Association study of microRNA polymorphisms with hepatocellular carcinoma in Korean population

Gene ◽  
2012 ◽  
Vol 504 (1) ◽  
pp. 92-97 ◽  
Author(s):  
Won Hee Kim ◽  
Kyung Tae Min ◽  
Young Joo Jeon ◽  
Chang-Il Kwon ◽  
Kwang Hyun Ko ◽  
...  
Keyword(s):  
Hepatocellular Carcinoma ◽  
Association Study ◽  
Korean Population

scholarly journals Association study between polymorphisms of CD28, CTLA4 and ICOS and non-segmental vitiligo in a Korean population

2011 ◽  
Vol 2 (6) ◽  
pp. 1145-1149 ◽  
Author(s):  
MIN KYUNG SHIN ◽  
SO HEE IM ◽  
HAE JEONG PARK ◽  
SU KANG KIM ◽  
SUNG VIN YIM ◽  
...  
Keyword(s):  
Association Study ◽  
Korean Population

TNFα promoter polymorphism is a risk factor for susceptibility in hepatocellular carcinoma in Korean population

2009 ◽  
Vol 407 (1-2) ◽  
pp. 16-19 ◽  
Author(s):  
Kang Wook Jung ◽  
Eunyoung Ha ◽  
Gyeong Im Yu ◽  
Sung Jin Kim ◽  
Woo Jin Chung ◽  
...  
Keyword(s):  
Hepatocellular Carcinoma ◽  
Risk Factor ◽  
Promoter Polymorphism ◽  
Korean Population

scholarly journals Association Study between 5-HT1A Receptor Gene C(-1019)G Polymorphism and Panic Disorder in a Korean Population

2010 ◽  
Vol 7 (2) ◽  
pp. 141 ◽  
Author(s):  
Won-Seok Choi ◽  
Bun-Hee Lee ◽  
Jong-Chul Yang ◽  
Yong-Ku Kim
Keyword(s):  
Panic Disorder ◽  
Association Study ◽  
Receptor Gene ◽  
Korean Population

scholarly journals PLCG1 (Phospholipase C, gamma 1) polymorphism and the risk of hepatocellular carcinoma in a Korean population.

2008 ◽  
Vol 22 (S1) ◽  
Author(s):  
Ah‐Reum Oh ◽  
Seung Ku Lee ◽  
Hyun Jun Kang ◽  
Min ho Kim ◽  
Hyoun Geun Kim ◽  
...  
Keyword(s):  
Hepatocellular Carcinoma ◽  
Phospholipase C ◽  
Korean Population ◽  
Phospholipase C Gamma

Association study of miR-146a, miR-149, miR-196a2, and miR-499 polymorphisms with venous thromboembolism in a Korean population

2019 ◽  
Vol 47 (2) ◽  
pp. 255-262
Author(s):  
Jung Oh Kim ◽  
Hyun Woo Kim ◽  
Hui Jeong An ◽  
Ok Joon Kim ◽  
Jisu Oh ◽  
...  
Keyword(s):  
Venous Thromboembolism ◽  
Association Study ◽  
Korean Population

Association study between glutathione S-transferase P1 polymorphism and schizophrenia in the Korean population

2003 ◽  
Vol 27 (3) ◽  
pp. 519-523 ◽  
Author(s):  
Chi-Un Pae ◽  
Jung-Jin Kim ◽  
Soo-Jung Lee ◽  
Chang-Uk Lee ◽  
Chul Lee ◽  
...  
Keyword(s):  
Association Study ◽  
Korean Population ◽  
Glutathione S Transferase

scholarly journals A non-synonymous variant rs12614 of complement factor B associated with risk of chronic hepatitis B in a Korean population

2020 ◽  
Vol 21 (1) ◽  
Author(s):  
Jung Yeon Seo ◽  
Joong-Gon Shin ◽  
Byeong Ju Youn ◽  
Suhg Namgoong ◽  
Hyun Sub Cheong ◽  
...  
Keyword(s):  
Chronic Hepatitis ◽  
Hepatitis B ◽  
Association Study ◽  
Genetic Effect ◽  
Korean Population ◽  
Complement Factor ◽  
Single Nucleotide ◽  
Factor B ◽  
Synonymous Variant ◽  
Population Controls

Abstract Background Hepatitis B is known to cause several forms of liver diseases including chronic hepatitis B (CHB), and hepatocellular carcinoma. Previous genome-wide association study of CHB risk has demonstrated that rs12614 of complement factor B (CFB) was significantly associated with CHB risk. In this study, fine-mapping study of previously reported GWAS single nucleotide polymorphism (SNP; CFB rs12614) was performed to validate genetic effect of rs12614 on CHB susceptibility and identify possible additional causal variants around rs12614 in a Korean population. This association study was conducted in order to identify genetic effects of CFB single nucleotide polymorphisms (SNPs) and to identify additional independent CHB susceptible causal markers within a Korean population. Methods A total of 10 CFB genetic polymorphisms were selected and genotyped in 1716 study subjects comprised of 955 CHB patients and 761 population controls. Results A non-synonymous variant, rs12614 (Arg32Trp) in exon2 of CFB, had significant associations with risk of CHB (odds ratio = 0.43, P = 5.91 × 10− 10). Additional linkage disequilibrium and conditional analysis confirmed that rs12614 had independent genetic effect on CHB susceptibility with previously identified CHB markers. The genetic risk scores (GRSs) were calculated and the CHB patients had higher GRSs than the population controls. Moreover, OR was found to increase significantly with cumulative GRS. Conclusions rs12614 showed significant genetic effect on CHB risk within the Korean population. As such rs12614 may be used as a possible causal genetic variant for CHB susceptibility.

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