Seok‐Jin Heo

1.6k total citations · 1 hit paper
19 papers, 1.1k citations indexed

About

Seok‐Jin Heo is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Seok‐Jin Heo has authored 19 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 3 papers in Genetics and 3 papers in Physiology. Recurrent topics in Seok‐Jin Heo's work include DNA Repair Mechanisms (6 papers), CRISPR and Genetic Engineering (4 papers) and Genomics and Chromatin Dynamics (4 papers). Seok‐Jin Heo is often cited by papers focused on DNA Repair Mechanisms (6 papers), CRISPR and Genetic Engineering (4 papers) and Genomics and Chromatin Dynamics (4 papers). Seok‐Jin Heo collaborates with scholars based in United States, Japan and Switzerland. Seok‐Jin Heo's co-authors include Dario Boffelli, David I. K. Martin, Yasuhiro Furuichi, Akira Shimamoto, Denise P. Muñoz, Judith Campisi, Christian Beauséjour, Sahn-Ho Kim, Patrick Kaminker and Albert R. Davalos and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and The Journal of Cell Biology.

In The Last Decade

Seok‐Jin Heo

19 papers receiving 1.1k citations

Hit Papers

Selection-free genome editing of the sickle mutation in h... 2016 2026 2019 2022 2016 100 200 300

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Seok‐Jin Heo United States 13 942 203 193 144 137 19 1.1k
Mitchell L. Leibowitz United States 8 1.0k 1.1× 36 0.2× 425 2.2× 252 1.8× 226 1.6× 9 1.3k
Daniel Capurso United States 9 794 0.8× 34 0.2× 172 0.9× 133 0.9× 115 0.8× 11 918
Isabelle Lamrissi‐Garcia France 14 661 0.7× 34 0.2× 182 0.9× 28 0.2× 74 0.5× 20 907
Sandeep K. Botla Germany 5 912 1.0× 28 0.1× 258 1.3× 42 0.3× 95 0.7× 5 1.0k
Julia M. Rogers United States 13 659 0.7× 36 0.2× 157 0.8× 83 0.6× 53 0.4× 22 955
Emma Haapaniemi Finland 4 829 0.9× 28 0.1× 260 1.3× 42 0.3× 34 0.2× 6 934
Alec B. Wilkens United States 3 1.3k 1.4× 36 0.2× 446 2.3× 45 0.3× 23 0.2× 4 1.5k
Wei Wen China 13 737 0.8× 22 0.1× 198 1.0× 44 0.3× 68 0.5× 18 803
Lin Ye United States 11 738 0.8× 85 0.4× 161 0.8× 28 0.2× 16 0.1× 27 828
Yick W. Fong United States 14 1.1k 1.2× 178 0.9× 84 0.4× 41 0.3× 94 0.7× 19 1.3k

Countries citing papers authored by Seok‐Jin Heo

Since Specialization
Citations

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

Fields of papers citing papers by Seok‐Jin Heo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Seok‐Jin Heo. 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 Seok‐Jin Heo. The network helps show where Seok‐Jin Heo may publish in the future.

