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Parkinsonism & Related Disorders|November 6, 2016
SMPD1 variants in Chinese Han patients with sporadic Parkinson's diseaseCheng-Yuan Mao, Jing Yang, Hui Wang, et al.Frontiers in Genetics|September 3, 2019
Prenatal Diagnosis of Fetuses With Increased Nuchal Translucency by Genome Sequencing AnalysisKwong Wai Choy, Huilin Wang, Mengmeng Shi, et al.Diagnostics (Basel, Switzerland)|June 12, 2026
Prenatal-Onset Recessive Titinopathies: Clinical Spectrum, Genotype-Phenotype Correlations, and OutcomesYu Zheng, Mengmeng Shi, Yilin Zhao, et al.Cell Reports. Medicine|November 20, 2024
Autologous transplantation of P63+ lung progenitor cells in patients with bronchiectasis: A randomized, single-blind, controlled trialJiayang Yan, Weipan Zhang, Yun Feng, et al.Stroke and Vascular Neurology|December 9, 2021
Genome sequencing reveals the role of rare genomic variants in Chinese patients with symptomatic intracranial atherosclerotic diseaseMengmeng Shi, Xinyi Leng, Ying Li, et al.Chinese Medical Journal|July 13, 2022
A trial of arbidol hydrochloride in adults with COVID-19Jingya Zhao, Jinnong Zhang, Yang Jin, et al.Pageof 9