Yiping Shen

890 total citations
12 papers, 275 citations indexed

About

Yiping Shen is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Yiping Shen has authored 12 papers receiving a total of 275 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 6 papers in Genetics and 2 papers in Oncology. Recurrent topics in Yiping Shen's work include Congenital heart defects research (4 papers), Genetics and Neurodevelopmental Disorders (3 papers) and RNA modifications and cancer (2 papers). Yiping Shen is often cited by papers focused on Congenital heart defects research (4 papers), Genetics and Neurodevelopmental Disorders (3 papers) and RNA modifications and cancer (2 papers). Yiping Shen collaborates with scholars based in China, United States and South Korea. Yiping Shen's co-authors include Jin Li, Bai-Lin Wu, Shuhua Xu, Haifeng Wang, Wenfei Jin, Yongguo Yu, Jennifer Moon, Timothy C. Miller, Emily C. Walvoord and Michael H. Guo and has published in prestigious journals such as PLoS ONE, Genome Research and Human Molecular Genetics.

In The Last Decade

Yiping Shen

10 papers receiving 273 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Yiping Shen China	9	151	144	42	39	23	12	275
G. Bryce Christensen United States	8	206 1.4×	142 1.0×	42 1.0×	20 0.5×	41 1.8×	12	362
Gianna Carvalheira Brazil	14	144 1.0×	182 1.3×	55 1.3×	36 0.9×	18 0.8×	25	381
Emilie Ait‐Yahya France	7	151 1.0×	171 1.2×	12 0.3×	51 1.3×	11 0.5×	18	366
Frédérique Sloan‐Béna Switzerland	9	87 0.6×	123 0.9×	8 0.2×	14 0.4×	24 1.0×	23	263
Irén Haltrich Hungary	9	93 0.6×	103 0.7×	8 0.2×	25 0.6×	33 1.4×	33	239
Sandesh C. Sreenath Nagamani United States	6	218 1.4×	194 1.3×	12 0.3×	13 0.3×	27 1.2×	8	349
Lea Velsher Canada	8	91 0.6×	61 0.4×	16 0.4×	22 0.6×	7 0.3×	18	181
Massimiliano Cocca Italy	9	92 0.6×	91 0.6×	19 0.5×	20 0.5×	26 1.1×	20	352
Oddveig Røsby Norway	10	114 0.8×	131 0.9×	21 0.5×	23 0.6×	5 0.2×	13	262
Nathalie Marle France	11	237 1.6×	170 1.2×	40 1.0×	10 0.3×	16 0.7×	23	373

Countries citing papers authored by Yiping Shen

Since Specialization

Citations

This map shows the geographic impact of Yiping Shen'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 Yiping Shen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Yiping Shen more than expected).

Fields of papers citing papers by Yiping Shen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Yiping Shen. 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 Yiping Shen. The network helps show where Yiping Shen may publish in the future.

Co-authorship network of co-authors of Yiping Shen

This figure shows the co-authorship network connecting the top 25 collaborators of Yiping Shen. A scholar is included among the top collaborators of Yiping Shen 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 Yiping Shen. Yiping Shen is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

12 of 12 papers shown

Shen, Yiping, et al.. (2023). Identification of acetyl-CoA carboxylase alpha as a prognostic and targeted candidate for hepatocellular carcinoma. Clinical & Translational Oncology. 25(8). 2499–2513. 8 indexed citations

Zhu, Mengqi, Jianping Zhang, Saiyan Bian, et al.. (2022). Circadian gene CSNK1D promoted the progression of hepatocellular carcinoma by activating Wnt/β-catenin pathway via stabilizing Dishevelled Segment Polarity Protein 3. Biological Procedures Online. 24(1). 21–21. 9 indexed citations

Bian, Saiyan, Wenkai Ni, Mengqi Zhu, et al.. (2022). Flap endonuclease 1 Facilitated Hepatocellular Carcinoma Progression by Enhancing USP7/MDM2-mediated P53 Inactivation. International Journal of Biological Sciences. 18(3). 1022–1038. 38 indexed citations

An, Yu, Wenyuan Duan, Guoying Huang, et al.. (2015). Genome-wide copy number variant analysis for congenital ventricular septal defects in Chinese Han population. BMC Medical Genomics. 9(1). 2–2. 20 indexed citations

Fu, Chunyun, Rongyu Chen, Shujie Zhang, et al.. (2015). PAX8 pathogenic variants in Chinese patients with congenital hypothyroidism. Clinica Chimica Acta. 450. 322–326. 17 indexed citations

Guo, Michael H., Yiping Shen, Emily C. Walvoord, et al.. (2014). Whole Exome Sequencing to Identify Genetic Causes of Short Stature. Hormone Research in Paediatrics. 82(1). 44–52. 58 indexed citations

Zhou, Weichen, Feng Zhang, Xiaoli Chen, et al.. (2013). Increased genome instability in human DNA segments with self-chains: homology-induced structural variations via replicative mechanisms. Human Molecular Genetics. 22(13). 2642–2651. 15 indexed citations

Yang, Likui, Qiulan Ding, Yiping Shen, Xuefeng Wang, & Alireza R. Rezaie. (2013). The missense Thr211Pro mutation in the factor X activation peptide of a bleeding patient causes molecular defect in the clotting cascade. Thrombosis and Haemostasis. 110(7). 53–61. 5 indexed citations

Gong, Xiaohong, Yuwu Jiang, Yu An, et al.. (2012). High Proportion of 22q13 Deletions and SHANK3 Mutations in Chinese Patients with Intellectual Disability. PLoS ONE. 7(4). e34739–e34739. 39 indexed citations

10.

Jin, Wenfei, Shuhua Xu, Haifeng Wang, et al.. (2011). Genome-wide detection of natural selection in African Americans pre- and post-admixture. Genome Research. 22(3). 519–527. 66 indexed citations

11.

Zhu, Haitao, et al.. (2010). Genetic Prognostic Markers in Neuroblastoma. North American Journal of Medicine and Science. 3(3). 123–123.

12.

Kao, Fa‐Ten, et al.. (1996). Construction and characterization of three region-specific microdissection libraries for human chromosome 18. Somatic Cell and Molecular Genetics. 22(3). 191–199.

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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