Xiaoang Sun
Shanghai, China
Last Updated: 09/26/2026
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Found 9 publications
Distinct phenotypes differentiate paroxysmal kinesigenic dyskinesia from epilepsy in children with PRRT2 variants.
Journal: Epileptic disorders : international epilepsy journal with videotape
Published: December 15, 2025
Novel SLC16A2 mutations impair thyroid hormone transport and drive neurodevelopmental deficits in Chinese patients with allan-herndon-dudley syndrome.
Journal: Scientific reports
Published: September 01, 2025
BiGATAE: a bipartite graph attention auto-encoder enhancing spatial domain identification from single-slice to multi-slices.
Journal: Briefings in bioinformatics
Published: November 12, 2023
Clinical features and underlying mechanisms of KAT6B disease in a Chinese boy.
Journal: Molecular genetics & genomic medicine
Published: August 22, 2022
Clinical characteristics and genetics of ten Chinese children with PRRT2-associated neurological diseases.
Journal: Frontiers in pediatrics
Published: July 18, 2022
Clinical Study of 8 Cases of CHD2 Gene Mutation-Related Neurological Diseases and Their Mechanisms.
Journal: Frontiers in cell and developmental biology
Published: January 12, 2022
Web-based calculator for biliary atresia screening in neonates and infants with cholestasis.
Journal: Translational pediatrics
Published: March 12, 2021
Effects of cytomegalovirus infection on the differential diagnosis between biliary atresia and intrahepatic cholestasis in a Chinese large cohort study.
Journal: Annals of hepatology
Published: July 17, 2020
Showing 1-9 of 9
Last Updated: 09/26/2026