Co-authorship network of co-authors of Seok‐Jin Heo

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

All Works

19 of 19 papers shown
1.
Heo, Seok‐Jin, Scot Federman, Phuong T. Nguyen, et al.. (2024). Compact CRISPR genetic screens enabled by improved guide RNA library cloning. Genome biology. 25(1). 25–25. 6 indexed citations
2.
Magis, Wendy, Mark A. DeWitt, Stacia K. Wyman, et al.. (2022). High-level correction of the sickle mutation is amplified in vivo during erythroid differentiation. iScience. 25(6). 104374–104374. 29 indexed citations
3.
Magis, Wendy, Mark A. DeWitt, Stacia K. Wyman, et al.. (2021). High-Level Correction of the Sickle Mutation is Amplified in Vivo During Erythroid Differentiation. SSRN Electronic Journal. 1 indexed citations
4.
Magis, Wendy, Jonathan T. Vu, Seok‐Jin Heo, et al.. (2019). CRISPR-Cas9 interrogation of a putative fetal globin repressor in human erythroid cells. PLoS ONE. 14(1). e0208237–e0208237. 21 indexed citations
5.
DeWitt, Mark A., Wendy Magis, Nicolas Bray, et al.. (2016). Selection-free genome editing of the sickle mutation in human adult hematopoietic stem/progenitor cells. Science Translational Medicine. 8(360). 360ra134–360ra134. 342 indexed citations breakdown →
6.
Heo, Seok‐Jin, et al.. (2015). piRNA-like small RNAs mark extended 3’UTRs present in germ and somatic cells. BMC Genomics. 16(1). 462–462. 12 indexed citations
7.
Yang, Song, Nir Oksenberg, Sachiko Takayama, et al.. (2015). Functionally conserved enhancers with divergent sequences in distant vertebrates. BMC Genomics. 16(1). 882–882. 12 indexed citations
8.
Takayama, Sachiko, Joseph M. Dhahbi, Adam Roberts, et al.. (2014). Genome methylation in D. melanogaster is found at specific short motifs and is independent of DNMT2 activity. Genome Research. 24(5). 821–830. 91 indexed citations
9.
Bolotin, Eugene, Kyungpil Kim, Seok‐Jin Heo, et al.. (2013). Statin-induced changes in gene expression in EBV-transformed and native B-cells. Human Molecular Genetics. 23(5). 1202–1210. 16 indexed citations
10.
Muñoz, Denise P., Sachiko Takayama, Jean‐Philippe Coppé, et al.. (2013). Activation-induced cytidine deaminase (AID) is necessary for the epithelial–mesenchymal transition in mammary epithelial cells. Proceedings of the National Academy of Sciences. 110(32). E2977–86. 57 indexed citations
11.
Bird, Joseph, Penelope A. Mason, J. Lowe, et al.. (2011). Recapitulation of Werner syndrome sensitivity to camptothecin by limited knockdown of the WRN helicase/exonuclease. Biogerontology. 13(1). 49–62. 2 indexed citations
12.
Davalos, Albert R., Seok‐Jin Heo, Françis Rodier, et al.. (2008). Telomere dysfunction and cell survival: roles for distinct TIN2-containing complexes. The Journal of Cell Biology. 181(3). 447–460. 1 indexed citations
13.
Kim, Sahn-Ho, Christian Beauséjour, Albert R. Davalos, et al.. (2004). TIN2 Mediates Functions of TRF2 at Human Telomeres. Journal of Biological Chemistry. 279(42). 43799–43804. 164 indexed citations
14.
Heo, Seok‐Jin, Seiichi Koshizuka, & Y. Oka. (2002). Numerical analysis of boiling on high heat-flux and high subcooling condition using MPS-MAFL. International Journal of Heat and Mass Transfer. 45(13). 2633–2642. 39 indexed citations
15.
Kawabe, Yoh-ichi, Dana Branzei, Tomoko Hayashi, et al.. (2001). A Novel Protein Interacts with the Werner's Syndrome Gene Product Physically and Functionally. Journal of Biological Chemistry. 276(23). 20364–20369. 56 indexed citations
16.
Sakamoto, Shuichi, Kaori Nishikawa, Seok‐Jin Heo, et al.. (2001). Werner helicase relocates into nuclear foci in response to DNA damaging agents and co‐localizes with RPA and Rad51. Genes to Cells. 6(5). 421–430. 148 indexed citations
17.
Heo, Seok‐Jin, et al.. (1999). Bloom's syndrome gene suppresses premature ageing caused by Sgs1 deficiency in yeast. Genes to Cells. 4(11). 619–625. 77 indexed citations
18.
Heo, Seok‐Jin, Kazuo Tatebayashi, & Hideo Ikeda. (1999). The budding yeast cohesin gene SCC1/MCD1/RHC21 genetically interacts with PKA, CDK and APC. Current Genetics. 36(6). 329–338. 18 indexed citations
19.
Heo, Seok‐Jin, Kazuo Tatebayashi, Junichi Kato, & H. Ikeda. (1998). The RHC21 gene of budding yeast, a homologue of the fission yeast rad21 +gene, is essential for chromosome segregation. Molecular and General Genetics MGG. 257(2). 149–156. 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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