Human Genome Epidemiology Literature Finder
Records 1 - 15 (of 15 Records) |
Query Trace: SIK3[original query] |
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A replication study of GWAS-derived lipid genes in Asian Indians: the chromosomal region 11q23.3 harbors loci contributing to triglycerides. PloS one 2012 7 (5): e37056. Braun Timothy R, Been Latonya F, Singhal Akhil, Worsham Jacob, Ralhan Sarju, Wander Gurpreet S, Chambers John C, Kooner Jaspal S, Aston Christopher E, Sanghera Dharambir |
Salt-inducible kinase 3, SIK3, is a new gene associated with hearing.
Human molecular genetics 2014 Dec 23 (23): 6407-18. Wolber Lisa E, Girotto Giorgia, Buniello Annalisa, Vuckovic Dragana, Pirastu Nicola, Lorente-Cánovas Beatriz, Rudan Igor, Hayward Caroline, Polasek Ozren, Ciullo Marina, Mangino Massimo, Steves Claire, Concas Maria Pina, Cocca Massilimiliano, Spector Tim D, Gasparini Paolo, Steel Karen P, Williams Frances M |
Amerindian-specific regions under positive selection harbour new lipid variants in Latinos.
Nature communications 2014 Jun 5 3983. Ko Arthur, Cantor Rita M, Weissglas-Volkov Daphna, Nikkola Elina, Reddy Prasad M V Linga, Sinsheimer Janet S, Pasaniuc Bogdan, Brown Robert, Alvarez Marcus, Rodriguez Alejandra, Rodriguez-Guillen Rosario, Bautista Ivette C, Arellano-Campos Olimpia, Muñoz-Hernández Linda L, Salomaa Veikko, Kaprio Jaakko, Jula Antti, Jauhiainen Matti, Heliövaara Markku, Raitakari Olli, Lehtimäki Terho, Eriksson Johan G, Perola Markus, Lohmueller Kirk E, Matikainen Niina, Taskinen Marja-Riitta, Rodriguez-Torres Maribel, Riba Laura, Tusie-Luna Teresa, Aguilar-Salinas Carlos A, Pajukanta Päi |
Multiple susceptibility loci at chromosome 11q23.3 are associated with plasma triglyceride in East Asians. Journal of lipid research 2015 Dec . Gombojav Bayasgalan, Lee Soo Ji, Kho Minjung, Song Yun-Mi, Lee Kayoung, Sung Jooh |
Genetic variants in SERPINA4 and SERPINA5, but not BCL2 and SIK3 are associated with acute kidney injury in critically ill patients with septic shock. Critical care (London, England) 2017 Mar 21 (1): 47. Vilander Laura M, Kaunisto Mari A, Vaara Suvi T, Pettilä Ville, |
Genetic variants and acute kidney injury: A review of the literature. Journal of critical care 2017 Nov 44 203-211. Larach Daniel B, Engoren Milo C, Schmidt Ellen M, Heung Micha |
Identification of female-specific genetic variants for metabolic syndrome and its component traits to improve the prediction of metabolic syndrome in females.
BMC medical genetics 2019 Jun 20 (1): 99. Kong Sokanha, Cho Yoon Sh |
Association of BUD13-ZNF259-APOA5-APOA1-SIK3 cluster polymorphism in 11q23.3 and structure of APOA5 with increased plasma triglyceride levels in a Korean population. Scientific reports 2019 Jun 9 (1): 8296. Kim Han-Kyul, Anwar Muhammad Ayaz, Choi Sangd |
Whole Exome Sequencing of Ulcerative Colitis-associated Colorectal Cancer Based on Novel Somatic Mutations Identified in Chinese Patients. Inflammatory bowel diseases 2019 2 25 (8): 1293-1301. Yan Pengguang, Wang Yanan, Meng Xiangchen, Yang Hong, Liu Zhanju, Qian Jiaming, Zhou Weixun, Li Jingn |
Quantitative and Qualitative Role of Antagonistic Heterogeneity in Genetics of Blood Lipids.
The journals of gerontology. Series A, Biological sciences and medical sciences 2020 Sep 75 (10): 1811-1819. Kulminski Alexander M, Loika Yury, Nazarian Alireza, Culminskaya Iri |
Salt-Inducible Kinase 3 Haplotypes Associated with Noise-Induced Hearing Loss in Chinese Workers. Audiology & neuro-otology 2020 Mar 1-9. Yin Haoyang, Guo Jiadi, Ding Enmin, Zhang Hengdong, Han Lei, Zhu Bao |
Contribution of APOA5, APOC3, CETP, ABCA1 and SIK3 genetic variants to hypertriglyceridemia development in Mexican HIV-patients receiving antiretroviral therapy. Pharmacogenetics and genomics 2021 Oct . Bautista-Martínez Jonathan Saúl, Mata-Marín José Antonio, Sandoval-Ramírez Jorge Luis, Chaparro-Sánchez Alberto, Manjarrez-Téllez Bulmaro, Uribe-Noguez Luis Antonio, Gaytán-Martínez Jesús, Núñez-Armendáriz Mireya, Cruz-Sánchez Arcenio, Núñez-Rodríguez Nohemí, Iván Martínez-Abarca, Morales-González Georgina Selene, Álvarez-Mendoza Juan Pablo, Pérez-Barragán Edgar, Ríos-De Los Ríos Jussara, Contreras-Chávez Gerson Gabriel, Tapia-Magallanes Denisse Marielle, Ribas-Aparicio Rosa Maria, Díaz-López Mónica, Olivares-Labastida Azucena, Gómez-Delgado Alejandro, Torres Javier, Miranda-Duarte Antonio, Zenteno Juan C, Pompa-Mera Ericka Nel |
A whole-exome case-control association study to characterize the contribution of rare coding variation to pancreatic cancer risk. HGG advances 2022 Jan 3 (1): 100078. Yu Yao, Chang Kyle, Chen Jiun-Sheng, Bohlender Ryan J, Fowler Jerry, Zhang Di, Huang Maosheng, Chang Ping, Li Yanan, Wong Justin, Wang Huamin, Gu Jian, Wu Xifeng, Schildkraut Joellen, Cannon-Albright Lisa, Ye Yuanqing, Zhao Hua, Hildebrandt Michelle A T, Permuth Jennifer B, Li Donghui, Scheet Paul, Huff Chad |
A Genome-Wide Association Study of Metabolic Syndrome in the Taiwanese Population. Nutrients 2024 1 16 (1): . Chih-Yi Ho, Jia-In Lee, Shu-Pin Huang, Szu-Chia Chen, Jiun-Hung Ge |
Interactions of genetic variations in FAS, GJB2 and PTPRN2 are associated with noise-induced hearing loss: a case-control study in China. BMC medical genomics 2024 1 17 (1): 18. Shan Wu, Zhidan Wu, Manlian Chen, Xiangbin Zhong, Haoyan Gu, Wenjing Du, Weidong Liu, Li Lang, Junyi Wa |
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- Page last updated:Mar 25, 2024
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