Duan Ma

2.3k total citations
82 papers, 1.1k citations indexed

About

Duan Ma is a scholar working on Molecular Biology, Cancer Research and Genetics. According to data from OpenAlex, Duan Ma has authored 82 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 56 papers in Molecular Biology, 19 papers in Cancer Research and 13 papers in Genetics. Recurrent topics in Duan Ma's work include Congenital heart defects research (12 papers), RNA modifications and cancer (11 papers) and Hearing, Cochlea, Tinnitus, Genetics (10 papers). Duan Ma is often cited by papers focused on Congenital heart defects research (12 papers), RNA modifications and cancer (11 papers) and Hearing, Cochlea, Tinnitus, Genetics (10 papers). Duan Ma collaborates with scholars based in China, South Korea and United States. Duan Ma's co-authors include Huijun Wang, Wenhao Zhou, Jing Ma, Nan Jiang, Yi Yang, Jinqiao Sun, Wenjun Xia, Jin Zhang, Guoying Huang and Fei Liu and has published in prestigious journals such as Journal of Clinical Oncology, PLoS ONE and Scientific Reports.

In The Last Decade

Duan Ma

79 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Duan Ma China	19	643	220	209	111	89	82	1.1k
Yoshitsugu Saishin Japan	22	749 1.2×	115 0.5×	105 0.5×	57 0.5×	75 0.8×	56	1.8k
Pei‐Lung Chen Taiwan	21	530 0.8×	287 1.3×	119 0.6×	82 0.7×	105 1.2×	102	1.4k
Mohammed Al‐Owain Saudi Arabia	25	1.1k 1.7×	595 2.7×	145 0.7×	110 1.0×	96 1.1×	87	2.0k
Françoise Wilkin Belgium	13	504 0.8×	132 0.6×	168 0.8×	46 0.4×	159 1.8×	19	1.2k
Nady Golestaneh United States	22	1.4k 2.2×	304 1.4×	177 0.8×	127 1.1×	110 1.2×	41	2.2k
Stephen Malin Sweden	19	785 1.2×	249 1.1×	115 0.6×	100 0.9×	264 3.0×	35	1.8k
Claudio Graziano Italy	20	695 1.1×	325 1.5×	73 0.3×	43 0.4×	61 0.7×	77	1.2k
Josef G. Heuer United States	20	818 1.3×	137 0.6×	164 0.8×	186 1.7×	79 0.9×	34	1.7k
Martina Kirstein Spain	15	541 0.8×	128 0.6×	181 0.9×	70 0.6×	110 1.2×	24	1.9k
Khushnooda Ramzan Saudi Arabia	18	644 1.0×	320 1.5×	84 0.4×	39 0.4×	64 0.7×	79	1.2k

Countries citing papers authored by Duan Ma

Since Specialization

Citations

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

Fields of papers citing papers by Duan Ma

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Duan Ma

This figure shows the co-authorship network connecting the top 25 collaborators of Duan Ma. A scholar is included among the top collaborators of Duan Ma 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 Duan Ma. Duan Ma 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

Li, Yajun, et al.. (2025). A novel mouse model of chronic neuronopathic Gaucher disease exhibits Parkinson's disease-like phenotypes. Neurobiology of Disease. 209. 106899–106899.

Song, Nan, Yang Xiang, Bing Mao, et al.. (2025). FOXK2 in skeletal muscle development: a new pathogenic gene for congenital myopathy with ptosis. EMBO Molecular Medicine. 17(7). 1599–1630.

Zhao, Zhiyang, Renjie Cui, Teng Wan, et al.. (2024). A novel IRF6 gene mutation impacting the regulation of TGFβ2-AS1 in the TGFβ pathway: A mechanism in the development of Van der Woude syndrome. Frontiers in Genetics. 15. 1397410–1397410. 1 indexed citations

Li, Yajun, et al.. (2024). Upregulation of NFE2L1 reduces ROS levels and α-synuclein aggregation caused by GBA1 knockdown. Biochemical and Biophysical Research Communications. 734. 150640–150640. 2 indexed citations

Liu, Jia, Xiaogang Bao, Yixuan Tan, et al.. (2023). TMEM135 maintains the equilibrium of osteogenesis and adipogenesis by regulating mitochondrial dynamics. Metabolism. 152. 155767–155767. 9 indexed citations

