Xiaodong Wang
Beijing, China
Last Updated: 09/26/2026
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Found 9 publications
Bi-allelic PRMT9 loss-of-function variants cause a syndromic form of intellectual disability.
Journal: American journal of human genetics
Published: July 22, 2024
Cohort Expansion and Genotype-Phenotype Analysis of RAB11A-Associated Neurodevelopmental Disorder.
Journal: Pediatric neurology
Published: May 16, 2023
Novel biallelic loss of EEF1B2 function links to autosomal recessive intellectual disability.
Journal: Human mutation
Published: September 28, 2021
Delineating the molecular and phenotypic spectrum of the SETD1B-related syndrome.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: March 05, 2021
A novel variant of CDK19 causes a severe neurodevelopmental disorder with infantile spasms.
Journal: Cold Spring Harbor molecular case studies
Published: December 15, 2020
Loss of function mutations in GEMIN5 cause a neurodevelopmental disorder.
Journal: Nature communications
Published: October 15, 2020
Identification of an Identical de Novo SCAMP5 Missense Variant in Four Unrelated Patients With Seizures and Severe Neurodevelopmental Delay.
Journal: Frontiers in pharmacology
Published: August 26, 2020
Missense variants in the N-terminal domain of the A isoform of FHF2/FGF13 cause an X-linked developmental and epileptic encephalopathy.
Journal: American journal of human genetics
Published: August 12, 2020
Clonality analysis of synchronous gastro-oesophageal junction carcinoma and distal gastric cancer by whole-exome sequencing.
Journal: The Journal of pathology
Published: February 01, 2017
Showing 1-9 of 9
Last Updated: 09/26/2026