Shiyue Y. Mei
Jianshe Road
Zhengzhou, 450052, China
Zhengzhou, 450052, China
Last Updated: 09/26/2026
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Found 55 publications
Multicenter international cohort study of HA20 reveals novel genetic architecture and phenotypic evolution.
Journal: The Journal of allergy and clinical immunology
Published: June 26, 2025
Multicenter international cohort study of haploinsufficiency of A20 reveals novel genetic architecture and phenotypic evolution.
Journal: The Journal of allergy and clinical immunology
Published: June 26, 2025
Identification of three novel GNAO1 variants in a Chinese cohort with GNAO1 encephalopathy: expanding the clinical and genetic spectrum.
Journal: Orphanet journal of rare diseases
Published: February 19, 2025
Optimizing optical neural network design for enhanced compatibility with analog computation.
Journal: Optics express
Published: January 29, 2025
Clinical features and genetic analysis of three patients with Infantile liver failure syndrome type 2 due to variants of NBAS gene
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: January 08, 2025
X-linked Deficiency in ELF4 in Females with Skewed X Chromosome Inactivation.
Journal: Journal of clinical immunology
Published: September 13, 2024
Comprehensive diagnosis and genetic analysis of two children with ring chromosome 18
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: September 01, 2024
Clinical phenotype and molecular genetic analysis of seven children with CHARGE syndrome
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: September 01, 2024
Genetic analysis of a child with Dias-Logan syndrome due to variant of BCL11A gene
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: September 01, 2024
Case Report: Clinical manifestations and treatment of two Chinese patients with FINCA syndrome carrying a novel variant of NHLRC2.
Journal: Frontiers in pediatrics
Published: March 17, 2024
Last Updated: 09/26/2026