Yiping Shen

14.8k citations

195 papers · 5.6k indexed · 1 hit paper · h-index 36

Molecular Biology top 2%
Genetics top 0.5%
Cognitive Neuroscience top 2%
Cellular and Molecular Neuroscience top 5%
Pediatrics, Perinatology and Child Health top 2%

Co-authors: James F. Gusella Bai-Lin Wu Mark A. Metcalf Pedro A. José Frederick J. Monsma Mark W. Hamblin David R. Sibley Karina F. Meiri
Topics: Genomic variations and chromosomal abnormalities (65 papers)Genomics and Rare Diseases (37 papers)Genetics and Neurodevelopmental Disorders (30 papers)
Cited by: Genetics Molecular Biology Cognitive Neuroscience
Journals: New England Journal of Medicine Proceedings of the National Academy of Sciences Journal of Biological Chemistry
Partner nations: United States China South Korea

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

#	Work	Indexed citations
1	Transcriptomic analysis of mRNA and miRNA reveals new insights into the regulatory mechanisms of Anadara granosa responses to heat stress 2024 ·Comparative Biochemistry and Physiology Part D Genomics and Proteomics ·Xin He,(unknown),Yiping Shen,(unknown),Shi Wang,Yongbo Bao	1
2	CTCF variant begets to short stature by down-regulation of IGF1 2023 ·Journal of Molecular Endocrinology ·Hong Chen,Weiyu Li,Suping Zhang,(unknown),Yiping Shen,Ruimin Chen	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 2023 ·Scientific Reports ·(unknown),Shotaro Kishikawa,Vijay Gupta,Natalia T. Leach,Yiping Shen,Oana Moldovan,Himanshu Goel,(unknown),(unknown),Nicolas Gruchy,Saskia M. Maas,Yves Lacassie,Soo‐Hyun Kim,Woo-Yang Kim,Bradley J. Quade,Cynthia C. Morton,Cheol‐Hee Kim,Lawrence C. Layman,Hyung‐Goo Kim	2
4	The phenotypic spectrum of Kabuki syndrome in patients of Chinese descent: A case series 2019 ·American Journal of Medical Genetics Part A ·Yirou Wang,Niu Li,Zhe Su,Yufei Xu,Shijian Liu,Yao Chen,(unknown),Yiping Shen,Christina Hung,Jian Wang,Xiumin Wang,Olaf A. Bodamer	10
5	Three additional de novo CTCF mutations in Chinese patients help to define an emerging neurodevelopmental disorder 2019 ·American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Fei Chen,(unknown),(unknown),Shaoke Chen,Qi Yang,Jin Wang,Qiang Zhang,(unknown),Xin Fan,Ruimin Chen,Yiping Shen	18
6	New insights from unbiased panel and whole-exome sequencing in a large Chinese cohort with disorders of sex development 2019 ·European Journal of Endocrinology ·Yufei Xu,Yirou Wang,Niu Li,Ruen Yao,Guoqiang Li,Juan Li,Yu Ding,Yao Chen,Xiaodong Huang,Yuling Chen,(unknown),Tingting Yu,Yongnian Shen,Xiumin Wang,Yiping Shen,Jian Wang	20
7	Non-invasive prenatal screening for fetal aneuploidy in twin pregnancies by cell-free DNA analysis 2018 ·Clinical and Experimental Obstetrics & Gynecology ·Yun Chen,Yunli Lai,Yi Shang,Yanqing Tang,(unknown),Yi Sheng,Yiping Shen,Hongwei Wei	2
8	Three‐generation family with novel contiguous gene deletion on chromosome 2p22 associated with thoracic aortic aneurysm syndrome 2018 ·American Journal of Medical Genetics Part A ·(unknown),Grace E. VanNoy,Meghan C. Towne,Yiping Shen,Michael Singh,Pankaj B. Agrawal,Sharon E. Smith	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 2018 ·Molecular and Cellular Endocrinology ·Tingting Yu,Guoying Chang,Qing Cheng,Ruen Yao,Juan Li,Yufei Xu,Guoqiang Li,Yu Ding,(unknown),Niu Li,Yiping Shen,Xiumin Wang,Jian Wang	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 2017 ·Genetics in Medicine ·Xuyun Hu,Niu Li,Yufei Xu,(unknown),Tingting Yu,Ruen Yao,Lijun Fu,Jiwen Wang,Lei Yin,Yong Yin,Ying Wang,Xingming Jin,Xiumin Wang,Jian Wang,Yiping Shen	59
