Jae Hoon Sul

13.5k total citations · 2 hit papers
32 papers, 3.1k citations indexed

About

Jae Hoon Sul is a scholar working on Genetics, Molecular Biology and Physiology. According to data from OpenAlex, Jae Hoon Sul has authored 32 papers receiving a total of 3.1k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Genetics, 17 papers in Molecular Biology and 3 papers in Physiology. Recurrent topics in Jae Hoon Sul's work include Genetic Associations and Epidemiology (19 papers), Genetic Mapping and Diversity in Plants and Animals (11 papers) and Genetic and phenotypic traits in livestock (6 papers). Jae Hoon Sul is often cited by papers focused on Genetic Associations and Epidemiology (19 papers), Genetic Mapping and Diversity in Plants and Animals (11 papers) and Genetic and phenotypic traits in livestock (6 papers). Jae Hoon Sul collaborates with scholars based in United States, South Korea and United Kingdom. Jae Hoon Sul's co-authors include Eleazar Eskin, Nelson B. Freimer, Chiara Sabatti, Susan K. Service, Noah Zaitlen, Hyun Min Kang, Lana S. Martin, Farhad Hormozdiari, Buhm Han and Xiao Li and has published in prestigious journals such as Nature Communications, Nature Genetics and Bioinformatics.

In The Last Decade

Jae Hoon Sul

30 papers receiving 3.1k citations

Hit Papers

Variance component model to account for sample structure ... 2010 2026 2015 2020 2010 2016 500 1000 1.5k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jae Hoon Sul United States 16 1.9k 1.1k 787 256 123 32 3.1k
Sha Tang China 36 1.1k 0.6× 2.1k 1.9× 1.5k 1.8× 233 0.9× 164 1.3× 126 4.0k
Jean‐Baptiste Veyrieras France 20 1.2k 0.6× 1.5k 1.3× 764 1.0× 276 1.1× 101 0.8× 28 2.6k
M. Yerle France 30 2.1k 1.1× 1.4k 1.2× 860 1.1× 188 0.7× 188 1.5× 143 3.2k
Mengjin Zhu China 21 970 0.5× 1.0k 0.9× 511 0.6× 502 2.0× 277 2.3× 106 2.4k
Eva K.F. Chan United States 27 799 0.4× 975 0.9× 589 0.7× 245 1.0× 53 0.4× 57 2.5k
Namshin Kim South Korea 34 677 0.4× 1.5k 1.4× 860 1.1× 486 1.9× 195 1.6× 91 2.9k
Joshua Starmer United States 28 1.2k 0.6× 1.7k 1.6× 331 0.4× 356 1.4× 359 2.9× 43 3.1k
Andrew Kirby United States 23 1.9k 1.0× 1.2k 1.0× 719 0.9× 108 0.4× 203 1.7× 29 3.2k
Joël Gellin France 26 2.4k 1.3× 1.7k 1.5× 857 1.1× 255 1.0× 157 1.3× 82 3.7k
Yukiko Yamazaki Japan 38 1.3k 0.7× 2.7k 2.4× 758 1.0× 98 0.4× 93 0.8× 100 3.9k

Countries citing papers authored by Jae Hoon Sul

Since Specialization
Citations

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

Fields of papers citing papers by Jae Hoon Sul

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jae Hoon Sul. 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 Jae Hoon Sul. The network helps show where Jae Hoon Sul may publish in the future.

