刘奇迹教授
刘奇迹，男，1970年出生，山东寿光人。山东大学教授，博士研究生导师，医学遗传学系主任，齐鲁医学院副院长，实验畸形学教育部重点实验室副主任, 山东省医学会医学遗传与优生学会主任委员，山东省干细胞学会副会长，山东省遗传学会常务理事，中华医学会医学遗传学分会青年委员，山东省中青年重点科技人才。主要研究方向为遗传病致病基因的发现及分子机制研究。 More+
- [21] 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.
- [22] 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.
- [23] 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.
- [24] 王梅天. Nongenetic Optical Modulation of Neural Stem Cell Proliferation and Neuronal/Glial Differentiatio.... BIOMATERIALS Journal, 225, 119539, 2019.
- [25] 段若楠. A De Novo Frameshift Mutation in TNFAIP3 Impairs A20 Deubiquitination Function to Cause Neuropsyc.... 2019.
- [26] 刘铎 , 李曦 , 刘巧 , 孙文杰 , 李江夏 , 龚瑶琴 , 杨坤 Exposure to blue light stimulates the proangiogenic capability of exosomes derived from human umb.... 10, 2019.
- [27] 龚瑶琴 , 刘奇迹 and Saadi, Ahlem. Ankylosing spondylitis: analysis of gene-gene interactions between IL-12 beta, JAK2, and STAT3 in.... CENTRAL EUROPEAN JOURNAL OF IMMUNOLOGY, 44, 65, 2019.
- [28] 孙文杰 , 刘奇迹 and 关景云. Generation of an iPSC line (SDQLCHi015-A) from peripheral blood mononuclear cells of a patient wi.... stem cell research, 2019.
- [29] 龚瑶琴 , 高贵敏 , 邵常顺 , 刘奇迹 and 胡慧丽. A Missense Mutation in SLC33A1, which Encodes the Acetyl-CoA Transporter, Causes Autosomal-Domina.... Am J Hum Genet., 83, 752, 2008.
- [30] 龚瑶琴 , 刘奇迹 and 邵常顺. Prenatal diagnosis of autosomal dominant hereditary spastic paraplegia (SPG42) caused by SLC33A1 .... Prenat Diagn., 30, 485, 2010.
- [31] 龚瑶琴 and 刘奇迹. A functional polymorphism in the SPINK5 gene is associated with asthma in a Chinese Han Populatio.... BMC Med Genet., 10, 1, 2009.
- [32] 龚瑶琴 , 刘奇迹 and 邵常顺. A novel deletion mutation in GJB1 causes X-linked Charcot-Marie-Tooth disease in a Han Chinese fa.... Muscle Nerve., 42, 922, 2014.
- [33] 龚瑶琴 , 蒋百春 , 邹永新 , 高贵敏 , 陈丙玺 and 刘奇迹. Sp1 and CREB regulate basal transcription of the human SNF2L gene.. Biochem Biophys Res Commun., 368, 438, 2008.
- [34] 龚瑶琴 , 周海滨 , 高贵敏 , 陈丙玺 , 刘奇迹 and 邵常顺. Serum withdrawal up-regulates human SIRT1 gene expression in a p53-dependent manner.. J Cell Mol Med., 13, 4176, 2009.
- [35] 龚瑶琴 , 邵常顺 , 刘奇迹 , 李江夏 and 蒋百春. Whole-exome Sequencing Identifies a Variant in TMEM132E Causing Autosomal-Recessive Nonsyndromic .... Hum Mutat, 36, 98, 2015.
- [36] 龚瑶琴 and 刘奇迹. Association of common polymorphisms in the LRP6 gene with sporadic coronary artery disease in a C.... CHINESE MEDICAL JOURNAL, 125, 444, 2012.
- [37] 龚瑶琴 , 刘奇迹 , 邵常顺 and 孙文杰. Identification and Functional Analysis of a SLC33A1: c.339T>G (p.Ser113Arg) Variant in the Origin.... Hum Mutat, 36, 240, 2015.
- [38] 龚瑶琴 , 蒋百春 , 胡慧丽 , 刘奇迹 and 邵常顺. Zebrafish cul4a, but not cul4b, modulates cardiac and forelimb development by upregulating tbx5a .... Hum Mol Genet., 24, 853, 2015.
- [39] 刘奇迹 and 李江夏. Gene-gene interaction of ATG5, ATG7, BLK and BANK1 in systemic lupus erythematosus.. International Journal of Rheumatic Disease, 2016.
- [40] 刘奇迹 , 邵常顺 , 李江夏 , 蒋百春 and 龚瑶琴. Whole-exome Sequencing Identifies a Variant in TMEM132E Causing Autosomal-Recessive Nonsyndromic.... Hum Mutat, 36, 98, 2015.