Author

Matthew Nelligan

Morgan Stanley Children's HospitalORCID 0009-0000-6824-2258Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 1 Approach:machine learning (classical)· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Ali G. GharaviiD· 1 shared Anna AlkelaiiD· 1 shared David B. GoldsteiniD· 1 shared Evin S. FeldmaniD· 1 shared Joseph A. HostykiD· 1 shared Joshua D. MilneriD· 1 shared Joshua E. MotelowiD· 1 shared Natalie C. LippaiD· 1 shared

Activity by Year

2022-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

1 shared paperGenetic & Genomic Medicine

Ali G. GharaviORCID

Mutual co-authors in cluster

Author profile →

1 paper

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintMay 1, 2022

Children with Critical Illness Carry Risk Variants Despite Non-Diagnostic Whole Exome Sequencing

Joshua E. Motelow, Natalie C. Lippa, Joseph A. Hostyk…·Steven G. Kernie

This study finds that children with critical illness and non-diagnostic whole exome sequencing may still carry risk variants in genes not previously associated with disease.

DOI 10.1101/2022.05.01.22274445

humanwhole-exome sequencing

𝕏 PostBluesky