coronary Artery Disease: A Systematic Review and Meta-Analysis. Cardiovascular therapeutics 2023 1 2023 4444708. Wei Baozhu, Liu Yang, Li Hang, Peng Yuanyuan, Luo Z |
PON1 rs662, rs854560 and TRIB1 rs17321515, rs2954029 Gene Polymorphisms Are Associated with Lipid Parameters in Patients with Unstable Angina. Genes 2024 7 15 (7): . Damian Malinowski, Krzysztof Safranow, Andrzej Pawl |
Exudative Age-Related Macular Degeneration: Association between Treatment Efficacy and Single-Nucleotide Variants in RAD51B, TRIB1, COL8A1, COL10A1, IL-9, IL-10, and VEGFA Genes. International journal of molecular sciences 2024 7 25 (13): . Alvita Vilkeviciute, Dzastina Cebatoriene, Loresa Kriauciuniene, Dalia Zaliuniene, Rasa Liutkevicie |
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