Comprehensive Analysis of Hemophilia A (CAHEA): Towards Full Characterization of the F8 Gene Variants by Long-Read Sequencing. Thromb Haemost. 2023 Dec;123(12):1151-1164.
Detection of complex chromosome rearrangements using optical genome mapping. Gene. 2023 Oct 30;884:147688.
Application of Chromosomal Microarray Analysis in Genetic Reasons of Miscarriage Tissues. Appl Clin Genet. 2024 May 31;17:85-93. doi: 10.2147/TACG.S461674.
Development of CRISPR Cas9, spin-off technologies and their application in model construction and potential therapeutic methods of Parkinson's disease. Front Neurosci. 2023 Jul 6;17:1223747.
Genetic analysis and prenatal diagnosis of short-rib thoracic dysplasia 3 with or without polydactyly caused by compound heterozygous variants of DYNC2H1 gene in four Chinese families. Front Genet. 2023 Mar 17;14:1075187.
Noninvasive prenatal testing for fetal subchromosomal copy number variations and chromosomal aneuploidy by low-pass whole-genome sequencing. Mol Genet Genomic Med. 2019 Jun;7(6):e674.
表型正常的夫妇反复妊娠21-三体胎儿的遗传学分析及文献复习[J]. 中华围产医学杂志,2024,27(10):842-848.
FANCB基因半合子变异致多发畸形胎儿1例的分析[J]. 中华医学遗传学杂志,2023,40(10):1257-1262.