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Yanling Yang

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Plos One|June 21, 2016

Ten Novel Mutations in Chinese Patients with Megalencephalic Leukoencephalopathy with Subcortical Cysts and a Long-Term Follow-Up ResearchBinbin Cao, Huifang Yan, Mangmang Guo, et al.

Scientific Reports|May 28, 2015

Exercise intolerance and developmental delay associated with a novel mitochondrial ND5 mutationHezhi Fang, Hao Shi, Xiyuan Li, et al.

Journal of Cancer|October 18, 2021

Association of dysbindin expression with individualized postoperative prognosis and chemotherapy benefit among patients with gastric adenocarcinomaHao Qian, Xiaohui Lv, Qiying Song, et al.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|May 11, 2021

[Consensus on screening, diagnosis and treatment of multiple acyl-CoA dehydrogenase deficiency]Division Of Genetics And Metabolomics Child Diseases And Health Care Branch Chinese Association For Maternal And Child Health, Xiaohong Chen, Yun Sun, et al.

Journal of Fungi (Basel, Switzerland)|February 26, 2026

Chromatin Remodeling Factor Arp8 Is Involved in the Regulation of Aflatoxin Biosynthesis and Fungal Pathogenicity of <i>Aspergillus flavus</i>Dongmei Ma, Yanfang Yao, Wenxin Luo, et al.

Zhonghua Yu Fang Yi Xue Za Zhi [Chinese Journal of Preventive Medicine]|February 3, 2016

[Analysis of the risky behaviors among HIV positive female sex workers]Jue Wang, Manhong Jia, Hongbing Luo, et al.

Frontiers in Endocrinology|March 8, 2021

Evaluation of SNA001, a Novel Recombinant Human Thyroid Stimulating Hormone Injection, in Patients With Differentiated Thyroid CarcinomaYushen Gu, Hongrong Xu, Yanling Yang, et al.

Journal of Pharmaceutical Analysis|November 10, 2025

Regulation of iron metabolism in ferroptosis: From mechanism research to clinical translationXin Zhang, Yang Xiang, Qingyan Wang, et al.

Heliyon|May 21, 2024

Association between sleep duration and serum neurofilament light chain levels among adults in the United StatesJiaxing Liang, Tengchi Ma, Youlei Li, et al.

Journal of Human Genetics|January 8, 2020

Mutations in TOMM70 lead to multi-OXPHOS deficiencies and cause severe anemia, lactic acidosis, and developmental delayXiujuan Wei, Miaomiao Du, Jie Xie, et al.