Professor | Liangliang Fan | Asia Growth Partners

Name	Liangliang Fan
Contact Information	swfanliangliang@csu.edu.cn
Language ability	English, Chinese
Province	Hunan

Name

Liangliang Fan

Contact Information

swfanliangliang@csu.edu.cn

Language ability

English, Chinese

Province

Hunan

University/Lab Affiliation and Title	Central South University
Faculty	Life Sciences
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
Work Experience	2019-present - Central South University, School of Life Sciences - Distinguished Associate Professor

University/Lab Affiliation and Title

Central South University

Faculty

Life Sciences

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

Work Experience

2019-present - Central South University, School of Life Sciences - Distinguished Associate Professor

Areas of Focus	Identification and molecular mechanisms of genetic pathogenic factors in cardiovascular and respiratory diseases
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

Areas of Focus

Identification and molecular mechanisms of genetic pathogenic factors in cardiovascular and respiratory diseases

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

Cardiovascular Diseases Respiratory Diseases Genetic Factors Pathogenic Molecular Mechanisms Identification Research Endoplasmic Reticulum Mitochondria Cellular Organelles

Gao Liangcai - East China Normal University

Zhang Wei - East China Normal University

Ke Tie - Huazhong University of Science and Technology

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