Yanling Yang

2.2k total citations
138 papers, 1.5k citations indexed

About

Yanling Yang is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Yanling Yang has authored 138 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 82 papers in Molecular Biology, 48 papers in Clinical Biochemistry and 21 papers in Genetics. Recurrent topics in Yanling Yang's work include Metabolism and Genetic Disorders (48 papers), Mitochondrial Function and Pathology (27 papers) and RNA modifications and cancer (14 papers). Yanling Yang is often cited by papers focused on Metabolism and Genetic Disorders (48 papers), Mitochondrial Function and Pathology (27 papers) and RNA modifications and cancer (14 papers). Yanling Yang collaborates with scholars based in China, Japan and United States. Yanling Yang's co-authors include Xiyuan Li, Jinqing Song, Yupeng Liu, Yuan Ding, Qiao Wang, Yanyan Ma, Seiji Yamaguchi, Yuki Hasegawa, Yuwu Jiang and Masahiko Kimura and has published in prestigious journals such as Journal of Biological Chemistry, Angewandte Chemie International Edition and SHILAP Revista de lepidopterología.

In The Last Decade

Yanling Yang

125 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yanling Yang China 19 857 505 209 136 134 138 1.5k
Klaas J. Wierenga United States 21 579 0.7× 305 0.6× 221 1.1× 211 1.6× 40 0.3× 43 1.4k
Akira Ohtake Japan 27 1.9k 2.3× 1.1k 2.3× 318 1.5× 140 1.0× 85 0.6× 138 2.7k
Natalia I. Krupenko United States 25 1.1k 1.2× 191 0.4× 79 0.4× 79 0.6× 212 1.6× 54 1.6k
Audrey Boutron France 21 1.2k 1.3× 627 1.2× 77 0.4× 79 0.6× 55 0.4× 47 1.6k
Jun Qin Mo United States 27 1.2k 1.4× 331 0.7× 113 0.5× 33 0.2× 173 1.3× 53 2.3k
E. Holme Sweden 22 1.1k 1.3× 926 1.8× 139 0.7× 121 0.9× 35 0.3× 45 1.7k
Tim U. Krohne Germany 29 1.2k 1.4× 112 0.2× 144 0.7× 142 1.0× 103 0.8× 99 2.9k
Lisa E. Kratz United States 28 1.3k 1.5× 191 0.4× 415 2.0× 87 0.6× 144 1.1× 63 2.0k
Stephanie Grünewald United Kingdom 28 1.4k 1.7× 558 1.1× 354 1.7× 139 1.0× 29 0.2× 85 2.1k
R. J. A. Wanders Netherlands 23 1.7k 1.9× 790 1.6× 71 0.3× 82 0.6× 109 0.8× 55 2.0k

Countries citing papers authored by Yanling Yang

Since Specialization
Citations

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

Fields of papers citing papers by Yanling Yang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yanling Yang

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

All Works

20 of 20 papers shown
1.
Chen, Yao, Lan‐Ping Xu, Xiaohui Zhang, et al.. (2024). Haploidentical hematopoietic stem cell transplantation with busulfan, cyclophosphamide, and fludarabine conditioning for X‐linked adrenal cerebral leukodystrophy. Pediatric Transplantation. 28(3). e14735–e14735.
2.
3.
Yang, Yanling, Yili Liu, Jianhui Weng, et al.. (2023). A carbonic anhydrase-targeted NIR-II fluorescent cisplatin theranostic nanoparticle for combined therapy of pancreatic tumors. Biomaterials. 305. 122454–122454. 17 indexed citations
4.
5.
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
6.
Li, Yuanyuan, Dongxiao Li, Jie Xie, et al.. (2018). SURF1 mutations in Chinese patients with Leigh syndrome: Novel mutations, mutation spectrum, and the functional consequences. Gene. 674. 15–24. 12 indexed citations
7.
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
8.
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
9.
10.
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
11.
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
12.
Oda, Tetsuya, Hui Xiong, Kazuhiro Kobayashi, et al.. (2015). A de novo mutation of the MYH7 gene in a large Chinese family with autosomal dominant myopathy. Human Genome Variation. 2(1). 15022–15022. 5 indexed citations
13.
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
14.
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
15.
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
16.
Xiong, Hui, Cuijie Wei, Xingzhi Chang, et al.. (2014). [Value of muscle enzyme analysis in differential diagnosis of childhood myopathic hyper-creatine kinase-emia].. PubMed. 46(1). 130–7. 1 indexed citations
17.
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
18.
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
19.
Hao, Xiaodan, Yanling Yang, Nelson L.S. Tang, et al.. (2012). Mitochondrial DNA haplogroup Y is associated to Leigh syndrome in Chinese population. Gene. 512(2). 460–463. 11 indexed citations
20.
Xu, Zhengmin, et al.. (2004). A new keratin 5 mutation (K199T) in a family with Weber-Cockayne epidermolysis bullosa simplex. Clinical and Experimental Dermatology. 29(1). 74–76.

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

Breakdown of academic impact, for papers by Klaas J. Wierenga Breakdown of academic impact, for papers by Akira Ohtake Breakdown of academic impact, for papers by Natalia I. Krupenko Breakdown of academic impact, for papers by Audrey Boutron Breakdown of academic impact, for papers by Jun Qin Mo Breakdown of academic impact, for papers by E. Holme Breakdown of academic impact, for papers by Tim U. Krohne Breakdown of academic impact, for papers by Lisa E. Kratz Breakdown of academic impact, for papers by Stephanie Grünewald Breakdown of academic impact, for papers by R. J. A. Wanders
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