Jihoon G. Yoon

1.1k total citations · 1 hit paper
41 papers, 697 citations indexed

About

Jihoon G. Yoon is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Jihoon G. Yoon has authored 41 papers receiving a total of 697 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 11 papers in Molecular Biology and 6 papers in Surgery. Recurrent topics in Jihoon G. Yoon's work include Genomics and Rare Diseases (8 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Genetic Neurodegenerative Diseases (5 papers). Jihoon G. Yoon is often cited by papers focused on Genomics and Rare Diseases (8 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Genetic Neurodegenerative Diseases (5 papers). Jihoon G. Yoon collaborates with scholars based in South Korea, United States and Ethiopia. Jihoon G. Yoon's co-authors include JoonNyung Heo, Hyo Suk Nam, Ji Hoe Heo, Hyungjong Park, Young Dae Kim, Min Goo Lee, Yangsoon Lee, Myung Sook Kim, Hee Bong Shin and Kyungwon Lee and has published in prestigious journals such as Nucleic Acids Research, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Jihoon G. Yoon

33 papers receiving 677 citations

Hit Papers

Machine Learning–Based Model for Prediction of Outcomes i... 2019 2026 2021 2023 2019 100 200 300 400

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jihoon G. Yoon South Korea 11 280 146 109 91 90 41 697
Yuan Xie China 18 503 1.8× 213 1.5× 275 2.5× 30 0.3× 77 0.9× 49 1.5k
Robyn L. Ball United States 17 170 0.6× 139 1.0× 68 0.6× 32 0.4× 11 0.1× 41 867
Nataša Popović Montenegro 16 135 0.5× 124 0.8× 209 1.9× 11 0.1× 17 0.2× 42 987
Yahia Imam Qatar 13 122 0.4× 47 0.3× 48 0.4× 17 0.2× 48 0.5× 51 361
Raghu Kolluri United States 19 66 0.2× 169 1.2× 612 5.6× 16 0.2× 31 0.3× 67 1.1k
Xiaoyi Wang China 18 69 0.2× 170 1.2× 107 1.0× 14 0.2× 12 0.1× 98 939
Alberto Bruno Italy 19 315 1.1× 176 1.2× 302 2.8× 6 0.1× 33 0.4× 53 1.4k
Kay Sin Tan Malaysia 12 685 2.4× 332 2.3× 45 0.4× 10 0.1× 93 1.0× 17 1.4k
Taku Harada Japan 14 71 0.3× 171 1.2× 164 1.5× 26 0.3× 6 0.1× 87 778
Ulf Mattsson Sweden 17 90 0.3× 43 0.3× 150 1.4× 17 0.2× 39 0.4× 39 810

Countries citing papers authored by Jihoon G. Yoon

Since Specialization
Citations

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

Fields of papers citing papers by Jihoon G. Yoon

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jihoon G. Yoon. 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 Jihoon G. Yoon. The network helps show where Jihoon G. Yoon may publish in the future.

