Yu Peng

820 total citations
12 papers, 239 citations indexed

About

Yu Peng is a scholar working on Cognitive Neuroscience, Genetics and Molecular Biology. According to data from OpenAlex, Yu Peng has authored 12 papers receiving a total of 239 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Cognitive Neuroscience, 6 papers in Genetics and 5 papers in Molecular Biology. Recurrent topics in Yu Peng's work include Genetics and Neurodevelopmental Disorders (6 papers), Autism Spectrum Disorder Research (6 papers) and Genomic variations and chromosomal abnormalities (3 papers). Yu Peng is often cited by papers focused on Genetics and Neurodevelopmental Disorders (6 papers), Autism Spectrum Disorder Research (6 papers) and Genomic variations and chromosomal abnormalities (3 papers). Yu Peng collaborates with scholars based in China, France and Taiwan. Yu Peng's co-authors include Zhengmao Hu, Kun Xia, Zhimin Xiong, Yalan Liu, Jingping Zhao, Xiaojuan Xu, Hui Guo, Lina Lu, Kun Xia and Lu Xia and has published in prestigious journals such as Scientific Reports, Journal of Psychiatric Research and JCI Insight.

In The Last Decade

Yu Peng

12 papers receiving 228 citations

Peers

Countries citing papers authored by Yu Peng

Since Specialization

Citations

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

Fields of papers citing papers by Yu Peng

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yu Peng

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

All Works

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12 of 12 papers shown

#	Work	Indexed citations
1	Intergenic sequences harboring potential enhancer elements contribute to Axenfeld-Rieger syndrome by regulating PITX2 2024 ·JCI Insight ·(unknown), Yu Peng, Qi Tian, (unknown), Bei Feng, (unknown), Lu Xia, Hui Guo, Kun Xia, Liang Zhou, Zhengmao Hu	1
2	Time of day-dependent alterations of ferroptosis in LPS-induced myocardial injury via Bmal-1/AKT/ Nrf2 in rat and H9c2 cell 2024 ·Heliyon ·(unknown), (unknown), (unknown), (unknown), Yu Peng, Xiaohu Chen	3
3	Rare NRXN1 missense variants identified in autism interfered protein degradation and Drosophila sleeping 2021 ·Journal of Psychiatric Research ·Yalan Liu, Lu Shen, Yaowen Zhang, Rongjuan Zhao, (unknown), (unknown), Jingjing Chen, Lu Xia, (unknown), Yu Peng, Kun Xia	3
4	Total cholesterol affects the outcome of patients with anterior cerebral artery-occluded acute ischemic stroke treated with thrombolysis. 2020 ·PubMed ·(unknown), Shan Jiang, (unknown), Yu Peng, Aihua Fei, (unknown), Yan Li, (unknown), Cathy Meaney, Changjun Gao, Shuming Pan	7
5	Exome sequencing identifies POU4F3 as the causative gene for a large Chinese family with non-syndromic hearing loss 2016 ·Journal of Human Genetics ·Xinzhang Cai, Ying Li, Lu Xia, Yu Peng, (unknown), Lu Jiang, Yong Feng, Kun Xia, Xue Zhong Liu, Ling Mei, Zheng Hu	23
6	Association of genetic variants of GRIN2B with autism 2015 ·Scientific Reports ·Yongcheng Pan, Jingjing Chen, Hui Guo, Jianjun Ou, Yu Peng, Qiong Liu, Yidong Shen, Lijuan Shi, Yalan Liu, Zhimin Xiong, Tengfei Zhu, (unknown), Zhengmao Hu, Jingping Zhao, Kun Xia	38
7	Variations analysis of NLGN3 and NLGN4X gene in Chinese autism patients 2014 ·Molecular Biology Reports ·Xiaojuan Xu, Zhimin Xiong, Lusi Zhang, Yalan Liu, Lina Lu, Yu Peng, Hui Guo, Jingping Zhao, Kun Xia, Zhengmao Hu	30
8	AMPD1 functional variants associated with autism in Han Chinese population 2014 ·European Archives of Psychiatry and Clinical Neuroscience ·Lusi Zhang, Jianjun Ou, Xiaojuan Xu, Yu Peng, Hui Guo, Yongcheng Pan, Jingjing Chen, Tianyun Wang, Hao Peng, Qiong Liu, Di Tian, Qian Pan, Xiaobin Zou, Jingping Zhao, Zhengmao Hu, Kun Xia	5
9	Homozygous loss‐of‐function mutation of the LEPREL1 gene causes severe non‐syndromic high myopia with early‐onset cataract 2013 ·Clinical Genetics ·(unknown), Ping Tong, Yu Peng, (unknown), Yong Liu, (unknown), (unknown), Qi Tian, Yuantai Hu, Yi-Cong Zheng, (unknown), Wei Xiong, Qian Pan, Zhengmao Hu, Kun Xia	44
10	Mutation analysis of the NRXN1 gene in a Chinese autism cohort 2012 ·Journal of Psychiatric Research ·Yalan Liu, Zhengmao Hu, Guanglei Xun, Yu Peng, Lina Lu, Xiaojuan Xu, Zhimin Xiong, Lu Xia, Deyuan Liu, Wei Li, Jingping Zhao, Kun Xia	35
11	Association analysis of CNTNAP2 polymorphisms with autism in the Chinese Han population 2010 ·Psychiatric Genetics ·Xiaoping Li, Zhengmao Hu, Yiqun He, Zhimin Xiong, Zhigao Long, Yu Peng, Fengxiao Bu, Jie Ling, Guanglei Xun, (unknown), Qian Pan, Jingping Zhao, Kun Xia	49
12	Near-Optimal Block Alignments 2008 ·IEICE Transactions on Information and Systems ·(unknown), (unknown), (unknown), Yu Peng	1

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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