Yue-Qiu Tan

409 total citations
16 papers, 241 citations indexed

About

Yue-Qiu Tan is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Yue-Qiu Tan has authored 16 papers receiving a total of 241 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Pediatrics, Perinatology and Child Health, 12 papers in Genetics and 5 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Yue-Qiu Tan's work include Prenatal Screening and Diagnostics (12 papers), Genomic variations and chromosomal abnormalities (10 papers) and Chromosomal and Genetic Variations (5 papers). Yue-Qiu Tan is often cited by papers focused on Prenatal Screening and Diagnostics (12 papers), Genomic variations and chromosomal abnormalities (10 papers) and Chromosomal and Genetic Variations (5 papers). Yue-Qiu Tan collaborates with scholars based in China and Saudi Arabia. Yue-Qiu Tan's co-authors include Ge Lin, Fei Gong, Guangxiu Lu, Liang Hu, Dehua Cheng, Changfu Lu, Keli Luo, Pingyuan Xie, Ke Tan and Yifan Gu and has published in prestigious journals such as PLoS ONE, Fertility and Sterility and EBioMedicine.

In The Last Decade

Yue-Qiu Tan

16 papers receiving 222 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yue-Qiu Tan China 11 153 134 70 60 42 16 241
K. Ketterson United States 3 231 1.5× 126 0.9× 88 1.3× 42 0.7× 23 0.5× 5 249
Brenda McInnes Canada 7 79 0.5× 165 1.2× 73 1.0× 47 0.8× 36 0.9× 8 242
Steven Tang Canada 5 218 1.4× 184 1.4× 128 1.8× 44 0.7× 64 1.5× 10 341
J. Lespinasse France 12 162 1.1× 195 1.5× 37 0.5× 69 1.1× 108 2.6× 25 310
Brittany L. Daughtry United States 7 103 0.7× 56 0.4× 122 1.7× 121 2.0× 20 0.5× 10 242
Aïda Pujol Spain 10 203 1.3× 145 1.1× 172 2.5× 76 1.3× 47 1.1× 15 340
Anastasia Mania United Kingdom 8 299 2.0× 139 1.0× 202 2.9× 73 1.2× 40 1.0× 11 410
Tongji Xing United States 4 128 0.8× 72 0.5× 56 0.8× 80 1.3× 11 0.3× 5 194
Theresa Naluai-Cecchini United States 4 57 0.4× 108 0.8× 62 0.9× 124 2.1× 36 0.9× 4 207
Elisabetta Cursio Italy 5 223 1.5× 80 0.6× 111 1.6× 63 1.1× 9 0.2× 5 274

Countries citing papers authored by Yue-Qiu Tan

Since Specialization
Citations

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

Fields of papers citing papers by Yue-Qiu Tan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Yue-Qiu Tan. 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 Yue-Qiu Tan. The network helps show where Yue-Qiu Tan may publish in the future.

Co-authorship network of co-authors of Yue-Qiu Tan

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

All Works

16 of 16 papers shown
1.
Cheng, Dehua, Keli Luo, Mengge Li, et al.. (2023). Evaluation of genetic risk of apparently balanced chromosomal rearrangement carriers by breakpoint characterization. Journal of Assisted Reproduction and Genetics. 41(1). 147–159. 1 indexed citations
2.
Yuan, Shi‐Min, Dehua Cheng, Xiurong Li, et al.. (2022). The de novo aberration rate of prenatal karyotype was comparable between 1496 fetuses conceived via IVF/ICSI and 1396 fetuses from natural conception. Journal of Assisted Reproduction and Genetics. 39(7). 1683–1689. 4 indexed citations
3.
Cheng, Dehua, Liang Hu, Fei Gong, et al.. (2021). Clinical outcomes following preimplantation genetic testing and microdissecting junction region in couples with balanced chromosome rearrangement. Journal of Assisted Reproduction and Genetics. 38(3). 735–742. 6 indexed citations
4.
Li, Yong, Weili Wang, Chaofeng Tu, et al.. (2020). A novel homozygous frameshift mutation in MNS1 associated with severe oligoasthenoteratozoospermia in humans. Asian Journal of Andrology. 23(2). 197–204. 18 indexed citations
5.
Hu, Liang, Fan Liang, Dehua Cheng, et al.. (2020). Location of Balanced Chromosome-Translocation Breakpoints by Long-Read Sequencing on the Oxford Nanopore Platform. Frontiers in Genetics. 10. 1313–1313. 38 indexed citations
6.
Cheng, Dehua, Shi‐Min Yuan, Liang Hu, et al.. (2020). The genetic cause of intellectual deficiency and/or congenital malformations in two parental reciprocal translocation carriers and implications for assisted reproduction. Journal of Assisted Reproduction and Genetics. 38(1). 243–250. 2 indexed citations
7.
Wang, Xingming, Ruixue Li, Zhizhong Liu, et al.. (2020). Improving native human sperm freezing protection by using a modified vitrification method. Asian Journal of Andrology. 23(1). 91–96. 13 indexed citations
8.
Xie, Pingyuan, Liang Hu, Yue-Qiu Tan, et al.. (2019). Retrospective analysis of meiotic segregation pattern and interchromosomal effects in blastocysts from inversion preimplantation genetic testing cycles. Fertility and Sterility. 112(2). 336–342.e3. 12 indexed citations
9.
Cheng, Dehua, Shi‐Min Yuan, Keli Luo, et al.. (2019). Analysis of molecular cytogenetic features and PGT-SR for two infertile patients with small supernumerary marker chromosomes. Journal of Assisted Reproduction and Genetics. 36(12). 2533–2539. 3 indexed citations
10.
Gu, Yifan, Changfu Lu, Fei Gong, et al.. (2018). Inner cell mass incarceration in 8-shaped blastocysts does not increase monozygotic twinning in preimplantation genetic diagnosis and screening patients. PLoS ONE. 13(1). e0190776–e0190776. 13 indexed citations
11.
Hu, Liang, Keli Luo, Pingyuan Xie, et al.. (2018). Clinical outcomes in carriers of complex chromosomal rearrangements: a retrospective analysis of comprehensive chromosome screening results in seven cases. Fertility and Sterility. 109(3). 486–492. 17 indexed citations
12.
Li, Xihong, Yan Ouyang, Yan Yi, Yue-Qiu Tan, & Guangxiu Lu. (2016). Correlation analysis between ultrasound findings and abnormal karyotypes in the embryos from early pregnancy loss after in vitro fertilization-embryo transfer. Journal of Assisted Reproduction and Genetics. 34(1). 43–50. 11 indexed citations
13.
Hu, Liang, Dehua Cheng, Fei Gong, et al.. (2016). Reciprocal Translocation Carrier Diagnosis in Preimplantation Human Embryos. EBioMedicine. 14. 139–147. 40 indexed citations
14.
Xiong, Bo, Ke Tan, Yue-Qiu Tan, et al.. (2014). Using SNP array to identify aneuploidy and segmental imbalance in translocation carriers. Genomics Data. 2. 92–95. 14 indexed citations
15.
Zhang, Shuoping, Ke Tan, Fei Gong, et al.. (2014). Blastocysts can be rebiopsied for preimplantation genetic diagnosis and screening. Fertility and Sterility. 102(6). 1641–1645. 30 indexed citations
16.
Xu, Fang, Yanan Zhang, Dehua Cheng, et al.. (2014). The first patient with a pure 1p36 microtriplication associated with severe clinical phenotypes. Molecular Cytogenetics. 7(1). 64–64. 19 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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2026