Publications by authors named "Shangying Yang"

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MRI cytometry imaging for cervical cancer differential diagnosis: a preliminary study.
Zhi-Lin Yuan, Di-Wei Shi, Hui Guan, Fan Liu, Zong-Shu Wang, Shang-Ying Yang

BMC Med Imaging· November 2025

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Evaluating the utility of enhanced T1 mapping MR imaging in assessing depth of myometrial invasion and detecting DNA mismatch repair status in endometrial cancer: a pilot study.
Xin-Yu Liu, Zhi-Lin Yuan, Shang-Ying Yang, Jing Ren, Yuan Li

Abdom Radiol (NY)· August 2025

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Whole-exome sequencing screening for candidate genes and potential pathogenic variants associated with early-onset high myopia in 47 Chinese families.
Xue Rui, Huiping Li, Runqing Ma, Shangying Yang, Yuanyuan Lian

Sci Rep· April 2025

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[Advances in Imaging-Based Evaluation of Solid Tumors Treated With Immune Checkpoint Inhibitors].
Shang-Ying Yang, Xin-Yu Liu, Hua-Dan Xue, Zheng-Yu Jin, Yong-Lan He

Zhongguo Yi Xue Ke Xue Yuan Xue Bao· August 2024

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De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia.
Xiaoyu Huang, Huiping Li, Shangying Yang, Meijiao Ma, Yuanyuan Lian

BMC Med Genomics· May 2024

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heterozygous copy number deletion on 7q31.31-7q31.32 involving gene with familial exudative vitreoretinopathy in a Chinese family.
Shuang Zhang, Hai-Ming Yong, Gang Zou, Mei-Jiao Ma, Xue Rui, Shang-Ying Yang

Int J Ophthalmol· December 2023

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Exome and genome sequencing to unravel the precise breakpoints of partial trisomy 6q and partial Monosomy 2q.
Shuang Zhang, Qianwei Cui, Shangying Yang, Fangxia Zhang, Chunxia Li

BMC Pediatr· November 2023

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BEST1 novel mutation causes Bestrophinopathies in six families with distinct phenotypic diversity.
Shangying Yang, Zhen Li, Wanyu Cheng, Meijiao Ma, Rui Qi

Mol Genet Genomic Med· January 2023

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Two novel variations in cause Donnai-Barrow syndrome in a Chinese family with severe early-onset high myopia.
Shiqin Yuan, Xiaoyu Huang, Shuang Zhang, Shangying Yang, Xue Rui

Front Genet· January 2023

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Novel Compound Heterozygous Variations in Gene Caused Isolated Bilateral Macular Coloboma in a Chinese Family.
Shuang Zhang, Fangxia Zhang, Juan Wang, Shangying Yang, Yinghua Ren

Cells· November 2022

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Identification of genetic variants in five chinese families with keratoconus: Pathogenicity analysis and characteristics of parental corneal topography.
Wan-Yu Cheng, Shang-Ying Yang, Xiao-Yu Huang, Fei-Yin Zi, Hui-Ping Li

Front Genet· October 2022

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T staging with functional and radiomics parameters of computed tomography in colorectal cancer patients.
Yafang Dou, Yingying Liu, Xiancheng Kong, Shangying Yang

Medicine (Baltimore)· May 2022

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