Jiangxia Li, Ph.D
Telephone: 86-531-88382190
E-mail: lijiangxia@sdu.edu.cn
Education
July 2010: Ph.D, Medical Genetics, School of Medicine, Shandong University
July. 2001, Master of Science, Medical Genetics, School of Medicine, Shandong University
July, 1998, Bachelor of Medicine, Shandong Medical University
Professional Experience
2015.09-present：Associate Professor, Department of Genetics, Shandong University
2003.12-2015.08：Lecturer, Department of Genetics, Shandong University
2006.6-2006.12: Visiting Scholar,University of California, Irvine
2001.7-2003.12: Instructor, Department of Genetics, Shandong University
Research Interests：
Identification and function analysis of the genes responsible for inherited diseases.
Selected Publications（＊Correspondence）：
1. Yuan Q, Li Y,Li J, Bian X, Long F, Duan R, Ma X, Gao F, Gao S, Wei S, Li X, Sun W, Liu Q*.WDFY4 Is Involved in Symptoms of Systemic Lupus Erythematosus by Modulating B Cell Fate via Noncanonical Autophagy. J Immunol. 2018 Nov 1;201(9):2570-257
2. Bian X, Lin P,Li J, Long F, Duan R, Yuan Q, Li Y, Gao F, Gao S, Wei S, Li X, Sun W, Gong Y, Yan C, Liu Q*. Whole-Genome Linkage Analysis with Whole-Exome Sequencing Identifies a Novel Frameshift Variant in NEFH in a Chinese Family with Charcot-Marie-Tooth 2: A Novel Variant in NEFH for Charcot-Marie-Tooth. Neurodegener Dis. 2018;18(2-3):74-83.
3. Dang J, Bian X, Ma X,Li J, Long F, Shan S, Yuan Q, Xin Q, Li Y, Gao F, Gong Y, Liu Q. ORMDL3 Facilitates the Survival of Splenic B Cells via an ATF6α-Endoplasmic Reticulum Stress-Beclin1 Autophagy Regulatory Pathway.J Immunol. 2017 Sep 1;199(5):1647-1659
4. Li J, Zhao X, Xin Q, Shan S, Jiang B, Jin Y, Yuan H, Dai P, Xiao R, Zhang Q, Xiao J, Shao C, Gong Y*, Liu Q*.Whole-Exome Sequencing Identifies a Variant in TMEM132E Causing Autosomal-Recessive Nonsyndromic Hearing Loss DFNB99.Hum Mutat.2015;36(1):98-105
5. Li J,Yang Y, Jiang B, Zhang X, Zou Y, Gong Y.Sp1 and KLF15 regulate basal transcription of the human LRP5 gene.BMC Genet. 2010 Feb 8;11:12.
6. Shan S, Dang J,Li J,Yang Z, Zhao H, Xin Q, Ma X, Liu Y, Bian X, Gong Y, Liu Q*.ETS1 variants confer susceptibility to ankylosing spondylitis in Han Chinese.Arthritis Res Ther. 2014 Apr 4;16(2):R87.
7. Wang X, Xin Q,Li L,Li J, Zhang C, Qiu R, Qian C, Zhao H, Liu Y, Shan S, Dang J, Bian X, Shao C, Gong Y, Liu Q*.Exome sequencing reveals a heterozygous DLX5 mutation in a Chinese family with autosomal-dominant split-hand/foot malformation.Eur J Hum Genet.2014 Sep;22(9):1105-10.
8. Liu Y, Zhang H,Li J,Zhao H, Xin Q, Shan S, Dang J, Bian X, Liu Q.Association of common variants in KIF21B and ankylosing spondylitis in a Chinese Han population: a replication study.Immunogenetics. 2013 Dec;65(12):835-9.
9. Wang X, Li L,Li J, Sun J, Heng X, Gong Y, Liu Q.Pathogenic gene screening and mutation detection in a Chinese family with multiple osteochondroma.Genet Test Mol Biomarkers. 2012 Jul;16(7):827-32.
10. Xin Q, Li L,Li J, Qiu R, Guo C, Gong Y, Liu Q.Eight-alanine duplication in homeobox D13 in a Chinese family with synpolydactyly.Gene. 2012 May 10;499(1):48-51.
11. Zhang X, Liu Q, Chen B, Guo C,Li J, Gao G, Guo Y, Gong Y.A locus for nonspecific X-linked mental retardation mapped to a 22.3 cM region of Xp11.3-q22.3.Am J Med Genet A. 2004 Sep 1;129A(3):286-9.
12. Lu Y, Guo C, Liu Q, Zhang X, Cheng L,Li J,Chen B, Gao G, Zhou H, Guo Y, Li Y, Gong Y.A novel mutation of keratin 9 in epidermolytic palmoplantar keratoderma combined with knuckle pads.Am J Med Genet A. 2003 Jul 30;120A(3):345-9
