Yongyi Ma

444 total citations
20 papers, 263 citations indexed

About

Yongyi Ma is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Yongyi Ma has authored 20 papers receiving a total of 263 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 8 papers in Molecular Biology and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Yongyi Ma's work include Prenatal Screening and Diagnostics (6 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers) and Sperm and Testicular Function (4 papers). Yongyi Ma is often cited by papers focused on Prenatal Screening and Diagnostics (6 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers) and Sperm and Testicular Function (4 papers). Yongyi Ma collaborates with scholars based in China, United States and Brazil. Yongyi Ma's co-authors include Yuan Yang, Ying Shen, Yunqiang Liu, Dong Yang, Wenling Tu, Qiang Dong, Zhiqing Liang, Zhiqiang Cai, Lin Wang and Chen Chen and has published in prestigious journals such as PLoS ONE, Scientific Reports and Science Advances.

In The Last Decade

Yongyi Ma

18 papers receiving 255 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yongyi Ma China 10 112 102 95 48 39 20 263
Molka Kammoun Tunisia 9 86 0.8× 128 1.3× 144 1.5× 111 2.3× 64 1.6× 18 368
Silke Mark Germany 7 95 0.8× 27 0.3× 93 1.0× 51 1.1× 16 0.4× 8 329
Emily Hardisty United States 8 80 0.7× 147 1.4× 239 2.5× 5 0.1× 29 0.7× 17 301
Elena S. Vashukova Russia 10 107 1.0× 27 0.3× 88 0.9× 18 0.4× 9 0.2× 37 288
Iris Roth United States 3 57 0.5× 14 0.1× 79 0.8× 38 0.8× 16 0.4× 5 340
Maria Daniel Poland 9 146 1.3× 104 1.0× 34 0.4× 8 0.2× 10 0.3× 19 290
Michael Fatouros Greece 9 50 0.4× 77 0.8× 20 0.2× 54 1.1× 88 2.3× 16 236
Yan-Li Dang China 3 170 1.5× 24 0.2× 178 1.9× 15 0.3× 8 0.2× 7 393
Lu Meng China 6 81 0.7× 153 1.5× 139 1.5× 4 0.1× 28 0.7× 7 257
Filippo Massa France 9 171 1.5× 62 0.6× 35 0.4× 6 0.1× 34 0.9× 15 282

Countries citing papers authored by Yongyi Ma

Since Specialization
Citations

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

Fields of papers citing papers by Yongyi Ma

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yongyi Ma

This figure shows the co-authorship network connecting the top 25 collaborators of Yongyi Ma. A scholar is included among the top collaborators of Yongyi Ma 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 Yongyi Ma. Yongyi Ma 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, Yongyi, Nan Liu, Yu Shi, et al.. (2024). BRD4L cooperates with MYC to block local tumor invasion via suppression of S100A10. Cellular Signalling. 119. 111173–111173.
2.
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Xu, Liang, et al.. (2023). Association between the first and second trimester cell free DNA fetal fraction and spontaneous preterm birth. Expert Review of Molecular Diagnostics. 23(7). 635–642. 3 indexed citations
4.
Zhang, Xueguang, Rui Zheng, Chen Liang, et al.. (2022). Loss-of-function mutations inCEP78cause male infertility in humans and mice. Science Advances. 8(40). eabn0968–eabn0968. 27 indexed citations
5.
Li, Xiaoduo, Li Liu, Xu Zhang, et al.. (2022). Prenatal diagnosis identifies compound heterozygous variants in RYR1 that causes ultrasound abnormalities in a fetus. BMC Medical Genomics. 15(1). 202–202. 1 indexed citations
6.
Ma, Yongyi, et al.. (2022). Case Report: Preimplantation Genetic Testing for Meckel Syndrome Induced by Novel Compound Heterozygous Mutations of MKS1. Frontiers in Genetics. 13. 843931–843931. 2 indexed citations
7.
Hu, Huamei, et al.. (2021). Prenatal Diagnosis and Genetic Analysis of 21q21.1–q21.2 Aberrations in Seven Chinese Pedigrees. Frontiers in Genetics. 12. 731815–731815. 2 indexed citations
8.
Li, Jia, et al.. (2021). X Chromosome Inactivation Pattern and Pregnancy Outcome of Female Carriers of Pathogenic Heterozygous X-Linked Deletions. Frontiers in Genetics. 12. 782629–782629. 7 indexed citations
9.
10.
Yang, Neng, et al.. (2020). Novel biallelic variants in COL7A1 cause recessive dystrophic epidermolysis bullosa. Molecular Genetics & Genomic Medicine. 8(8). e1347–e1347. 2 indexed citations
11.
Yao, Hong, et al.. (2020). Fetal Phenotype and Prenatal Diagnosis of Kabuki Syndrome. Maternal-Fetal Medicine. 5(3). 187–191.
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13.
Zhang, Rong, et al.. (2020). [Factors affecting the failure of non-invasive prenatal testing and the feasibility analysis of retesting].. PubMed. 37(6). 603–608. 1 indexed citations
14.
Li, Penghao, Yaxin Yao, Tianhua Huang, et al.. (2018). Preimplantation Genetic Screening with Spent Culture Medium/Blastocoel Fluid for in Vitro Fertilization. Scientific Reports. 8(1). 9275–9275. 45 indexed citations
15.
16.
Shen, Ying, Yunqiang Liu, Yongyi Ma, et al.. (2017). Evidence for the involvement of the proximal copy of the MAGEA9 gene in Xq28-linked CNV67 specific to spermatogenic failure†. Biology of Reproduction. 96(3). 610–616. 10 indexed citations
17.
Liu, Yunqiang, Ying Shen, Wenling Tu, et al.. (2017). Copy number variation of functional RBMY1 is associated with sperm motility: an azoospermia factor-linked candidate for asthenozoospermia. Human Reproduction. 32(7). 1521–1531. 29 indexed citations
18.
Cai, Zhiqiang, Shubin Si, Chen Chen, et al.. (2015). Analysis of Prognostic Factors for Survival after Hepatectomy for Hepatocellular Carcinoma Based on a Bayesian Network. PLoS ONE. 10(3). e0120805–e0120805. 33 indexed citations
19.
Yang, Bo, Yongyi Ma, Lei Li, et al.. (2015). Common AZFc structure may possess the optimal spermatogenesis efficiency relative to the rearranged structures mediated by non-allele homologous recombination. Scientific Reports. 5(1). 10551–10551. 15 indexed citations
20.
Ma, Yongyi, Yunqiang Liu, Hongde Hu, et al.. (2013). Combined analysis of genome-wide-linked susceptibility loci to Kawasaki disease in Han Chinese. Human Genetics. 132(6). 669–680. 32 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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