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American Journal of Obstetrics & Gynecology MFM|July 1, 2023
Association analysis between chromosomal abnormalities and fetal ultrasonographic soft markers based on 15,263 fetusesLijuan Pan, Jiayu Wu, Desheng Liang, et al.
Clinical Chemistry|June 17, 2022
Comprehensive Analysis of Congenital Adrenal Hyperplasia Using Long-Read SequencingYingdi Liu, Miaomiao Chen, Jing Liu, et al.
Clinical Chemistry|September 28, 2022
Comprehensive Analysis of Fragile X Syndrome: Full Characterization of the FMR1 Locus by Long-Read SequencingQiaowei Liang, Yingdi Liu, Yaning Liu, et al.
IEEE Transactions on Medical Imaging|April 20, 2023
KaryoNet: Chromosome Recognition With End-to-End Combinatorial Optimization NetworkChao Xia, Jiyue Wang, Yulei Qin, et al.
Frontiers in Genetics|July 4, 2025
Two novel variants in <i>CNNM2</i> disrupts magnesium efflux leading to neurodevelopmental disordersHuijuan Li, Jing Liu, Yingdi Liu, et al.
IEEE Transactions on Medical Imaging|March 26, 2019
Varifocal-Net: A Chromosome Classification Approach Using Deep Convolutional NetworksYulei Qin, Juan Wen, Hao Zheng, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 11, 2022
The exploration of genetic aetiology and diagnostic strategy for 321 Chinese individuals with intellectual disabilityHongyun Zhang, Xin Chen, Hu Tan, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|September 1, 2024
[Expert consensus on the clinical application of efficient intelligent chromosomal karyotyping precise auxiliary diagnosis system]Efficient Intelligent Chromosomal Karyotyping Precise Auxiliary Diagnosis System Clinical Application Collaboration Group, Hao Wang, Juan Wen, et al.
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