Yiping Shen

14.8k total citations · 1 hit paper
195 papers, 5.6k citations indexed

About

Yiping Shen is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Yiping Shen has authored 195 papers receiving a total of 5.6k indexed citations (citations by other indexed papers that have themselves been cited), including 111 papers in Genetics, 93 papers in Molecular Biology and 27 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Yiping Shen's work include Genomic variations and chromosomal abnormalities (65 papers), Genomics and Rare Diseases (37 papers) and Genetics and Neurodevelopmental Disorders (30 papers). Yiping Shen is often cited by papers focused on Genomic variations and chromosomal abnormalities (65 papers), Genomics and Rare Diseases (37 papers) and Genetics and Neurodevelopmental Disorders (30 papers). Yiping Shen collaborates with scholars based in United States, China and South Korea. Yiping Shen's co-authors include James F. Gusella, Bai-Lin Wu, Mark A. Metcalf, Pedro A. José, Frederick J. Monsma, Mark W. Hamblin, David R. Sibley, Karina F. Meiri, Orah S. Platt and Shyamala Mani and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Yiping Shen

188 papers receiving 5.4k citations

Hit Papers

Association between Microdeletion and Microduplication at... 2008 2026 2014 2020 2008 250 500 750 1000
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Association between Microdeletion and Microduplication at 16p11.2 and Autism
    2008 1.1k citations Yiping Shen, Orah S. Platt et al. profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yiping Shen United States 36 2.8k 2.6k 728 582 569 195 5.6k
Gerald V. Raymond United States 46 5.1k 1.8× 970 0.4× 406 0.6× 333 0.6× 471 0.8× 137 7.2k
Hossein Najmabadi Iran 41 3.5k 1.2× 1.7k 0.7× 252 0.3× 426 0.7× 396 0.7× 292 6.5k
Lodewijk A. Sandkuijl Netherlands 44 3.9k 1.4× 1.9k 0.7× 317 0.4× 755 1.3× 221 0.4× 94 7.7k
Jenny Hsieh United States 32 3.9k 1.4× 1.3k 0.5× 273 0.4× 1.6k 2.8× 317 0.6× 64 6.2k
Xuekun Li China 34 5.2k 1.8× 1.5k 0.6× 335 0.5× 952 1.6× 297 0.5× 93 6.9k
Richard J. Sinke Netherlands 39 2.2k 0.8× 1.2k 0.5× 231 0.3× 1.2k 2.0× 286 0.5× 119 4.4k
Nine V.A.M. Knoers Netherlands 54 6.4k 2.3× 2.4k 0.9× 137 0.2× 599 1.0× 943 1.7× 152 9.2k
Kazuaki Yoshikawa Japan 43 3.6k 1.3× 1.3k 0.5× 163 0.2× 1.2k 2.0× 246 0.4× 142 5.7k
Zeynep Tümer Denmark 39 3.4k 1.2× 1.9k 0.7× 252 0.3× 283 0.5× 517 0.9× 180 5.7k

