Results 281 to 290 of about 771,775 (343)

Genetic association of long non-coding RNA ANRIL polymorphism with the risk of type 2 diabetes mellitus in the Chinese Han population. [PDF]

Diabetol Metab Syndr
Li X, Yang A, Liu X, Zhang R, Zhou H, Xu S.   +5 more
europepmc   +1 more source

LncRNA RNF144A-AS1 gene polymorphisms and their influence on lung cancer patients in the Chinese Han population. [PDF]

Noncoding RNA Res
Wu H, Xie Y, Li A, Liu X, Guo L, Wu F, Yang Z, Zhang Z, Zhang X.   +8 more
europepmc   +1 more source

Association of ADAMTS-5 gene polymorphisms with the susceptibility to knee osteoarthritis in a Chinese Han population. [PDF]

J Orthop Surg Res
Gao S, Jia M, Wang J, Sun Q, Liu F, Yu L, Guo Y, Li N, Wei L.   +8 more
europepmc   +1 more source

Associations Between Serum IL-17A, Renal Function and Diabetic Retinopathy in Type 2 Diabetes Mellitus: Evidence From a Chinese Han Population. [PDF]

Endocrinol Diabetes Metab
Wang W, Huang Y, Shen J, Jin L, Chen Z.
europepmc   +1 more source

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Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus

Nature Genetics, 2009
Jian-Wen Han, Houfeng Zheng, Yong Cui, Liangdan Sun, D. Ye, Zhilin Hu, Jin-hua Xu, Z. Cai, Wei Huang, Guoping Zhao, Hong-Fu Xie, H. Fang, Q. Lu, Jian-hua Xu, Xiang-Pei Li, Yun-feng Pan, D. Deng, F. Zeng, Zhi‐zhong Ye, Xiao-Yan Zhang, Qing-Wen Wang, Fei Hao, Li Ma, X. Zuo, F. Zhou, W. Du, Yi-lin Cheng, Jian-Qiang Yang, Song-ke Shen, Jian Li, Y. Sheng, Xiaowei Zuo, Weidong Zhu, F. Gao, Pei-lian Zhang, Qing Guo, Bo Li, Min Gao, F. Xiao, C. Quan, Chi Zhang, Zheng Zhang, K. Zhu, Yang Li, D. Hu, Wen-sheng Lu, Jian-lin Huang, Sheng-Xiu Liu, Hui Li, Yunqing Ren, Zaixing Wang, Chun-Jun Yang, Peiguang Wang, Wen Zhou, Y. Lv, An-Sheng Zhang, Shengquan Zhang, Da Lin, Y. Li, H. Low, M. Shen, Z. Zhai, Ying Wang, Feng-yu Zhang, Sen Yang, Jian-jun Liu, Xuejun Zhang   +66 more
semanticscholar   +3 more sources

DNA-based eyelid trait prediction in Chinese Han population

International Journal of Legal Medicine, 2021
The eyelid folding represents one of the most distinguishing features of East Asian faces, involving the absence or presence of the eyelid crease, i.e., single vs. double eyelid. Recently, a genome-wide association study (GWAS) identified two SNPs (rs12570134 and rs1415425) showing genome-wide significant association with the double eyelid phenotype in
Qian Wang, Bo Jin, Fan Liu, Zhilong Li, Yu Tan, Weibo Liang, Feijun Huang   +6 more
openaire   +2 more sources

The evaluation of seven age-related CpGs for forensic purpose in blood from Chinese Han population.

Forensic Science International: Genetics, 2020
Age prediction of biological samples is one of the important tasks in forensic DNA phenotyping, and DNA methylation is regarded as the most promising biomarker for forensic age prediction.
Chao Pan, S. Yi, Chao Xiao, Yujie Huang, Xiaoying Chen, Daixin Huang   +5 more
semanticscholar   +1 more source

Prevalence of BRCA1/BRCA2 pathogenic variation in Chinese Han population

Journal of Medical Genetics, 2020
Background Pathogenic variation in BRCA1 and BRCA2 (BRCA) is one of the most frequent genetic predispositions for hereditary breast cancer. The identification of the variant carriers plays an important role in prevention and treatment of cancer.
Hui Dong, Khyati Chandratre, Yu’e Qin, Jing Zhang, Xiao-Jian Tian, Ce Rong, Ning Wang, Maoni Guo, Guoping Zhao, S. Wang   +9 more
semanticscholar   +1 more source

Apolipoprotein E and longevity among Han Chinese population

Mechanisms of Ageing and Development, 1998
The apolipoprotein E gene (APOE), which locates on chromosome 19, has three common APOE alleles encoding APOE*2, APOE*3, APOE*4. It has been considered to be closely associated with human longevity among Western population. However, the allele frequency varies among racial and ethnic groups.
Z, Jian-Gang, M, Yong-Xing, W, Chuan-Fu, L, Pei-Fang, Z, Song-Bai, G, Nui-Fan, F, Guo-Yin, H, Lin   +7 more
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Spinocerebellar ataxia type 11 in the Chinese Han population

Neurological Sciences, 2009
The spinocerebellar ataxias (SCAs) are a clinically and genetically heterogeneous group of neurodegenerative diseases. Researchers have recently found that SCA type 11 (SCA11) is associated with mutations in the TTBK2 gene. In our previous work, we performed mutation detection in SCA1, 2, 3, 6, 7, 8, 10, 12, 17 and dentatorubral-pallidoluysian atrophy ...
Qian, Xu, Xiaohui, Li, Junling, Wang, JiPing, Yi, Lifang, Lei, Lu, Shen, Hong, Jiang, Kun, Xia, Qian, Pan, Beisha, Tang   +9 more
openaire   +2 more sources