Xiangyi Jing

841 total citations
52 papers, 410 citations indexed

About

Xiangyi Jing is a scholar working on Pediatrics, Perinatology and Child Health, Molecular Biology and Genetics. According to data from OpenAlex, Xiangyi Jing has authored 52 papers receiving a total of 410 indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Pediatrics, Perinatology and Child Health, 27 papers in Molecular Biology and 22 papers in Genetics. Recurrent topics in Xiangyi Jing's work include Prenatal Screening and Diagnostics (31 papers), Genomic variations and chromosomal abnormalities (13 papers) and Congenital heart defects research (10 papers). Xiangyi Jing is often cited by papers focused on Prenatal Screening and Diagnostics (31 papers), Genomic variations and chromosomal abnormalities (13 papers) and Congenital heart defects research (10 papers). Xiangyi Jing collaborates with scholars based in China, Hong Kong and United Kingdom. Xiangyi Jing's co-authors include Fang Fu, Dong‐Zhi Li, Xin Yang, Yongling Zhang, Tingying Lei, Ru Li, Jin Han, Can Liao, Can Liao and Min Pan and has published in prestigious journals such as The Journal of Pediatrics, Gene and Nephrology Dialysis Transplantation.

In The Last Decade

Xiangyi Jing

46 papers receiving 406 citations

Peers

Countries citing papers authored by Xiangyi Jing

Since Specialization

Citations

This map shows the geographic impact of Xiangyi Jing's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Xiangyi Jing with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Xiangyi Jing more than expected).

Fields of papers citing papers by Xiangyi Jing

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Xiangyi Jing. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Xiangyi Jing. The network helps show where Xiangyi Jing may publish in the future.

