Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 78 Records) |
Query Trace: SLC22A12[original query] |
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Variants of ALPK1 with ABCG2, SLC2A9, and SLC22A12 increased the positive predictive value for gout. Journal of human genetics 2017 Nov . Tu Hung-Pin, Min-Shan Ko Albert, Lee Su-Shin, Lee Chi-Pin, Kuo Tzer-Min, Huang Chung-Ming, Ko Ying-Ch |
Long-term effects of the SLC2A9 G844A and SLC22A12 C246T variants on serum uric acid concentrations in children. BMC pediatrics 2018 09 18 (1): 296. Lee Hye Ah, Park Bo Hyun, Park Eun Ae, Cho Su Jin, Kim Hae Soon, Park Hyeso |
Prevalence of hyperuricemia among the Chinese population of the southeast coastal region and association with single nucleotide polymorphisms in urate?anion exchanger genes: SLC22A12, ABCG2 and SLC2A9. Molecular medicine reports 2018 Jul . Yang Xinran, Xiao Yingxiu, Liu Kaixi, Jiao Xiaoyang, Lin Xiaozhe, Wang Yongni, Zhang Qiaox |
A heterozygous variant in the SLC22A12 gene in a Sri Lanka family associated with mild renal hypouricemia. BMC pediatrics 2018 7 18 (1): 210. Vidanapathirana Dinesha Maduri, Jayasena Subashinie, Jasinge Eresha, Stiburkova Blan |
[Association between SLC22A12 rs1529909 and rs7929627 polymorphism and hyperuricemia]. Wei sheng yan jiu = Journal of hygiene research 2017 Jul 46 (4): 589-594. Zhang Yadi, Zhang Fandi, Zhao Li, Du Jiancai, Wang Yun, Guo Zhongq |
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 |
Uromodulin in a Pathway Between Decreased Renal Urate Excretion and Albuminuria. American journal of hypertension 2019 Mar 32 (4): 384-392. Krajcoviechova Alena, Marois-Blanchet Francois-Christophe, Troyanov Stephan, Harvey Francois, Dumas Pierre, Tremblay Johanne, Cifkova Renata, Awadalla Philip, Madore Francois, Hamet Pav |
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 |
Associations between the SLC22A12 gene and gout susceptibility: a meta-analysis. Clinical and experimental rheumatology 2018 Jan . Zou Yao, Du Jinfeng, Zhu Yantong, Xie Xi, Chen Jinwei, Ling Guangh |
The association between genotypes of urate transporter-1, Serum uric acid, and mortality in the community-based population: the Yamagata (Takahata) Study. Clinical and experimental nephrology 2019 Sep . Kon Soichiro, Konta Tsuneo, Ichikawa Kazunobu, Watanabe Masafumi, Sato Hidenori, Ishizawa Kenichi, Ueno Yoshiyuki, Yamashita Hidetoshi, Kayama Takama |
Amplicon targeted resequencing for SLC2A9 and SLC22A12 identified novel mutations in hypouricemia subjects. Molecular genetics & genomic medicine 2019 May e722. Zhou Zhaowei, Wang Ke, Zhou Juan, Wang Can, Li Xinde, Cui Lingling, Han Lin, Liu Zhen, Ren Wei, Wang Xuefeng, Zhang Keke, Li Zhiqiang, Pan Dun, Li Changgui, Shi Yongyo |
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 |
Contribution of SLC22A12 on hypouricemia and its clinical significance for screening purposes. Scientific reports 2019 Oct 9 (1): 14360. Cha Do Hyeon, Gee Heon Yung, Cachau Raul, Choi Jong Mun, Park Daeui, Jee Sun Ha, Ryu Seungho, Kim Kyeong Kyu, Won Hong-Hee, Limou Sophie, Myung Woojae, Winkler Cheryl A, Cho Sung Kwe |
Polymorphisms of ABCG2 and SLC22A12 Genes Associated with Gout Risk in Vietnamese Population. Medicina (Kaunas, Lithuania) 2019 1 55 (1): . Duong Nguyen Thuy, Ngoc Nguyen Thy, Thang Nguyen Tran Minh, Phuong Bach Thi Hoai, Nga Nguyen Thanh, Tinh Nguyen Doan, Quynh Do Hai, Ton Nguyen Dang, Hai Nong V |
Evaluation of the Influence of Genetic Variants of SLC2A9 (GLUT9) and SLC22A12 (URAT1) on the Development of Hyperuricemia and Gout. Journal of clinical medicine 2020 8 9 (8): . Pavelcova Katerina, Bohata Jana, Pavlikova Marketa, Bubenikova Eliska, Pavelka Karel, Stiburkova Blan |
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 |
A population-specific low-frequency variant of SLC22A12 (p.W258*) explains nearby genome-wide association signals for serum uric acid concentrations among Koreans.
PloS one 2020 15 (4): e0231336. Im Sun-Wha, Chae Jeesoo, Son Ho-Young, Cho Belong, Kim Jong-Il, Park Jin- |
ABCG2 rs2231142 variant in hyperuricemia is modified by SLC2A9 and SLC22A12 polymorphisms and cardiovascular risk factors in an elderly community-dwelling population. BMC medical genetics 2020 3 21 (1): 54. Liu Jia, Yang Wei, Li Yun, Wei Zhanyun, Dan Xiaoju |
Contribution of Rare Variants of the SLC22A12 Gene to the Missing Heritability of Serum Urate Levels. Genetics 2020 Jan . Misawa Kazuharu, Hasegawa Takanori, Mishima Eikan, Jutabha Promsuk, Ouchi Motoshi, Kojima Kaname, Kawai Yosuke, Matsuo Masafumi, Anzai Naohiko, Nagasaki Mas |
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 |
Correction to: Genetic Association Between SLC22A12 Variants and Susceptibility to Hyperuricemia:A Meta-Analysis by Zhen et al. Genet Test Mol Biomarkers 2022;26(2):81-95; DOI: 10.1089/gtmb.2021.0175. Genetic testing and molecular biomarkers 2022 4 26 (4): 249. Authors are not available |
Genetic Association Between SLC22A12 Variants and Susceptibility to Hyperuricemia: A Meta-Analysis. Genetic testing and molecular biomarkers 2022 2 26 (2): 81-95. Zheng Qu, Keliang Wu, Hongtao Qiu, Xiaosheng L |
The impact of genetic variability in urate transporters on oxypurinol pharmacokinetics. Clinical and translational science 2022 11 . Hishe Hailemichael Z, Stocker Sophie L, Stamp Lisa K, Dalbeth Nicola, Merriman Tony R, Phipps-Green Amanda, Wright Daniel F |
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 |
Pathogenic Variants of SLC22A12 (URAT1) and SLC2A9 (GLUT9) in Spanish Patients with Renal Hypouricemia: Founder Effect of SLC2A9 Variant c.374C>T; p.(T125M). International journal of molecular sciences 2023 5 24 (9): . Ana Perdomo-Ramirez, Elizabeth Cordoba-Lanus, Carmen Jane Trujillo-Frias, Carolina Gonzalez-Navasa, Elena Ramos-Trujillo, Maria Isabel Luis-Yanes, Victor Garcia-Nieto, Felix Claverie-Martin, |
Genotype and Phenotype of Renal Hypouricemia: A Single-Center Study from China. Molecular diagnosis & therapy 2023 11 . Lijun Mou, Lina Zhu, Xujiao Chen, Ying Hu, Hong Zhu, Ying |
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- Page last updated:Mar 25, 2024
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