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Journal of Cardiovascular Electrophysiology|March 13, 2020
The long-term therapeutic effects of His-Purkinje system pacing on bradycardia and cardiac conduction dysfunction compared with right ventricular pacing: A systematic review and meta-analysisJin-Yu Sun, Ye-Qin Sha, Qing-Yang Sun, et al.Neural Plasticity|December 13, 2019
Auditory Neuropathy Spectrum Disorder due to Two Novel Compound Heterozygous <i>OTOF</i> Mutations in Two Chinese FamiliesYue Qiu, Sen Chen, Le Xie, et al.Clinical Genetics|February 11, 2024
A hemizygous loss-of-function variant in BCORL1 is associated with male infertility and oligoasthenoteratozoospermiaChen Luo, Zixu Chen, Lanlan Meng, et al.Iranian Journal of Basic Medical Sciences|January 31, 2022
Tertiary butylhydroquinone alleviated liver steatosis and increased cell survival via β-arrestin-2/PI3K/AKT pathwayTian-Tian Zhu, Chao-Nan Zhu, Yue Qiu, et al.Molecular Genetics & Genomic Medicine|February 25, 2022
A novel FAM83H variant causes familial amelogenesis imperfecta with incomplete penetranceRui-Qi Bai, Wen-Bin He, Qian Peng, et al.Evidence-Based Complementary and Alternative Medicine : Ecam|June 13, 2012
Interleukin-10 genotype correlated to deficiency syndrome in hepatitis B cirrhosisQing-Ya Li, Zhi-Zhong Guo, Jian Liang, et al.Pituitary|February 17, 2020
A novel diagnostic method for pituitary adenoma based on magnetic resonance imaging using a convolutional neural networkYu Qian, Yue Qiu, Cheng-Cheng Li, et al.Journal of Assisted Reproduction and Genetics|April 16, 2025
Novel mutations in ZMYND15 are associated with male infertility with oligozoospermia/azoospermiaChunjia Wei, Yingchi Lu, Sibing Yi, et al.Molecular Medicine Reports|March 31, 2017
Exome sequencing reveals novel IRXI mutation in congenital heart diseaseChanglong Guo, Qidi Wang, Yuting Wang, et al.Frontiers in Genetics|August 22, 2022
Novel <i>MEIOB</i> variants cause primary ovarian insufficiency and non-obstructive azoospermiaYurong Wang, Ling Liu, Chen Tan, et al.Pageof 94