Lingling Hu

Analysis of human upstream open reading frames and impact on gene expression

Lingling Hu, Zhenhai Zhang, Haoli Li, 2015, Human Genetics.

Novel loss-of-function PRRT2 mutation causes paroxysmal kinesigenic dyskinesia in a Han Chinese family

Lingling Hu, J. Xiong, Quanxi Su, 2014, BMC Neurology.

Two novel copy number variations involving the α-globin gene cluster on chromosome 16 cause thalassemia in two Chinese families

Decheng Cai, Yidan Liang, Lingling Hu, 2016, Molecular Genetics and Genomics.

MALDI-TOF-MS for Rapid Screening and Typing of β-Globin Variant and β-Thalassemia through Direct Measurements of Intact Globin Chains.

Tizhen Yan, S. Zou, Yan Li, 2022, Clinical chemistry.

Analysis of human upstream open reading frames and impact on gene expression

Zhenhai Zhang, Haoli Li, Yuhua Ye, 2015, Human Genetics.

Mutation in SSUH2 Causes Autosomal‐Dominant Dentin Dysplasia Type I

Qiuxia Yu, Lingling Hu, Xiangmin Xu, 2017, Human mutation.

A splicing mutation in VPS4B causes dentin dysplasia I

Wanjun Zhou, Jinzhong Liu, Yuhua Ye, 2016, Journal of Medical Genetics.