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Biomed Research International|December 13, 2018
A Novel MLH1 Initiation Codon Mutation (c.3G>T) in a Large Chinese Lynch Syndrome Family with Different Onset Age and mRNA Expression LevelYanni Zhang, Huishuang Chen, Zhiyu Peng, et al.
BMC Medical Genomics|October 10, 2021
Noninvasive prenatal diagnosis of monogenic disorders based on direct haplotype phasing through targeted linked-read sequencingChao Chen, Min Chen, Yaping Zhu, et al.
BMC Medical Genomics|June 6, 2022
The effect of hemolysis on quality control metrics for noninvasive prenatal testingYaya Guo, Dandan Yu, Kaisu Zhou, et al.
BMC Genomics|March 14, 2015
A systems genetics study of swine illustrates mechanisms underlying human phenotypic traitsJun Zhu, Congying Chen, Bin Yang, et al.
Academic Radiology|April 22, 2025
The Predictive Value of Preoperative Coronary Artery Calcium Score for Long-term Survival in Elderly Patients with Lung Cancer After SurgeryZetao Liu, Linyan Huang, Xiongmu Tan, et al.
Scientific Reports|January 8, 2022
Next generation sequencing is a highly reliable method to analyze exon 7 deletion of survival motor neuron 1 (SMN1) geneSumin Zhao, Yaoshen Wang, Xiuqing Xin, et al.
The Plant Cell|March 23, 2012
Genome-wide analysis of DNA methylation and gene expression changes in two Arabidopsis ecotypes and their reciprocal hybridsHuaishun Shen, Hang He, Jigang Li, et al.
Human Mutation|April 14, 2025
Genome Sequencing Unveils the Role of Copy Number Variants in Hearing Loss and Identifies Novel Deletions With Founder Effect in the DFNB1 LocusZibin Lin, Jiale Xiang, Xiangzhong Sun, et al.
Frontiers in Immunology|February 28, 2025
PDK2-enhanced glycolysis aggravates fibrosis via IL11 signaling pathway in Graves' orbitopathyZhiyu Peng, Rui Huang, Lu Gan, et al.
BMC Medical Genomics|May 30, 2019
Increased diagnostic yield by reanalysis of data from a hearing loss gene panelYu Sun, Jiale Xiang, Yidong Liu, et al.
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