Human Genome Epidemiology Literature Finder
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Records 1 - 19 (of 19 Records) |
| Query Trace: Disease and SLC22A12[original query] |
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Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations.
PLoS genetics 2009 Jun 5 (6): e1000504. Kolz Melanie, Johnson Toby, Sanna Serena, Teumer Alexander, Vitart Veronique, Perola Markus, Mangino Massimo, Albrecht Eva, Wallace Chris, Farrall Martin, Johansson Asa, Nyholt Dale R, Aulchenko Yurii, Beckmann Jacques S, Bergmann Sven, Bochud Murielle, Brown Morris, Campbell Harry, , Connell John, Dominiczak Anna, Homuth Georg, Lamina Claudia, McCarthy Mark I, , Meitinger Thomas, Mooser Vincent, Munroe Patricia, Nauck Matthias, Peden John, Prokisch Holger, Salo Perttu, Salomaa Veikko, Samani Nilesh J, Schlessinger David, Uda Manuela, Völker Uwe, Waeber Gérard, Waterworth Dawn, Wang-Sattler Rui, Wright Alan F, Adamski Jerzy, Whitfield John B, Gyllensten Ulf, Wilson James F, Rudan Igor, Pramstaller Peter, Watkins Hugh, , Doering Angela, Wichmann H-Erich, , Spector Tim D, Peltonen Leena, Völzke Henry, Nagaraja Ramaiah, Vollenweider Peter, Caulfield Mark, , Illig Thomas, Gieger Christi |
| Common polymorphisms influencing serum uric acid levels contribute to susceptibility to gout, but not to coronary artery disease. PloS one 2009 4 (11): e7729. Stark Klaus, Reinhard Wibke, Grassl Martina, Erdmann Jeanette, Schunkert Heribert, Illig Thomas, Hengstenberg Christi |
| Genetic impact on uric acid concentration and hyperuricemia in the Japanese population. Journal of atherosclerosis and thrombosis 2012 Dec . Takeuchi F, Yamamoto K, Isono M, Katsuya T, Akiyama K, Ohnaka K, Rakugi H, Yamori Y, Ogihara T, Takayanagi R, Kato N |
| Absence of the SLC22A12 gene mutation in Turkish population with primary gout disease. Rheumatology international 2012 Nov . Yakut S, Cetin Z, Arman M, Akbas H, Manguoglu AE, Luleci G |
| Genetic variability related to serum uric acid concentration and risk of Parkinson's disease. Movement disorders : official journal of the Movement Disorder Society 2013 Oct 28 (12): 1737-40. González-Aramburu Isabel, Sánchez-Juan Pascual, Jesús Silvia, Gorostidi Ana, Fernández-Juan Eduardo, Carrillo Fátima, Sierra María, Gómez-Garre Pilar, Cáceres-Redondo María T, Berciano José, Ruiz-Martínez Javier, Combarros Onofre, Mir Pablo, Infante J |
| Serum uric acid and risk of dementia in Parkinson's disease. Parkinsonism & related disorders 2014 Jun 20 (6): 637-9. González-Aramburu Isabel, Sánchez-Juan Pascual, Sierra María, Fernández-Juan Eduardo, Sánchez-Quintana Coro, Berciano José, Combarros Onofre, Infante J |
| Polymorphisms in GCKR, SLC17A1 and SLC22A12 were associated with phenotype gout in Han Chinese males: a case-control study. BMC medical genetics 2015 16 (1): 66. Zhou Zhao-Wei, Cui Ling-Ling, Han Lin, Wang Can, Song Zhi-Jian, Shen Jia-Wei, Li Zhi-Qiang, Chen Jian-Hua, Wen Zu-Jia, Wang Xiao-Min, Shi Yong-Yong, Li Chang-G |
| Analysis of ABCG2 and other urate transporters in uric acid homeostasis in chronic kidney disease: potential role of remote sensing and signaling. Clinical kidney journal 2016 Jun 9 (3): 444-53. Bhatnagar Vibha, Richard Erin L, Wu Wei, Nievergelt Caroline M, Lipkowitz Michael S, Jeff Janina, Maihofer Adam X, Nigam Sanjay |
| Genome-wide association analysis identifies multiple loci associated with kidney disease-related traits in Korean populations.
