Ming-min Gu

454 total citations
19 papers, 355 citations indexed

About

Ming-min Gu is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Ming-min Gu has authored 19 papers receiving a total of 355 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 6 papers in Cellular and Molecular Neuroscience and 5 papers in Genetics. Recurrent topics in Ming-min Gu's work include Hereditary Neurological Disorders (4 papers), Connective tissue disorders research (3 papers) and Aluminum Alloys Composites Properties (3 papers). Ming-min Gu is often cited by papers focused on Hereditary Neurological Disorders (4 papers), Connective tissue disorders research (3 papers) and Aluminum Alloys Composites Properties (3 papers). Ming-min Gu collaborates with scholars based in China, United States and United Kingdom. Ming-min Gu's co-authors include Zhugang Wang, Juhua Luo, Ziyang Dai, Mengna Feng, Yu Xie, Houbao Zhu, Hongxin Zhang, Yimin He, D.Z. Wang and Yuting Yao and has published in prestigious journals such as SHILAP Revista de lepidopterología, FEBS Letters and The American Journal of Human Genetics.

In The Last Decade

Ming-min Gu

16 papers receiving 352 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ming-min Gu China	9	181	75	65	50	47	19	355
Tarfa Al‐Sheddi Saudi Arabia	13	456 2.5×	166 2.2×	19 0.3×	80 1.6×	34 0.7×	21	664
Vishwanath Kumble Bhat India	11	155 0.9×	52 0.7×	108 1.7×	12 0.2×	12 0.3×	17	410
Yoshihiro Ujihara Japan	11	264 1.5×	31 0.4×	9 0.1×	13 0.3×	17 0.4×	48	510
Pingting Liu China	10	172 1.0×	25 0.3×	21 0.3×	4 0.1×	9 0.2×	20	330
Kaouther Ajroud United States	5	217 1.2×	14 0.2×	19 0.3×	8 0.2×	3 0.1×	8	439
Shingo Hirashima Japan	10	157 0.9×	32 0.4×	11 0.2×	24 0.5×	2 0.0×	28	351
Aiping Lin China	9	111 0.6×	15 0.2×	33 0.5×	5 0.1×	3 0.1×	17	304
Yejin Yun South Korea	9	209 1.2×	18 0.2×	31 0.5×	2 0.0×	19 0.4×	23	350
Guillermo Menéndez Spain	8	201 1.1×	32 0.4×	33 0.5×	2 0.0×	37 0.8×	16	576
Kyung‐Yong Kim South Korea	11	120 0.7×	46 0.6×	139 2.1×	7 0.1×	2 0.0×	35	482

Countries citing papers authored by Ming-min Gu

Since Specialization

Citations

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

Fields of papers citing papers by Ming-min Gu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ming-min Gu. 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 Ming-min Gu. The network helps show where Ming-min Gu may publish in the future.

Co-authorship network of co-authors of Ming-min Gu

This figure shows the co-authorship network connecting the top 25 collaborators of Ming-min Gu. A scholar is included among the top collaborators of Ming-min Gu 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 Ming-min Gu. Ming-min Gu 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:

19 of 19 papers shown

Chen, Xuejiao, Yan Chen, Runzhe Shu, et al.. (2025). Investigating the effects of global gene knockout of MrgF on motor performance and pain sensitivity in mice. Hereditas. 162(1). 31–31.

Luo, Juhua, Ziyang Dai, Mengna Feng, Ming-min Gu, & Yu Xie. (2022). Graphitic carbon nitride/ferroferric oxide/reduced graphene oxide nanocomposite as highly active visible light photocatalyst. Nano Research. 16(1). 371–376. 55 indexed citations

Guo, Wenting, Lei Chen, Yimin He, et al.. (2020). CMT2Q-causing mutation in the Dhtkd1 gene lead to sensory defects, mitochondrial accumulation and altered metabolism in a knock-in mouse model. Acta Neuropathologica Communications. 8(1). 32–32. 9 indexed citations

Chen, Chong, Qiao Sun, Ming-min Gu, et al.. (2020). Multimodal imaging and genetic characteristics of Chinese patients with USH2A ‐associated nonsyndromic retinitis pigmentosa. Molecular Genetics & Genomic Medicine. 8(11). e1479–e1479. 4 indexed citations

Gu, Ming-min, et al.. (2018). Research progress in early diagnosis of Alzheimer's disease. SHILAP Revista de lepidopterología.

He, Yimin & Ming-min Gu. (2017). Research progress of myosin heavy chain genes in human genetic diseases.. PubMed. 39(10). 877–887. 15 indexed citations

Tang, Lingyun, Xiaolin Wu, Hongxin Zhang, et al.. (2017). A point mutation in Fgf9 impedes joint interzone formation leading to multiple synostoses syndrome. Human Molecular Genetics. 26(7). 1280–1293. 26 indexed citations

Yang, Fu, et al.. (2016). The functional mechanisms and clinical application of read-through drugs.. PubMed. 38(7). 623–633. 1 indexed citations

Zhang, Jiaying, Ye Xu, Boyu Yang, et al.. (2016). [Mutation analysis for a family affected with Charcot-Marie-Tooth disease type 4C].. PubMed. 33(1). 57–60. 1 indexed citations

10.

Shen, Wei Feng, Lei Chen, Yi Gu, et al.. (2015). Two nonsense mutations cause protein C deficiency by nonsense-mediated mRNA decay. Thrombosis Research. 135(4). 733–738. 3 indexed citations

11.

Chen, Chong, et al.. (2015). A novel Cx50 (GJA8) p.H277Y mutation associated with autosomal dominant congenital cataract identified with targeted next-generation sequencing. Graefe s Archive for Clinical and Experimental Ophthalmology. 253(6). 915–924. 14 indexed citations

12.

Gu, Ming-min, et al.. (2014). Research progress in the mouse models of Charcot-Marie-Tooth disease type 2 (CMT2). Hereditas (Beijing). 36(1). 21–29.

13.

Zhu, Houbao, Ming-min Gu, Qingqiong Luo, et al.. (2013). DHTKD1 is essential for mitochondrial biogenesis and function maintenance. FEBS Letters. 587(21). 3587–3592. 52 indexed citations

14.

Gu, Ming-min, Lianhua Sun, Wenting Guo, et al.. (2012). A Nonsense Mutation in DHTKD1 Causes Charcot-Marie-Tooth Disease Type 2 in a Large Chinese Pedigree. The American Journal of Human Genetics. 91(6). 1088–1094. 62 indexed citations

15.

Guo, Wenting, et al.. (2012). Nonsense-mediated mRNA decay and human monogenic disease. Hereditas (Beijing). 34(8). 935–942. 1 indexed citations

16.

Wu, Xiaolin, Ming-min Gu, Lei Huang, et al.. (2009). Multiple Synostoses Syndrome Is Due to a Missense Mutation in Exon 2 of FGF9 Gene. The American Journal of Human Genetics. 85(1). 53–63. 70 indexed citations

17.

Yang, Feifei, et al.. (2006). Recrystallization Kinetics of Cold-rolled Squeeze-cast Al/SiC/15w Composites. Journal of Composite Materials. 40(12). 1117–1131. 7 indexed citations

18.

Gu, Ming-min, et al.. (2005). Compressive stress-strain response of directionally aligned SiCw/Al composite. Journal of Materials Science. 40(23). 6091–6097. 3 indexed citations

19.

Gu, Ming-min, et al.. (2004). Rolling and annealing textures of a SiCw/Al composite. Materials Letters. 58(27-28). 3414–3418. 32 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.

Explore authors with similar magnitude of impact