Dong Wu

545 total citations
41 papers, 423 citations indexed

About

Dong Wu is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Dong Wu has authored 41 papers receiving a total of 423 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 19 papers in Genetics and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Dong Wu's work include Genomic variations and chromosomal abnormalities (7 papers), Congenital heart defects research (5 papers) and Prenatal Screening and Diagnostics (5 papers). Dong Wu is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Congenital heart defects research (5 papers) and Prenatal Screening and Diagnostics (5 papers). Dong Wu collaborates with scholars based in China, United States and Hong Kong. Dong Wu's co-authors include Takashi Okamoto, Gordon Sato, Jun Sato, Hongdan Wang, Jian Zhai, Shuping Qu, Tao Li, Xiaowei Li, Xiaoxia Chen and Shixiu Liao and has published in prestigious journals such as Journal of Biological Chemistry, Blood and PLoS ONE.

In The Last Decade

Dong Wu

40 papers receiving 416 citations

Peers

Dong Wu

GENET

ONCOL

Michelle M. Thiaville United States

Kunhua Qin United States

Chuanqing Wu China

Ezequiel Luis Calvo France

René Meyer United States

Nanding Zhao United States

Jinhua Xu United States

Teri M. Plona United States

Scott Houghtaling United States

Sheryl Gere United States

Michelle M. Thiaville United States

Dong Wu

422 ×1.3

93 ×0.9

GENET

77 ×0.9

137 ×2.3

57 ×1.0

ONCOL

Citations per year, relative to Dong Wu Dong Wu (= 1×) peers Michelle M. Thiaville

Countries citing papers authored by Dong Wu

Since Specialization

Citations

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

Fields of papers citing papers by Dong Wu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dong Wu

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

All Works

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20 of 20 papers shown

Kang, Bing, et al.. (2022). Case Report: Twin Pregnancy Gives Birth to a Girl with Partial Trisomy 21 Mosaicism after in vitro Fertilization and Embryo Transfer. Frontiers in Genetics. 12. 740415–740415. 1 indexed citations

Huo, Xiaodong, et al.. (2021). A Novel Variant of the <b><i>KIF11</i></b> Gene, c.2922G>T, Is Associated with Microcephaly by Affecting RNA Splicing. Developmental Neuroscience. 44(2). 113–120. 5 indexed citations

Qu, Shuping, Xiaobing Zhang, Yue Wu, et al.. (2021). miR-361-3p Regulates Liver Tumor-initiating Cells Expansion and Chemo-resistance. Journal of Cancer. 12(5). 1483–1492. 13 indexed citations

Huang, Jia, Hongyan Liu, Rongrong Wang, et al.. (2019). A 3.06-Mb interstitial deletion on 12p11.22-12.1 caused brachydactyly type E combined with pectus carinatum. Chinese Medical Journal. 132(14). 1681–1688. 2 indexed citations

Wu, Dong, Tao Li, Xiaodong Huo, et al.. (2018). [Genetic analysis of a child with cleidocranial dysplasia and 6q21-q22.31 microdeletion].. PubMed. 35(2). 253–256. 1 indexed citations

Liu, Di, Wenpeng Wang, Dong Wu, et al.. (2017). Elucidating Bottlenecks to the Efficient Preparation of AB5-Hexamer Mucosal Adjuvant Protein LTm by Genetic Engineering. Journal of Microbiology and Biotechnology. 27(8). 1461–1471. 1 indexed citations

Liu, Hongyan, Jia Huang, Yue Wang, et al.. (2017). Diagnosis with Multiple Epiphyseal Dysplasia Using Whole-exome Sequencing in a Chinese Family. Chinese Medical Journal. 130(1). 104–107. 3 indexed citations

Li, Tao, Xin Ma, Hongyan Liu, et al.. (2017). Prenatal diagnosis for a Chinese family with a de novo DMD gene mutation. Medicine. 96(50). e8814–e8814. 5 indexed citations

Wu, Dong, et al.. (2017). Genotype/phenotype analysis in a male patient with partial trisomy 4p and monosomy 20q due to maternal reciprocal translocation (4;20): A case report. Molecular Medicine Reports. 16(5). 6222–6227. 2 indexed citations

10.

Liu, Hong Yan, Jia Huang, Tao Li, et al.. (2016). Clinical and molecular cytogenetic analyses of four patients with imbalanced translocations. Molecular Cytogenetics. 9(1). 31–31. 5 indexed citations

11.

Liu, Hong Yan, Jia Huang, Yue Wang, et al.. (2016). A novel missense mutation of NDP in a Chinese family with X-linked familial exudative vitreoretinopathy. Journal of the Chinese Medical Association. 79(11). 633–638. 1 indexed citations

12.

Wu, Dong, et al.. (2016). Clinical findings and molecular cytogenetic study of de novo pure chromosome 9p deletion: Pre- and postnatal diagnosis. Taiwanese Journal of Obstetrics and Gynecology. 55(6). 867–870. 5 indexed citations

13.

Wang, Hongdan, et al.. (2016). Integrated miRNA and mRNA expression profiling in fetal hippocampus with Down syndrome. Journal of Biomedical Science. 23(1). 48–48. 19 indexed citations

14.

Liu, Lin, Hongdan Wang, Dong Wu, et al.. (2016). Application of array-comparative genomic hybridization in tetralogy of Fallot. Medicine. 95(49). e5552–e5552. 8 indexed citations

15.

Zhai, Jian, Shuping Qu, Xiaowei Li, et al.. (2015). miR-129 suppresses tumor cell growth and invasion by targeting PAK5 in hepatocellular carcinoma. Biochemical and Biophysical Research Communications. 464(1). 161–167. 39 indexed citations

16.

Liu, Hongyan, Jia Huang, Dong Wu, et al.. (2015). Collagen Type I Alpha 1 Mutation Causes Osteogenesis Imperfecta from Mild to Perinatal Death in a Chinese Family. Chinese Medical Journal. 129(1). 88–91. 5 indexed citations

17.

Wang, Hongdan, Tao Li, Dong Wu, et al.. (2014). DNA methylation study of fetus genome through a genome-wide analysis. BMC Medical Genomics. 7(1). 18–18. 9 indexed citations

18.

Tao, Yanfang, Jun Lu, Xiaojuan Du, et al.. (2012). Survivin selective inhibitor YM155 induce apoptosis in SK-NEP-1 Wilms tumor cells. BMC Cancer. 12(1). 619–619. 40 indexed citations

19.

Zhang, Changsong, Lieying Fan, Tingting Fan, et al.. (2012). Decreased PADI4 mRNA Association with Global Hypomethylation in Hepatocellular Carcinoma During HBV Exposure. Cell Biochemistry and Biophysics. 65(2). 187–195. 13 indexed citations

20.

Hu, Shengping, et al.. (2004). Genetic profile of 15 STR loci in the Min Nan population in Southeast China. Forensic Science International. 152(2-3). 263–265. 17 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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