Yanling Yang

1.3k total citations
56 papers, 856 citations indexed

About

Yanling Yang is a scholar working on Molecular Biology, Clinical Biochemistry and Rheumatology. According to data from OpenAlex, Yanling Yang has authored 56 papers receiving a total of 856 indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Molecular Biology, 31 papers in Clinical Biochemistry and 10 papers in Rheumatology. Recurrent topics in Yanling Yang's work include Metabolism and Genetic Disorders (31 papers), Mitochondrial Function and Pathology (22 papers) and ATP Synthase and ATPases Research (13 papers). Yanling Yang is often cited by papers focused on Metabolism and Genetic Disorders (31 papers), Mitochondrial Function and Pathology (22 papers) and ATP Synthase and ATPases Research (13 papers). Yanling Yang collaborates with scholars based in China, United States and Japan. Yanling Yang's co-authors include Guilin Li, Lei Li, Peng Geng, Yuan Liu, Y Liu, Yuehua Zhang, Jiong Qin, Jinqing Song, Yuwu Jiang and Xiru Wu and has published in prestigious journals such as Scientific Reports, Annals of Oncology and Science Translational Medicine.

In The Last Decade

Yanling Yang

52 papers receiving 839 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 17 576 373 183 125 97 56 856
Esmeralda Martins Portugal 20 484 0.8× 495 1.3× 40 0.2× 219 1.8× 132 1.4× 77 988
Shobhana Vora United States 19 504 0.9× 187 0.5× 210 1.1× 190 1.5× 61 0.6× 25 870
Dimitar K. Gavrilov United States 10 202 0.4× 214 0.6× 32 0.2× 95 0.8× 85 0.9× 21 428
Andrea Zaťková Slovakia 17 502 0.9× 361 1.0× 81 0.4× 36 0.3× 12 0.1× 40 795
Janet Haasjes Netherlands 9 525 0.9× 66 0.2× 61 0.3× 32 0.3× 49 0.5× 11 904
Alain Lemonnier France 12 214 0.4× 80 0.2× 192 1.0× 52 0.4× 41 0.4× 22 654
A Grenier Canada 13 231 0.4× 402 1.1× 28 0.2× 92 0.7× 107 1.1× 24 616
Toshihiro Imamura Japan 14 592 1.0× 59 0.2× 122 0.7× 48 0.4× 23 0.2× 27 880
Greice Andreotti de Molfetta Brazil 13 414 0.7× 37 0.1× 339 1.9× 65 0.5× 27 0.3× 34 649
Khaja Basheeruddin United States 15 239 0.4× 43 0.1× 80 0.4× 68 0.5× 31 0.3× 25 605

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.
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.
2.
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
3.
Zhu, Jin, Weihong Wang, Lian Zeng, et al.. (2024). Exosomal lncRNA HCP5 derived from human bone marrow mesenchymal stem cells improves chronic periodontitis by miR-24-3p/HO1/P38/ELK1 pathway. Heliyon. 10(14). e34203–e34203. 4 indexed citations
4.
5.
Jin, Ying, Mengqiu Li, Jinqing Song, et al.. (2024). The utility of methylmalonic acid, methylcitrate acid, and homocysteine in dried blood spots for therapeutic monitoring of three inherited metabolic diseases. Frontiers in Nutrition. 11. 1414681–1414681. 1 indexed citations
6.
Fang, Hezhi, Miaomiao Du, Wei‐Dong Yu, et al.. (2022). SERAC1 is a component of the mitochondrial serine transporter complex required for the maintenance of mitochondrial DNA. Science Translational Medicine. 14(634). eabl6992–eabl6992. 12 indexed citations
7.
Zhang, Luyi, Zhehui Chen, Dongxiao Li, et al.. (2022). Novel biallelic mutations in TMEM126B cause splicing defects and lead to Leigh-like syndrome with severe complex I deficiency. Journal of Human Genetics. 68(4). 239–246. 2 indexed citations
8.
Du, Miaomiao, Jie Xie, Yan Zhou, et al.. (2020). Mutations in TOMM70 lead to multi-OXPHOS deficiencies and cause severe anemia, lactic acidosis, and developmental delay. Journal of Human Genetics. 65(3). 231–240. 24 indexed citations
9.
Liu, Yi, Ying Jin, Mengqiu Li, et al.. (2020). Mutations of MACF1, Encoding Microtubule-Actin Crosslinking-Factor 1, Cause Spectraplakinopathy. Frontiers in Neurology. 10. 1335–1335. 9 indexed citations
10.
Liu, Yuan, Xin Jin, Yang Liu, et al.. (2019). Long non‐coding RNA LINC01535 promotes cervical cancer progression via targeting the miR‐214/EZH2 feedback loop. Journal of Cellular and Molecular Medicine. 23(9). 6098–6111. 31 indexed citations
11.
Liu, Y, Yanling Yang, Lei Li, et al.. (2017). LncRNA SNHG1 enhances cell proliferation, migration, and invasion in cervical cancer. Biochemistry and Cell Biology. 96(1). 38–43. 119 indexed citations
12.
Yang, Haipo, Shuo Wang, Aijie Liu, et al.. (2017). Novel copy number variation of POMGNT1 associated with muscle-eye-brain disease detected by next-generation sequencing. Scientific Reports. 7(1). 7056–7056. 4 indexed citations
13.
Mariathasan, Sanjeev, Shannon J. Turley, Dorothee Nickles, et al.. (2017). TGF-β signalling attenuates tumour response to PD-L1 checkpoint blockade by contributing to retention of T cells in the peritumoural stroma. Annals of Oncology. 28. xi30–xi30. 8 indexed citations
14.
Li, Xiyuan, et al.. (2016). Novel mutation of ND4 gene identified by targeted next-generation sequencing in patient with Leigh syndrome. Journal of Human Genetics. 62(2). 291–297. 13 indexed citations
15.
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
16.
Yang, Yanling & Yun Ye. (2014). [Consensus about the diagnosis and treatment of hyperphenylalaninemia].. PubMed. 52(6). 420–5. 13 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.
Qi, Yu, Ying Zhang, Zhaoxia Wang, et al.. (2006). Screening of common mitochondrial mutations in Chinese patients with mitochondrial encephalomyopathies. Mitochondrion. 7(1-2). 147–150. 20 indexed citations
19.
Yang, Yanling, Fang Sun, Qian Ning, et al.. (2005). [Clinical and laboratory screening studies on urea cycle defects].. PubMed. 43(5). 331–4. 4 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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