Zuozhen Yang

1.5k total citations
40 papers, 482 citations indexed

About

Zuozhen Yang is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Zuozhen Yang has authored 40 papers receiving a total of 482 indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 15 papers in Genetics and 6 papers in Oncology. Recurrent topics in Zuozhen Yang's work include Genomics and Rare Diseases (11 papers), Genetics and Neurodevelopmental Disorders (9 papers) and RNA and protein synthesis mechanisms (6 papers). Zuozhen Yang is often cited by papers focused on Genomics and Rare Diseases (11 papers), Genetics and Neurodevelopmental Disorders (9 papers) and RNA and protein synthesis mechanisms (6 papers). Zuozhen Yang collaborates with scholars based in China, Australia and United States. Zuozhen Yang's co-authors include Min Liu, Tao Liu, Shuang Chen, Hua Tang, Xin Li, Yixuan Li, Xiuru Zhang, Y. Zhang, Ping Yang and Hongmei Jing and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and Nature Cell Biology.

In The Last Decade

Zuozhen Yang

37 papers receiving 476 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Zuozhen Yang China 10 363 191 72 53 48 40 482
Stephanie Greer United States 9 229 0.6× 90 0.5× 62 0.9× 58 1.1× 27 0.6× 18 339
Hanna M. Petrykowska United States 14 469 1.3× 114 0.6× 95 1.3× 28 0.5× 24 0.5× 22 538
Veronika I. Zabarovska Sweden 13 508 1.4× 146 0.8× 88 1.2× 98 1.8× 30 0.6× 19 635
Sree Rama Chaitanya Sridhara Portugal 9 552 1.5× 64 0.3× 50 0.7× 45 0.8× 33 0.7× 12 640
Li-Juan Ji China 9 413 1.1× 212 1.1× 54 0.8× 53 1.0× 42 0.9× 10 495
Ashley Cass United States 8 319 0.9× 105 0.5× 48 0.7× 59 1.1× 25 0.5× 13 429
Stefania Oliveto Italy 11 448 1.2× 271 1.4× 21 0.3× 52 1.0× 33 0.7× 18 629
Erik J. Coffman United States 5 543 1.5× 115 0.6× 89 1.2× 54 1.0× 44 0.9× 6 598
Maxim Pilyugin Switzerland 10 351 1.0× 96 0.5× 67 0.9× 68 1.3× 15 0.3× 16 413

Countries citing papers authored by Zuozhen Yang

Since Specialization
Citations

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

Fields of papers citing papers by Zuozhen Yang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Zuozhen Yang

