Min Liang

787 citations

29 papers · 573 indexed · h-index 15

Co-authors: Min‐Xin Guan Xiangtian Zhou Jia Qu Fuxin Zhao Juanjuan Zhang Yanchun Ji Yi Tong Pingping Jiang
Topics: Mitochondrial Function and Pathology (18 papers)ATP Synthase and ATPases Research (14 papers)Metabolism and Genetic Disorders (10 papers)
Cited by: Clinical Biochemistry Molecular Biology Ophthalmology
Journals: Journal of Biological Chemistry Biochemical and Biophysical Research Communications International Journal of Molecular Sciences
Partner nations: China United States Sweden

In The Last Decade

Min Liang

28 papers receiving 570 citations

Peers

Countries citing papers authored by Min Liang

Since Specialization

Citations

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

Fields of papers citing papers by Min Liang

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Min Liang

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

#	Work	Indexed citations
1	Discovery and characterization of a novel alginate lyase PeAly15 and its truncated protein DUF4962 domain from Paenibacillus elgii HSFD1: Elucidation the molecular mechanism of endolytic mode 2025 ·International Journal of Biological Macromolecules ·(unknown),Zhenhua Li,Min Liang,Naikun Shen,Lixia Pan,Mingguo Jiang,(unknown)	0
2	Mir-381-3p aggravates ovariectomy-induced osteoporosis by inhibiting osteogenic differentiation through targeting KLF5/Wnt/β-catenin signaling pathway 2024 ·Journal of Orthopaedic Surgery and Research ·(unknown),Jingsong Liu,(unknown),Min Liang,Rui Li,(unknown),Yansong Wang	2
3	Mutation of CRYAB encoding a conserved mitochondrial chaperone and antiapoptotic protein causes hereditary optic atrophy 2024 ·JCI Insight ·Chenghui Wang,(unknown),(unknown),Min Liang,Hanqing Liu,(unknown),(unknown),Cheng Ai,Juanjuan Zhang,(unknown),Yanchun Ji,Min‐Xin Guan	4
4	Leber’s hereditary optic neuropathy-associated ND6 14484T > C mutation caused pleiotropic effects on the complex I, RNA homeostasis, apoptosis and mitophagy 2022 ·Human Molecular Genetics ·Min Liang,Yanchun Ji,(unknown),Xuan Wang,(unknown),Juanjuan Zhang,Yiwei Zhu,Jun Qin Mo,Min‐Xin Guan	19
5	Mitochondrial tRNA variants in 811 Chinese probands with Leber’s hereditary optic neuropathy 2022 ·Mitochondrion ·Yanchun Ji,Juanjuan Zhang,Min Liang,Feilong Meng,Minglian Zhang,Jun Qin Mo,Meng Wang,Min‐Xin Guan	5
6	Vestibular evoked myogenic potential may predict the hearing recovery in patients with unilateral idiopathic sudden sensorineural hearing loss 2022 ·Frontiers in Neurology ·Min Liang,Hui Wu,Jianyong Chen,(unknown),Shuna Li,Guiliang Zheng,(unknown),Xiangping Chen,Maoli Duan,Jun Yang,Yulian Jin	3
7	Compound Heterozygosity for KLF1 Mutations Causing Hemolytic Anemia in Children: A Case Report and Literature Review 2021 ·Frontiers in Genetics ·(unknown),(unknown),Yanxia Zhang,(unknown),Min Liang,Xiaofeng Wei,(unknown),Xuedong Wu,Xuan Shang	6
8	Identification of MYO6 copy number variation associated with cochlear aplasia by targeted sequencing 2019 ·International Journal of Pediatric Otorhinolaryngology ·Lianhua Sun,Xiaowen Wang,(unknown),Min Liang,Jun Yang	2
9	Secondary Metabolites from the Twigs of Cinnamomum camphora 2019 ·Chemistry of Natural Compounds ·Lei Wu,Wei Xiong,Ju-Wu Hu,(unknown),(unknown),Yue Gao,Dan Liu,Ying Liu,Wei Liu,Min Liang,Chuanling Si,Young‐Soo Bae	14
10	Biochemical evidence for a mitochondrial genetic modifier in the phenotypic manifestation of Leber’s hereditary optic neuropathy-associated mitochondrial DNA mutation 2016 ·Human Molecular Genetics ·Pingping Jiang,Min Liang,Chaofan Zhang,Xiaoxu Zhao,(unknown),(unknown),Xiaoling Liu,(unknown),Qun Fu,Yanchun Ji,Yidong Bai,Taosheng Huang,Min‐Xin Guan	33
