Jong-Yeon Shin

2.0k total citations
32 papers, 601 citations indexed

About

Jong-Yeon Shin is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Jong-Yeon Shin has authored 32 papers receiving a total of 601 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 10 papers in Genetics and 7 papers in Oncology. Recurrent topics in Jong-Yeon Shin's work include Cancer Genomics and Diagnostics (5 papers), Cancer-related Molecular Pathways (5 papers) and Epigenetics and DNA Methylation (5 papers). Jong-Yeon Shin is often cited by papers focused on Cancer Genomics and Diagnostics (5 papers), Cancer-related Molecular Pathways (5 papers) and Epigenetics and DNA Methylation (5 papers). Jong-Yeon Shin collaborates with scholars based in South Korea, United States and Uruguay. Jong-Yeon Shin's co-authors include Michael J. Higgins, Jeong‐Sun Seo, Jeong‐Sun Seo, Jae‐Bong Park, Jaebong Kim, Elena M. Pugacheva, Victor V. Lobanenkov, Ziedulla Abdullaev, Youwen Yang and Hyun‐Seok Kim and has published in prestigious journals such as The Journal of Cell Biology, The EMBO Journal and Journal of the American College of Cardiology.

In The Last Decade

Jong-Yeon Shin

31 papers receiving 590 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jong-Yeon Shin South Korea 15 391 217 107 93 82 32 601
K N Harikrishnan Australia 12 552 1.4× 249 1.1× 73 0.7× 52 0.6× 41 0.5× 16 722
Ana Moreira Portugal 13 211 0.5× 231 1.1× 63 0.6× 106 1.1× 63 0.8× 22 670
Junehawk Lee South Korea 9 371 0.9× 221 1.0× 128 1.2× 34 0.4× 46 0.6× 20 569
Yew Kok Lee Singapore 6 473 1.2× 268 1.2× 55 0.5× 96 1.0× 38 0.5× 6 598
Kinga Hadzsiev Hungary 14 316 0.8× 212 1.0× 34 0.3× 55 0.6× 27 0.3× 73 624
Cíntia Barros Santos-Rebouças Brazil 17 378 1.0× 311 1.4× 51 0.5× 82 0.9× 36 0.4× 64 767
Chee‐Seng Ku Singapore 11 295 0.8× 402 1.9× 105 1.0× 32 0.3× 41 0.5× 14 661
Albandary AlBakheet Saudi Arabia 13 360 0.9× 132 0.6× 82 0.8× 16 0.2× 76 0.9× 34 576
Kristy Crooks United States 12 183 0.5× 282 1.3× 53 0.5× 56 0.6× 20 0.2× 27 623

Countries citing papers authored by Jong-Yeon Shin

Since Specialization
Citations

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

Fields of papers citing papers by Jong-Yeon Shin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jong-Yeon Shin. 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 Jong-Yeon Shin. The network helps show where Jong-Yeon Shin may publish in the future.

