Author

Justine H. Ryu

Beth Israel Deaconess Medical Center

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:differential expression· 1 Research Focus:GWAS / association mapping· 1 Assay:whole-exome sequencing· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Ágnes Tóth-PetróczyiD· 1 shared Alissa K. RobbinsiD· 1 shared Andrea H. RamireziD· 1 shared Betty RouaisneliD· 1 shared Bryce E. Pasko· 1 shared Elizabeth L. FiegiD· 1 shared Greg A. TalaveraiD· 1 shared Henry Robert Condon· 1 shared

Activity by Year

2022-2022 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Ágnes Tóth-PetróczyORCID

Mutual co-authors in cluster

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2 papers

Recent·Most cited

Common and Rare Variants Associated with Cardiometabolic Traits across 98,622 Whole-Genome Sequences in the All of Us Research Program

Xin Wang, Justine H. Ryu, Jihoon Kim, Andrea H. Ramirez, Kelsey Mayo, Henry Robert Condon, Nataraja Sarma Vaitinadin, Lucila Ohno-machado A, Greg A. Talavera, Patrick T. Ellinor, Steven A. Lubitz, Seung Hoan Choi

The paper analyzes whole-genome sequences from 98,622 participants to identify common and rare variants associated with cardiometabolic traits, replicating known associations and finding new loci.

medRxiv · Nov 23, 2022 · PreprintGenetic & Genomic Medicine

Pathway-based Rare Variant Burden Analysis Identifies a Role for the Complement System in an Extreme Phenotype of Sepsis with Coagulopathy

Pavan K. Bendapudi, Sumaiya Nazeen, Justine H. Ryu, Onuralp Söylemez, Betty Rouaisnel, Meaghan E. Colling, Bryce E. Pasko, Alissa K. Robbins, Michael Bouzinier, Lindsay Tomczak, Lindsay Collier, Sanjay Ram, Ágnes Tóth-Petróczy, Joel B. Krier, Elizabeth L. Fieg, , Julie-Aurore Losman

The paper identifies rare variants in the complement system associated with severe sepsis with coagulopathy using pathway-based analysis of whole exome sequencing data.

medRxiv · Feb 24, 2022 · PreprintGenetic & Genomic Medicine