Dejian Yuan

515 total citations
28 papers, 224 citations indexed

About

Dejian Yuan is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Dejian Yuan has authored 28 papers receiving a total of 224 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 13 papers in Molecular Biology and 6 papers in Genetics. Recurrent topics in Dejian Yuan's work include Genomic variations and chromosomal abnormalities (6 papers), Hemoglobinopathies and Related Disorders (6 papers) and Genetic Associations and Epidemiology (5 papers). Dejian Yuan is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Hemoglobinopathies and Related Disorders (6 papers) and Genetic Associations and Epidemiology (5 papers). Dejian Yuan collaborates with scholars based in China, United States and Germany. Dejian Yuan's co-authors include Shi Huang, Zuobin Zhu, Tizhen Yan, Ning Tang, Xingyuan Chen, Dingyuan Zeng, Aiping Mao, Xiaoyun Lei, Yimin Huang and Mengping Long and has published in prestigious journals such as PLoS ONE, Scientific Reports and Biology of Reproduction.

In The Last Decade

Dejian Yuan

23 papers receiving 223 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Dejian Yuan China 10 107 86 56 38 32 28 224
Shelly C. Bernstein United States 9 104 1.0× 121 1.4× 42 0.8× 33 0.9× 57 1.8× 13 340
Joshi Stephen United States 11 112 1.0× 119 1.4× 12 0.2× 10 0.3× 34 1.1× 17 259
Laura V. Milko United States 12 277 2.6× 132 1.5× 28 0.5× 7 0.2× 52 1.6× 23 407
Emily Greenfest‐Allen United States 9 46 0.4× 170 2.0× 28 0.5× 32 0.8× 10 0.3× 18 297
Philip L. Beales United Kingdom 7 152 1.4× 102 1.2× 7 0.1× 14 0.4× 32 1.0× 8 263
Andrey Khrunin Russia 10 186 1.7× 225 2.6× 11 0.2× 21 0.6× 28 0.9× 39 536
Bixia Xiang United States 10 196 1.8× 136 1.6× 13 0.2× 25 0.7× 94 2.9× 15 362
Franca Bernardi Italy 10 246 2.3× 116 1.3× 30 0.5× 37 1.0× 93 2.9× 13 367
Shirley Oren Israel 7 90 0.8× 170 2.0× 27 0.5× 29 0.8× 16 0.5× 8 416
M. Acuña Chile 10 88 0.8× 70 0.8× 6 0.1× 13 0.3× 15 0.5× 34 268

Countries citing papers authored by Dejian Yuan

Since Specialization
Citations

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

Fields of papers citing papers by Dejian Yuan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dejian Yuan

This figure shows the co-authorship network connecting the top 25 collaborators of Dejian Yuan. A scholar is included among the top collaborators of Dejian Yuan 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 Dejian Yuan. Dejian Yuan 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.
Zhang, Xinrong, et al.. (2024). Pathogenic relationship between phenotypes of ARPKD and novel compound heterozygous mutations of PKHD1. Frontiers in Genetics. 15. 1429336–1429336.
2.
Yuan, Dejian, Aiping Mao, Dingyuan Zeng, et al.. (2024). Improved Genetic Characterization of Congenital Adrenal Hyperplasia by Long-Read Sequencing Compared with Multiplex Ligation-Dependent Probe Amplification Plus Sanger Sequencing. Journal of Molecular Diagnostics. 26(9). 770–780. 2 indexed citations
3.
Mei, Hualin, et al.. (2024). A Novel Homozygous Synonymous Variant in CCDC134 as a Cause of Osteogenesis Imperfecta Type XXII. Clinical Genetics. 107(4). 446–452. 1 indexed citations
4.
5.
Chen, Xingyuan, Dingyuan Zeng, Ning Tang, et al.. (2022). Detection of four rare thalassemia variants using Single-molecule realtime sequencing. Frontiers in Genetics. 13. 974999–974999. 10 indexed citations
6.
Yang, Jin‐Ling, Dejian Yuan, Xiaohui Tan, et al.. (2021). Analysis of a family with mitochondrial trifunctional protein deficiency caused by HADHA gene mutations. Molecular Medicine Reports. 25(2). 8 indexed citations
7.
Chen, Xingyuan, Dingyuan Zeng, Ning Tang, et al.. (2021). The value of single-molecule real-time technology in the diagnosis of rare thalassemia variants and analysis of phenotype–genotype correlation. Journal of Human Genetics. 67(4). 183–195. 42 indexed citations
8.
9.
Zhu, Liangjun, David J. Cooper, Dejian Yuan, et al.. (2020). Regional Scale Temperature Rather than Precipitation Determines Vessel Features in Earlywood of Manchurian Ash in Temperate Forests. Journal of Geophysical Research Biogeosciences. 125(11). 13 indexed citations
10.
Chen, Xingyuan, et al.. (2020). Application of Copy Number Variation Sequencing in Genetic Analysis of Miscarriages in Early and Middle Pregnancy. Cytogenetic and Genome Research. 160(11-12). 634–642. 9 indexed citations
11.
Chen, Xingyuan, Jun Huang, Dejian Yuan, et al.. (2020). Diagnosis and Prenatal Diagnosis in a Chinese Family Carrying the Rare α-Thalassemia Gene HBA2: c.1A>G Mutation. Hemoglobin. 44(1). 51–54. 1 indexed citations
12.
Chen, Hongyao, Xiaoyun Lei, Dejian Yuan, & Shi Huang. (2020). The relationship between the minor allele content and Alzheimer's disease. Genomics. 112(3). 2426–2432. 5 indexed citations
13.
Yan, Tizhen, et al.. (2020). [Analysis of PLA2G6 gene variant in a family affected with infantile neuroaxonal dystrophy].. PubMed. 37(1). 21–24. 3 indexed citations
14.
Yuan, Dejian & Shi Huang. (2017). Genetic equidistance at nucleotide level. Genomics. 109(3-4). 192–195. 1 indexed citations
15.
16.
Zhu, Zuobin, et al.. (2015). Enrichment of Minor Alleles of Common SNPs and Improved Risk Prediction for Parkinson's Disease. PLoS ONE. 10(7). e0133421–e0133421. 18 indexed citations
17.
Zhu, Zuobin, et al.. (2015). Collective effects of SNPs on transgenerational inheritance in Caenorhabditis elegans and budding yeast. Genomics. 106(1). 23–29. 10 indexed citations
18.
Yuan, Dejian, Zuobin Zhu, Jie Liang, et al.. (2014). Scoring the collective effects of SNPs: association of minor alleles with complex traits in model organisms. Science China Life Sciences. 57(9). 876–888. 18 indexed citations
19.
Hu, Taobo, et al.. (2013). The genetic equidistance result: misreading by the molecular clock and neutral theory and reinterpretation nearly half of a century later. Science China Life Sciences. 56(3). 254–261. 16 indexed citations
20.
Watkins, M. M., et al.. (2005). GRACE Harmonic and Mascon Solutions at JPL. AGU Fall Meeting Abstracts. 2005. 3 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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