Ruen Yao
14PUBLICATIONS
37CO-AUTHORS
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Publications (14)
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|Aug 28, 2025
Combined Genetic and Transcriptional Study Unveils the Role of DGAT1 Gene Mutations in Congenital Diarrhea.Jingqing Zeng, Jing Ma, Lan Wang
|Apr 30, 2025
Focusing on Rare Variants Related to Maturity-Onset Diabetes of the Young in Children.Yu Ding, Qianwen Zhang, Shiyang Gao
|Oct 05, 2024
Pharmacokinetic, Pharmacodynamic and Pharmacogenetic Studies Related to Vincristine-Induced Peripheral Neuropathy in Chinese Pediatric ALL Patients.Yawen Yuan, Wenting Hu, Changcheng Chen
|Jul 20, 2023
A novel heterozygous variant of FOXJ1 in a Chinese female with primary ciliary dyskinesia and hydrocephalus: A case report and literature review.Shiyang Gao, Qianwen Zhang, Biyun Feng
|Dec 23, 2022
Assessment of Rare Genetic Variants to Identify Candidate Modifier Genes Underlying Neurological Manifestations in Neurofibromatosis 1 Patients.Jie Tang, Niu Li, Guoqiang Li
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