Fei-Feng Li

机构：Hubei University of Medicine · ORCID：0000-0002-7056-6101

发表论文 37 篇 · 总被引 536 次 · h-index 17

代表论文

• Characterization of Transcriptional Repressor Gene MSX1 Variations for Possible Associations with Congenital Heart Diseases (2015 · PLoS ONE · 被引 34)
• Characterization of SMAD3 Gene Variants for Possible Roles in Ventricular Septal Defects and Other Congenital Heart Diseases (2015 · PLoS ONE · 被引 28)
• Characterization of variations in IL23A and IL23R genes: possible roles in multiple sclerosis and other neuroinflammatory demyelinating diseases (2016 · Aging · 被引 23)
• Polymorphisms in the CHIT1 gene: Associations with colorectal cancer (2016 · Oncotarget · 被引 23)
• Identification of two novel critical mutations in PCNT gene resulting in microcephalic osteodysplastic primordial dwarfism type II associated with multiple intracranial aneurysms (2015 · Metabolic Brain Disease · 被引 23)
• Identification of epigenetic factor KAT2B gene variants for possible roles in congenital heart diseases (2020 · Bioscience Reports · 被引 19)