Chun‐Ming Pan

3.6k total citations · 1 hit paper
33 papers, 1.1k citations indexed

About

Chun‐Ming Pan is a scholar working on Molecular Biology, Genetics and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Chun‐Ming Pan has authored 33 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 9 papers in Genetics and 8 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Chun‐Ming Pan's work include Diabetes and associated disorders (8 papers), Hormonal Regulation and Hypertension (5 papers) and Immunodeficiency and Autoimmune Disorders (4 papers). Chun‐Ming Pan is often cited by papers focused on Diabetes and associated disorders (8 papers), Hormonal Regulation and Hypertension (5 papers) and Immunodeficiency and Autoimmune Disorders (4 papers). Chun‐Ming Pan collaborates with scholars based in China, Czechia and United Kingdom. Chun‐Ming Pan's co-authors include Huai‐Dong Song, Zhaohui Gu, Jingyi Shi, Chen Zhu, Sai‐Juan Chen, Yang Shen, Xiaowei Zhang, Keqin Li, Jian‐Qing Mi and Lin Tang and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and PLoS ONE.

In The Last Decade

Chun‐Ming Pan

33 papers receiving 1.1k 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.

Exome sequencing identifies somatic mutations of DNA methyltransferase gene DNMT3A in acute monocytic leukemia

2011 587 citations Xiaojing Yan, Jie Xu et al. Nature Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Chun‐Ming Pan China	16	656	355	203	195	176	33	1.1k
Maria Lombardi Netherlands	17	329 0.5×	245 0.7×	88 0.4×	222 1.1×	72 0.4×	45	1.1k
Panagiotis Flevaris United States	13	378 0.6×	312 0.9×	85 0.4×	54 0.3×	105 0.6×	14	930
Kaavya Paruchuri United States	9	476 0.7×	189 0.5×	177 0.9×	76 0.4×	36 0.2×	20	1.2k
Lars Palmqvist Sweden	23	722 1.1×	666 1.9×	132 0.7×	117 0.6×	21 0.1×	67	1.6k
Jacob van den Born Netherlands	17	485 0.7×	173 0.5×	51 0.3×	104 0.5×	39 0.2×	23	1.3k
Lingyun Wu China	18	441 0.7×	571 1.6×	111 0.5×	53 0.3×	19 0.1×	62	971
Jean-Paul Beressi France	11	316 0.5×	131 0.4×	52 0.3×	553 2.8×	460 2.6×	20	1.2k
Thomas Nührenberg Germany	20	492 0.8×	136 0.4×	127 0.6×	63 0.3×	36 0.2×	57	1.2k
Theresa M. Palabrica United States	13	238 0.4×	544 1.5×	178 0.9×	61 0.3×	38 0.2×	17	1.8k

Countries citing papers authored by Chun‐Ming Pan

Since Specialization

Citations

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

Fields of papers citing papers by Chun‐Ming Pan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Chun‐Ming Pan. 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 Chun‐Ming Pan. The network helps show where Chun‐Ming Pan may publish in the future.

Co-authorship network of co-authors of Chun‐Ming Pan

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Cao, Huang‐Ming, Xiao-Ping Ye, Junhua Ma, et al.. (2015). Mimecan, a Hormone Abundantly Expressed in Adipose Tissue, Reduced Food Intake Independently of Leptin Signaling. EBioMedicine. 2(11). 1718–1724. 17 indexed citations

Gong, Yi, Guochao Shi, Wan Huan-ying, et al.. (2013). Association between the interleukin-13 gene and development of chronic obstructive pulmonary disease in southern Chinese Han population: a case-control study. Chinese Medical Journal. 126(23). 4403–4408. 10 indexed citations

Han, Bing, Wei Liu, Chao Zuo, et al.. (2013). Identifying a novel mutation of CYP17A1 gene from five Chinese 17α-hydroxylase/17, 20-lyase deficiency patients. Gene. 516(2). 345–350. 13 indexed citations

Zhao, Shuang‐Xia, Wei Liu, Ming Zhan, et al.. (2013). A Refined Study of FCRL Genes from a Genome-Wide Association Study for Graves’ Disease. PLoS ONE. 8(3). e57758–e57758. 23 indexed citations

