Yu Ding

536 total citations
38 papers, 359 citations indexed

About

Yu Ding is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Yu Ding has authored 38 papers receiving a total of 359 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 23 papers in Genetics and 6 papers in Surgery. Recurrent topics in Yu Ding's work include Genetic Syndromes and Imprinting (6 papers), Genomics and Rare Diseases (6 papers) and Genomic variations and chromosomal abnormalities (4 papers). Yu Ding is often cited by papers focused on Genetic Syndromes and Imprinting (6 papers), Genomics and Rare Diseases (6 papers) and Genomic variations and chromosomal abnormalities (4 papers). Yu Ding collaborates with scholars based in China and United States. Yu Ding's co-authors include Niu Li, Yiping Shen, Jian Wang, Guoying Chang, Tingting Yu, Xiumin Wang, Ruen Yao, Yongnian Shen, Yufei Xu and Xiaodong Huang and has published in prestigious journals such as PLoS ONE, The Journal of Clinical Endocrinology & Metabolism and International Journal of Molecular Sciences.

In The Last Decade

Yu Ding

32 papers receiving 356 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yu Ding China 12 219 170 55 38 35 38 359
Amy Knight Johnson United States 12 196 0.9× 164 1.0× 26 0.5× 16 0.4× 67 1.9× 16 396
Lilia Romdhane Tunisia 12 150 0.7× 189 1.1× 20 0.4× 17 0.4× 40 1.1× 29 394
Mohammad Miryounesi Iran 10 191 0.9× 83 0.5× 15 0.3× 22 0.6× 63 1.8× 70 337
Sara Bertok Slovenia 10 166 0.8× 122 0.7× 27 0.5× 42 1.1× 10 0.3× 35 354
Catherine Naud-Saudreau France 5 287 1.3× 95 0.6× 47 0.9× 107 2.8× 18 0.5× 5 380
Shinsuke Ninomiya Japan 14 268 1.2× 210 1.2× 11 0.2× 41 1.1× 48 1.4× 31 444
C Lecointre France 10 336 1.5× 203 1.2× 155 2.8× 27 0.7× 19 0.5× 15 506
Majdi Nagara Tunisia 10 161 0.7× 140 0.8× 18 0.3× 11 0.3× 26 0.7× 25 343
Katsura Ishizu Japan 12 213 1.0× 136 0.8× 222 4.0× 16 0.4× 15 0.4× 25 404
Maribeth A. Lazzaro Canada 9 296 1.4× 73 0.4× 17 0.3× 10 0.3× 31 0.9× 9 428