This figure shows the co-authorship network connecting the top 25 collaborators of Zuozhen Yang. A scholar is included among the top collaborators of Zuozhen 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 Zuozhen Yang. Zuozhen 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.
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Cai, Qianyun, Yanmei Tian, Rong Luo, et al.. (2024). A case report on deficiency of adenosine deaminase 2 with relapse–remission course and analysis of genotype–phenotype correlation. American Journal of Medical Genetics Part A. 194(6). e63568–e63568. 1 indexed citations
3.
He, Xinyu, Fan Xiao, Lei Qu, et al.. (2023). LncRNA modulates Hippo-YAP signaling to reprogram iron metabolism. Nature Communications. 14(1). 2253–2253. 34 indexed citations
4.
Jia, Xiaoyi, et al.. (2023). A novel variant in BCL11B in an individual with neurodevelopmental delay: A case report. Molecular Genetics & Genomic Medicine. 11(4). e2132–e2132. 4 indexed citations
5.
6.
Chen, Jun, Jianjun Wang, Jing Gan, et al.. (2023). Anti-AQP4–IgG-positive Leigh syndrome: A case report and review of the literature. Frontiers in Pediatrics. 11.
7.
Fang, Chunyan, et al.. (2023). A de novo variant of BICRA results in Coffin–Siris syndrome 12. Molecular Genetics & Genomic Medicine. 11(11). e2250–e2250. 1 indexed citations
8.
Zheng, Yanyan, Mengmeng Niu, Siyu Zhao, et al.. (2023). Identification of a de novo variant in the ASXL2 gene related to Shashi‐Pena syndrome. Molecular Genetics & Genomic Medicine. 11(11). e2251–e2251. 2 indexed citations
9.
Jin, Hongfang, Xin Wang, Jing Wang, et al.. (2022). Compound Heterozygous Variants in a Surviving Patient With Alkuraya-Kučinskas Syndrome: A New Case Report and a Review of the Literature. Frontiers in Pediatrics. 10. 806752–806752. 1 indexed citations
10.
Cai, Qianyun, et al.. (2022). Novel GRIA2 variant in a patient with atypical autism spectrum disorder and psychiatric symptoms: a case report. BMC Pediatrics. 22(1). 629–629. 2 indexed citations
11.
Wang, Liping, et al.. (2022). Hemizygous deletion in the OTC gene results in ornithine transcarbamylase deficiency: A case report. World Journal of Clinical Cases. 10(4). 1417–1422. 1 indexed citations
12.
Zhang, Xiaoping, Zuozhen Yang, Xiaoyan Li, et al.. (2022). Bioinformatics Analysis Reveals Cell Cycle-Related Gene Upregulation in Ascending Aortic Tissues From Murine Models. Frontiers in Genetics. 13. 823769–823769. 3 indexed citations
13.
Yang, Fan, et al.. (2022). Treating GNAO1 mutation-related severe movement disorders with oxcarbazepine: a case report. Translational Pediatrics. 11(9). 1577–1587. 5 indexed citations
14.
Li, Yang, Lijuan Fan, Rong Luo, et al.. (2021). Case Report: De novo Variants of KMT2E Cause O'Donnell-Luria-Rodan Syndrome: Additional Cases and Literature Review. Frontiers in Pediatrics. 9. 641841–641841. 7 indexed citations
15.
Zhang, Jia, Zuozhen Yang, Fan Yang, et al.. (2021). A splicing variation in NPRL2 causing familial focal epilepsy with variable foci: additional cases and literature review. Journal of Human Genetics. 67(2). 79–85. 7 indexed citations
16.
Yang, Zuozhen, et al.. (2020). Dysregulated Expression and Methylation Analysis Identified TLX1NB as a Novel Recurrence Marker in Low-Grade Gliomas. International Journal of Genomics. 2020. 1–8. 2 indexed citations
17.
Zhang, Weilong, Rui Lai, Xue He, et al.. (2019). Clinical prognostic implications of EPB41L4A expression in multiple myeloma. Journal of Cancer. 11(3). 619–629. 8 indexed citations
18.
Zhang, Weilong, Ling Cao, Xiaoni Liu, et al.. (2019). High expression of CHML predicts poor prognosis of multiple myeloma. Journal of Cancer. 10(24). 6048–6056. 1 indexed citations
19.
Zhang, Weilong, Xiaoni Liu, Xue He, et al.. (2018). Prediction and prognostic significance of BCAR3 expression in patients with multiple myeloma. Journal of Translational Medicine. 16(1). 363–363. 12 indexed citations
20.
Yang, Zuozhen, Shuang Chen, Yixuan Li, et al.. (2009). MicroRNA‐214 is aberrantly expressed in cervical cancers and inhibits the growth of HeLa cells. IUBMB Life. 61(11). 1075–1082. 113 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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Breakdown of academic impact, for papers by Stephanie Greer Breakdown of academic impact, for papers by Hanna M. Petrykowska Breakdown of academic impact, for papers by Veronika I. Zabarovska Breakdown of academic impact, for papers by Sree Rama Chaitanya Sridhara Breakdown of academic impact, for papers by Li-Juan Ji Breakdown of academic impact, for papers by Ashley Cass Breakdown of academic impact, for papers by Stefania Oliveto Breakdown of academic impact, for papers by Erik J. Coffman Breakdown of academic impact, for papers by Maxim Pilyugin
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