Wu, Suwen, Huanqiang Zhao, Lili Gong, et al.. (2022). Trophoblast Exosomal UCA1 Induces Endothelial Injury through the PFN1‐RhoA/ROCK Pathway in Preeclampsia: A Human‐Specific Adaptive Pathogenic Mechanism. Oxidative Medicine and Cellular Longevity. 2022(1). 2198923–2198923. 14 indexed citations

Xia, Wenjun, Jing Ma, Jianbo Huang, et al.. (2019). Novel TRRAP mutation causes autosomal dominant non‐syndromic hearing loss. Clinical Genetics. 96(4). 300–308. 13 indexed citations

Xia, Wenjun, Jing Ma, Jianbo Huang, et al.. (2019). Mutations in TOP 2B cause autosomal‐dominant hereditary hearing loss via inhibition of the PI 3K‐Akt signalling pathway. FEBS Letters. 593(15). 2008–2018. 17 indexed citations

Yang, Jichun, Jing Ma, Yu Xiong, et al.. (2018). Epigenetic regulation of megakaryocytic and erythroid differentiation by PHF2 histone demethylase. Journal of Cellular Physiology. 233(9). 6841–6852. 10 indexed citations

10.

Cui, Renjie, Nan Jiang, Meiqin Zhang, et al.. (2018). Delivery of Glucosylceramidase Beta Gene Using AAV9 Vector Therapy as a Treatment Strategy in Mouse Models of Gaucher Disease. Human Gene Therapy. 30(2). 155–167. 24 indexed citations

11.

Liu, Fei, et al.. (2015). Exome Sequencing Identifies a Mutation in EYA4 as a Novel Cause of Autosomal Dominant Non-Syndromic Hearing Loss. PLoS ONE. 10(5). e0126602–e0126602. 20 indexed citations

12.

Yang, Lin, et al.. (2013). Psychiatric Illness and Intellectual Disability in the Prader–Willi Syndrome with Different Molecular Defects - A Meta Analysis. PLoS ONE. 8(8). e72640–e72640. 56 indexed citations

13.

Zhang, Tianyu, Zhengmin Wang, Yi Jiang, et al.. (2011). A novel mutation in the MITF may be digenic with GJB2 mutations in a large Chinese family of Waardenburg syndrome type II. Journal of genetics and genomics. 38(12). 585–591. 17 indexed citations

14.

Xu, Wangjie, Ying Zhou, Zijue Zhu, et al.. (2010). The role of Dby mRNA in early development of male mouse zygotes. Asian Journal of Andrology. 12(4). 567–577. 18 indexed citations

15.

Ma, Duan, et al.. (2010). Research progress in modification of histone lysine methylation and congenital heart defect. Hereditas (Beijing). 32(7). 650–655. 1 indexed citations

16.

Liu, Rui, Yiming Li, Tianru Jin, et al.. (2010). A site-specific genomic integration strategy for sustained expression of glucagon-like peptide-1 in mouse muscle for controlling energy homeostasis. Biochemical and Biophysical Research Communications. 403(2). 172–177. 7 indexed citations

17.

Wang, Suxia, Huijuan Wu, Yujing Liu, et al.. (2010). Expression of USP2-69 in mesangial cellsin vivoandin vitro. Pathology International. 60(3). 184–192. 10 indexed citations

18.

Wang, Zhaoxia, Minghao Yin, Wangjie Xu, et al.. (2009). A study of Y chromosome gene mRNA in human ejaculated spermatozoa. Molecular Reproduction and Development. 77(2). 158–166. 10 indexed citations

19.

Zhu, Ying, Xinping Luo, & Duan Ma. (2007). Tissue Factor and Tissue Factor Pathway Inhibitor in Coronary Atherosclerotic Plaque. 28(5). 759–762. 1 indexed citations

20.

Ling, Chang‐Chun, Yao Xiao, Duan Ma, et al.. (2006). Exogenous Tissue Plasminogen Activator Enhances Peripheral Nerve Regeneration and Functional Recovery After Injury In Mice. Journal of Neuropathology & Experimental Neurology. 65(1). 78–86. 46 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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