Areas of Focus
- Identification and molecular mechanisms of genetic pathogenic factors in cardiovascular and respiratory diseases
Work Experience
- 2019-present - Central South University, School of Life Sciences - Distinguished Associate Professor
Academic Background & Achievements
- 2009-2013 Bachelor in Life Sciences, Central South University
- 2013-2019 Master-PhD in Cell Biology, Central South University
- Joint training at Cleveland Medical Center, USA and University of Connecticut Medical School, USA
Publications
- Increased RTN3 Leads to Obesity and Hypertriglyceridemia by Interacting with HSPA5, Xiang R, Fan L L, Huang H, et al., 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, et al., 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, et al., 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, et al., 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, et al., 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, et al., 2018
- Novel mutations of low-density lipoprotein receptor gene in China patients with familial hypercholesterolemia, Fan L L, Lin M, Chen Y, et al., 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, et al., 2017
- Whole-exome sequencing identifies two novel TTN mutations in Chinese families with dilated cardiomyopathy, Liu J S, Fan L L, Zhang H, et al., 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, et al., 2018
