Author

Bader M. Alghamdi

King Saud bin Abdulaziz University for Health SciencesORCID 0000-0001-5701-0216Unclaimed 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:statistical model· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Abdulaziz AlmalikiD· 1 shared Abdulraheem AlshareefiD· 1 shared Ali G. GharaviiD· 1 shared Asma A. Al Thani· 1 shared Atlas KhaniD· 1 shared Bandar A. SulimaniD· 1 shared Bartha Maria KnoppersiD· 1 shared Chadi SaadiD· 1 shared

Activity by Year

2021-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Abdulaziz AlmalikORCID

Mutual co-authors in cluster

Author profile →

1 paper

Recent·Most cited

Genetic & Genomic MedicineJournal of Clinical InvestigationPeer-reviewedMay 27, 2021

Failure to replicate the association of rare loss-of-function variants in type I IFN immunity genes with severe COVID-19

Gundula Povysil, Guillaume Butler‐Laporte, Ning Shang…·Krzysztof Kiryluk

The paper investigates the association of rare loss-of-function variants in type I IFN immunity genes with severe COVID-19 and finds no significant association.

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humanwhole-exome sequencing

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