Co-authorship network of co-authors of Jihoon G. Yoon

This figure shows the co-authorship network connecting the top 25 collaborators of Jihoon G. Yoon. A scholar is included among the top collaborators of Jihoon G. Yoon 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 Jihoon G. Yoon. Jihoon G. Yoon 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.
Yoon, Jihoon G., et al.. (2026). A predictive framework for stop-loss variants with C-terminal extensions. Nucleic Acids Research. 54(2).
2.
Yoon, Jihoon G., Seungbok Lee, Soojin Park, et al.. (2025). Identification of a novel non-coding deletion in Allan-Herndon-Dudley syndrome by long-read HiFi genome sequencing. BMC Medical Genomics. 18(1). 41–41.
3.
Yoon, Jihoon G., Cheng‐Bo Han, Shin Hye Noh, et al.. (2025). Digenic impairments of haploinsufficient genes in patients with craniosynostosis. JCI Insight. 10(4).
4.
Kim, Kyung‐A, Suho Lee, Chang Sik Kim, et al.. (2025). A Duplex qPCR Assay Targeting the fadA Gene Enables Robust Detection of Fusobacterium in Clinical Samples. International Journal of Molecular Sciences. 26(23). 11319–11319.
5.
Lee, Seungbok, Seungbok Lee, Jihoon G. Yoon, et al.. (2024). Prevalence and Characterization of NOTCH2NLC GGC Repeat Expansions in Koreans. Neurology Genetics. 10(3). e200147–e200147. 7 indexed citations
6.
Lee, Seungbok, Jihoon G. Yoon, Sheehyun Kim, et al.. (2024). Broadening the scope of multigene panel analysis for adult epilepsy patients. Epilepsia Open. 9(4). 1538–1549. 1 indexed citations
7.
Yoon, Jihoon G., et al.. (2024). Late-Onset Ataxia-Telangiectasia Presenting With Dystonia and Tremor. Neurology Genetics. 10(2). e200141–e200141. 3 indexed citations
8.
Yoon, Jihoon G., Seungbok Lee, Soo Yeon Kim, et al.. (2024). De novo missense variants in HDAC3 leading to epigenetic machinery dysfunction are associated with a variable neurodevelopmental disorder. The American Journal of Human Genetics. 111(8). 1588–1604. 1 indexed citations
9.
Lee, Seungbok, Jihoon G. Yoon, Sheehyun Kim, et al.. (2024). Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay Masquerading as Charcot-Marie-Tooth Disease: A Case Study and Literature Review of Korean Patients. Journal of Movement Disorders. 18(1). 93–95.
10.
11.
Kim, Soo Yeon, Seungbok Lee, Jihoon G. Yoon, et al.. (2023). Epilepsy phenotype and gene ontology analysis of the 129 genes in a large neurodevelopmental disorders cohort. Frontiers in Neurology. 14. 1218706–1218706. 2 indexed citations
12.
Yoon, Jihoon G., Man Jin Kim, Yong Jin Kwon, & Jong‐Hee Chae. (2023). Clinical applications of next-generation sequencing in the diagnosis of genetic disorders in Korea: a narrative review. Journal of Korean Medical Association. 66(10). 613–623.
13.
Kim, Man Jin, Sheehyun Kim, Seungbok Lee, et al.. (2023). Prevalence and founder effect of DRC1 exon 1–4 deletion in Korean patients with primary ciliary dyskinesia. Journal of Human Genetics. 68(6). 369–374. 6 indexed citations
14.
Yoon, Jihoon G., et al.. (2023). Multi‐locus pathogenic variation identified in a patient with craniosynostosis. American Journal of Medical Genetics Part A. 194(5). e63521–e63521.
15.
Lee, Seung Min, Kwangsoo Kim, Jihoon G. Yoon, et al.. (2020). Association between Use of Hydrochlorothiazide and Nonmelanoma Skin Cancer: Common Data Model Cohort Study in Asian Population. Journal of Clinical Medicine. 9(9). 2910–2910. 14 indexed citations
16.
Kim, Yonjung, Ikhyun Jun, Dong Hoon Shin, et al.. (2019). Regulation of CFTR Bicarbonate Channel Activity by WNK1: Implications for Pancreatitis and CFTR-Related Disorders. Cellular and Molecular Gastroenterology and Hepatology. 9(1). 79–103. 26 indexed citations
17.
Yoon, Jihoon G., Sungkyoung Choi, Soo‐Jeong Kim, et al.. (2019). Molecular Diagnosis of Craniosynostosis Using Targeted Next-Generation Sequencing. Neurosurgery. 87(2). 294–302. 15 indexed citations
18.
Yoon, Jihoon G., et al.. (2016). Magnetic bead-based nucleic acid purification kit: Clinical application and performance evaluation in stool specimens. Journal of Microbiological Methods. 124. 62–68. 10 indexed citations
19.
Park, Jong‐Hwan, et al.. (2005). A Case of Esophageal Tuberculous Abscess.. Clinical Endoscopy. 31(4). 252–256. 1 indexed citations
20.
Lee, Jungnam, et al.. (2005). A Case of Hepatic Angiosarcoma Presenting as Submucosal Tumor Resulting from Gastric Invasion.. Clinical Endoscopy. 31(4). 257–262. 1 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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