Minyue Ma

482 total citations
18 papers, 347 citations indexed

About

Minyue Ma is a scholar working on Pediatrics, Perinatology and Child Health, Molecular Biology and Genetics. According to data from OpenAlex, Minyue Ma has authored 18 papers receiving a total of 347 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Pediatrics, Perinatology and Child Health, 9 papers in Molecular Biology and 8 papers in Genetics. Recurrent topics in Minyue Ma's work include Prenatal Screening and Diagnostics (12 papers), Genomic variations and chromosomal abnormalities (7 papers) and Reproductive Biology and Fertility (4 papers). Minyue Ma is often cited by papers focused on Prenatal Screening and Diagnostics (12 papers), Genomic variations and chromosomal abnormalities (7 papers) and Reproductive Biology and Fertility (4 papers). Minyue Ma collaborates with scholars based in China, Hong Kong and Australia. Minyue Ma's co-authors include Yuanqing Yao, Hui Wang, David S. Cram, Wenke Zhang, Li Wang, Qi Zhou, Zuomin Zhou, Shuling Wang, Li Wang and Na Duan and has published in prestigious journals such as PLoS ONE, Cellular and Molecular Life Sciences and Human Reproduction.

In The Last Decade

Minyue Ma

17 papers receiving 334 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Minyue Ma China 9 188 153 128 126 48 18 347
Olga Tšuiko Belgium 16 353 1.9× 195 1.3× 218 1.7× 227 1.8× 94 2.0× 30 583
Andrea R. Victor United States 11 499 2.7× 152 1.0× 184 1.4× 258 2.0× 65 1.4× 20 585
Anastasia Mania United Kingdom 8 299 1.6× 73 0.5× 139 1.1× 202 1.6× 107 2.2× 11 410
Lizhi Leng China 10 93 0.5× 240 1.6× 77 0.6× 149 1.2× 55 1.1× 18 360
Bhavini Rana United States 4 128 0.7× 191 1.2× 122 1.0× 40 0.3× 31 0.6× 8 330
Ilaria Stanghellini Italy 9 71 0.4× 269 1.8× 53 0.4× 94 0.7× 60 1.3× 15 400
Mark Grossmann Spain 8 116 0.6× 214 1.4× 123 1.0× 160 1.3× 170 3.5× 14 397
D. Potter United States 3 246 1.3× 79 0.5× 148 1.2× 96 0.8× 17 0.4× 5 301
Songbang Ou China 8 93 0.5× 117 0.8× 63 0.5× 211 1.7× 135 2.8× 28 321
Jennifer R. Gruhn Denmark 8 95 0.5× 171 1.1× 87 0.7× 93 0.7× 30 0.6× 11 288

