| Prokineticins and their G protein-coupled receptors in health and disease Y Zhao, J Wu, X Wang, H Jia, DN Chen, JD Li Progress in Molecular Biology and Translational Science 161, 149-179, 2019 | 37 | 2019 |
| PROKR2 mutations in idiopathic hypogonadotropic hypogonadism: selective disruption of the binding to a Gα‐protein leads to biased signaling Y Zhao, J Wu, H Jia, X Wang, R Zheng, F Jiang, DN Chen, Z Chen, JD Li The FASEB Journal 33 (3), 4538-4546, 2019 | 29 | 2019 |
| Genotypic and phenotypic spectra of FGFR1, FGF8, and FGF17 mutations in a Chinese cohort with idiopathic hypogonadotropic hypogonadism M Men, J Wu, Y Zhao, X Xing, F Jiang, R Zheng, JD Li Fertility and sterility 113 (1), 158-166, 2020 | 26 | 2020 |
| A novel PNPLA6 compound heterozygous mutation identified in a Chinese patient with Boucher‑Neuhäuser syndrome R Zheng, Y Zhao, J Wu, Y Wang, JL Liu, ZL Zhou, XT Zhou, DN Chen, ... Molecular Medicine Reports 18 (1), 261-267, 2018 | 26 | 2018 |
| Functional analysis of SOX10 mutations identified in Chinese patients with Kallmann syndrome W Dai, J Wu, Y Zhao, F Jiang, R Zheng, DN Chen, M Men, JD Li Gene 702, 99-106, 2019 | 23 | 2019 |
| A dominant negative FGFR1 mutation identified in a Kallmann syndrome patient H Luo, R Zheng, Y Zhao, J Wu, J Li, F Jiang, DN Chen, XT Zhou, JD Li Gene 621, 1-4, 2017 | 20 | 2017 |
| Phenotypic Spectrum of Idiopathic Hypogonadotropic Hypogonadism Patients With CHD7 Variants From a Large Chinese Cohort JD Li, J Wu, Y Zhao, X Wang, F Jiang, Q Hou, DN Chen, R Zheng, R Yu, ... The Journal of Clinical Endocrinology & Metabolism 105 (5), 1515-1526, 2020 | 17 | 2020 |
| Effect of cisplatin on the clock genes expression in the liver, heart and kidney BB Cao, D Li, X Xing, Y Zhao, K Wu, F Jiang, W Yin, JD Li Biochemical and biophysical research communications 501 (2), 593-597, 2018 | 16 | 2018 |
| Functional analysis of SEMA3A variants identified in Chinese patients with isolated hypogonadotropic hypogonadism W Dai, JD Li, Y Zhao, J Wu, F Jiang, DN Chen, R Zheng, M Men Clinical genetics 97 (5), 696-703, 2020 | 14 | 2020 |
| SLIT2 rare sequencing variants identified in idiopathic hypogonadotropic hypogonadism J Wu, Z Fang, X Wang, W Zeng, Y Zhao, F Jiang, DN Chen, R Zheng, J Li, ... Hormone research in paediatrics 95 (4), 384-392, 2022 | 11 | 2022 |
| Genotypic and phenotypic spectrum of CCDC141 variants in a Chinese cohort with congenital hypogonadotropic hypogonadism Q Hou, J Wu, Y Zhao, X Wang, F Jiang, DN Chen, R Zheng, M Men, JD Li European Journal of Endocrinology 183 (3), 245-254, 2020 | 9 | 2020 |
| SUMOylation in skeletal development, homeostasis, and disease H Liu, SEL Craig, V Molchanov, JS Floramo, Y Zhao, T Yang Cells 11 (17), 2710, 2022 | 6 | 2022 |
| TRIM28 secures skeletal stem cell fate during skeletogenesis by silencing neural gene expression and repressing GREM1/AKT/mTOR signaling axis H Liu, Y Liu, SG Jin, J Johnson, H Xuan, D Lu, J Li, L Zhai, X Li, Y Zhao, ... Cell Reports 42 (1), 2023 | 5 | 2023 |
| A functional spectrum of PROKR2 mutations identified in isolated hypogonadotropic hypogonadism X Wang, D Chen, Y Zhao, M Men, Z Chen, F Jiang, R Zheng, MI Stamou, ... Human Molecular Genetics 32 (10), 1722-1729, 2023 | 2 | 2023 |
| Phenotypic spectrum of idiopathic hypogonadotropic hypogonadism patients with J Wu, Y Zhao, X Wang, F Jiang, Q Hou, DN Chen, R Zheng, R Yu, W Zhou, ... | | 2019 |
