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Biochemical and Biophysical Research Communications|August 3, 2022
Actl7a deficiency in mice leads to male infertility and fertilization failureXiaopei Zhou, Zhenxing Liu, Weimin Jia, et al.IEEE Transactions on Neural Networks and Learning Systems|May 21, 2019
Fast Semisupervised Learning With Bipartite Graph for Large-Scale DataFang He, Feiping Nie, Rong Wang, et al.Neuro-Degenerative Diseases|May 24, 2022
Juvenile-Onset Kufs Disease in a Chinese Consanguineous Family due to CLN6 MutationWeimin Jia, Yalin Luo, Jiuxiang Wang, et al.The Journal of Gene Medicine|March 30, 2020
A novel UBE2A mutation in a Chinese family with X-linked intellectual disabilityWeimin Jia, Qi Hu, Yanling Wu, et al.Molecules (Basel, Switzerland)|July 29, 2023
Investigation on the Mechanism of PAL (100) Surface Modified by APTESWeimin Jia, Bomiao Qi, Yanbin Wang, et al.Journal of Assisted Reproduction and Genetics|October 30, 2024
Novel splicing mutations in PATL2 and WEE2 cause oocyte degradation and fertilization failureZhenxing Liu, Lixia Zhu, Hui He, et al.Nephrology (Carlton, Vic.)|October 10, 2025
Novel Compound Heterozygous Mutation in the KCNJ1 Gene Causes Bartter SyndromeLinglu Xiao, Yanqin Ying, Weimin Jia, et al.American Journal of Medical Genetics. Part A|September 1, 2021
A novel microdeletion upstream of HOXD13 in a Chinese family with synpolydactylyWeimin Jia, Xiaopei Zhou, Naiqiang Guo, et al.Human Genetics|November 4, 2025
Deficiency of SCAMP5 causes Parkinson's disease due to loss of dopamine neuronsHuihui Liu, Shunnan Ge, Zhenxing Liu, et al.Journal of Assisted Reproduction and Genetics|April 3, 2022
Novel mutations in ZP2 and ZP3 cause female infertility in three patientsWeimin Jia, Qingsong Xi, Lixia Zhu, et al.Pageof 2