Yeqing Qian

Jiangnan University — China

Medicine · Health Sciences

16h-index826citations103works1.52yr avg
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Research Topics

Prenatal Screening and Diagnostics(35), Genomic variations and chromosomal abnormalities(23), Fetal and Pediatric Neurological Disorders(19), RNA modifications and cancer(8), Congenital heart defects research(8)

Publications103 total

Performance testing for the sensitivity and resolution of low-pass WGS for small CNV detection
BMC Medical Genomics·2025Open Access
ALA-PDT used as a long-term management approach for refractory lichen sclerosus
Photodiagnosis and Photodynamic Therapy·2025Open Access
Emerging regulated cell death mechanisms in bone remodeling: decoding ferroptosis, cuproptosis, disulfidptosis, and PANoptosis as therapeutic targets for skeletal disorders
Cell Death Discovery·2025· 9 citedOpen Access
Decoding TAGLN2 in cancer: the molecular linchpin bridging actin remodeling, immune dysregulation and therapeutic challenges
International Journal of Biological Macromolecules·2025Open Access
The persistent risk of secondary malignancies in gastric neuroendocrine tumor survivors: a population-based analysis
Clinical and Experimental Medicine·2025· 1 citedOpen Access
Effect of <italic>Acanthopanacis Cortex</italic> on reproductive damage induced by cyclophosphamide in male rats
Lishizhen medicine and materia medica research·2025Open Access
Salvia miltiorrhiza in angina pectoris and myocardial infarction: A bibliometric analysis
European Journal of Integrative Medicine·2025Open Access
[Preliminary study on the significance of serum thyroid antibody in the selection of treatment for oral lichen planus].
PubMed·2025
Fine-tuning of Wnt signaling by RNA surveillance factor Smg5 in the mouse craniofacial development
iScience·2025· 5 citedOpen Access
Squamous cell carcinoma of the cervix associated with choriocarcinomatous differentiation: a case report and review of the literature
Journal of International Medical Research·2024Open Access
Molecular diagnostic yield of exome sequencing in a Chinese cohort of 512 fetuses with anomalies
BMC Pregnancy and Childbirth·2024· 5 citedOpen Access
Post-implantation analysis of genomic variations in the progeny from developing fetus to birth
Human Genomics·2024Open Access
SLC10A5 deficiency causes hypercholanemia
Hepatology·2024Open Access
Synonymous variant at the terminal nucleotide in exon 3 of <i>F7</i> causes abnormal splicing: A case report
Molecular Genetics & Genomic Medicine·2024Open Access
Validation and depth evaluation of recurrent neural network‐based ultra low‐pass genome sequencing for the detection of absence of heterozygosity: A multi‐centre study of 409 cases
Clinical and Translational Medicine·2024Open Access
Identification of four TTN variants in three families with fetal akinesia deformation sequence
BMC Medical Genomics·2024· 1 citedOpen Access
An efficient molecular genetic testing strategy for incontinentia pigmenti based on single-tube long fragment read sequencing
npj Genomic Medicine·2024· 3 citedOpen Access
Performance of noninvasive prenatal screening for fetal sex chromosome aneuploidies in a cohort of 116,862 pregnancies
Expert Review of Molecular Diagnostics·2024· 3 cited
Limb girdle muscular dystrophy 23 caused by compound heterozygous mutations of LAMA2 gene
Frontiers in Pediatrics·2023· 2 citedOpen Access
Validation and depth evaluation of low-pass genome sequencing in prenatal diagnosis using 387 amniotic fluid samples
Journal of Medical Genetics·2023· 9 cited
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Frequent Co-authors

Minyue Dong(29), Yanmei Yang(12), Yixi Sun(11), Yuqin Luo(10), Wei‐Jun Yang(9), Pengzhen Jin(9), Liya Wang(9), Hongge Li(8), Kai Yan(7), Yingzhi Huang(7), Min Chen(7), Yuqing Xu(6), Fan Jin(6), Yanfei Xu(5), Min Chen(5), Fan Yang(5), Chenming Xu(4), Hefeng Huang(4), Wen‐Ming Ma(4), Jin‐Shu Yang(4)