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Stem Cell Research|September 16, 2021
Establishment of human induced pluripotent stem cell line (SDQLCHi040-A) from a patient with Infantile-onset inflammatory bowel disease carrying a homozygous mutation in IL10RA geneNing Liu, Xiaomeng Yang, Lu Yang, et al.
Stroke and Vascular Neurology|April 30, 2026
Low-FREquency Deep TRanscranial Magnetic Stimulation in ACute Ischaemic StrokE within 48 Hours (RETRACE-I): rationale and design of a randomised, multicentre, open-label, blinded endpoint trialLingling Ding, Shuyu Lv, Wenjie Wang, et al.
BMC Neurology|March 9, 2022
Association of triglyceride-glucose index and stroke recurrence among nondiabetic patients with acute ischemic strokeXiaomeng Yang, Guangyao Wang, Jing Jing, et al.
Food & Function|April 17, 2023
Dietary flavonoid intake is associated with a lower risk of diabetic nephropathy in US adults: data from NHANES 2007-2008, 2009-2010, and 2017-2018Fang Liu, Jiaqi Nie, Ming-Gang Deng, et al.
Stroke|December 24, 2015
Use of Warfarin at Discharge Among Acute Ischemic Stroke Patients With Nonvalvular Atrial Fibrillation in ChinaXiaomeng Yang, Zixiao Li, Xingquan Zhao, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|May 5, 2026
A Soft Mechanoluminescent Skin for High-Resolution Optical Tactile Sensing in Human-Machine InteractionYu Feng, Qiaojiao Wang, Yehui Liu, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 21, 2017
Association of IMMP2L deletions with autism spectrum disorder: A trio family study and meta-analysisYanqing Zhang, Yi Liu, Mehdi Zarrei, et al.
Scientific Reports|July 27, 2025
Genetic findings of children with congenital heart diseases using chromosomal microarray and trio-based whole exome sequencingRui Guo, Chunhong Duan, Mehdi Zarrei, et al.
Genes|September 28, 2023
Genome-Wide Association Study Reveals the Genetic Basis of Total Flavonoid Content in Brown RiceHaijian Xia, Xiaoying Pu, Xiaoyang Zhu, et al.
Geroscience|January 11, 2021
SMAD4 mutations and cross-talk between TGF-β/IFNγ signaling accelerate rates of DNA damage and cellular senescence, resulting in a segmental progeroid syndrome-the Myhre syndromeRenuka Kandhaya-Pillai, Deyin Hou, Jiaming Zhang, et al.
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