Countries citing papers authored by Yu Ding

Since Specialization
Citations

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

Fields of papers citing papers by Yu Ding

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yu Ding

This figure shows the co-authorship network connecting the top 25 collaborators of Yu Ding. A scholar is included among the top collaborators of Yu Ding 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 Yu Ding. Yu Ding 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.
Ding, Yu, Shiyang Gao, Guoying Chang, et al.. (2025). Focusing on Rare Variants Related to Maturity‐Onset Diabetes of the Young in Children. Pediatric Diabetes. 2025(1). 8155443–8155443.
2.
Yang, Min, et al.. (2025). The Effect of Valine on the Synthesis of α-Casein in MAC-T Cells and the Expression and Phosphorylation of Genes Related to the mTOR Signaling Pathway. International Journal of Molecular Sciences. 26(7). 3179–3179. 1 indexed citations
3.
Gao, Shiyang, Yu Ding, Zhiying Li, et al.. (2024). Molecular and phenotypic characteristics of Bardet-Biedl syndrome in Chinese patients. Orphanet Journal of Rare Diseases. 19(1). 149–149. 2 indexed citations
4.
5.
Chang, Guoying, Lingwen Ying, Ruen Yao, et al.. (2024). Genetic variants of ABCC8 and clinical manifestations in eight Chinese children with hyperinsulinemic hypoglycemia. BMC Endocrine Disorders. 24(1). 8–8. 2 indexed citations
6.
7.
Gao, Shiyang, et al.. (2023). A novel heterozygous variant of FOXJ1 in a Chinese female with primary ciliary dyskinesia and hydrocephalus: A case report and literature review. Molecular Genetics & Genomic Medicine. 11(9). e2235–e2235. 2 indexed citations
8.
Chang, Guoying, Yijun Tang, Yu Ding, et al.. (2023). Genotypic and phenotypic features of dyslipidemia in a sample of pediatric patients in China. BMC Pediatrics. 23(1).
9.
Ding, Yu, Niu Li, Dan Lou, et al.. (2020). Clinical and genetic analysis in a Chinese cohort of children and adolescents with diabetes/persistent hyperglycemia. Journal of Diabetes Investigation. 12(1). 48–62. 7 indexed citations
10.
Li, Xin, Ruen Yao, Xin Tan, et al.. (2019). Molecular and phenotypic spectrum of Noonan syndrome in Chinese patients. Clinical Genetics. 96(4). 290–299. 32 indexed citations
11.
Li, Xin, Ruen Yao, Xin Tan, et al.. (2019). Molecular and Phenotypic Spectrum of Noonan Syndrome in Chinese Patients. 2 indexed citations
12.
Xu, Yufei, Yirou Wang, Niu Li, et al.. (2019). New insights from unbiased panel and whole-exome sequencing in a large Chinese cohort with disorders of sex development. European Journal of Endocrinology. 181(3). 311–323. 20 indexed citations
13.
Li, Xin, Qing Cheng, Yu Ding, et al.. (2019). TRMA syndrome with a severe phenotype, cerebral infarction, and novel compound heterozygous SLC19A2 mutation: a case report. BMC Pediatrics. 19(1). 233–233. 6 indexed citations
14.
15.
Li, Niu, Yirou Wang, Yu Yang, et al.. (2018). Description of the molecular and phenotypic spectrum of Wiedemann-Steiner syndrome in Chinese patients. Orphanet Journal of Rare Diseases. 13(1). 178–178. 29 indexed citations
16.
Yu, Tingting, J Li, Yu Ding, et al.. (2016). Obesity and developmental delay in a patient with uniparental disomy of chromosome 2. International Journal of Obesity. 40(12). 1935–1941. 11 indexed citations
17.
Li, Niu, Yu Ding, Tingting Yu, et al.. (2016). Causal variants screened by whole exome sequencing in a patient with maternal uniparental isodisomy of chromosome 10 and a complicated phenotype. Experimental and Therapeutic Medicine. 11(6). 2247–2253. 4 indexed citations
18.
Li, Niu, Juan Li, Yu Ding, et al.. (2016). Novel mutations in the CYP11B2 gene causing aldosterone synthase deficiency. Molecular Medicine Reports. 13(4). 3127–3132. 9 indexed citations
19.
Zheng, Zhaojing, Li Hong, Xiaodong Huang, et al.. (2013). Screening for Coding Variants in FTO and SH2B1 Genes in Chinese Patients with Obesity. PLoS ONE. 8(6). e67039–e67039. 19 indexed citations
20.
Lu, Zhaohui, Zhongwei Lv, Tingting Yu, et al.. (2013). The Fas/Fas Ligand Death Receptor Pathway Contributes to Phenylalanine-Induced Apoptosis in Cortical Neurons. PLoS ONE. 8(8). e71553–e71553. 28 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Amy Knight Johnson Breakdown of academic impact, for papers by Lilia Romdhane Breakdown of academic impact, for papers by Mohammad Miryounesi Breakdown of academic impact, for papers by Sara Bertok Breakdown of academic impact, for papers by Catherine Naud-Saudreau Breakdown of academic impact, for papers by Shinsuke Ninomiya Breakdown of academic impact, for papers by C Lecointre Breakdown of academic impact, for papers by Majdi Nagara Breakdown of academic impact, for papers by Katsura Ishizu Breakdown of academic impact, for papers by Maribeth A. Lazzaro
Rankless by CCL
2026