Jinqing Song

811 total citations
61 papers, 478 citations indexed

About

Jinqing Song is a scholar working on Clinical Biochemistry, Molecular Biology and Rheumatology. According to data from OpenAlex, Jinqing Song has authored 61 papers receiving a total of 478 indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Clinical Biochemistry, 37 papers in Molecular Biology and 19 papers in Rheumatology. Recurrent topics in Jinqing Song's work include Metabolism and Genetic Disorders (47 papers), Mitochondrial Function and Pathology (21 papers) and Folate and B Vitamins Research (18 papers). Jinqing Song is often cited by papers focused on Metabolism and Genetic Disorders (47 papers), Mitochondrial Function and Pathology (21 papers) and Folate and B Vitamins Research (18 papers). Jinqing Song collaborates with scholars based in China, Hungary and Japan. Jinqing Song's co-authors include Yanling Yang, Xiyuan Li, Yupeng Liu, Yuan Ding, Yanyan Ma, Kai Wang, Jinjing Zhao, Shuyi Pan, Qiao Wang and Qiao Wang and has published in prestigious journals such as PLoS ONE, Gene and Clinica Chimica Acta.

In The Last Decade

Jinqing Song

56 papers receiving 470 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jinqing Song China	12	303	281	85	68	62	61	478
Brandi Wasek United States	14	195 0.6×	61 0.2×	143 1.7×	32 0.5×	53 0.9×	34	441
C. R. Roe United States	9	409 1.3×	524 1.9×	72 0.8×	85 1.3×	182 2.9×	10	691
T. Baykal Türkiye	14	228 0.8×	237 0.8×	88 1.0×	30 0.4×	61 1.0×	18	449
Mitsuharu Kajita Japan	12	166 0.5×	132 0.5×	22 0.3×	45 0.7×	45 0.7×	26	363
E. Mönch Germany	13	347 1.1×	519 1.8×	84 1.0×	51 0.8×	97 1.6×	37	686
M. Blaskovics United States	12	248 0.8×	340 1.2×	86 1.0×	52 0.8×	98 1.6×	21	534
Denise M. McGuire United States	9	147 0.5×	110 0.4×	50 0.6×	20 0.3×	14 0.2×	11	358
Kathryn Moseley United States	17	416 1.4×	672 2.4×	178 2.1×	61 0.9×	137 2.2×	26	833
Ronald L. George United States	6	128 0.4×	109 0.4×	23 0.3×	10 0.1×	71 1.1×	6	343
Barbara S. Miles United States	10	357 1.2×	304 1.1×	32 0.4×	37 0.5×	28 0.5×	12	462

Countries citing papers authored by Jinqing Song

Since Specialization

Citations

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

Fields of papers citing papers by Jinqing Song

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jinqing Song

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

Ma, Xue, Zhehui Chen, Jinqing Song, et al.. (2024). Hypermethioninemia due to methionine adenosyltransferase I/III deficiency and brain damage. BMC Pediatrics. 24(1). 713–713.

Dong, Hui, Jinqing Song, Zhehui Chen, et al.. (2024). Clinical features and CPS1 variants in Chinese patients with carbamoyl phosphate synthetase 1 deficiency. BMC Pediatrics. 24(1). 539–539. 1 indexed citations

Mi, Xia, et al.. (2023). Visible-Light-Promoted Direct C3-H Cyanomethylation of 2H-Indazoles. ACS Omega. 8(12). 11192–11200. 1 indexed citations

Li, Yanhan, Ying Jin, Yi Liu, et al.. (2019). Case report of congenital chloride diarrhea and literature review. Zhonghua shiyong erke linchuang zazhi. 34(11). 862–865. 1 indexed citations

Zhang, Yao, et al.. (2018). Clinical and genetic study on 5 children with dopa-responsive dystonia due to tyrosine hydroxylase deficiency. Zhonghua shiyong erke linchuang zazhi. 33(6). 462–464. 1 indexed citations

