Q. Xin

发表

Gene–gene interaction of ATG5, ATG7, BLK and BANK1 in systemic lupus erythematosus

Xiaochun Ma, X. Bian, Jiangxia Li, 2016, International journal of rheumatic diseases.

Association of common variants in KIF21B and ankylosing spondylitis in a Chinese Han population: a replication study

X. Bian, Jiangxia Li, Qiji Liu, 2013, Immunogenetics.

ORMDL3 Facilitates the Survival of Splenic B Cells via an ATF6α–Endoplasmic Reticulum Stress–Beclin1 Autophagy Regulatory Pathway

Y. Gong, F. Gao, Xiaochun Ma, 2017, The Journal of Immunology.

miR-155 Deficiency Ameliorates Autoimmune Inflammation of Systemic Lupus Erythematosus by Targeting S1pr1 in Faslpr/lpr Mice

Zhaojian Liu, Y. Gong, Guangyi Liu, 2015, The Journal of Immunology.

Gene-gene interactions of IRF5, STAT4, IKZF1 and ETS1 in systemic lupus erythematosus.

H. Zhao, J. Li, X. Bian, 2014, Tissue antigens.

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.

ETS1 variants confer susceptibility to ankylosing spondylitis in Han Chinese

Y. Gong, Xiaochun Ma, Ze Yang, 2014, Arthritis Research & Therapy.

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.

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.

Novel deletion of SPAST in a Chinese family with hereditary spastic paraplegia.

Y. Gong, Qiji Liu, Q. Xin, 2013, Singapore medical journal.

Association of common variants in KIF21B and ankylosing spondylitis in a Chinese Han population: a replication study

X. Bian, Jiangxia Li, Qiji Liu, 2013, Immunogenetics.

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.

Whole‐Exome Sequencing Identifies a Variant in TMEM132E Causing Autosomal‐Recessive Nonsyndromic Hearing Loss DFNB99

Y. Gong, C. Shao, Baichun Jiang, 2015, Human mutation.