Xinna Ji
Beijing, China
Last Updated: 09/26/2026
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Found 12 publications
Genetic testing and analysis of 1024 children with global developmental delay or intellectual disability: a single-center cohort study.
Journal: European journal of pediatrics
Published: January 06, 2026
Diagnostic Genetic Findings From Exome Sequencing in a Cohort of 1,109 Children With Epilepsy.
Journal: Neurology. Genetics
Published: June 10, 2025
Prevalence, clinical characteristics and outcomes of seizures in neurofibromatosis type 1: A systematic review and single arm meta-analysis.
Journal: Epilepsy research
Published: June 07, 2024
Generation of a human iPSC line CIPi004-A from a patient with neurofibromatosis type 1 and epilepsy harboring a heterozygous mutation in NF1 gene.
Journal: Stem cell research
Published: May 10, 2024
Accelerating the diagnosis of Chinese cblC type MMA patients by multiplex PCR sequencing method.
Journal: Pediatric research
Published: February 20, 2024
Whole exome sequencing identifies KCNH7 variants associated with epilepsy in children.
Journal: Genes & diseases
Published: January 22, 2024
A de novo heterozygous variant in ACOX1 gene cause Mitchell syndrome: the first case in China and literature review.
Journal: BMC medical genomics
Published: September 22, 2022
Generation of a human induced pluripotent stem cell line (CIPi002-A) from an early infantile epileptic encephalopathy patient with a heterozygous mutation in SCN8A.
Journal: Stem cell research
Published: June 08, 2022
Drug-resistant epilepsy in children with hemophilia: how can we do it surgically?
Journal: British journal of neurosurgery
Published: February 17, 2022
Pediatric Autoimmune Encephalitis: Case Series From Two Chinese Tertiary Pediatric Neurology Centers.
Journal: Frontiers in neurology
Published: October 10, 2018
Showing 1-12 of 12
Last Updated: 09/26/2026