Yanyan W. Qian
399 Wanyuan Road
Shanghai, 201102, China
Shanghai, 201102, China
Last Updated: 09/26/2026
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Found 48 publications
Causal Association Between Chronic Inflammatory Arthropathies and Sarcopenia and the Mediation Role of Inflammatory Factors.
Journal: International journal of rheumatic diseases
Published: October 22, 2024
Thirteen New Patients of PPP2R5D Gene Mutation and the Fine Profile of Genotype-Phenotype Correlation Unraveling the Pathogenic Mechanism Underlying Macrocephaly Phenotype.
Journal: Children (Basel, Switzerland)
Published: June 17, 2024
Derivation of an induced pluripotent stem cell line (FDCHi014-A) from PBMCs of a seven-year-old patient with a truncating NOVA2 variant (c.625del).
Journal: Stem cell research
Published: January 22, 2024
Genetic Spectrum of Congenital Anomalies of the Kidney and Urinary Tract in Chinese Newborn Genome Project.
Journal: Kidney international reports
Published: July 21, 2023
Novel Variants of PPP2R1A in Catalytic Subunit Binding Domain and Genotype-Phenotype Analysis in Neurodevelopmentally Delayed Patients.
Journal: Genes
Published: July 20, 2023
Genetic spectrums and clinical profiles of critically ill neonates with congenital auricular deformity in the China Neonatal Genomes Project.
Journal: Human genetics
Published: July 13, 2023
Further delineation of EBF3-related syndromic neurodevelopmental disorder in twelve Chinese patients.
Journal: Frontiers in pediatrics
Published: November 07, 2022
Case report: A novel truncating variant of BCL11B associated with rare feature of craniosynostosis and global developmental delay.
Journal: Frontiers in pediatrics
Published: June 30, 2022
In the developing cerebral cortex: axonogenesis, synapse formation, and synaptic plasticity are regulated by SATB2 target genes.
Journal: Pediatric research
Published: April 27, 2022
WDR62 variants contribute to congenital heart disease by inhibiting cardiomyocyte proliferation.
Journal: Clinical and translational medicine
Published: February 08, 2022
Genetic architecture in neonatal intensive care unit patients with congenital heart defects: a retrospective study from the China Neonatal Genomes Project.
Journal: Journal of medical genetics
Published: November 25, 2021
mTOR pathway repressing expression of FoxO3 is a potential mechanism involved in neonatal white matter dysplasia.
Journal: Human molecular genetics
Published: November 24, 2021
Last Updated: 09/26/2026