Liu, Bingli, Shaoying Yang, Wei Liu, et al.. (2013). Refined association of TSH receptor susceptibility locus to Graves' disease in the Chinese Han population. European Journal of Endocrinology. 170(1). 109–119. 11 indexed citations

Xue, Liqiong, Chun‐Ming Pan, Zhaohui Gu, et al.. (2013). Genetic Heterogeneity of Susceptibility Gene in Different Ethnic Populations: Refining Association Study of PTPN22 for Graves’ Disease in a Chinese Han Population. PLoS ONE. 8(12). e84514–e84514. 13 indexed citations

Liu, Wei, Haining Wang, Zhaohui Gu, et al.. (2013). Identification of BACH2 as a susceptibility gene for Graves’ disease in the Chinese Han population based on a three-stage genome-wide association study. Human Genetics. 133(5). 661–671. 18 indexed citations

Xue, Liqiong, Bing Han, Chun‐Ming Pan, & Huai‐Dong Song. (2013). The association of SCGB3A2 polymorphisms with the risk of Graves’ disease: a meta-analysis. Endocrine. 45(3). 365–369. 3 indexed citations

Zheng, Cuixia, Zhaohui Gu, Bing Han, et al.. (2013). Whole-exome sequencing to identify novel somatic mutations in squamous cell lung cancers. International Journal of Oncology. 43(3). 755–764. 17 indexed citations

10.

Zhao, Lin, Minjia Zhang, Chun‐Ming Pan, et al.. (2012). The influence of the genetic and non-genetic factors on bone mineral density and osteoporotic fractures in Chinese women. Endocrine. 43(1). 127–135. 12 indexed citations

11.

Guo, Yi, Yi Gong, Chun‐Ming Pan, et al.. (2012). Association of genetic polymorphisms with chronic obstructive pulmonary disease in the Chinese Han population: a case–control study. BMC Medical Genomics. 5(1). 64–64. 26 indexed citations

12.

Xue, Liqiong, Bing Han, Libo Chen, et al.. (2012). Identification of a novel mutation in CYP17A1 gene. Translational research. 161(1). 44–49. 3 indexed citations

13.

Cao, Hua, et al.. (2012). Identification of a locus (DSP2) for disseminated superficial porokeratosis at chromosome 12q21.2-24.21. Clinical and Experimental Dermatology. 37(6). 672–676. 7 indexed citations

14.

Wang, Zhiquan, Liqiong Xue, Cuicui Guo, et al.. (2012). Stevioside ameliorates high-fat diet-induced insulin resistance and adipose tissue inflammation by downregulating the NF-κB pathway. Biochemical and Biophysical Research Communications. 417(4). 1280–1285. 39 indexed citations

15.

Yang, Shaoying, Wei Liu, Liqiong Xue, et al.. (2011). Association of TSHR gene intron 1 polymorphisms with Graves′ disease. Zhonghua neifenmi daixie zazhi. 27(6). 478–481. 2 indexed citations

16.

Gong, Yi, Fan Liang, Wan Huan-ying, et al.. (2011). Lack of Association Between the TGF-β1 Gene and Development of COPD in Asians: A Case–Control Study and Meta-analysis. Lung. 189(3). 213–223. 14 indexed citations

17.

Yan, Xiaojing, Jie Xu, Zhaohui Gu, et al.. (2011). Exome sequencing identifies somatic mutations of DNA methyltransferase gene DNMT3A in acute monocytic leukemia. Nature Genetics. 43(4). 309–315. 587 indexed citations breakdown →

18.

Qiao, Jie, Bing Han, Bingli Liu, et al.. (2011). A unique exonic splicing mutation in the CYP17A1 gene as the cause for steroid 17α-hydroxylase deficiency. European Journal of Endocrinology. 164(4). 627–633. 20 indexed citations

19.

Pan, Chun‐Ming, Huang‐Ming Cao, Bing Han, et al.. (2010). Association of the CTLA4 Gene with Graves' Disease in the Chinese Han Population. PLoS ONE. 5(3). e9821–e9821. 39 indexed citations

20.

Ma, Qinyun, Chao Zuo, Junhua Ma, et al.. (2010). Glucocorticoid up-regulates mimecan expression in corticotroph cells. Molecular and Cellular Endocrinology. 321(2). 239–244. 12 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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