Author

Meaghan E. Colling

Harvard UniversityORCID 0000-0002-8362-0613Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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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 Bryce E. Pasko· 1 shared Elizabeth L. FiegiD· 1 shared James C. HudspethiD· 1 shared Joel B. KrieriD· 1 shared Julie-Aurore LosmaniD· 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

Genetic & Genomic MedicinemedRxivPreprintFeb 24, 2022

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…·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.

2 citations

humanwhole-exome sequencing