11	The exome sequencing identified the mutation in YARS2 encoding the mitochondrial tyrosyl-tRNA synthetase as a nuclear modifier for the phenotypic manifestation of Leber's hereditary optic neuropathy-associated mitochondrial DNA mutation 2015 ·Human Molecular Genetics ·Pingping Jiang,Xiaofen Jin,Yanyan Peng,Meng Wang,Hao Liu,Xiaoling Liu,(unknown),Yanchun Ji,Juanjuan Zhang,Min Liang,Fuxin Zhao,Yanhong Sun,Minglian Zhang,Xiangtian Zhou,Ye Chen,Jun Qin Mo,Taosheng Huang,Jia Qu,Min‐Xin Guan	84
12	[A novel mutation T8821G in mitochondrial DNA may be associated with Leber's hereditary optic neuropathy]. 2015 ·PubMed ·Min Gao,Sai Zhang,(unknown),Fuxin Zhao,Juanjuan Zhang,Min Liang,Xiaoling Liu,Qi-Ping Wei,Yi Tong,Jia Qu,Min‐Xin Guan	1
13	Mitochondrial haplotypes may modulate the phenotypic manifestation of the LHON-associated ND1 G3460A mutation in Chinese families 2014 ·Journal of Human Genetics ·Yanchun Ji,Min Liang,Juanjuan Zhang,Minglian Zhang,Jinping Zhu,(unknown),Sai Zhang,Min Gao,Fuxin Zhao,Qi-Ping Wei,Pingping Jiang,Yi Tong,Xiaoling Liu,Jun Qin Mo,Min‐Xin Guan	17
14	Mitochondrial haplotypes may modulate the phenotypic manifestation of the LHON-associated m.14484T>C (MT-ND6) mutation in Chinese families 2013 ·Mitochondrion ·Juanjuan Zhang,Fuxin Zhao,Qun Fu,Min Liang,Yi Tong,Xiaoling Liu,(unknown),(unknown),Minglian Zhang,Qi-Ping Wei,Ling Xue,Pingping Jiang,Xiangtian Zhou,Jun Qin Mo,Taosheng Huang,Jia Qu,Min‐Xin Guan	21
15	Application of DNA barcoding technology for species identification of common thrips (Insecta: Thysanoptera) in China. 2012 ·Acta Entomologica Sinica ·(unknown),(unknown),Aibing Zhang,Min Liang,Guifen Zhang	5
16	The altered activity of complex III may contribute to the high penetrance of Leber's hereditary optic neuropathy in a Chinese family carrying the ND4 G11778A mutation 2011 ·Mitochondrion ·Yaping Qian,Xiangtian Zhou,Min Liang,Jia Qu,Min‐Xin Guan	23
17	SCAR marker for rapid identification of the western flower thrips, Frankliniella occidentalis (Pergande) (Thysanoptera: Thripidae). 2010 ·Acta Entomologica Sinica ·(unknown),Min Liang,(unknown),Zhongshi Zhou,Wenkai Wang,Guifen Zhang	2
18	Mitochondrial haplogroup M9a specific variant ND1 T3394C may have a modifying role in the phenotypic expression of the LHON-associated ND4 G11778A mutation 2010 ·Molecular Genetics and Metabolism ·Minglian Zhang,Xiangtian Zhou,Chengwu Li,Fuxin Zhao,Juanjuan Zhang,(unknown),Yanhong Sun,Jingzheng Wang,Yi Tong,Min Liang,Li Yang,Wanshi Cai,Lifei Wang,Jia Qu,Min‐Xin Guan	31
19	Low penetrance of Leber's hereditary optic neuropathy in ten Han Chinese families carrying the ND6 T11484C mutation 2009 ·Biochimica et Biophysica Acta (BBA) - General Subjects ·Jia Qu,Xiangtian Zhou,Fuxin Zhao,Xiaoling Liu,Minglian Zhang,Yanhong Sun,Min Liang,(unknown),Qi Liu,Yi Tong,Qi-Ping Wei,Li Yang,Min‐Xin Guan	15
20	Leber’s hereditary optic neuropathy is associated with mitochondrial ND1 T3394C mutation 2009 ·Biochemical and Biophysical Research Communications ·Min Liang,(unknown),Fuxin Zhao,Xiangtian Zhou,(unknown),Yi Tong,Li Yang,Qi-Ping Wei,Yanhong Sun,Fan Lü,Jia Qu,Min‐Xin Guan	60

About Min Liang

Min Liang is a scholar working on Clinical Biochemistry, General Decision Sciences and Molecular Biology, having authored 29 papers that have together received 573 indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (18 papers), ATP Synthase and ATPases Research (14 papers) and Metabolism and Genetic Disorders (10 papers). The work is most often cited by research in Clinical Biochemistry (212 citations), Molecular Biology (516 citations) and Ophthalmology (37 citations). Min Liang has collaborated with scholars based in China, United States and Sweden. Frequent co-authors include Min‐Xin Guan, Xiangtian Zhou, Jia Qu, Fuxin Zhao, Juanjuan Zhang, Yanchun Ji, Yi Tong, Pingping Jiang, Yanhong Sun and Minglian Zhang. Their work appears in journals such as Journal of Biological Chemistry, Biochemical and Biophysical Research Communications and International Journal of Molecular Sciences.

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