Co-authorship network of co-authors of Jong-Yeon Shin

This figure shows the co-authorship network connecting the top 25 collaborators of Jong-Yeon Shin. A scholar is included among the top collaborators of Jong-Yeon Shin 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 Jong-Yeon Shin. Jong-Yeon Shin 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.
Lee, Seung‐been, Jong-Yeon Shin, Nak‐Jung Kwon, Changhoon Kim, & Jeong‐Sun Seo. (2022). ClinPharmSeq: A targeted sequencing panel for clinical pharmacogenetics implementation. PLoS ONE. 17(7). e0272129–e0272129. 31 indexed citations
2.
Shin, Jong-Yeon, et al.. (2021). Genomic and transcriptomic analyses reveal a tandem amplification unit of 11 genes and mutations in mismatch repair genes in methotrexate-resistant HT-29 cells. Experimental & Molecular Medicine. 53(9). 1344–1355. 5 indexed citations
3.
Kim, Sungjae, Jong-Yeon Shin, Nak‐Jung Kwon, et al.. (2021). Evaluation of low-pass genome sequencing in polygenic risk score calculation for Parkinson’s disease. Human Genomics. 15(1). 58–58. 3 indexed citations
4.
Spangenberg, Lucía, María Inés Fariello, Gonzalo Greif, et al.. (2021). Indigenous Ancestry and Admixture in the Uruguayan Population. Frontiers in Genetics. 12. 733195–733195. 6 indexed citations
5.
Raggio, Víctor, Gonzalo Costa, Gonzalo Greif, et al.. (2021). Whole genome sequencing reveals a frameshift mutation and a large deletion in YY1AP1 in a girl with a panvascular artery disease. Human Genomics. 15(1). 28–28. 5 indexed citations
6.
Kim, Sungjae, et al.. (2020). The tumor immune microenvironmental analysis of 2,033 transcriptomes across 7 cancer types. Scientific Reports. 10(1). 9536–9536. 22 indexed citations
7.
Cho, Hyesun, Seung Jae Hyeon, Jong-Yeon Shin, et al.. (2020). Alterations of transcriptome signatures in head trauma-related neurodegenerative disorders. Scientific Reports. 10(1). 8811–8811. 19 indexed citations
8.
Lee, Ji Won, Jong-Yeon Shin, & Jeong‐Sun Seo. (2018). Identification of novel mutations in FFPE lung adenocarcinomas using DEPArray sorting technology and next-generation sequencing. Journal of Applied Genetics. 59(3). 269–277. 7 indexed citations
9.
Kim, Seunghyo, Ha Young Kim, Dongsup Kim, et al.. (2016). FARS2 mutation and epilepsy: Possible link with early-onset epileptic encephalopathy. Epilepsy Research. 129. 118–124. 19 indexed citations
10.
Kim, Hyun-Jung, Jong-Yeon Shin, Jong‐Il Kim, et al.. (2014). Somatic deletions implicated in functional diversity of brain cells of individuals with schizophrenia and unaffected controls. Scientific Reports. 4(1). 3807–3807. 19 indexed citations
12.
Lee, Se‐Hoon, et al.. (2014). Abstract 4191: Whole exome sequencing of a case of olfactory neuroblastoma. Cancer Research. 74(19_Supplement). 4191–4191.
13.
Oh, Soo Jin, Yoonjung Kho, Jeong‐Hyeon Kim, et al.. (2012). ATM mediates interdependent activation of p53 and ERK through formation of a ternary complex with p-p53 and p-ERK in response to DNA damage. Molecular Biology Reports. 39(8). 8007–8014. 23 indexed citations
14.
Park, Hansoo, Seungbok Lee, Hyunjin Kim, et al.. (2012). Comprehensive genomic analyses associate UGT8 variants with musical ability in a Mongolian population. Journal of Medical Genetics. 49(12). 747–752. 41 indexed citations
15.
Oh, Soo Jin, Yoonjung Kho, Jeong‐Hyeon Kim, et al.. (2010). ERK mediates anti-apoptotic effect through phosphorylation and cytoplasmic localization of p21Waf1/Cip1/Sdi in response to DNA damage in normal human embryonic fibroblast (HEF) cells. Molecular Biology Reports. 38(4). 2785–2791. 14 indexed citations
16.
Shin, Jong-Yeon, et al.. (2010). Swedish mutation within amyloid precursor protein modulates global gene expression towards the pathogenesis of Alzheimer's disease. BMB Reports. 43(10). 704–709. 27 indexed citations
17.
Hiura, Hitoshi, Simon J. Tunster, Takahiro Arima, et al.. (2010). Autonomous silencing of the imprintedCdkn1cgene in stem cells. Epigenetics. 5(3). 214–221. 17 indexed citations
18.
Shin, Jong-Yeon, et al.. (2007). Two distinct mechanisms of silencing by the KvDMR1 imprinting control region. The EMBO Journal. 27(1). 168–178. 105 indexed citations
19.
Kim, Hyun-Seok, et al.. (2001). Immortalization of human embryonic fibroblasts by overexpression of c-myc and simian virus 40 large T antigen. Experimental & Molecular Medicine. 33(4). 293–298. 15 indexed citations
20.
Shin, Jong-Yeon, Hyun‐Seok Kim, Jaebong Kim, et al.. (2000). Mutation and expression of the p27KIP1 and p57KIP2 genes in human gastric cancer. Experimental & Molecular Medicine. 32(2). 79–83. 49 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026