Author

Bryce E. Pasko

University of Colorado Anschutz

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· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 1 Organism:human· 1 Approach:statistical model· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Ágnes Tóth-PetróczyiD· 1 shared Alissa K. RobbinsiD· 1 shared Betty RouaisneliD· 1 shared Elizabeth L. FiegiD· 1 shared James C. HudspethiD· 1 shared Joel B. KrieriD· 1 shared Julie-Aurore LosmaniD· 1 shared Justine H. Ryu· 1 shared

Activity by Year

2022-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 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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1 paper

Recent·Most cited

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