Lin Yang

ORCID

Publication Activity (10 Years)

Years Active: 2019-2021
Publications (10 Years): 5

Top Venues

Clinical genetics

Human mutation

Journal of medical genetics

BMC medical genetics

Children's Hospital of Fudan University (PHD)

This page only lists publications with an associated author ORCID identifier.

Education History

Children's Hospital of Fudan University

China

PHD

Publications

Lin Yang, Zejun Wei, Xiang Chen, Liyuan Hu, Xiaomin Peng, Jin Wang, Chunmei Lu, Yanting Kong, Xinran Dong, Qi Ni, Yulan Lu, Bingbing Wu, Huijun Wang, Katia Meirelles, Xia Tian, Jing Zhang, Fengqi Chang, Liu Liu, Changhua Li, Wesley You, Guoqiang Cheng, Laishuan Wang, Yun Cao, Chao Chen, Ping Fang, Sha Tang, Wen-Hao Zhou
Use of medical exome sequencing for identification of underlying genetic defects in NICU: Experience in a cohort of 2303 neonates in China. Clinical genetics 101 (1) (2021)
Huijun Wang, Feifan Xiao, Xinran Dong, Yulan Lu, Guoqiang Cheng, Laishuan Wang, Wei Lu, Lin Yang, Liping Chen, Wenqing Kang, Long Li, Xinnian Pan, Qiufen Wei, Deyi Zhuang, Dongmei Chen, Zhaoqing Yin, Ling Yang, Qi Ni, Renchao Liu, Gang Li, Ping Zhang, Yanyan Qian, Xu Li, Xiaomin Peng, Yao Wang, Fang Liu, Dahui Wang, Hao Li, Chun Shen, Liling Qian, Yun Cao, Bingbing Wu, Wen-Hao Zhou
Diagnostic and clinical utility of next-generation sequencing in children born with multiple congenital anomalies in the China neonatal genomes project. Human mutation 42 (4) (2021)
Lin Yang, Xiang Chen, Xu Liu, Xinran Dong, Chang Ye, Dongli Deng, Yulan Lu, Yifeng Lin, Wen-Hao Zhou
Clinical features and underlying genetic causes in neonatal encephalopathy: A large cohort study. Clinical genetics 98 (4) (2020)
Xinran Dong, Bo Liu, Lin Yang, Huijun Wang, Bingbing Wu, Renchao Liu, Hongbo Chen, Xiang Chen, Sha Yu, Bin Chen, Sujuan Wang, Xiu Xu, Wenhao Zhou, Yulan Lu
Clinical exome sequencing as the first-tier test for diagnosing developmental disorders covering both CNV and SNV: a Chinese cohort. Journal of medical genetics 57 (8) (2020)
Xiang Chen, Kai Yan, Yanyan Gao, Huijun Wang, Guoqiang Chen, Bingbing Wu, Qian Qin, Lin Yang, Wenhao Zhou
Feeding difficulty is the dominant feature in 12 Chinese newborns with CHD7 pathogenic variants. BMC medical genetics 20 (1) (2019)

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Publication Activity (10 Years)

Top Topics

Top Venues

Lin Yang