11	Evaluation of three read-depth based CNV detection tools using whole-exome sequencing data 2017 ·Molecular Cytogenetics ·Ruen Yao,Cheng Zhang,Tingting Yu,Niu Li,Xuyun Hu,Xiumin Wang,Jian Wang,Yiping Shen	67
12	Maternal uniparental disomy 14 and mosaic trisomy 14 in a Chinese boy with moderate to severe intellectual disability 2016 ·Molecular Cytogenetics ·Shujie Zhang,(unknown),Jin Wang,(unknown),Shiyu Luo,Chunyun Fu,Xin Fan,Jiasun Su,Rongyu Chen,Bobo Xie,Xuyun Hu,Shaoke Chen,Yiping Shen	10
13	A behavioral defect of temporal association memory in mice that partly lack dopamine reuptake transporter 2015 ·Scientific Reports ·Shining Deng,Lingli Zhang,(unknown),Yanmei Liu,Hailong Zhang,Yiping Shen,Wei‐Guang Li,Fēi Li	13
14	Exome sequencing reveals a novel PTHLH mutation in a Chinese pedigree with brachydactyly type E and short stature 2015 ·Clinica Chimica Acta ·Jian Wang,Zhigang Wang,Yu An,(unknown),Yunlan Xu,Qihua Fu,Yiping Shen,Qinghua Zhang	17
15	Novel frame-shift mutations of GLI3 gene in non-syndromic postaxial polydactyly patients 2014 ·Clinica Chimica Acta ·Zhigang Wang,Jian Wang,Yuchan Li,Juan Geng,Qihua Fu,Yunlan Xu,Yiping Shen	17
16	Detection of Copy Number Variants Reveals Association of Cilia Genes with Neural Tube Defects 2013 ·PLoS ONE ·Xiaoli Chen,Yiping Shen,Yonghui Gao,Huizhi Zhao,Xiaoming Sheng,Jizhen Zou,Va Lip,Hua Xie,Jin Guo,(unknown),Yihua Bao,Jianliang Shen,Bo Niu,James F. Gusella,Bai-Lin Wu,Ting Zhang	31
17	Genome-wide Association of Copy-Number Variation Reveals an Association between Short Stature and the Presence of Low-Frequency Genomic Deletions 2011 ·The American Journal of Human Genetics ·Andrew Dauber,Yongguo Yu,Michael C. Turchin,Charleston W. K. Chiang,Yan Meng,Ellen W. Demerath,Sanjay R. Patel,Stephen S. Rich,Jerome I. Rotter,Pamela J. Schreiner,James Wilson,Yiping Shen,Bai-Lin Wu,Joel N. Hirschhorn	56
18	Next-Generation Sequencing Strategies Enable Routine Detection of Balanced Chromosome Rearrangements for Clinical Diagnostics and Genetic Research 2011 ·The American Journal of Human Genetics ·Michael E. Talkowski,Carl Ernst,Adrian Heilbut,Colby Chiang,Carrie Hanscom,Amelia M. Lindgren,Andrew Kirby,Shangtao Liu,(unknown),Toshiro K. Ohsumi,Yiping Shen,Mark L. Borowsky,Mark J. Daly,Cynthia C. Morton,James F. Gusella	120
19	Age- and gender-dependent obesity in individuals with 16p11.2 deletion 2011 ·Journal of genetics and genomics ·Yongguo Yu,Haitao Zhu,David T. Miller,James F. Gusella,Orah S. Platt,Bai-Lin Wu,Yiping Shen	14
20	Intra-family phenotypic heterogeneity of 16p11.2 deletion carriers in a three-generation Chinese family 2010 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Yiping Shen,Xiaoli Chen,Liwen Wang,Jin Guo,Jianliang Shen,Yu An,Haitao Zhu,Yanli Zhu,Ruolei Xin,Yihua Bao,James F. Gusella,Ting Zhang,Bai-Lin Wu	27

About Yiping Shen

Yiping Shen is a scholar working on Genetics, Developmental Biology and Pediatrics, Perinatology and Child Health, having authored 195 papers that have together received 5.6k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (65 papers), Genomics and Rare Diseases (37 papers) and Genetics and Neurodevelopmental Disorders (30 papers). The work is most often cited by research in Genetics (2.6k citations), Molecular Biology (2.8k citations) and Cognitive Neuroscience (728 citations). Yiping Shen has collaborated with scholars based in United States, China and South Korea. Frequent 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. Their work appears in journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

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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