Judong Shen

3.6k total citations · 1 hit paper
30 papers, 1.6k citations indexed

About

Judong Shen is a scholar working on Genetics, Molecular Biology and Statistics and Probability. According to data from OpenAlex, Judong Shen has authored 30 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 14 papers in Molecular Biology and 7 papers in Statistics and Probability. Recurrent topics in Judong Shen's work include Genetic Associations and Epidemiology (14 papers), Bioinformatics and Genomic Networks (7 papers) and Helicobacter pylori-related gastroenterology studies (5 papers). Judong Shen is often cited by papers focused on Genetic Associations and Epidemiology (14 papers), Bioinformatics and Genomic Networks (7 papers) and Helicobacter pylori-related gastroenterology studies (5 papers). Judong Shen collaborates with scholars based in United States, United Kingdom and China. Judong Shen's co-authors include Matthew R. Nelson, John C. Whittaker, Lon R. Cardon, Pak C. Sham, Aris Floratos, Paola Nicoletti, Mulin Jun Li, Junwen Wang, Hannah Tipney and Jeffery L. Painter and has published in prestigious journals such as Nature Communications, Nature Genetics and Journal of Clinical Oncology.

In The Last Decade

Judong Shen

29 papers receiving 1.5k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

The support of human genetic evidence for approved drug indications

2015 874 citations Matthew R. Nelson, Hannah Tipney et al. Nature Genetics profile →

Peers

Countries citing papers authored by Judong Shen

Since Specialization

Citations

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

Fields of papers citing papers by Judong Shen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Judong Shen. 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 Judong Shen. The network helps show where Judong Shen may publish in the future.

