Dandan Yan
Beijing, 100049, China
Last Updated: 09/26/2026
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Found 13 publications
Durable Organic Coating-Free Superhydrophobic Metal Surface by Paracrystalline State Formation.
Journal: Advanced materials (Deerfield Beach, Fla.)
Published: August 28, 2024
Dense Amorphous Passivation Layer Formed on Aluminum Alloy Surfaces by Femtosecond Laser-Assisted Oxygen-Rich Doping.
Journal: Langmuir : the ACS journal of surfaces and colloids
Published: April 03, 2024
Succinic semialdehyde dehydrogenase deficiency: exploring the relationship between ALDH5A1 variants and molecular effect on SSADH.
Journal: Orphanet journal of rare diseases
Published: January 29, 2024
DEPDC5 plays a vital role in epilepsy: Genotypic and phenotypic features in cohort and literature.
Journal: Epileptic disorders : international epilepsy journal with videotape
Published: December 27, 2023
Case Report: A developmental and epileptic encephalopathy 45 due to de novo variant of GABRB1.
Journal: Frontiers in pediatrics
Published: November 30, 2023
A novel variant in ALG1 gene associated with congenital disorder of glycosylation: A case report and short literature review.
Journal: Molecular genetics & genomic medicine
Published: November 23, 2022
Long-Time Persisting Superhydrophilicity on Sapphire Surface via Femtosecond Laser Processing with the Varnish of TiO2.
Journal: Nanomaterials (Basel, Switzerland)
Published: August 19, 2022
Analysis of a child with severe combined immunodeficiency due to variants of DCLRE1C gene
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: July 10, 2022
Analysis of gene variant in an infant with succinic semialdehyde dehydrogenase deficiency
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: January 25, 2022
Complicated Hereditary Spastic Paraplegia Caused by SERAC1 Variants in a Chinese Family.
Journal: Frontiers in pediatrics
Published: November 16, 2021
A functional study for verifying the pathogenicity of a TRPM6 variant of uncertain significance: A novel non-canonical splicing-site variant in primary hypomagnesemia with secondary hypocalcemia.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: October 08, 2021
Last Updated: 09/26/2026