Haipo Yang

575 total citations
29 papers, 220 citations indexed

About

Haipo Yang is a scholar working on Molecular Biology, Psychiatry and Mental health and Cellular and Molecular Neuroscience. According to data from OpenAlex, Haipo Yang has authored 29 papers receiving a total of 220 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 8 papers in Psychiatry and Mental health and 7 papers in Cellular and Molecular Neuroscience. Recurrent topics in Haipo Yang's work include Muscle Physiology and Disorders (13 papers), Epilepsy research and treatment (7 papers) and RNA Research and Splicing (7 papers). Haipo Yang is often cited by papers focused on Muscle Physiology and Disorders (13 papers), Epilepsy research and treatment (7 papers) and RNA Research and Splicing (7 papers). Haipo Yang collaborates with scholars based in China, United States and Japan. Haipo Yang's co-authors include Hui Xiong, Yanping Wang, Zhulong Chan, Xiru Wu, Lin Meng, Lin Xiang, Zhixian Yang, Xiaoyan Liu, Xue Jiao and Carsten G. Bönnemann and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and PLANT PHYSIOLOGY.

In The Last Decade

Haipo Yang

26 papers receiving 212 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Haipo Yang China 10 145 50 44 40 34 29 220
Viola Doccini Italy 9 109 0.8× 58 1.2× 25 0.6× 92 2.3× 17 0.5× 10 317
Lijuan Yan China 7 234 1.6× 46 0.9× 48 1.1× 10 0.3× 4 0.1× 15 296
Thuong Ha Australia 6 77 0.5× 13 0.3× 5 0.1× 9 0.2× 5 0.1× 13 136
Nicoletta Zanotta Italy 8 70 0.5× 59 1.2× 4 0.1× 69 1.7× 11 0.3× 16 169
Mette Gilling Denmark 6 64 0.4× 41 0.8× 14 0.3× 3 0.1× 19 0.6× 7 124
Rita Teek Estonia 9 126 0.9× 34 0.7× 10 0.2× 14 0.3× 5 0.1× 14 221
Dana Marafi United States 8 88 0.6× 22 0.4× 5 0.1× 13 0.3× 10 0.3× 24 171
Theresa Scattergood United States 5 117 0.8× 100 2.0× 3 0.1× 85 2.1× 21 0.6× 7 220
A. Nazlı Başak Türkiye 7 50 0.3× 44 0.9× 15 0.3× 11 0.3× 2 0.1× 14 158
Patrícia B. S. Celestino-Soper United States 5 97 0.7× 26 0.5× 8 0.2× 6 0.1× 33 1.0× 8 166

Countries citing papers authored by Haipo Yang

Since Specialization
Citations

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

Fields of papers citing papers by Haipo Yang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Haipo Yang

