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Frontiers in Oncology|June 9, 2020
Development and Validation of a Comprehensive Multivariate Dosimetric Model for Predicting Late Genitourinary Toxicity Following Prostate Cancer Stereotactic Body RadiotherapyLuca F Valle, Dan Ruan, Audrey Dang, et al.
Scientific Reports|April 1, 2024
Clinical phenotype and genetic function analysis of a family with hypomyelinating leukodystrophy-7 caused by POLR3A mutationDan-Dan Ruan, Xing-Lin Ruan, Ruo-Li Wang, et al.
Frontiers in Neuroscience|August 15, 2024
In vitro study of ATP1A3 p.Ala275Pro mutant causing alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonismDan-Dan Ruan, Jing Zou, Li-Sheng Liao, et al.
Digestive Diseases and Sciences|April 2, 2024
Pedigree Analysis of Nonclassical Cholesteryl Ester Storage Disease with Dominant Inheritance in a LIPA I378T Heterozygous CarrierJian-Hui Zhang, Ai-Ping Lin, Li Zhang, et al.
Experimental and Therapeutic Medicine|July 9, 2025
Genetic and clinical insights into acute kidney injury in maturity-onset diabetes of the young caused by the ABCC8 c.2500C>T mutation: Potential risk factors associated with SGLT2 inhibitorsJing Zou, Xiang Chen, Hong-Ping Yu, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|February 15, 2020
A Phase II Trial of 5-Day Neoadjuvant Radiotherapy for Patients with High-Risk Primary Soft Tissue SarcomaAnusha Kalbasi, Mitchell Kamrava, Fang-I Chu, et al.
Nature Communications|December 2, 2025
CIP2A mediates mitotic recruitment of SLX4/MUS81/XPF to resolve replication stress-induced DNA lesionsLauren de Haan, Sietse J Dijt, Alejandro García-López, et al.
Medscience|February 24, 2026
Differential genetic analysis of ectrodactyly in a Fanconi anemia pedigree with FANCA mutationsJian-Hui Zhang, Zi-Yan Xu, Hong-Ping Yu, et al.
Gene|September 25, 2025
Genetic analysis of a family with skeletal muscle ion channelopathy and hereditary spastic paraplegia type 7 caused by SCN4A and SPG7 double mutationsHong-Ping Yu, Zi-Yan Xu, Meng-Qian Wu, et al.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences|March 17, 2026
Phosphoproteomics elucidates the functional impact of the PTPN11 p.Asn308Ser variant in a Noonan syndrome pedigreeWei-Jing Xu, Li-Jun Xie, Wen-Jun Chen, et al.
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