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

20 of 20 papers shown
1.
He, Xin, et al.. (2024). Transcriptomic analysis of mRNA and miRNA reveals new insights into the regulatory mechanisms of Anadara granosa responses to heat stress. Comparative Biochemistry and Physiology Part D Genomics and Proteomics. 52. 101311–101311. 1 indexed citations
2.
Chen, Hong, et al.. (2023). CTCF variant begets to short stature by down-regulation of IGF1. Journal of Molecular Endocrinology. 70(4). 1 indexed citations
3.
Kishikawa, Shotaro, Vijay Gupta, Natalia T. Leach, et al.. (2023). A cryptic microdeletion del(12)(p11.21p11.23) within an unbalanced translocation t(7;12)(q21.13;q23.1) implicates new candidate loci for intellectual disability and Kallmann syndrome. Scientific Reports. 13(1). 12984–12984. 2 indexed citations
4.
Wang, Yirou, Niu Li, Zhe Su, et al.. (2019). The phenotypic spectrum of Kabuki syndrome in patients of Chinese descent: A case series. American Journal of Medical Genetics Part A. 182(4). 640–651. 10 indexed citations
5.
Chen, Fei, Shaoke Chen, Qi Yang, et al.. (2019). Three additional de novo CTCF mutations in Chinese patients help to define an emerging neurodevelopmental disorder. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 181(2). 218–225. 18 indexed citations
6.
Xu, Yufei, Yirou Wang, Niu Li, et al.. (2019). New insights from unbiased panel and whole-exome sequencing in a large Chinese cohort with disorders of sex development. European Journal of Endocrinology. 181(3). 311–323. 20 indexed citations
7.
Chen, Yun, Yunli Lai, Yi Shang, et al.. (2018). Non-invasive prenatal screening for fetal aneuploidy in twin pregnancies by cell-free DNA analysis. Clinical and Experimental Obstetrics & Gynecology. 45(5). 656–660. 2 indexed citations
8.
VanNoy, Grace E., Meghan C. Towne, Yiping Shen, et al.. (2018). Three‐generation family with novel contiguous gene deletion on chromosome 2p22 associated with thoracic aortic aneurysm syndrome. American Journal of Medical Genetics Part A. 176(3). 560–569. 11 indexed citations
9.
10.
11.
Yao, Ruen, Cheng Zhang, Tingting Yu, et al.. (2017). Evaluation of three read-depth based CNV detection tools using whole-exome sequencing data. Molecular Cytogenetics. 10(1). 30–30. 67 indexed citations
12.
Zhang, Shujie, Jin Wang, Shiyu Luo, et al.. (2016). Maternal uniparental disomy 14 and mosaic trisomy 14 in a Chinese boy with moderate to severe intellectual disability. Molecular Cytogenetics. 9(1). 66–66. 10 indexed citations
13.
Deng, Shining, Lingli Zhang, Yanmei Liu, et al.. (2015). A behavioral defect of temporal association memory in mice that partly lack dopamine reuptake transporter. Scientific Reports. 5(1). 17461–17461. 13 indexed citations
14.
Wang, Jian, Zhigang Wang, Yu An, et al.. (2015). Exome sequencing reveals a novel PTHLH mutation in a Chinese pedigree with brachydactyly type E and short stature. Clinica Chimica Acta. 446. 9–14. 17 indexed citations
15.
Wang, Zhigang, Jian Wang, Yuchan Li, et al.. (2014). Novel frame-shift mutations of GLI3 gene in non-syndromic postaxial polydactyly patients. Clinica Chimica Acta. 433. 195–199. 17 indexed citations
16.
Chen, Xiaoli, Yiping Shen, Yonghui Gao, et al.. (2013). Detection of Copy Number Variants Reveals Association of Cilia Genes with Neural Tube Defects. PLoS ONE. 8(1). e54492–e54492. 31 indexed citations
17.
Dauber, Andrew, Yongguo Yu, Michael C. Turchin, et al.. (2011). Genome-wide Association of Copy-Number Variation Reveals an Association between Short Stature and the Presence of Low-Frequency Genomic Deletions. The American Journal of Human Genetics. 89(6). 751–759. 56 indexed citations
18.
Talkowski, Michael E., Carl Ernst, Adrian Heilbut, et al.. (2011). Next-Generation Sequencing Strategies Enable Routine Detection of Balanced Chromosome Rearrangements for Clinical Diagnostics and Genetic Research. The American Journal of Human Genetics. 88(4). 469–481. 120 indexed citations
19.
Yu, Yongguo, Haitao Zhu, David T. Miller, et al.. (2011). Age- and gender-dependent obesity in individuals with 16p11.2 deletion. Journal of genetics and genomics. 38(9). 403–409. 14 indexed citations
20.
Shen, Yiping, Xiaoli Chen, Liwen Wang, et al.. (2010). Intra-family phenotypic heterogeneity of 16p11.2 deletion carriers in a three-generation Chinese family. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 156(2). 225–232. 27 indexed citations

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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