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Your search keyword '"Guo, Xuejiang"' showing total 5 results
Start Over Author "Guo, Xuejiang" Journal nature genetics
5 results on '"Guo, Xuejiang"'

3. A genome-wide association study identifies two risk loci for congenital heart malformations in Han Chinese populations

Author

Hu, Zhibin, primary, Shi, Yongyong, additional, Mo, Xuming, additional, Xu, Jing, additional, Zhao, Bijun, additional, Lin, Yuan, additional, Yang, Shiwei, additional, Xu, Zhengfeng, additional, Dai, Juncheng, additional, Pan, Shandong, additional, Da, Min, additional, Wang, Xiaowei, additional, Qian, Bo, additional, Wen, Yang, additional, Wen, Juan, additional, Xing, Jinliang, additional, Guo, Xuejiang, additional, Xia, Yankai, additional, Ma, Hongxia, additional, Jin, Guangfu, additional, Yu, Shiqiang, additional, Liu, Jiayin, additional, Zhou, Zuomin, additional, Wang, Xinru, additional, Chen, Yijiang, additional, Sha, Jiahao, additional, and Shen, Hongbing, additional

Published
2013
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4. A genome-wide association study in Chinese men identifies three risk loci for non-obstructive azoospermia

Author

Hu, Zhibin, primary, Xia, Yankai, additional, Guo, Xuejiang, additional, Dai, Juncheng, additional, Li, HongGang, additional, Hu, Hongliang, additional, Jiang, Yue, additional, Lu, Feng, additional, Wu, Yibo, additional, Yang, Xiaoyu, additional, Li, Huizhang, additional, Yao, Bing, additional, Lu, Chuncheng, additional, Xiong, Chenliang, additional, Li, Zheng, additional, Gui, Yaoting, additional, Liu, Jiayin, additional, Zhou, Zuomin, additional, Shen, Hongbing, additional, Wang, Xinru, additional, and Sha, Jiahao, additional

Published
2011
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5. A genome-wide association study in Chinese men identifies three risk loci for non-obstructive azoospermia.

Author

Hu, Zhibin, Xia, Yankai, Guo, Xuejiang, Dai, Juncheng, Li, HongGang, Hu, Hongliang, Jiang, Yue, Lu, Feng, Wu, Yibo, Yang, Xiaoyu, Li, Huizhang, Yao, Bing, Lu, Chuncheng, Xiong, Chenliang, Li, Zheng, Gui, Yaoting, Liu, Jiayin, Zhou, Zuomin, Shen, Hongbing, and Wang, Xinru

Subjects
MALE infertility, MALE reproductive organ diseases, HUMAN genetic variation, CHINESE people, PLOIDY
Abstract

Non-obstructive azoospermia (NOA) is one of the most severe forms of male infertility. Its pathophysiology is largely unknown, and few genetic influences have been defined. To identify common variants contributing to NOA in Han Chinese men, we performed a three-stage genome-wide association study of 2,927 individuals with NOA and 5,734 controls. The combined analyses identified significant (P < 5.0 × 10?8) associations between NOA risk and common variants near PRMT6 (rs12097821 at 1p13.3: odds ratio (OR) = 1.25, P = 5.7 × 10?10), PEX10 (rs2477686 at 1p36.32: OR = 1.39, P = 5.7 × 10?12) and SOX5 (rs10842262 at 12p12.1: OR = 1.23, P = 2.3 × 10?9). These findings implicate genetic variants at 1p13.3, 1p36.32 and 12p12.1 in the etiology of NOA in Han Chinese men. [ABSTRACT FROM AUTHOR]

Published
2012
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