Yifei Li

A novel frameshift mutation of DVL1 ‐induced Robinow syndrome: A case report and literature review

Ruolan Hu, Y. Qiu, Yifei Li, 2022, Molecular genetics & genomic medicine.

Exome sequencing contributes to identify comorbidities in a rare case of infant ARDS induced by the CD40LG mutation

L. Qiao, Yulin Zhang, Xue Gong, 2022, BMC medical genomics.

Molecular mechanisms of endothelial dysfunction in Kawasaki-disease-associated vasculitis

Yue Zhang, Y. Hua, Yulin Zhang, 2022, Frontiers in Cardiovascular Medicine.

Invisible bronchial foreign bodies of rare small objects from living plants causing delayed diagnosis and destroyed lobes

L. Zhong, Yifei Li, Y. Qiu, 2021, Asian Journal of Surgery.

Circ_0039569 promotes renal cell carcinoma growth and metastasis by regulating miR-34a-5p/CCL22.

Wei Liu, Bai Zhao, Yakun Zhao, 2019, American journal of translational research.

Mechanism of tumor-derived extracellular vesicles in regulating renal cell carcinoma progression by the delivery of MALAT1

Wei Liu, Bai Zhao, Yakun Zhao, 2021, Oncology reports.

A rare early-onset neonatal case of Birk-Barel syndrome presenting severe obstructive sleep apnea: a case report

Fan Yang, Ruolan Hu, Yifei Li, 2023, Frontiers in Medicine.

Case report: Additional variants induced sudden cardiac death among pediatric ACM with DSG2 homozygous mutant genotype: a report of three cases

K. Zhou, Xiaoliang Liu, Lei Liu, 2024, Frontiers in genetics.