教育经历

2009.9-2013.6  伟德BETVLCTOR1946/生命科学/本科

2013.9-2019.6  伟德BETVLCTOR1946/细胞生物学/硕博连读

2017.10-20.8.4  美国克里夫兰医学中心/联合培养

2018.5-2019.1  美国康涅狄格大学医学院/联合培养

工作经历

2019.6-至今 伟德BETVLCTOR1946/特聘副教授

研究方向

研究重点关注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，从人-小鼠-线虫-细胞多层次探索内质网、线粒体等细胞器在心血管疾病和呼吸系统疾病中的作用。目前，以第一作者在Circulation, Chemistry and Laboratory Medicine, Journal of Human Genetics 等发表SCI论文十余篇。

代表性论文

1. Xiang R, Fan L L, Huang H, et al. Increased RTN3 Leads to Obesity and Hypertriglyceridemia by Interacting with HSPA5[J]. Circulation, 2018: 138(17):1828-1838.（共同第一）

2. Fan L L, Ding D B, Huang H, et al. A de novo mutation of SMYD1 (p. F272L) is responsible for hypertrophic cardiomyopathy in a Chinese patient[J]. Clinical Chemistry and Laboratory Medicine (CCLM), 2019, 57(4): 532-539.

3. Ding D B, Fan L L, Xiao Z, et al. A novel mutation of dipeptidyl aminopeptidase-like protein-6 in a family with suspicious idiopathic ventricular fibrillation[J]. QJM: An International Journal of Medicine, 2018, 111(6): 373-377.（共同第一）

4. Fan L L, Chen Y Q, Huang H, et al. Exome sequencing identifies a novel nonsense mutation of Ring Finger Protein 207 in a Chinese family with Long QT syndrome and syncope[J]. Journal of human genetics, 2019, 64(3): 233.

5. Liu J S, Fan L L, Li J J, et al. Whole-exome sequencing identifies a novel mutation of desmocollin 2 in a Chinese family with arrhythmogenic right ventricular cardiomyopathy[J]. The American journal of cardiology, 2017, 119(9): 1485-1489. （共同第一）

6. Fan L L, Huang H, Jin J Y, et al. Whole exome sequencing identifies a novel mutation (c. 333+ 2T> C) of TNNI3K in a Chinese family with dilated cardiomyopathy and cardiac conduction disease[J]. Gene, 2018, 648: 63-67.

7. Fan L L, Lin M, Chen Y, et al. Novel mutations of low-density lipoprotein receptor gene in China patients with familial hypercholesterolemia[J]. Applied biochemistry and biotechnology, 2015, 176(1): 101-109.

8. Fan L L, Liu J S, Huang H, et al. Whole exome sequencing identified a novel mutation (p. Ala1884Pro) of β‐spectrin in a Chinese family with hereditary spherocytosis[J]. The Journal of Gene Medicine, e3073.

 9. Liu J S, Fan L L, Zhang H, et al. Whole-exome sequencing identifies two novel TTN mutations in Chinese families with dilated cardiomyopathy[J]. Cardiology, 2017, 136(1): 10-14. （共同第一）

10. Fan L L, Huang H, Jin J Y, et al. Whole Exome Sequencing identifies a Novel Mutation (p.L320R) of Actinin Alpha 2 in a Chinese Family with Dilated Cardiomyopathy and Ventricular Tachycardia. (Online, Cytogenetic and Genome Research)