Areas of Focus
- 心血管疾病和呼吸系统疾病的遗传致病因素鉴定和致病分子机理探索
Work Experience
- 2019-至今 中南大学生命科学学院/特聘副教授
Academic Background & Achievements
- 2009-2013 中南大学生命科学学院/生命科学/本科
- 2013-2019 中南大学生命科学学院/细胞生物学/硕博连读
- 美国克里夫兰医学中心/联合培养, 美国康涅狄格大学医学院/联合培养
Publications
- Increased RTN3 Leads to Obesity and Hypertriglyceridemia by Interacting with HSPA5, Xiang R, Fan L L, Huang H, 等., 2018
- A de novo mutation of SMYD1 (p. F272L) is responsible for hypertrophic cardiomyopathy in a Chinese patient, Fan L L, Ding D B, Huang H, 等., 2019
- A novel mutation of dipeptidyl aminopeptidase-like protein-6 in a family with suspicious idiopathic ventricular fibrillation, Ding D B, Fan L L, Xiao Z, 等., 2018
- Exome sequencing identifies a novel nonsense mutation of Ring Finger Protein 207 in a Chinese family with Long QT syndrome and syncope, Fan L L, Chen Y Q, Huang H, 等., 2019
- Whole-exome sequencing identifies a novel mutation of desmocollin 2 in a Chinese family with arrhythmogenic right ventricular cardiomyopathy, Liu J S, Fan L L, Li J J, 等., 2017
- Whole exome sequencing identifies a novel mutation (c. 333+ 2T> C) of TNNI3K in a Chinese family with dilated cardiomyopathy and cardiac conduction disease, Fan L L, Huang H, Jin J Y, 等., 2018
- Novel mutations of low-density lipoprotein receptor gene in China patients with familial hypercholesterolemia, Fan L L, Lin M, Chen Y, 等., 2015
- Whole exome sequencing identified a novel mutation (p. Ala1884Pro) of β‐spectrin in a Chinese family with hereditary spherocytosis, Fan L L, Liu J S, Huang H, 等., 2017
- Whole-exome sequencing identifies two novel TTN mutations in Chinese families with dilated cardiomyopathy, Liu J S, Fan L L, Zhang H, 等., 2017
- Whole Exome Sequencing identifies a Novel Mutation (p.L320R) of Actinin Alpha 2 in a Chinese Family with Dilated Cardiomyopathy and Ventricular Tachycardia, Fan L L, Huang H, Jin J Y, 等., 2018
