Professor | Xueyan Yang | Asia Growth Partners

	Upload Avatar (500 x 500)
Name	Xueyan Yang
Contact Information	xueyanyang@fudan.edu.cn
Language ability	English, Chinese
Province	Shanghai

Upload Avatar (500 x 500)

Name

Xueyan Yang

Contact Information

xueyanyang@fudan.edu.cn

Language ability

English, Chinese

Province

Shanghai

University/Lab Affiliation and Title	Fudan University
Faculty	Life Sciences
Academic Background & Achievements	1995-1999 Bachelor: Huazhong Agricultural University 1999-2005 PhD: Fudan University 2005-2008 Postdoctoral Research: University of Bath 2013-2014 Visiting Scholar: National Institute of Health (NIH)
Work Experience	2008-Present - Fudan University - Lecturer, Associate Researcher
Awards	2020: Second Prize in Shanghai and Third Prize Nationally in National College Student Biology Competition 2019: Third Prize in National University Life Sciences Microlecture Teaching Competition

University/Lab Affiliation and Title

Fudan University

Faculty

Life Sciences

Academic Background & Achievements

1995-1999 Bachelor: Huazhong Agricultural University
1999-2005 PhD: Fudan University
2005-2008 Postdoctoral Research: University of Bath
2013-2014 Visiting Scholar: National Institute of Health (NIH)

Work Experience

2008-Present - Fudan University - Lecturer, Associate Researcher

Awards

2020: Second Prize in Shanghai and Third Prize Nationally in National College Student Biology Competition
2019: Third Prize in National University Life Sciences Microlecture Teaching Competition

Areas of Focus	Genetic basis and pathogenesis of major birth defects
Publications	A mutation in TBXT causes congenital vertebral malformations in humans and mice, Chen S, Lei Y, Yang Y, Liu C, Kuang L, Jin L, Finnell RH, Yang X, Wang H, 2023 Deleterious Rare Mutations of GLI1 Dysregulate Sonic Hedgehog Signaling in Human Congenital Heart Disease, Peng R, Li B, Chen S, Shi Z, Yu L, Gao Y, Yang X, Lu L, Wang H, 2022 Rare variants in TULP3 abolish the suppressive effect on sonic hedgehog signaling and contribute to human neural tube defects, Kuang L, Jiang Y, Chen S, Su K, Peng R, Yang X, Wang H, 2021 Genetic variants of TBX6 and TBXT identified in patients with congenital scoliosis in Southern China, Feng X, Cheung JPY, Je JSH, Cheung PWH, Chen S, Yue M, Wang N, Choi VNT, Yang X, Song YQ, Luk KDK, Gao B, 2021 Rare mutations in the autophagy-regulating gene AMBRA1 contribute to human neural tube defects, Ye J, Tong Y, Lv J, Peng R, Chen S, Kuang L, Su K, Zheng Y, Zhang T, Zhang F, Jin L, Yang X, Wang H, 2020 Association between rare variants in specific functional pathways and human neural tube defects multiple subphenotypes, Zou J, Wang F, Yang X, Wang H, Niswander L, Zhang T, Li H, 2020 A functional indel polymorphism rs34396413 in TFAP2A intron-5 significantly increases female encephalocele risk in Han Chinese population, Su K, Chen S, Ye J, Kuang L, Zhang T, Wang H, Yang X*, 2019 Novel mutations of AXIN2 identified in a Chinese Congenital Heart Disease Cohort, Zhu MJ, Ma XY, Ding PC, Tang HF, Peng R, Lu L, Li PQ, Qiao B, Yang XY, Zheng YF, Wang HY, Gao YQ, Chen FS, 2019

Areas of Focus

Genetic basis and pathogenesis of major birth defects

Publications

A mutation in TBXT causes congenital vertebral malformations in humans and mice, Chen S, Lei Y, Yang Y, Liu C, Kuang L, Jin L, Finnell RH, Yang X*, Wang H*, 2023
Deleterious Rare Mutations of GLI1 Dysregulate Sonic Hedgehog Signaling in Human Congenital Heart Disease, Peng R, Li B, Chen S, Shi Z, Yu L, Gao Y, Yang X, Lu L, Wang H, 2022
Rare variants in TULP3 abolish the suppressive effect on sonic hedgehog signaling and contribute to human neural tube defects, Kuang L, Jiang Y, Chen S, Su K, Peng R, Yang X*, Wang H*, 2021
Genetic variants of TBX6 and TBXT identified in patients with congenital scoliosis in Southern China, Feng X, Cheung JPY, Je JSH, Cheung PWH, Chen S, Yue M, Wang N, Choi VNT, Yang X, Song YQ, Luk KDK, Gao B, 2021
Rare mutations in the autophagy-regulating gene AMBRA1 contribute to human neural tube defects, Ye J, Tong Y, Lv J, Peng R, Chen S, Kuang L, Su K, Zheng Y, Zhang T, Zhang F, Jin L, Yang X*, Wang H*, 2020
Association between rare variants in specific functional pathways and human neural tube defects multiple subphenotypes, Zou J, Wang F, Yang X, Wang H, Niswander L, Zhang T, Li H, 2020
A functional indel polymorphism rs34396413 in TFAP2A intron-5 significantly increases female encephalocele risk in Han Chinese population, Su K, Chen S, Ye J, Kuang L, Zhang T, Wang H, Yang X*, 2019
Novel mutations of AXIN2 identified in a Chinese Congenital Heart Disease Cohort, Zhu MJ, Ma XY, Ding PC, Tang HF, Peng R, Lu L, Li PQ, Qiao B, Yang XY, Zheng YF, Wang HY, Gao YQ, Chen FS, 2019

Genetics Birth Defects Neural Tube Defects Congenital Heart Disease Pathogenesis Mutation Genetic Research Developmental Biology Human Genetics Medical Genetics

Zhang Feng - Fudan University

Xuemin Mo - Nanjing University

Guangrong Qiu - China Medical University

View All

Personal Information

Academic Information

Research

Contact us

No account yet?

Personal Information

Academic Information

Research

Contact us