R. Qiu

发表

Association of the ANTXR2 gene polymorphism and ankylosing spondylitis in Chinese Han

H. Zhao, Q. Liu, C. Guo, 2012, Scandinavian journal of rheumatology.

Association of genetic variants in chromosome 17 q 21 and adult-onset asthma in a Chinese Han population

Y. Gong, Qiji Liu, Hailing Zhao, 2011 .

Two single nucleotide polymorphisms in TSLP gene are associated with asthma susceptibility in Chinese Han population

Qi-Ji Liu, Liang Dong, Mingjie Ding, 2012, Experimental lung research.

A missense mutation in SLC33A1, which encodes the acetyl-CoA transporter, causes autosomal-dominant spastic paraplegia (SPG42).

Huili Hu, Y. Gong, C. Shao, 2008, American journal of human genetics.

Eight-alanine duplication in homeobox D13 in a Chinese family with synpolydactyly.

Y. Gong, Jiangxia Li, Qiji Liu, 2012, Gene.

Exome sequencing reveals a heterozygous DLX5 mutation in a Chinese family with autosomal-dominant split-hand/foot malformation

Y. Gong, C. Shao, X. Bian, 2014, European Journal of Human Genetics.

ORMDL3 contributes to the risk of atherosclerosis in Chinese Han population and mediates oxidized low-density lipoprotein-induced autophagy in endothelial cells

Y. Gong, Xiaochun Ma, X. Bian, 2015, Scientific Reports.

Genetic variants on 17q21 are associated with ankylosing spondylitis susceptibility and severity in a Chinese Han population

H. Zhao, H. Zhang, Q. Liu, 2013, Scandinavian journal of rheumatology.

Signal transducer and activator of transcription 6 directly regulates human ORMDL3 expression

Y. Gong, Jiangxia Li, Qiji Liu, 2013, The FEBS journal.

An intronic variant associated with systemic lupus erythematosus changes the binding affinity of Yinyang1 to downregulate WDFY4

W. Yang, Y. Gong, Wanling Yang, 2012, Genes and Immunity.

Evidence for Genetic Association of CARD9 and SNAPC4 with Ankylosing Spondylitis in a Chinese Han Population

Y. Gong, Xiaochun Ma, Ze Yang, 2014, The Journal of Rheumatology.