Jiada H. Li
110 Xiangya Road
Changsha, China
Changsha, China
Last Updated: 09/26/2026
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Found 58 publications
Electricity-Driven Radical Carbonyl Catalysis for Asymmetric Synthesis of α-Tertiary Amino Esters.
Journal: Angewandte Chemie (International ed. in English)
Published: April 02, 2026
Altered spontaneous brain activity is associated with cognitive impairment in patients with Kallmann syndrome.
Journal: Reproductive biology and endocrinology : RB&E
Published: January 27, 2026
Evidence supporting the role of GIGYF2 in synapse development and autism.
Journal: Molecular psychiatry
Published: July 07, 2025
Knockout of Bmal1 in dopaminergic neurons induces ADHD-like symptoms via hyperactive dopamine signaling in male mice.
Journal: Behavioral and brain functions : BBF
Published: April 14, 2025
Disrupting integrator complex subunit INTS6 causes neurodevelopmental disorders and impairs neurogenesis and synapse development.
Journal: The Journal of clinical investigation
Published: January 28, 2025
KCTD10 p.C124W variant contributes to schizophrenia by attenuating LLPS-mediated synapse formation.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: November 20, 2024
Metabonomics analysis of decidual tissue in patients with recurrent spontaneous abortion.
Journal: Journal of reproductive immunology
Published: September 22, 2024
Loss of Necdin causes social deficit and aberrant synaptic function through destabilization of SynGAP.
Journal: Molecular psychiatry
Published: June 28, 2024
KCTD10 regulates brain development by destabilizing brain disorder-associated protein KCTD13.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: March 15, 2024
EXTL3 and NPC1 are mammalian host factors for Autographa californica multiple nucleopolyhedrovirus infection.
Journal: Nature communications
Published: January 25, 2024
Targeting BMAL1 reverses drug resistance of acute myeloid leukemia cells and promotes ferroptosis through HMGB1-GPX4 signaling pathway.
Journal: Journal of cancer research and clinical oncology
Published: January 19, 2024
Mutations in CLCN6 as a Novel Genetic Cause of Neuronal Ceroid Lipofuscinosis in Patients and a Murine Model.
Journal: Annals of neurology
Published: October 16, 2023
Last Updated: 09/26/2026