PloS one 2018 13 (3): e0194044. Lee Jeonghwan, Lee Young, Park Boram, Won Sungho, Han Jin Suk, Heo Nam |
| Large-scale whole-exome sequencing association studies identify rare functional variants influencing serum urate levels. Nature communications 2018 10 9 (1): 4228. Tin Adrienne, Li Yong, Brody Jennifer A, Nutile Teresa, Chu Audrey Y, Huffman Jennifer E, Yang Qiong, Chen Ming-Huei, Robinson-Cohen Cassianne, Macé Aurélien, Liu Jun, Demirkan Ay?e, Sorice Rossella, Sedaghat Sanaz, Swen Melody, Yu Bing, Ghasemi Sahar, Teumer Alexanda, Vollenweider Peter, Ciullo Marina, Li Meng, Uitterlinden André G, Kraaij Robert, Amin Najaf, van Rooij Jeroen, Kutalik Zoltán, Dehghan Abbas, McKnight Barbara, van Duijn Cornelia M, Morrison Alanna, Psaty Bruce M, Boerwinkle Eric, Fox Caroline S, Woodward Owen M, Köttgen An |
| Refining genome-wide associated loci for serum uric acid in individuals with African ancestry.
Human molecular genetics 2020 Feb 29 (3): 506-514. Chen Guanjie, Shriner Daniel, Doumatey Ayo P, Zhou Jie, Bentley Amy R, Lei Lin, Adeyemo Adebowale, Rotimi Charles |
| Polygenic analysis of the effect of common and low-frequency genetic variants on serum uric acid levels in Korean individuals.
Scientific reports 2020 Jun 10 (1): 9179. Cho Sung Kweon, Kim Beomsu, Myung Woojae, Chang Yoosoo, Ryu Seungho, Kim Han-Na, Kim Hyung-Lae, Kuo Po-Hsiu, Winkler Cheryl A, Won Hong-H |
| Causal Associations of Urate With Cardiovascular Risk Factors: Two-Sample Mendelian Randomization. Frontiers in genetics 2021 12 687279. Lukkunaprasit Thitiya, Rattanasiri Sasivimol, Ongphiphadhanakul Boonsong, McKay Gareth J, Attia John, Thakkinstian Ammar |
| Genetic epidemiological analysis of hypouricaemia from 4993 Japanese on non-functional variants of URAT1/SLC22A12 gene. Rheumatology (Oxford, England) 2021 7 61 (3): 1276-1281. Nakayama Akiyoshi, Kawamura Yusuke, Toyoda Yu, Shimizu Seiko, Kawaguchi Makoto, Aoki Yuka, Takeuchi Kenji, Okada Rieko, Kubo Yoko, Imakiire Toshihiko, Iwasawa Satoko, Nakashima Hiroshi, Tsunoda Masashi, Ito Keiichi, Kumagai Hiroo, Takada Tappei, Ichida Kimiyoshi, Shinomiya Nariyoshi, Matsuo Hirota |
| The Epidemiology and Genetics of Hyperuricemia and Gout across Major Racial Groups: A Literature Review and Population Genetics Secondary Database Analysis. Journal of personalized medicine 2021 4 11 (3): . Butler Faven, Alghubayshi Ali, Roman Youss |
| Renal Hypouricemia 1: Rare Disorder as Common Disease in Eastern Slovakia Roma Population. Biomedicines 2021 11 9 (11): . Stiburkova Blanka, Bohatá Jana, Pavelcová Kate?ina, Tasic Velibor, Plaseska-Karanfilska Dijana, Cho Sung-Kweon, Poto?naková Ludmila, Šaligová Ja |
| Polymorphisms of the genes ABCG2, SLC22A12 and XDH and their relation with hyperuricemia and hypercholesterolemia in Mexican young adults. F1000Research 2021 10 10 217. Vargas-Morales Juan Manuel, Guevara-Cruz Martha, Aradillas-García Celia, G Noriega Lilia, Tovar Armando, Alegría-Torres Jorge Alejand |
| GLUT9 as a potential drug target for chronic kidney disease: Drug target validation by a Mendelian randomization study. Journal of human genetics 2023 6 . Masatoshi Ueda, Kenji Fukui, Naoyuki Kamatani, Shigeo Kamitsuji, Akira Matsuo, Tomohiko Sasase, Jun Nishiu, Mutsuyoshi Matsushi |
| Ischemic stroke susceptibility associated with ALPK1 single nucleotide polymorphisms by inhibiting URAT1 in uric acid hemostasis. Gene 2024 10 934 149017. Luying Qiu, Xiaoqin Lu, Weishuang Xue, Hefei Fu, Shumin Deng, Long Li, Meilin Chen, Yanzhe Wa |
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