Author

Evin S. Feldman

Morgan Stanley Children's HospitalORCID 0000-0002-9896-2405Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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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 Joseph A. HostykiD· 1 shared Joshua D. MilneriD· 1 shared Joshua E. MotelowiD· 1 shared Matthew NelliganiD· 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

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1 shared paperGenetic & Genomic Medicine

Ali G. GharaviORCID

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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

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