Application of Sensory Descriptive Analysis and Consumer Studies to Investigate Traditional and Authentic Foods: A Review

od Yang, Jiyun, Lee, Jeehyun
Wydane w Foods (2019)

MicroRNA-126 Inhibits Tumor Cell Growth and Its Expression Level Correlates with Poor Survival in Non-Small Cell Lung Cancer Patients

od Yang, Jiyun, Lan, Haitao, Huang, Xiaobing, Liu, Baoyu, Tong, Yu
Wydane 2012

Genetic Variant in Interleukin-18 Is Associated with Idiopathic Recurrent Miscarriage in Chinese Han Population

od Yue, Jun, Tong, Yu, Zhou, Jing, Liu, Qingqing, Yang, Jiyun
Wydane w Int J Mol Sci (2015)

Genetic variant in IL-33 is associated with idiopathic recurrent miscarriage in Chinese Han population

od Yue, Jun, Tong, Yu, Xie, Lan, Ma, Tao, Yang, Jiyun
Wydane w Sci Rep (2016)

Two novel likely pathogenic variants of HARS2 identified in a Chinese family with sensorineural hearing loss

od Yu, Jing, Jiang, Wei, Cao, Li, Na, Xiaoxue, Yang, Jiyun
Wydane w Hereditas (2020)

Identification of two novel PRPF31 mutations in Chinese families with non‐syndromic autosomal dominant retinitis pigmentosa

od Cao, Li, Peng, Chunyan, Yu, Jing, Jiang, Wei, Yang, Jiyun
Wydane w Mol Genet Genomic Med (2020)

Mutation screening of the USH2A gene in retinitis pigmentosa and USHER patients in a Han Chinese population

od Huang, Lulin, Mao, Yao, Yang, Jiyun, Li, Yuanfeng, Li, Yang, Yang, Zhenglin
Wydane w Eye (Lond) (2018)

Prenatal diagnosis of familial exudative vitreoretinopathy and Norrie disease

od Liu, Jingjing, Zhu, Jing, Yang, Jiyun, Zhang, Xiang, Zhang, Qi, Zhao, Peiquan
Wydane w Mol Genet Genomic Med (2018)

Association between TCF7L2 gene polymorphisms and susceptibility to Type 2 Diabetes Mellitus: a large Human Genome Epidemiology (HuGE) review and meta-analysis

od Tong, Yu, Lin, Ying, Zhang, Yuan, Yang, Jiyun, Zhang, Yawei, Liu, Hengchuan, Zhang, Ben
Wydane 2009

Whole-exome sequencing identifies a novel homozygous frameshift mutation in the PROM1 gene as a causative mutation in two patients with sporadic retinitis pigmentosa

od LIU, SANMEI, XIE, LAN, YUE, JUN, MA, TAO, PENG, CHUNYAN, QIU, BIYUAN, YANG, ZHENGLIN, YANG, JIYUN
Wydane w Int J Mol Med (2016)

Reinterpretation of common pathogenic variants in ClinVar revealed a high proportion of downgrades

od Xiang, Jiale, Yang, Jiyun, Chen, Lisha, Chen, Qiang, Yang, Haiyan, Sun, Chengcheng, Zhou, Qing, Peng, Zhiyu
Wydane w Sci Rep (2020)

Author Correction: Reinterpretation of common pathogenic variants in ClinVar revealed a high proportion of downgrades

od Xiang, Jiale, Yang, Jiyun, Chen, Lisha, Chen, Qiang, Yang, Haiyan, Sun, Chengcheng, Zhou, Qing, Peng, Zhiyu
Wydane w Sci Rep (2020)

Association Study of Polymorphisms in Selenoprotein Genes and Kashin–Beck Disease and Serum Selenium/Iodine Concentration in a Tibetan Population

od Huang, Lulin, Shi, Yi, Lu, Fang, Zheng, Hong, Liu, Xiaoqi, Gong, Bo, Yang, Jiyun, Lin, Ying, Cheng, Jing, Ma, Shi, Lin, He, Yang, Zhenglin
Wydane 2013

Mutation screening in genes known to be responsible for Retinitis Pigmentosa in 98 Small Han Chinese Families

od Huang, Lulin, Zhang, Qi, Huang, Xin, Qu, Chao, Ma, Shi, Mao, Yao, Yang, Jiyun, Li, You, Li, Yuanfeng, Tan, Chang, Zhao, Peiquan, Yang, Zhenglin
Wydane w Sci Rep (2017)

The essential effector SCRE1 in Ustilaginoidea virens suppresses rice immunity via a small peptide region

od Zhang, Nan, Yang, Jiyun, Fang, Anfei, Wang, Jiyang, Li, Dayong, Li, Yuejiao, Wang, Shanzhi, Cui, Fuhao, Yu, Junjie, Liu, Yongfeng, Peng, You‐Liang, Sun, Wenxian
Wydane w Mol Plant Pathol (2020)

A novel deleterious mutation in the COMP gene that causes pseudoachondroplasia

od Luo, Huaichao, Yu, Sisi, Lin, Ying, Guo, Qi, Ma, Rongchuan, Ye, Zimeng, Di, Yanan, Li, Ning, Miao, Yuanying, Zhou, Yu, Li, Yuanfeng, Yang, Jiyun, Yang, Zhenglin
Wydane w Hum Genome Var (2016)

A genome-wide scan maps a novel autosomal dominant juvenile-onset open-angle glaucoma locus to 2p15-16

od Lin, Ying, Liu, Ting, Li, Jing, Yang, Jiyun, Du, Qiong, Wang, Junfang, Yang, Yang, Liu, Xiaoqi, Fan, Yuanfu, Lu, Fang, Chen, Yilian, Pu, Yonghong, Zhang, Kang, He, Xiangge, Yang, Zhenglin
Wydane 2008

An association study of SERPING1 gene and age-related macular degeneration in a Han Chinese population

od Lu, Fang, Zhao, Peiquan, Fan, Yinchuan, Tang, Shibo, Hu, Jianbin, Liu, Xiaoqi, Yang, Xian, Chen, Yiye, Li, Tao, Lei, Chuntao, Yang, Jiyun, Lin, Ying, Ma, Shi, Li, Chunyong, Shi, Yi, Yang, Zhenglin
Wydane 2010

A Novel PRPF31 Mutation in a Large Chinese Family with Autosomal Dominant Retinitis Pigmentosa and Macular Degeneration

od Lu, Fang, Huang, Lulin, Lei, Chuntao, Sha, Guiquan, Zheng, Hong, Liu, Xiaoqi, Yang, Jiyun, Shi, Yi, Lin, Ying, Gong, Bo, Zhu, Xianjun, Ma, Shi, Qiao, Lifeng, Lin, He, Cheng, Jing, Yang, Zhenglin
Wydane 2013

Association study of genetic variants in eight genes/loci with type 2 diabetes in a Han Chinese population

od Lin, Ying, Li, Pengqiu, Cai, Li, Zhang, Ben, Tang, Xin, Zhang, Xuejun, Li, Ying, Xian, Yang, Yang, Yang, Wang, Li, Lu, Fang, Liu, Xiaoqi, Rao, Shaoqin, Chen, Ming, Ma, Shi, Shi, Yi, Bao, Mingjing, Wu, Jichuan, Yang, Yan, Yang, Jiyun, Yang, Zhenglin
Wydane 2010