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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 6 (of 6 Records)

Query Trace: Disease and SIK3[original query]
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
Amerindian-specific regions under positive selection harbour new lipid variants in Latinos. GWAS Catalog
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
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,
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
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
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
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