Jun Qin Mo

3.0k total citations · 1 hit paper
53 papers, 2.3k citations indexed

About

Jun Qin Mo is a scholar working on Molecular Biology, Surgery and Hematology. According to data from OpenAlex, Jun Qin Mo has authored 53 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Molecular Biology, 8 papers in Surgery and 8 papers in Hematology. Recurrent topics in Jun Qin Mo's work include Mitochondrial Function and Pathology (27 papers), RNA modifications and cancer (14 papers) and ATP Synthase and ATPases Research (11 papers). Jun Qin Mo is often cited by papers focused on Mitochondrial Function and Pathology (27 papers), RNA modifications and cancer (14 papers) and ATP Synthase and ATPases Research (11 papers). Jun Qin Mo collaborates with scholars based in United States, China and Canada. Jun Qin Mo's co-authors include Min‐Xin Guan, Julie K. Andersen, Haytham Dimashkieh, Veena Viswanath, Kevin E. Bove, Pingping Jiang, Yaping Qian, Xiangtian Zhou, Ashley I. Bush and Lisa Ellerby and has published in prestigious journals such as Journal of Biological Chemistry, Neuron and Circulation Research.

In The Last Decade

Jun Qin Mo

53 papers receiving 2.3k 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.

Genetic or Pharmacological Iron Chelation Prevents MPTP-Induced Neurotoxicity In Vivo

2003 526 citations Jun Qin Mo, Julie K. Andersen et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jun Qin Mo United States	27	1.2k	381	331	299	281	53	2.3k
Rohini Sidhu United States	25	1.3k 1.0×	207 0.5×	114 0.3×	283 0.9×	1.1k 4.0×	39	2.7k
David Watkins Canada	30	1.6k 1.4×	298 0.8×	1.1k 3.4×	77 0.3×	147 0.5×	99	3.0k
Isa Bernardini United States	33	1.0k 0.9×	82 0.2×	1.0k 3.1×	113 0.4×	465 1.7×	64	3.6k
Daniel Leclerc Canada	30	1.5k 1.3×	288 0.8×	600 1.8×	93 0.3×	343 1.2×	65	3.2k
Klaas J. Wierenga United States	21	579 0.5×	270 0.7×	305 0.9×	45 0.2×	137 0.5×	43	1.4k
Randall A. Heidenreich United States	25	722 0.6×	327 0.9×	353 1.1×	75 0.3×	798 2.8×	46	2.0k
Ben J. H. M. Poorthuis Netherlands	36	1.5k 1.2×	166 0.4×	530 1.6×	105 0.4×	3.2k 11.5×	61	4.8k
Stephan Rust Germany	30	2.0k 1.7×	99 0.3×	135 0.4×	397 1.3×	287 1.0×	63	3.9k
Oliver Speer Switzerland	27	746 0.6×	216 0.6×	237 0.7×	69 0.2×	366 1.3×	49	1.8k
Yuki Hattori Japan	23	521 0.4×	193 0.5×	39 0.1×	284 0.9×	170 0.6×	85	1.7k

Countries citing papers authored by Jun Qin Mo

Since Specialization

Citations

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

Fields of papers citing papers by Jun Qin Mo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jun Qin Mo. 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 Jun Qin Mo. The network helps show where Jun Qin Mo may publish in the future.

Co-authorship network of co-authors of Jun Qin Mo

This figure shows the co-authorship network connecting the top 25 collaborators of Jun Qin Mo. A scholar is included among the top collaborators of Jun Qin Mo 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 Jun Qin Mo. Jun Qin Mo 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

Chen, Xiaowan, Feilong Meng, Chao Chen, et al.. (2024). Deafness-associated tRNAPhe mutation impaired mitochondrial and cellular integrity. Journal of Biological Chemistry. 300(5). 107235–107235. 6 indexed citations

Wang, Jing, Yanchun Ji, Cheng Ai, et al.. (2023). Optimized allotopic expression of mitochondrial ND6 transgene restored complex I and apoptosis deficiencies caused by LHON-linked ND6 14484T > C mutation. Journal of Biomedical Science. 30(1). 63–63. 11 indexed citations

Liang, Min, Yanchun Ji, Xuan Wang, et al.. (2022). Leber’s hereditary optic neuropathy-associated ND6 14484T > C mutation caused pleiotropic effects on the complex I, RNA homeostasis, apoptosis and mitophagy. Human Molecular Genetics. 31(19). 3299–3312. 19 indexed citations

Ji, Yanchun, Juanjuan Zhang, Min Liang, et al.. (2022). Mitochondrial tRNA variants in 811 Chinese probands with Leber’s hereditary optic neuropathy. Mitochondrion. 65. 56–66. 5 indexed citations

