Dehua Cheng

1.3k total citations
44 papers, 618 citations indexed

About

Dehua Cheng is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Dehua Cheng has authored 44 papers receiving a total of 618 indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Genetics, 21 papers in Pediatrics, Perinatology and Child Health and 17 papers in Molecular Biology. Recurrent topics in Dehua Cheng's work include Prenatal Screening and Diagnostics (21 papers), Genomic variations and chromosomal abnormalities (19 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (11 papers). Dehua Cheng is often cited by papers focused on Prenatal Screening and Diagnostics (21 papers), Genomic variations and chromosomal abnormalities (19 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (11 papers). Dehua Cheng collaborates with scholars based in China, United States and Australia. Dehua Cheng's co-authors include Yue‐Qiu Tan, Ge Lin, Fei Gong, Guangxiu Lu, Changfu Lu, Guangxiu Lu, Keli Luo, Ke Tan, Liang Hu and Pingyuan Xie and has published in prestigious journals such as Scientific Reports, Gene and Human Reproduction.

In The Last Decade

Dehua Cheng

42 papers receiving 574 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Dehua Cheng China 12 307 300 242 162 80 44 618
Eftychia Dimitriadou Belgium 15 488 1.6× 315 1.1× 251 1.0× 175 1.1× 51 0.6× 26 715
Judy Chernos Canada 15 286 0.9× 521 1.7× 375 1.5× 180 1.1× 219 2.7× 38 859
Pingyuan Xie China 13 196 0.6× 151 0.5× 182 0.8× 93 0.6× 34 0.4× 36 388
Denise Molina‐Gomes France 12 130 0.4× 162 0.5× 101 0.4× 133 0.8× 157 2.0× 32 406
G. L. Terzoli Italy 10 517 1.7× 397 1.3× 237 1.0× 84 0.5× 64 0.8× 14 843
M. Bras Netherlands 14 344 1.1× 136 0.5× 171 0.7× 464 2.9× 292 3.6× 20 745
T.-N. Dao Canada 5 211 0.7× 309 1.0× 162 0.7× 144 0.9× 180 2.3× 6 527
Celia Donaghue United Kingdom 14 437 1.4× 479 1.6× 155 0.6× 44 0.3× 14 0.2× 16 629
Sandra Peacock United States 9 207 0.7× 308 1.0× 183 0.8× 16 0.1× 34 0.4× 11 489
E. J. Maher United Kingdom 8 342 1.1× 440 1.5× 173 0.7× 36 0.2× 21 0.3× 11 613

Countries citing papers authored by Dehua Cheng

Since Specialization
Citations

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

Fields of papers citing papers by Dehua Cheng

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dehua Cheng

This figure shows the co-authorship network connecting the top 25 collaborators of Dehua Cheng. A scholar is included among the top collaborators of Dehua Cheng 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 Dehua Cheng. Dehua Cheng 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.
2.
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
3.
Wang, Weili, Lanlan Meng, Jiaxin He, et al.. (2023). Biallelic variants in KCTD19 associated with male factor infertility and oligoasthenoteratozoospermia. Human Reproduction. 38(7). 1399–1411. 11 indexed citations
4.
Wu, Huixia, Wei Zheng, Dehua Cheng, et al.. (2023). Novel biallelic ASTL variants are associated with polyspermy and female infertility: A successful live birth following ICSI treatment. Gene. 887. 147745–147745. 5 indexed citations
5.
6.
Xie, Pingyuan, Ping Liu, Shuoping Zhang, et al.. (2022). Segmental aneuploidies with 1 Mb resolution in human preimplantation blastocysts. Genetics in Medicine. 24(11). 2285–2295. 11 indexed citations
7.
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
8.
Yuan, Shi‐Min, Dehua Cheng, Keli Luo, et al.. (2021). Reproductive risks and preimplantation genetic testing intervention for X–autosome translocation carriers. Reproductive BioMedicine Online. 43(1). 73–80. 2 indexed citations
9.
Tan, Yue‐Qiu, et al.. (2020). Whole-genome mate-pair sequencing of apparently balanced chromosome rearrangements reveals complex structural variations: two case studies. Molecular Cytogenetics. 13(1). 15–15. 8 indexed citations
10.
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
11.
Li, Haiyu, Juan Du, Wen Li, et al.. (2018). Rare partial octosomy and hexasomy of 15q11-q13 associated with intellectual impairment and development delay: report of two cases and review of literature. Molecular Cytogenetics. 11(1). 15–15. 7 indexed citations
12.
Luo, Aixiang, Dehua Cheng, Shi‐Min Yuan, et al.. (2018). Maternal interchromosomal insertional translocation leading to 1q43-q44 deletion and duplication in two siblings. Molecular Cytogenetics. 11(1). 24–24. 9 indexed citations
13.
Zhou, Shuang, Dehua Cheng, Qi Ouyang, et al.. (2018). Prevalence and authenticity of de-novo segmental aneuploidy (>16 Mb) in human blastocysts as detected by next-generation sequencing. Reproductive BioMedicine Online. 37(5). 511–520. 22 indexed citations
14.
Leng, Lizhi, Qi Ouyang, Fei Gong, et al.. (2017). Self-diploidization of human haploid parthenogenetic embryos through the Rho pathway regulates endomitosis and failed cytokinesis. Scientific Reports. 7(1). 4242–4242. 8 indexed citations
15.
Zhang, Shuoping, Keli Luo, Dehua Cheng, et al.. (2016). Number of biopsied trophectoderm cells is likely to affect the implantation potential of blastocysts with poor trophectoderm quality. Fertility and Sterility. 105(5). 1222–1227.e4. 73 indexed citations
16.
Hu, Liang, Dehua Cheng, Fei Gong, et al.. (2016). Reciprocal Translocation Carrier Diagnosis in Preimplantation Human Embryos. EBioMedicine. 14. 139–147. 40 indexed citations
17.
Zhou, Di, Ge Lin, Sicong Zeng, et al.. (2014). Trace levels of mitomycin C disrupt genomic integrity and lead to DNA damage response defect in long-term-cultured human embryonic stem cells. Archives of Toxicology. 89(1). 33–45. 8 indexed citations
18.
Chen, Jing, Zhu-Wen Yi, Xiqiang Dang, et al.. (2013). Genetic analysis of a 12-year-old boy with X-linked ichthyosis in association with sclerosing glomerulonephritis. Molecular Medicine Reports. 8(4). 1183–1187. 5 indexed citations
19.
Cheng, Dehua, et al.. (2012). Risk evaluation and preimplantation genetic diagnosis in an infertile man with an unbalanced translocation t(10;15) resulting in a healthy baby. Journal of Assisted Reproduction and Genetics. 29(11). 1299–1304. 9 indexed citations
20.
Cheng, Dehua, et al.. (2009). Crypt Y chromosome fragment resulting from an X;Y translocation in a patient with premature ovarian failure. Fertility and Sterility. 92(2). 828.e3–828.e6. 20 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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