Li, Dongxiao, Hui Dong, Hong Zheng, et al.. (2017). A chinese boy with geleophysic dysplasia caused by compound heterozygous mutations in ADAMTSL2. European Journal of Medical Genetics. 60(12). 685–689. 6 indexed citations

Li, Xiyuan, Yuan Ding, Yupeng Liu, et al.. (2016). Clinical, biochemical and genetic features of 13 children with maple syrup urine disease. Zhonghua shiyong erke linchuang zazhi. 31(8). 569–572. 2 indexed citations

Li, Dongxiao, Yupeng Liu, Yuan Ding, et al.. (2016). A patient with initial symptom of epilepsy from age of 12 years old due to early-onset Alzheimer disease caused by presenilin 1 mutation. 12(6). 621–626.

Ding, Yuan, Xiyuan Li, Yupeng Liu, et al.. (2016). Seven novel mutations of the SMPD1 gene in four Chinese patients with Niemann-Pick disease type A and prenatal diagnosis for four fetuses. European Journal of Medical Genetics. 59(4). 263–268. 4 indexed citations

10.

Liu, Yupeng, Haijun Wang, Yuan Ding, et al.. (2015). [Acute encephalopathy induced by vaccination in an infant with methylmalonic aciduria cblA].. PubMed. 53(1). 62–5. 4 indexed citations

11.

Li, Xiyuan, Ding Yuan, Yupeng Liu, et al.. (2015). Five Chinese patients with 5-oxoprolinuria due to glutathione synthetase and 5-oxoprolinase deficiencies. Brain and Development. 37(10). 952–959. 16 indexed citations

12.

Li, Xiyuan, Yuan Ding, Yupeng Liu, et al.. (2015). Analysis of four Chinese patients with neonatal–onset isovaleric acidemia. Zhonghua weichan yixue zazhi. 18(3). 188–194. 3 indexed citations

13.

Li, Xiyuan, Yuan Ding, Yanyan Ma, et al.. (2015). Very long-chain acyl-coenzyme A dehydrogenase deficiency in Chinese patients: Eight case reports, including one case of prenatal diagnosis. European Journal of Medical Genetics. 58(3). 134–139. 10 indexed citations

14.

Li, Xiyuan, Yuan Ding, Yupeng Liu, et al.. (2015). Succinic semialdehyde dehydrogenase deficiency of four Chinese patients and prenatal diagnosis for three fetuses. Gene. 574(1). 41–47. 8 indexed citations

15.

Liu, Yupeng, Xiyuan Li, Qiao Wang, et al.. (2015). Five novel SUCLG1 mutations in three Chinese patients with succinate-CoA ligase deficiency noticed by mild methylmalonic aciduria. Brain and Development. 38(1). 61–67. 8 indexed citations

16.

Ma, Yanyan, Yupeng Liu, Xiyuan Li, et al.. (2013). Two compound frame-shift mutations in succinate dehydrogenase gene of a Chinese boy with encephalopathy. Brain and Development. 36(5). 394–398. 17 indexed citations

17.

Ma, Yanyan, Yupeng Liu, Qiao Wang, et al.. (2013). [Clinical, biochemical and genetic analysis of the mitochondrial disorders presenting with cardiac damage].. PubMed. 51(12). 909–14. 1 indexed citations

18.

Li, Xiyuan, Qiao Wang, Yupeng Liu, et al.. (2013). [HEXB gene study and prenatal diagnosis for a family affected by infantile Sandhoff disease].. PubMed. 42(4). 403–10. 3 indexed citations

19.

Liu, Yupeng, Yanyan Ma, Qiao Wang, et al.. (2012). [Mitochondrial respiratory chain complex I deficiency due to 10191T>C mutation in ND3 gene].. PubMed. 14(8). 561–6. 5 indexed citations

20.

Yang, Yanling, Fang Sun, Yun Yuan, et al.. (2004). A Clinical Survey of 65 Patients with Leigh Syndrome. 20(1). 59–62.

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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