Co-authorship network of co-authors of Jae Hoon Sul

This figure shows the co-authorship network connecting the top 25 collaborators of Jae Hoon Sul. A scholar is included among the top collaborators of Jae Hoon Sul 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 Jae Hoon Sul. Jae Hoon Sul 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.
Manipur, Ichcha, Jae Hoon Sul, Myung K. Shin, et al.. (2024). CoPheScan: phenome-wide association studies accounting for linkage disequilibrium. Nature Communications. 15(1). 5862–5862. 2 indexed citations
2.
Lluri, Gentian, et al.. (2022). Polygenic risk scores of endo-phenotypes identify the effect of genetic background in congenital heart disease. Human Genetics and Genomics Advances. 3(3). 100112–100112. 5 indexed citations
3.
Jew, Brandon, et al.. (2021). Rare variants in the endocytic pathway are associated with Alzheimer’s disease, its related phenotypes, and functional consequences. PLoS Genetics. 17(9). e1009772–e1009772. 5 indexed citations
4.
Han, Buhm, et al.. (2021). Rare variants regulate expression of nearby individual genes in multiple tissues. PLoS Genetics. 17(6). e1009596–e1009596. 6 indexed citations
5.
Jew, Brandon, Marcus Alvarez, Elior Rahmani, et al.. (2020). Accurate estimation of cell composition in bulk expression through robust integration of single-cell information. Nature Communications. 11(1). 1971–1971. 212 indexed citations
6.
Hormozdiari, Farhad, Brandon Jew, Stephane E. Castel, et al.. (2019). Leveraging allelic imbalance to refine fine-mapping for eQTL studies. PLoS Genetics. 15(12). e1008481–e1008481. 21 indexed citations
7.
Sul, Jae Hoon, Lana S. Martin, & Eleazar Eskin. (2018). Population structure in genetic studies: Confounding factors and mixed models. PLoS Genetics. 14(12). e1007309–e1007309. 132 indexed citations
8.
Duong, Dat, Sagi Snir, Eun Yong Kang, et al.. (2017). Applying meta-analysis to genotype-tissue expression data from multiple tissues to identify eQTLs and increase the number of eGenes. Bioinformatics. 33(14). i67–i74. 14 indexed citations
9.
Hormozdiari, Farhad, Martijn van de Bunt, Ayellet V. Segrè, et al.. (2016). Colocalization of GWAS and eQTL Signals Detects Target Genes. The American Journal of Human Genetics. 99(6). 1245–1260. 380 indexed citations breakdown →
10.
Han, Buhm, Dat Duong, Jae Hoon Sul, et al.. (2016). A general framework for meta-analyzing dependent studies with overlapping subjects in association mapping. Human Molecular Genetics. 25(9). 1857–1866. 21 indexed citations
11.
Bae, Joon Seol, Hyun Sub Cheong, Jeong-Meen Seo, et al.. (2016). A genome-wide association analysis of chromosomal aberrations and Hirschsprung disease. Translational research. 177. 31–40.e6. 9 indexed citations
12.
Sul, Jae Hoon, Brian E. Cade, Michael H. Cho, et al.. (2016). Increasing Generality and Power of Rare-Variant Tests by Utilizing Extended Pedigrees. The American Journal of Human Genetics. 99(4). 846–859. 11 indexed citations
13.
Sul, Jae Hoon, Wen-Yun Yang, Emrah Kostem, et al.. (2016). Accounting for Population Structure in Gene-by-Environment Interactions in Genome-Wide Association Studies Using Mixed Models. PLoS Genetics. 12(3). e1005849–e1005849. 36 indexed citations
14.
Sul, Jae Hoon, Towfique Raj, Simone de Jong, et al.. (2015). Accurate and Fast Multiple-Testing Correction in eQTL Studies. The American Journal of Human Genetics. 96(6). 857–868. 20 indexed citations
15.
Sul, Jae Hoon, et al.. (2014). Effectively identifying regulatory hotspots while capturing expression heterogeneity in gene expression studies. Genome biology. 15(4). r61–r61. 23 indexed citations
16.
Kim, Jeong‐Hyun, Hyun Sub Cheong, Jae Hoon Sul, et al.. (2014). A Genome-Wide Association Study Identifies Potential Susceptibility Loci for Hirschsprung Disease. PLoS ONE. 9(10). e110292–e110292. 35 indexed citations
17.
Sul, Jae Hoon, et al.. (2013). School Zone Safety Improvement Using Smart Bollard. Journal of the Korean Society of Civil Engineers. 33(1). 251–259.
18.
Sul, Jae Hoon, Buhm Han, Lucía Conde, et al.. (2013). Rare Variant Association Testing Under Low-Coverage Sequencing. Genetics. 194(3). 769–779. 11 indexed citations
19.
Miller, Michael B., Saonli Basu, Julie M. Cunningham, et al.. (2012). The Minnesota Center for Twin and Family Research Genome-Wide Association Study. Twin Research and Human Genetics. 15(6). 767–774. 53 indexed citations
20.
Sul, Jae Hoon, Buhm Han, & Eleazar Eskin. (2011). Increasing Power of Groupwise Association Test with Likelihood Ratio Test. Journal of Computational Biology. 18(11). 1611–1624. 7 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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