Co-authorship network of co-authors of Judong Shen

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Statistical assessment of biomarker replicability using MAJAR method 2023 ·Statistical Methods in Medical Research ·(unknown), (unknown), Wei Jiang, Hongyu Zhao, Devan V. Mehrotra, Judong Shen	1
2	Applying polygenic risk score methods to pharmacogenomics GWAS: challenges and opportunities 2023 ·Briefings in Bioinformatics ·(unknown), Devan V. Mehrotra, Judong Shen	5
3	AWOT and CWOT for genotype and genotype-by-treatment interaction joint analysis in pharmacogenetics GWAS 2023 ·Bioinformatics ·Hong Zhang, Devan V. Mehrotra, Judong Shen	0
4	GWAS of longitudinal trajectories at biobank scale 2022 ·The American Journal of Human Genetics ·(unknown), Chris German, A. E. Jensen, Judong Shen, Anran Wang, Devan V. Mehrotra, Yan V. Sun, Janet S. Sinsheimer, Hua Zhou, Jin Zhou	18
5	A statistical perspective on baseline adjustment in pharmacogenomic genome-wide association studies of quantitative change 2022 ·npj Genomic Medicine ·Hong Zhang, Aparna Chhibber, Peter Shaw, Devan V. Mehrotra, Judong Shen	4
6	Germline HLA landscape does not predict efficacy of pembrolizumab monotherapy across solid tumor types 2022 ·Immunity ·Aparna Chhibber, Lingkang Huang, Hong Zhang, Jialin Xu, Răzvan Cristescu, Xiao Liu, Devan V. Mehrotra, Judong Shen, Peter Shaw, Matthew D. Hellmann, Alexandra Snyder	21
7	Pharmacogenomics polygenic risk score for drug response prediction using PRS-PGx methods 2022 ·Nature Communications ·(unknown), Hong Zhang, Devan V. Mehrotra, Judong Shen	28
8	Global Landscape of Clostridioides Difficile Phylogeography, Antibiotic Susceptibility, and Toxin Polymorphisms by Post-Hoc Whole-Genome Sequencing from the MODIFY I/II Studies 2021 ·Infectious Diseases and Therapy ·Hailong Zhao, David C. Nickle, Zhen Zeng, Pierra Y. Law, Mark H. Wilcox, Lan Chen, Ye Peng, Jie Meng, Ziqing Deng, Andrew Albright, Huanzi Zhong, Xun Xu, Shida Zhu, Judong Shen, Rebecca Blanchard, Marcus Dörr, Peter Shaw, Junhua Li	20
9	VCSEL: Prioritizing SNP-set by penalized variance component selection 2021 ·The Annals of Applied Statistics ·Juhyun Kim, Judong Shen, Anran Wang, Devan V. Mehrotra, (unknown), Jin Zhou, Hua Zhou	1
10	Multi-trait analysis of rare-variant association summary statistics using MTAR 2020 ·Nature Communications ·(unknown), Judong Shen, Hong Zhang, Aparna Chhibber, Devan V. Mehrotra, Zheng-Zheng Tang	24
11	Composite Kernel Association Test (CKAT) for SNP-set joint assessment of genotype and genotype-by-treatment interaction in Pharmacogenetics studies 2020 ·Bioinformatics ·Hong Zhang, Ni Zhao, Devan V. Mehrotra, Judong Shen	3
12	Bezlotoxumab for prevention of Clostridium difficile infection recurrence: Distinguishing relapse from reinfection with whole genome sequencing 2019 ·Anaerobe ·Zhen Zeng, Hailong Zhao, Marcus Dörr, Judong Shen, Mark H. Wilcox, Ian R. Poxton, Dalya Güriş, Junhua Li, Peter Shaw	6
13	STOPGAP: a database for systematic target opportunity assessment by genetic association predictions 2017 ·Bioinformatics ·Judong Shen, Kijoung Song, Andrew J. Slater, Enrico Ferrero, Matthew R. Nelson	16
14	No evidence of large genetic effects on steroid response in asthma patients 2016 ·Journal of Allergy and Clinical Immunology ·Michael Mosteller, Louise K. Hosking, (unknown), Judong Shen, Kijoung Song, Matthew R. Nelson, Soumitra Ghosh	25
15	Comprehensive genome-wide evaluation of lapatinib-induced liver injury yields a single genetic signal centered on known risk allele HLA-DRB107:01 2015 ·The Pharmacogenomics Journal* ·(unknown), Linda P. Briley, (unknown), Judong Shen, Paul J. Newcombe, Karen S. King, Andrew J. Slater, Alexander Dilthey, Zamin Iqbal, Gil McVean, Charles Cox, Matthew R. Nelson, Colin F. Spraggs	45
16	The support of human genetic evidence for approved drug indications breakdown → 2015 ·Nature Genetics ·Matthew R. Nelson, Hannah Tipney, Jeffery L. Painter, Judong Shen, Paola Nicoletti, Yufeng Shen, Aris Floratos, Pak C. Sham, Mulin Jun Li, Junwen Wang, Lon R. Cardon, John C. Whittaker, Philippe Sanséau	874
17	Pharmacogenetic investigation of dabrafenib efficacy in a meta-analysis of three melanoma studies. 2014 ·Journal of Clinical Oncology ·Diptee Kulkarni, Judong Shen, Linda P. Briley, Karen S. King, S. Swann, Gursel Aktan, Kiran Patel, Colin F. Spraggs	1
18	HIBAG—HLA genotype imputation with attribute bagging 2013 ·The Pharmacogenomics Journal ·Xiuwen Zheng, Judong Shen, Charles Cox, J. C. Wakefield, Margaret G. Ehm, Matthew R. Nelson, B. S. Weir	245
19	Multi-Population Classical HLA Type Imputation 2013 ·PLoS Computational Biology ·Alexander Dilthey, Stephen Leslie, Loukas Moutsianas, Judong Shen, Charles Cox, Matthew R. Nelson, Gil McVean	125
20	Deep sequencing of theLRRK2gene in 14,002 individuals reveals evidence of purifying selection and independent origin of the p.Arg1628Pro mutation in Europe 2012 ·Human Mutation ·Justin P. Rubio, Simon Topp, Liling Warren, Pamela L. St. Jean, Daniel Wegmann, Darren Kessner, John Novembre, Judong Shen, Dana J. Fraser, Jennifer L. Aponte, (unknown), Lon R. Cardon, Margaret G. Ehm, Stephanie L. Chissoe, John C. Whittaker, Matthew R. Nelson, Vincent Mooser	24

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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