Chin‐Tong Ong

5.4k total citations · 3 hit papers
28 papers, 3.9k citations indexed

About

Chin‐Tong Ong is a scholar working on Molecular Biology, Plant Science and Genetics. According to data from OpenAlex, Chin‐Tong Ong has authored 28 papers receiving a total of 3.9k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 4 papers in Plant Science and 2 papers in Genetics. Recurrent topics in Chin‐Tong Ong's work include RNA Research and Splicing (12 papers), Genomics and Chromatin Dynamics (10 papers) and Epigenetics and DNA Methylation (5 papers). Chin‐Tong Ong is often cited by papers focused on RNA Research and Splicing (12 papers), Genomics and Chromatin Dynamics (10 papers) and Epigenetics and DNA Methylation (5 papers). Chin‐Tong Ong collaborates with scholars based in Singapore, United States and Canada. Chin‐Tong Ong's co-authors include Victor G. Corces, Raphael Kopan, Zhaohui Qin, Naomi Takenaka, M. Bland, Job Dekker, Tracy A. Hookway, Stephen Dalton, Jennifer E. Phillips‐Cremins and Ranjan Sen and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Chin‐Tong Ong

28 papers receiving 3.8k citations

Hit Papers

Architectural Protein Subclasses Shape 3D Organization of... 2011 2026 2016 2021 2013 2014 2011 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Chin‐Tong Ong Singapore 19 3.3k 675 493 361 304 28 3.9k
Robert‐Jan Palstra Netherlands 24 3.4k 1.0× 645 1.0× 630 1.3× 216 0.6× 340 1.1× 33 4.0k
Hans Teunissen Netherlands 20 3.2k 1.0× 764 1.1× 634 1.3× 240 0.7× 205 0.7× 33 3.8k
Stéphanie Le Gras France 32 2.0k 0.6× 347 0.5× 437 0.9× 304 0.8× 443 1.5× 57 2.9k
Lan Lin United States 23 2.4k 0.7× 339 0.5× 239 0.5× 668 1.9× 207 0.7× 39 3.2k
Ephraim Kenigsberg United States 11 2.9k 0.9× 623 0.9× 394 0.8× 390 1.1× 670 2.2× 15 3.5k
Jafar Sharif Japan 26 3.1k 0.9× 318 0.5× 706 1.4× 382 1.1× 179 0.6× 44 3.4k
Mikhail Spivakov United Kingdom 29 4.1k 1.2× 579 0.9× 700 1.4× 388 1.1× 1.1k 3.5× 39 5.1k
Ivan Ovcharenko United States 29 3.7k 1.1× 707 1.0× 1.1k 2.2× 386 1.1× 295 1.0× 71 4.4k
Gabriel E. Zentner United States 30 2.9k 0.9× 439 0.7× 484 1.0× 215 0.6× 144 0.5× 55 3.5k
Wendy Talhout Netherlands 13 3.1k 0.9× 673 1.0× 374 0.8× 115 0.3× 115 0.4× 16 3.4k

Countries citing papers authored by Chin‐Tong Ong

Since Specialization
Citations

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

Fields of papers citing papers by Chin‐Tong Ong

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Chin‐Tong Ong. 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 Chin‐Tong Ong. The network helps show where Chin‐Tong Ong may publish in the future.

