- [1] 刘奇迹. A functional polymorphism in the SPINK5 gene is associated with asthma in a Chinese Han Populatio.... BMC Medical Genetics, 10, 2009.
- [2] . Generation of an iPSC line (SDQLCHi015-A) from peripheral blood mononuclear cells of a patient wi.... 41, 2019.
- [3] 龚瑶琴. Ablation of ORMDL3 impairs adipose tissue thermogenesis and insulin sensitivity by increasing cer.... MOLECULAR METABOLISM, 101423, 2022.
- [4] 赵晓晗. Zebrafish cul4a, but not cul4b, modulates cardiac and forelimb development by upregulating tbx5a .... Human Molecular Genetics, 24, 853-864, 2015.
- [5] 毛飞. Identification and Functional Analysis of a SLC33A1: c.339T > G (p.Ser113Arg) Variant in the O.... HUMAN MUTATION, 240-249, 2015.
- [6] 龙逢. An iPS cell line SDUBMSi0011-A from a multiple epiphyseal dysplasia patient carrying c. 1076T > G.... STEM CELL RESEARCH, 53, 2021.
- [7] 段若楠. Smek1 deficiency exacerbates experimental autoimmune encephalomyelitis by activating proinflammat.... JOURNAL OF NEUROINFLAMMATION, 18, 2021.
- [8] 李妍. Generation of an induced pluripotent stem cell line SDUBMSi005-A from a patient with double prima.... STEM CELL RESEARCH, 53, 2021.
- [9] 刘晓林. Establishment of patient-specific induced pluripotent stem cell line SDUBMSi009-A from a patient .... STEM CELL RESEARCH, 51, 2021.
- [10] 段若楠. A De Novo Frameshift Mutation in TNFAIP3 Impairs A20 Deubiquitination Function to Cause Neuropsyc.... 40, 1062, 2020.
- [11] 汪小晶. Generation of a human induced pluripotent stem cell line (SDUBMSi001-A) from a hereditary spastic.... 43, 2020.
- [12] 龙逢. A SMOC2 variant inhibits BMP signaling by competitively binding to BMPR1B and causes growth plate.... 142, 2021.
- [13] 汪小晶. Generation of a human induced pluripotent stem cell line (SDUMSi001-A) from a hereditary spastic .... stem cell research, 2020.
- [14] 龚瑶琴 and 刘奇迹. Novel deletion of SPAST in a Chinese family with hereditary spastic paraplegia. Singapore Med J, 54, 251, 2013.
- [15] 党洁. ORMDL3 Facilitates the Survival of Splenic B Cells via an ATF6 alpha-Endoplasmic Reticulum Stress.... Journal of Immunology, 199, 1647, 2017.
- [16] 龚瑶琴 , 李江夏 and 刘奇迹. Evidence for genetic association of CARD9 and SNAPC4 with ankylosing spondylitis in a Chinese Han.... Journal of Rheumatology, 2014.
- [17] 刘奇迹. Gene-gene interactions of IRF5, STAT4, IKZF1 and ETS1 in systemic lupus erythematosus.. Tissue Antigens, 83, 401, 2014.
- [18] 邵常顺 , 李江夏 and 刘奇迹. Exome sequencing reveals a heterozygous DLX5 mutation in a Chinese family with autosomal-dominant.... European Journal of Human Genetics, 2014.
- [19] 龚瑶琴 , 李江夏 and 刘奇迹. ETS1 variants confer susceptibility to ankylosing spondylitis in Han Chinese.. Arthritis Research & Therapy, 16, 2014.
- [20] 李曦 , 孙文杰 , 李江夏 and 袁倩倩. WDFY4 Is Involved in Symptoms of Systemic Lupus Erythematosus by Modulating B Cell Fate via Nonca.... Journal of Immunology, 201, 2570, 2018.