Zi-long Ye
Guangzhou, China
Last Updated: 09/26/2026
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Found 9 publications
Child Neurology: Multiple Genetic Etiologies Causing Dandy-Walker Variant With Microcephaly, Epilepsy, and Global Developmental Delay.
Journal: Neurology
Published: March 06, 2026
Reply: USP25 in genetic generalized epilepsy: a gene under scrutiny.
Journal: Brain : a journal of neurology
Published: August 15, 2025
De novo heterozygous missense variants in ATP11A are associated with refractory focal epilepsy.
Journal: Journal of medical genetics
Published: November 25, 2024
Variants in EP400, encoding a chromatin remodeler, cause epilepsy with neurodevelopmental disorders.
Variants in EP400, encoding a chromatin remodeler, cause epilepsy with neurodevelopmental disorders.
Journal: American journal of human genetics
Published: June 18, 2024
Heterozygous variants in USP25 cause genetic generalized epilepsy.
Journal: Brain : a journal of neurology
Published: January 24, 2024
NEXMIF variants are associated with epilepsy with or without intellectual disability.
Journal: Seizure
Published: May 09, 2023
Recessive LAMA5 Variants Associated With Partial Epilepsy and Spasms in Infancy.
Journal: Frontiers in molecular neuroscience
Published: November 30, 2021
CELSR1 variants are associated with partial epilepsy of childhood.
Journal: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics
Published: August 31, 2021
Showing 1-9 of 9
Last Updated: 09/26/2026