This figure shows the co-authorship network connecting the top 25 collaborators of Haipo Yang. A scholar is included among the top collaborators of Haipo Yang 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 Haipo Yang. Haipo Yang 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.
Arens, Paul, Liangsheng Zhang, Haipo Yang, et al.. (2025). Sugar transport in tulip is modulated by TgRR12TgTCP2 signaling through TgSUT4 . New Phytologist. 249(3). 1342–1359.
2.
Wang, Ting, et al.. (2025). A zebrafish model unravels the role of PHF21A in neurodevelopment and epilepsy. Neuroscience. 584. 138–147.
3.
Meng, Lin, Haipo Yang, Yaping Wang, et al.. (2024). Tulip transcription factor TgWRKY75 activates salicylic acid and abscisic acid biosynthesis to synergistically promote petal senescence. Journal of Experimental Botany. 75(8). 2435–2450. 11 indexed citations
4.
Yang, Haipo & Shuang Wang. (2024). Generalized paroxysmal fast activity in a cohort of patients with epilepsy with eyelid myoclonia. Clinical Neurophysiology. 167. 192–197.
5.
Huang, Xiuli, Dandan Tan, Zaiqiang Zhang, et al.. (2023). Unique genotype-phenotype correlations within LAMA2-related limb girdle muscular dystrophy in Chinese patients. Frontiers in Neurology. 14. 1158094–1158094. 3 indexed citations
6.
Yang, Haipo, Xiaoyu Chen, Ying Zhu, et al.. (2022). Seizures and EEG characteristics in a cohort of pediatric patients with dystroglycanopathies. Seizure. 101. 39–47. 3 indexed citations
7.
Yang, Haipo, et al.. (2021). The relationship between the characteristics of burst suppression pattern and different etiologies in epilepsy. Scientific Reports. 11(1). 15903–15903. 3 indexed citations
8.
Yang, Haipo, et al.. (2021). De Novo Variants in the DYNC1H1 Gene Associated With Infantile Spasms. Frontiers in Neurology. 12. 733178–733178. 2 indexed citations
9.
Liao, Ying, Jianguang Qi, Qingyou Zhang, et al.. (2021). Comorbidity of chronic fatigue syndrome, postural tachycardia syndrome, and narcolepsy with 5,10-methylenetetrahydrofolate reductase (MTHFR) mutation in an adolescent: a case report. Chinese Medical Journal. 134(12). 1495–1497. 2 indexed citations
10.
Fan, Yanbin, Dandan Tan, Xu Zhang, et al.. (2020). Nuclear Factor-κB Pathway Mediates the Molecular Pathogenesis of LMNA-Related Muscular Dystrophies. Biochemical Genetics. 58(6). 966–980. 5 indexed citations
11.
Lin, Ge, Aijie Liu, Kai Gao, et al.. (2018). Deletion of exon 4 in LAMA2 is the most frequent mutation in Chinese patients with laminin α2-related muscular dystrophy. Scientific Reports. 8(1). 14989–14989. 14 indexed citations
12.
Jiao, Xue, Ping Qian, Haipo Yang, et al.. (2018). Scalp-recorded high-frequency oscillations in childhood epileptic encephalopathy with continuous spike-and-wave during sleep with different etiologies. Brain and Development. 40(4). 299–310. 27 indexed citations
13.
Yang, Haipo, Shuo Wang, Aijie Liu, et al.. (2017). Novel copy number variation of POMGNT1 associated with muscle-eye-brain disease detected by next-generation sequencing. Scientific Reports. 7(1). 7056–7056. 4 indexed citations
14.
Jiao, Xue, Ping Qian, Hui Li, et al.. (2016). Atonic elements combined or uncombined with epileptic spasms in infantile spasms. Clinical Neurophysiology. 128(1). 220–226. 4 indexed citations
15.
Yang, Haipo, Hiroshi Manya, Kazuhiro Kobayashi, et al.. (2016). Analysis of phenotype, enzyme activity and genotype of Chinese patients with POMT1 mutation. Journal of Human Genetics. 61(8). 753–759. 13 indexed citations
16.
Yang, Haipo, Cuijie Wei, Shuo Wang, et al.. (2016). FKRP mutations, including a founder mutation, cause phenotype variability in Chinese patients with dystroglycanopathies. Journal of Human Genetics. 61(12). 1013–1020. 12 indexed citations
17.
Yang, Haipo, Kazuhiro Kobayashi, Shuo Wang, et al.. (2015). Founder mutation causes classical Fukuyama congenital muscular dystrophy (FCMD) in Chinese patients. Brain and Development. 37(9). 880–886. 4 indexed citations
18.
Zhao, Dandan, Renqian Du, Yuehua Zhang, et al.. (2015). Clinical and molecular genetic analysis of a family with late-onset LAMA2-related muscular dystrophy. Brain and Development. 38(2). 242–249. 10 indexed citations
19.
Wei, Cuijie, Haipo Yang, Aijie Liu, et al.. (2015). [Duchenne and Becker muscular dystrophy complicated with epilepsy].. PubMed. 53(4). 274–9. 2 indexed citations
20.
Zhao, Danhua, Haipo Yang, Aijie Liu, et al.. (2014). Novel collagen VI mutations identified in Chinese patients with Ullrich congenital muscular dystrophy. World Journal of Pediatrics. 10(2). 126–132. 14 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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