Co-authorship network of co-authors of Chin‐Tong Ong

This figure shows the co-authorship network connecting the top 25 collaborators of Chin‐Tong Ong. A scholar is included among the top collaborators of Chin‐Tong Ong 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 Chin‐Tong Ong. Chin‐Tong Ong 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.
Ong, Chin‐Tong, et al.. (2025). Higher Intron Retention Levels in Female Alzheimer's Brains May Be Linked to Disease Prevalence. Aging Cell. 24(2). e14457–e14457. 1 indexed citations
2.
Chong, Suet Yen, et al.. (2024). ApoE maintains neuronal integrity via microRNA and H3K27me3-mediated repression. iScience. 27(3). 109231–109231. 2 indexed citations
3.
Grinchuk, Oleg V., Roberto Tirado-Magallanes, Emmy Xue Yun Tay, et al.. (2022). E2F and STAT3 provide transcriptional synergy for histone variant H2AZ activation to sustain glioblastoma chromatin accessibility and tumorigenicity. Cell Death and Differentiation. 29(7). 1379–1394. 20 indexed citations
4.
Koh, Tong‐Wey, et al.. (2022). Altered stability of nuclear lamin-B marks the onset of aging in male Drosophila. PLoS ONE. 17(3). e0265223–e0265223. 7 indexed citations
5.
Ong, Chin‐Tong, et al.. (2021). NELF‐A controls Drosophila healthspan by regulating heat‐shock protein‐mediated cellular protection and heterochromatin maintenance. Aging Cell. 20(5). e13348–e13348. 6 indexed citations
6.
Rao, Vinay Kumar, et al.. (2019). Phosphorylation of Tet3 by cdk5 is critical for robust activation of BRN2 during neuronal differentiation. Nucleic Acids Research. 48(3). 1225–1238. 14 indexed citations
7.
Yang, Qiaoyun, et al.. (2018). Poly(ADP-ribosyl)ation of OVOL2 regulates aneuploidy and cell death in cancer cells. Oncogene. 38(15). 2750–2766. 8 indexed citations
8.
Li, Li, Xiaowen Lyu, Chunhui Hou, et al.. (2015). Widespread Rearrangement of 3D Chromatin Organization Underlies Polycomb-Mediated Stress-Induced Silencing. Molecular Cell. 58(2). 216–231. 226 indexed citations
9.
Ong, Chin‐Tong & Victor G. Corces. (2014). CTCF: an architectural protein bridging genome topology and function. Nature Reviews Genetics. 15(4). 234–246. 717 indexed citations breakdown →
10.
Ong, Chin‐Tong, Kevin Van Bortle, Edward Ramos, & Victor G. Corces. (2013). Poly(ADP-ribosyl)ation Regulates Insulator Function and Intrachromosomal Interactions in Drosophila. Cell. 155(1). 148–159. 59 indexed citations
11.
Phillips‐Cremins, Jennifer E., Michael E.G. Sauria, Amartya Sanyal, et al.. (2013). Architectural Protein Subclasses Shape 3D Organization of Genomes during Lineage Commitment. Cell. 153(6). 1281–1295. 871 indexed citations breakdown →
12.
Ong, Chin‐Tong, Antonino Carbone, A. Mukhopadhyay, et al.. (2011). Interleukin-18 system plays an important role in keloid pathogenesis via epithelial-mesenchymal interactions. British Journal of Dermatology. 166(6). 1275–1288. 42 indexed citations
13.
Ong, Chin‐Tong & Victor G. Corces. (2011). Enhancer function: new insights into the regulation of tissue-specific gene expression. Nature Reviews Genetics. 12(4). 283–293. 655 indexed citations breakdown →
14.
Ong, Chin‐Tong & Victor G. Corces. (2009). Insulators as mediators of intra- and inter-chromosomal interactions: a common evolutionary theme. Journal of Biology. 8(8). 73–73. 19 indexed citations
15.
Ong, Chin‐Tong, John R. Šedý, Kenneth M. Murphy, & Raphael Kopan. (2008). Notch and Presenilin Regulate Cellular Expansion and Cytokine Secretion but Cannot Instruct Th1/Th2 Fate Acquisition. PLoS ONE. 3(7). e2823–e2823. 77 indexed citations
16.
Ong, Chin‐Tong & Victor G. Corces. (2008). Modulation of CTCF Insulator Function by Transcription of a Noncoding RNA. Developmental Cell. 15(4). 489–490. 7 indexed citations
17.
Bai, Shuting, Raphael Kopan, Wei Zou, et al.. (2007). NOTCH1 Regulates Osteoclastogenesis Directly in Osteoclast Precursors and Indirectly via Osteoblast Lineage Cells. Journal of Biological Chemistry. 283(10). 6509–6518. 193 indexed citations
18.
Ong, Chin‐Tong, et al.. (2007). mTOR as a potential therapeutic target for treatment of keloids and excessive scars. Experimental Dermatology. 16(5). 394–404. 82 indexed citations
19.
Ong, Chin‐Tong, Hui‐Teng Cheng, Li‐Wei Chang, et al.. (2005). Target Selectivity of Vertebrate Notch Proteins. Journal of Biological Chemistry. 281(8). 5106–5119. 183 indexed citations
20.
Yu, Fengwei, Chin‐Tong Ong, William Chia, & Xiaohang Yang. (2002). Membrane Targeting and Asymmetric Localization of Drosophila Partner of Inscuteable Are Discrete Steps Controlled by Distinct Regions of the Protein. Molecular and Cellular Biology. 22(12). 4230–4240. 28 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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