Qingping Zhang
Publications by Year
Research Areas
Genetics and Neurodevelopmental Disorders, Epilepsy research and treatment, Hereditary Neurological Disorders, Genomics and Rare Diseases, Neuroscience and Neuropharmacology Research
Most-Cited Works
- → Modeling Rett Syndrome Using TALEN-Edited MECP2 Mutant Cynomolgus Monkeys(2017)196 cited
- → Gene mutational analysis in a cohort of Chinese children with unexplained epilepsy: Identification of a new KCND3 phenotype and novel genes causing Dravet syndrome(2019)42 cited
- → Clinical features and gene mutational spectrum of CDKL5-related diseases in a cohort of Chinese patients(2014)41 cited
- → Genomic mosaicism in the pathogenesis and inheritance of a Rett syndrome cohort(2018)41 cited
- → Rett and Rett‐like syndrome: Expanding the genetic spectrum to KIF1A and GRIN1 gene(2019)39 cited
- → Novel MEF2C point mutations in Chinese patients with Rett (−like) syndrome or non-syndromic intellectual disability: insights into genotype-phenotype correlation(2018)31 cited
- → The genetic and clinical characteristics of aromatic L-amino acid decarboxylase deficiency in mainland China(2020)26 cited
- → Familial cases and male cases with MECP2 mutations(2017)23 cited
- → CACNA1A Gene Variants in Eight Chinese Patients With a Wide Range of Phenotypes(2020)20 cited
- → Clinical and Genetic Heterogeneity in a Cohort of Chinese Children With Dopa-Responsive Dystonia(2020)14 cited