Co-authorship network of co-authors of Xiangyi Jing

This figure shows the co-authorship network connecting the top 25 collaborators of Xiangyi Jing. A scholar is included among the top collaborators of Xiangyi Jing based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Xiangyi Jing. Xiangyi Jing is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Macrocyclic peptides as a new class of targeted protein degraders 2025 ·RSC Chemical Biology ·Xiangyi Jing, Joel P. Mackay, Toby Passioura	3
2	Prenatal Diagnosis of KBG Syndrome: Phenotypic and Genotypic Features of 12 Fetal Cases With the Disorder 2025 ·Prenatal Diagnosis ·Xiangyi Jing, Qiuxia Yu, (unknown), (unknown), Dong‐Zhi Li	0
3	Prenatal diagnosis and perinatal outcomes of fetuses with congenital duodenal obstruction: A nine‐year retrospective study from China 2025 ·Acta Obstetricia Et Gynecologica Scandinavica ·Jiaming Lu, Fang Fu, (unknown), Hang Zhou, (unknown), (unknown), (unknown), Liyuan Liu, Xiangyi Jing, Simin Yuan, Xiang Zhou, Qiuxia Yu, Meng Yang, Jin Han, Dong‐Zhi Li, Ru Li, Can Liao	0
4	Invasive genetic testing for isolated increased nuchal translucency of 3.0–3.4 mm: Results from cohort analysis with 604 fetuses 2024 ·International Journal of Gynecology & Obstetrics ·Xiangyi Jing, (unknown), (unknown)	0
5	Prenatal diagnosis of 17q12 copy number variants in fetuses via chromosomal microarray analysis - A retrospective cohort study and literature review 2024 ·Heliyon ·(unknown), (unknown), (unknown), Fang Fu, (unknown), Liyuan Liu, Lushan Li, Shujuan Yan, Jianqin Lu, Hang Zhou, (unknown), Fei Guo, Xiangyi Jing, Fucheng Li, Zhen Li, (unknown), Ru Li, Can Liao	0
6	Prenatal diagnosis of ultrasound soft markers in a single medical center of mainland China 2023 ·Molecular Cytogenetics ·Yanhong Zhou, Siqi Wu, Jin Han, Zhen Li, Xin Yang, Ru Li, Yongling Zhang, Xiangyi Jing, Fucheng Li, Huishu Liu	3
7	Prenatal diagnosis of 21 fetuses with balanced chromosomal abnormalities (BCAs) using whole-genome sequencing 2022 ·Frontiers in Genetics ·Fang Fu, Ru Li, (unknown), Qiuxia Yu, Ke Xu, Weiyue Gu, Dan Wang, Xin Yang, Min Pan, (unknown), Yongling Zhang, Fatao Li, Xiangyi Jing, Fucheng Li, Dong‐Zhi Li, Can Liao	1
8	Sotos syndrome: A study of antenatal presentation 2022 ·European Journal of Obstetrics & Gynecology and Reproductive Biology ·Yongling Zhang, Xiangyi Jing, Guilan Chen, Zhen Li, Dong‐Zhi Li	5
9	The Genetic and Clinical Outcomes in Fetuses With Isolated Fetal Growth Restriction: A Chinese Single-Center Retrospective Study 2022 ·Frontiers in Genetics ·Hang Zhou, (unknown), (unknown), Fang Fu, Ru Li, Yongling Zhang, Xin Yang, Xiangyi Jing, Fucheng Li, Jin Han, Min Pan, Zhen Li, Dong‐Zhi Li, Can Liao	9
10	Prenatal Silver-Russell Syndrome in a Chinese Family Identified by Non-Invasive Prenatal Testing 2022 ·Molecular Syndromology ·Yongling Zhang, Xiangyi Jing, (unknown), Min Pan, Dong‐Zhi Li	2
11	Prenatal diagnosis of Williams-Beuren syndrome by ultrasound and chromosomal microarray analysis 2022 ·Molecular Cytogenetics ·(unknown), Hang Zhou, Fang Fu, Ru Li, Tingying Lei, (unknown), (unknown), You Wang, Xin Yang, Lushan Li, Xiangyi Jing, Yongling Zhang, Fucheng Li, Dong‐Zhi Li, Can Liao	6
12	Evaluation of the Z‐score accuracy of noninvasive prenatal testing for fetal trisomies 13, 18 and 21 at a single center 2021 ·Prenatal Diagnosis ·(unknown), Ru Li, Qiuxia Yu, Dan Wang, (unknown), Yongling Zhang, Xiangyi Jing, Fatao Li, (unknown), Guilan Chen, (unknown), Fucheng Li, Fang Fu, Yan Li, Lina Zhang, (unknown), Jian Li, (unknown), Can Liao	22
13	Genetic tests aid in counseling of fetuses with cerebellar vermis defects 2020 ·Prenatal Diagnosis ·Lushan Li, Fang Fu, Ru Li, (unknown), Qiuxia Yu, Dan Wang, Xiangyi Jing, Yongning Zhang, Xin Yang, Min Pan, (unknown), Can Liao	14
14	Pregnancy outcome of autosomal aneuploidies other than common trisomies detected by noninvasive prenatal testing in routine clinical practice 2018 ·Prenatal Diagnosis ·(unknown), Ru Li, Yongling Zhang, Xiangyi Jing, Qiuxia Yu, Fatao Li, Yan Li, Lina Zhang, (unknown), Jian Li, Dong‐Zhi Li, Can Liao	25
15	Application of chromosome microarray analysis in patients with unexplained developmental delay/intellectual disability in South China 2018 ·Pediatrics & Neonatology ·Rongyue Wang, Tingying Lei, Fang Fu, Ru Li, Xiangyi Jing, Xin Yang, (unknown), (unknown), Can Liao	22
16	Clinical application of SNP array analysis in fetuses with ventricular septal defects and normal karyotypes 2017 ·Archives of Gynecology and Obstetrics ·Fang Fu, Qiong Deng, Tingying Lei, Ru Li, Xiangyi Jing, Xin Yang, Can Liao	23
17	Whole-exome sequencing for prenatal diagnosis of fetuses with congenital anomalies of the kidney and urinary tract 2017 ·Nephrology Dialysis Transplantation ·Tingying Lei, Fang Fu, Ru Li, Dan Wang, (unknown), Xiangyi Jing, Qiong Deng, (unknown), (unknown), Xin Yang, Dong‐Zhi Li, Can Liao	50
18	Dent Disease in Chinese Children and Findings from Heterozygous Mothers: Phenotypic Heterogeneity, Fetal Growth, and 10 Novel Mutations 2016 ·The Journal of Pediatrics ·Fucheng Li, (unknown), Tingting Xu, Minghui Chen, (unknown), Ting Liu, Xiangyi Jing, (unknown), Bin Hu, Yuling Liu, Haiyan Wang, Kar Neng Lai, Liangzhong Sun, Jinsong Liu, Patrick H. Maxwell, Yiming Wang	14
19	Novel genes and variants associated with IgA nephropathy by co-segregating with the disease phenotypes in 10 IgAN families 2015 ·Gene ·(unknown), Bin Hu, Qibin Li, Xiangyi Jing, Cheng Zhong, Yu Mei Chang, (unknown), Man Fai Lam, Joseph C.K. Leung, Kar Neng Lai, Yiming Wang	10
20	Characterization of 26 deletion CNVs reveals the frequent occurrence of micro-mutations within the breakpoint-flanking regions and frequent repair of double-strand breaks by templated insertions derived from remote genomic regions 2015 ·Human Genetics ·Ye Wang, Peiqiang Su, Bin Hu, Wenjuan Zhu, Qibin Li, Ping Yuan, Jiangchao Li, Xin‐Yuan Guan, Fucheng Li, Xiangyi Jing, Ru Li, Yongling Zhang, Claude Férec, D.N. Cooper, Jun Wang, Dongsheng Huang, Jian‐Min Chen, Yiming Wang	20

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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