Countries citing papers authored by Minyue Ma

Since Specialization
Citations

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

Fields of papers citing papers by Minyue Ma

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Minyue Ma

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

All Works

18 of 18 papers shown
1.
Guan, Jing, Minyue Ma, Xiaonan Wu, et al.. (2025). Clinical application of preimplantation genetic testing based on low-coverage next-generation sequencing with linkage analyses in hereditary hearing loss families. Journal of Assisted Reproduction and Genetics. 42(6). 1989–2002.
2.
Ma, Minyue, Hui Wang, William S.B. Yeung, et al.. (2023). Preimplantation genetic testing for aneuploidy helps to achieve a live birth with fewer transfer cycles for the blastocyst FET patients with unexplained recurrent implantation failure. Archives of Gynecology and Obstetrics. 308(2). 599–610. 3 indexed citations
3.
Huang, Shasha, Hui Wang, Xue Gao, et al.. (2023). Preimplantation genetic testing for hereditary hearing loss in Chinese population. Journal of Assisted Reproduction and Genetics. 40(7). 1721–1732. 3 indexed citations
4.
Gao, Yuan, Hui Wang, Yanfei Cheng, et al.. (2022). Single-Cell Sequencing Reveals Clearance of Blastula Chromosomal Mosaicism in In Vitro Fertilization Babies. Genomics Proteomics & Bioinformatics. 20(6). 1224–1231. 5 indexed citations
5.
Cheng, Yanfei, Qian Yu, Minyue Ma, et al.. (2021). Variant haplophasing by long-read sequencing: a new approach to preimplantation genetic testing workups. Fertility and Sterility. 116(3). 774–783. 22 indexed citations
6.
Ma, Minyue, et al.. (2018). Chromosome constitution of equal-sized three-cell embryos using next-generation sequencing technology. Journal of Assisted Reproduction and Genetics. 36(2). 307–314. 1 indexed citations
7.
Wang, Li, Jiandong Shen, David S. Cram, et al.. (2017). Preferential selection and transfer of euploid noncarrier embryos in preimplantation genetic diagnosis cycles for reciprocal translocations. Fertility and Sterility. 108(4). 620–627.e4. 21 indexed citations
8.
Liu, Yifan, Ming Han, Xiaoshuang Li, et al.. (2017). Age-related changes in the mitochondria of human mural granulosa cells. Human Reproduction. 32(12). 2465–2473. 65 indexed citations
9.
Wang, Shuling, Ziru Niu, Hui Wang, et al.. (2017). De Novo Paternal FBN1 Mutation Detected in Embryos Before Implantation. Medical Science Monitor. 23. 3136–3146. 5 indexed citations
10.
Zhang, Yixin, Li Wang, Huiying Sun, et al.. (2016). Molecular analysis of DNA in blastocoele fluid using next-generation sequencing. Journal of Assisted Reproduction and Genetics. 33(5). 637–645. 44 indexed citations
11.
Zhang, Wenke, Li Wang, Hui Wang, et al.. (2016). Clinical application of next-generation sequencing in preimplantation genetic diagnosis cycles for Robertsonian and reciprocal translocations. Journal of Assisted Reproduction and Genetics. 33(7). 899–906. 39 indexed citations
12.
Shi, Zhonghua, Chun Zhao, Ye Yang, et al.. (2015). Maternal PCBP1 determines the normal timing of pronucleus formation in mouse eggs. Cellular and Molecular Life Sciences. 72(18). 3575–3586. 4 indexed citations
13.
Wang, Li, Hui Wang, Minyue Ma, et al.. (2015). The clinical utility of next-generation sequencing for identifying chromosome disease syndromes in human embryos. Reproductive BioMedicine Online. 31(1). 62–70. 18 indexed citations
14.
Wang, Li, Hui Wang, Minyue Ma, et al.. (2015). The Performance of Whole Genome Amplification Methods and Next-Generation Sequencing for Pre-Implantation Genetic Diagnosis of Chromosomal Abnormalities. Journal of genetics and genomics. 42(4). 151–159. 31 indexed citations
15.
Lu, Yanping, Hongmei Peng, Jing Cheng, et al.. (2013). Preimplantation Genetic Diagnosis for a Chinese Family with Autosomal Recessive Meckel-Gruber Syndrome Type 3 (MKS3). PLoS ONE. 8(9). e73245–e73245. 8 indexed citations
16.
Ma, Minyue, Lin Zhou, Xuejiang Guo, et al.. (2009). Decreased cofilin1 expression is important for compaction during early mouse embryo development. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1793(12). 1804–1810. 23 indexed citations
17.
Ma, Minyue, Jiahao Sha, Zuomin Zhou, Qi Zhou, & Qingzhang Li. (2008). Generation of patient-specific pluripotent stem cells and directed differentiation of embryonic stem cells for regenerative medicine. 22(3). 135–142. 4 indexed citations
18.
Ma, Minyue, Xuejiang Guo, Fuqiang Wang, et al.. (2008). Protein Expression Profile of the Mouse Metaphase-II Oocyte. Journal of Proteome Research. 7(11). 4821–4830. 51 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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