Zechen Chong

43.3k total citations · 1 hit paper
32 papers, 1.6k citations indexed

About

Zechen Chong is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Zechen Chong has authored 32 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 9 papers in Genetics and 8 papers in Cancer Research. Recurrent topics in Zechen Chong's work include Genomics and Phylogenetic Studies (13 papers), Epigenetics and DNA Methylation (8 papers) and Cancer Genomics and Diagnostics (7 papers). Zechen Chong is often cited by papers focused on Genomics and Phylogenetic Studies (13 papers), Epigenetics and DNA Methylation (8 papers) and Cancer Genomics and Diagnostics (7 papers). Zechen Chong collaborates with scholars based in United States, China and United Kingdom. Zechen Chong's co-authors include Yun‐Gui Yang, Jue Ruan, Danni Wu, Hailin Wang, Bailin Zhao, Hua Huang, Guo-Liang Xu, Chao Zhao, Ruichuan Yin and Ying Yang and has published in prestigious journals such as Journal of the American Chemical Society, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Zechen Chong

30 papers receiving 1.6k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Ascorbic Acid Enhances Tet-Mediated 5-Methylcytosine Oxidation and Promotes DNA Demethylation in Mammals

2013 486 citations Ruichuan Yin, Bailin Zhao et al. profile →

Peers

Zechen Chong

MB

GENET

CR

PS

ONCOL

René Bartz United States

Ataman Sendoel Switzerland

Zhen‐Bo Wang China

Myung-Jin Kim South Korea

Eric M. Kallin United States

Pat P. Ongusaha United States

Bradley A. Ozenberger United States

Lina Li China

Elena Grigorieva United Kingdom

René Bartz United States

Zechen Chong

1.5k ×1.3

MB

155 ×0.6

GENET

109 ×0.5

CR

130 ×0.9

PS

117 ×1.0

ONCOL

Citations per year, relative to Zechen Chong Zechen Chong (= 1×) peers René Bartz

Countries citing papers authored by Zechen Chong

Since Specialization

Citations

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

Fields of papers citing papers by Zechen Chong

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Zechen Chong

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

1.

Hale, Andrew T., Phan Q. Duy, Michael C. Dewan, et al.. (2024). The genetic basis of hydrocephalus: genes, pathways, mechanisms, and global impact. Fluids and Barriers of the CNS. 21(1). 24–24. 9 indexed citations

2.

Xu, Peng, et al.. (2024). Body Weight Correlates with Molecular Variances in Patients with Cancer. Cancer Research. 84(5). 757–770. 2 indexed citations

3.

Hale, Andrew T., Shanrun Liu, Michael R. Crowley, et al.. (2024). Endoluminal Biopsy for Vein of Galen Malformation. Neurosurgery. 95(5). 1082–1088.

4.

Chen, Yu, Amy Wang, Yixin Zhang, et al.. (2023). Deciphering the exact breakpoints of structural variations using long sequencing reads with DeBreak. Nature Communications. 14(1). 283–283. 34 indexed citations

5.

Chen, Yu, et al.. (2022). Gene Fusion Detection and Characterization in Long-Read Cancer Transcriptome Sequencing Data with FusionSeeker. Cancer Research. 83(1). 28–33. 22 indexed citations

6.

Zhao, Xinyang, Zechen Chong, Yabing Chen, et al.. (2022). Protein arginine methyltransferase 1 in the generation of immune megakaryocytes: A perspective review. Journal of Biological Chemistry. 298(11). 102517–102517. 6 indexed citations

7.

Wang, Jun, Holly R. Thomas, Yu Chen, et al.. (2022). Reduced sister chromatid cohesion acts as a tumor penetrance modifier. PLoS Genetics. 18(8). e1010341–e1010341. 4 indexed citations

8.

Xiao, Li, Min Gao, Kevin Dybvig, et al.. (2022). B-assembler: a circular bacterial genome assembler. BMC Genomics. 23(S4). 361–361. 4 indexed citations

9.

Xu, Peng, et al.. (2019). MRLR: unraveling high-resolution meiotic recombination by linked reads. Bioinformatics. 36(1). 10–16. 4 indexed citations

10.

Grochowski, Christopher M., Shen Gu, Bo Yuan, et al.. (2018). Marker chromosome genomic structure and temporal origin implicate a chromoanasynthesis event in a family with pleiotropic psychiatric phenotypes. Human Mutation. 39(7). 939–946. 19 indexed citations

11.

Chong, Zechen & Ken Chen. (2018). Structural Variant Breakpoint Detection with novoBreak. Methods in molecular biology. 1833. 129–141. 2 indexed citations

12.

Chong, Zechen, Jue Ruan, Min Gao, et al.. (2016). novoBreak: local assembly for breakpoint detection in cancer genomes. Nature Methods. 14(1). 65–67. 54 indexed citations

13.

Chen, Tenghui, Zixing Wang, Wanding Zhou, et al.. (2016). Hotspot mutations delineating diverse mutational signatures and biological utilities across cancer types. BMC Genomics. 17(S2). 394–394. 25 indexed citations

14.

Dogruluk, Turgut, Yiu Huen Tsang, Fengju Chen, et al.. (2015). Identification of Variant-Specific Functions of PIK3CA by Rapid Phenotyping of Rare Mutations. Cancer Research. 75(24). 5341–5354. 118 indexed citations

15.

Zhou, Wanding, Hao Zhao, Zechen Chong, et al.. (2015). ClinSeK: a targeted variant characterization framework for clinical sequencing. Genome Medicine. 7(1). 34–34. 11 indexed citations

16.

Zhou, Zhong‐Wei, Yue Shi, Zechen Chong, et al.. (2014). Trrap-Dependent Histone Acetylation Specifically Regulates Cell-Cycle Gene Transcription to Control Neural Progenitor Fate Decisions. Cell stem cell. 14(5). 632–643. 50 indexed citations

17.

Fan, Xian, Wanding Zhou, Zechen Chong, Luay Nakhleh, & Ken Chen. (2014). Towards accurate characterization of clonal heterogeneity based on structural variation. BMC Bioinformatics. 15(1). 299–299. 7 indexed citations

18.

Gao, Min, Wei Wei, Zhaoqing Ba, et al.. (2014). Ago2 facilitates Rad51 recruitment and DNA double-strand break repair by homologous recombination. Cell Research. 24(5). 532–541. 147 indexed citations

19.

Ruan, Jue, Lan Jiang, Zechen Chong, et al.. (2013). Pseudo-Sanger sequencing: massively parallel production of long and near error-free reads using NGS technology. BMC Genomics. 14(1). 711–711. 6 indexed citations

20.

Zhao, Bailin, Ying Yang, Xiaoli Wang, et al.. (2013). Redox-active quinones induces genome-wide DNA methylation changes by an iron-mediated and Tet-dependent mechanism. Nucleic Acids Research. 42(3). 1593–1605. 113 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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