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

align trajectories

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.

Association between Microdeletion and Microduplication at 16p11.2 and Autism

2008 1.1k citations Yiping Shen, Orah S. Platt et al. profile →

Peers

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

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20 of 20 papers shown

#	Title	Journal	Authors	Indexed citations
1	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	Xin He, Yiping Shen et al.	1
2	CTCF variant begets to short stature by down-regulation of IGF1	Journal of Molecular Endocrinology	Hong Chen, Weiyu Li et al.	1
3	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	Shotaro Kishikawa, Vijay Gupta et al.	2
4	The phenotypic spectrum of Kabuki syndrome in patients of Chinese descent: A case series	American Journal of Medical Genetics Part A	Yirou Wang, Niu Li et al.	10
5	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	Fei Chen, Shaoke Chen et al.	18
6	New insights from unbiased panel and whole-exome sequencing in a large Chinese cohort with disorders of sex development	European Journal of Endocrinology	Yufei Xu, Yirou Wang et al.	20
7	Non-invasive prenatal screening for fetal aneuploidy in twin pregnancies by cell-free DNA analysis	Clinical and Experimental Obstetrics & Gynecology	Yun Chen, Yunli Lai et al.	2
8	Three‐generation family with novel contiguous gene deletion on chromosome 2p22 associated with thoracic aortic aneurysm syndrome	American Journal of Medical Genetics Part A	Grace E. VanNoy, Meghan C. Towne et al.	11
9	Increased transactivation and impaired repression of β-catenin-mediated transcription associated with a novel SOX3 missense mutation in an X-linked hypopituitarism pedigree with modest growth failure	Molecular and Cellular Endocrinology	Tingting Yu, Guoying Chang et al.	4
10	Proband-only medical exome sequencing as a cost-effective first-tier genetic diagnostic test for patients without prior molecular tests and clinical diagnosis in a developing country: the China experience	Genetics in Medicine	Xuyun Hu, Niu Li et al.	59
11	Evaluation of three read-depth based CNV detection tools using whole-exome sequencing data	Molecular Cytogenetics	Ruen Yao, Cheng Zhang et al.	67
12	Maternal uniparental disomy 14 and mosaic trisomy 14 in a Chinese boy with moderate to severe intellectual disability	Molecular Cytogenetics	Shujie Zhang, Jin Wang et al.	10
13	A behavioral defect of temporal association memory in mice that partly lack dopamine reuptake transporter	Scientific Reports	Shining Deng, Lingli Zhang et al.	13
14	Exome sequencing reveals a novel PTHLH mutation in a Chinese pedigree with brachydactyly type E and short stature	Clinica Chimica Acta	Jian Wang, Zhigang Wang et al.	17
15	Novel frame-shift mutations of GLI3 gene in non-syndromic postaxial polydactyly patients	Clinica Chimica Acta	Zhigang Wang, Jian Wang et al.	17
16	Detection of Copy Number Variants Reveals Association of Cilia Genes with Neural Tube Defects	PLoS ONE	Xiaoli Chen, Yiping Shen et al.	31
17	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	Andrew Dauber, Yongguo Yu et al.	56
18	Next-Generation Sequencing Strategies Enable Routine Detection of Balanced Chromosome Rearrangements for Clinical Diagnostics and Genetic Research	The American Journal of Human Genetics	Michael E. Talkowski, Carl Ernst et al.	120
19	Age- and gender-dependent obesity in individuals with 16p11.2 deletion	Journal of genetics and genomics	Yongguo Yu, Haitao Zhu et al.	14
20	Intra-family phenotypic heterogeneity of 16p11.2 deletion carriers in a three-generation Chinese family	American Journal of Medical Genetics Part B Neuropsychiatric Genetics	Yiping Shen, Xiaoli Chen et al.	27

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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