Nation, Javan, et al.. (2019). Sinonasal Non-Intestinal Type Adenocarcinoma of the Nasopharynx: A Case Report. 4(1). 1 indexed citations

Zheng, Jing, Min Wang, Xiaohui Cang, et al.. (2019). Contribution of a mitochondrial tyrosyl-tRNA synthetase mutation to the phenotypic expression of the deafness-associated tRNASer(UCN) 7511A>G mutation. Journal of Biological Chemistry. 294(50). 19292–19305. 22 indexed citations

Xue, Ling, Meng Wang, Haiying Li, et al.. (2016). Mitochondrial tRNA mutations in 2070 Chinese Han subjects with hypertension. Mitochondrion. 30. 208–221. 28 indexed citations

Liu, Hao, Ronghua Li, Weixing Li, et al.. (2015). Maternally inherited diabetes is associated with a homoplasmic T10003C mutation in the mitochondrial tRNAGly gene. Mitochondrion. 21. 49–57. 26 indexed citations

Ji, Yanchun, Min Liang, Juanjuan Zhang, et al.. (2014). Mitochondrial haplotypes may modulate the phenotypic manifestation of the LHON-associated ND1 G3460A mutation in Chinese families. Journal of Human Genetics. 59(3). 134–140. 17 indexed citations

10.

Chandrakasan, Shanmuganathan, Nihal Bakeer, Jun Qin Mo, Carrye Cost, & Charles T. Quinn. (2013). Iron-Refractory Microcytic Anemia as the Presenting Feature of Unicentric Castleman Disease in Children. The Journal of Pediatrics. 164(4). 928–930. 6 indexed citations

11.

Zhang, Juanjuan, Fuxin Zhao, Qun Fu, et al.. (2013). Mitochondrial haplotypes may modulate the phenotypic manifestation of the LHON-associated m.14484T>C (MT-ND6) mutation in Chinese families. Mitochondrion. 13(6). 772–781. 21 indexed citations

12.

Marsh, Rebecca, Carl E. Allen, Kenneth L. McClain, et al.. (2012). Salvage therapy of refractory hemophagocytic lymphohistiocytosis with alemtuzumab. Pediatric Blood & Cancer. 60(1). 101–109. 217 indexed citations

13.

Hinze, Claas, Ndate Fall, Sherry Thornton, et al.. (2010). Immature cell populations and an erythropoiesis gene-expression signature in systemic juvenile idiopathic arthritis: implications for pathogenesis. Arthritis Research & Therapy. 12(3). R123–R123. 42 indexed citations

14.

Towbin, Alexander J., et al.. (2010). Focal nodular hyperplasia in children, adolescents, and young adults. Pediatric Radiology. 41(3). 341–349. 45 indexed citations

15.

Chen, Jey-Hsin, Mark D. Fleming, Geraldine S. Pinkus, et al.. (2010). Pathology of the Liver in Familial Hemophagocytic Lymphohistiocytosis. The American Journal of Surgical Pathology. 34(6). 852–867. 43 indexed citations

16.

Lee, Ki‐Won, Yin Liu, Jun Qin Mo, et al.. (2008). Vav3 oncogene activates estrogen receptor and its overexpression may be involved in human breast cancer. BMC Cancer. 8(1). 158–158. 54 indexed citations

17.

Lee, Ki‐Won, Yin Liu, Amy Wang, et al.. (2007). Vav3 oncogene, a quanine nucleotide exchange factor for Rac/Rho GTPases, is a coactivator for nuclear receptors and involved in human breast cancer.. Cancer Research. 67. 2518–2518. 1 indexed citations

18.

Yuan, Huijun, Yaping Qian, Weidong Shen, et al.. (2005). Cosegregation of the G7444A mutation in the mitochondrial COI/tRNA^Ser(UCN) genes with the 12S rRNA A1555G mutation in a Chinese family with aminoglycoside‐induced and nonsyndromic hearing loss. American Journal of Medical Genetics Part A. 138A(2). 133–140. 72 indexed citations

19.

Mo, Jun Qin, Haytham Dimashkieh, & Kevin E. Bove. (2004). GLUT1 endothelial reactivity distinguishes hepatic infantile hemangioma from congenital hepatic vascular malformation with associated capillary proliferation. Human Pathology. 35(2). 200–209. 85 indexed citations

20.

Jiang, Dongmei, et al.. (1997). Elevated expression of glutathione peroxidase in PC12 cells results in protection against methamphetamine but not MPTP toxicity. Molecular Brain Research. 46(1-2). 154–160. 38 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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