Qiong Zhang

发表

Evaluation of VEGFA gene variants for possible roles in cerebral infarction diseases

Jié Zhou, Shu-Lin Liu, Chunji Zhu, 2019 .

Characterization of soluble N-ethylmaleimide-sensitive factor attachment protein receptor gene STX18 variations for possible roles in congenital heart diseases.

Rui Cheng, Shu-Lin Liu, Xia Li, 2017, Gene.

Autosomal Dominant Congenital Nuclear Cataracts Caused by a CRYAA Gene Mutation

Meng Zhang, Xu Ma, Si-quan Zhu, 2010, Current eye research.

RBPJ polymorphisms associated with cerebral infarction diseases in Chinese Han population

Jié Zhou, Shu-Lin Liu, Hong Lei, 2018, Medicine.

Structural Genomic Analysis of SARS-CoV-2 and Other Coronaviruses

Fei Li, Qiong Zhang, Yaowen Zhang, 2022, Frontiers in Genetics.

Perceptions towards online learning among medical students during the COVID-19 pandemic

P. Ma, Xiangru Liu, Yue Li, 2023, Heliyon.

Identification of two novel critical mutations in PCNT gene resulting in microcephalic osteodysplastic primordial dwarfism type II associated with multiple intracranial aneurysms

Shu-Lin Liu, Xudong Wang, Fei-feng Li, 2015, Metabolic Brain Disease.

Different effection of p.1125Val>Ala and rs11954856 in APC on Wnt signaling pathway

Xiao-ning Zhang, Chang-hao Sun, Xi-shan Wang, 2017, Oncotarget.

Comparative analysis of SARS-CoV-2 and its receptor ACE2 with evolutionarily related coronaviruses

Shu-Lin Liu, Fei-feng Li, Qiong Zhang, 2020, Aging.

Identification of two novel critical mutations in PCNT gene resulting in microcephalic osteodysplastic primordial dwarfism type II associated with multiple intracranial aneurysms

Shu-Lin Liu, Xudong Wang, Fei-feng Li, 2015, Metabolic Brain Disease.