Author

Abdulaziz Almalik

King Abdulaziz City for Science and TechnologyORCID 0000-0002-4656-0674Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 2 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Approach:statistical model· 3 Organism:Arabidopsis· 2 Research Focus:benchmarking· 1 Assay:DNA methylation· 1 Organism:human· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Ary A. HoffmanniD· 2 shared Samia ElfékihiD· 2 shared Abdulraheem AlshareefiD· 1 shared AboElgasim Ali· 1 shared Ali G. GharaviiD· 1 shared Asma A. Al Thani· 1 shared Atlas KhaniD· 1 shared Bader M. AlghamdiiD· 1 shared

Activity by Year

2021-2022 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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2 shared papersGenetics

Ary A. HoffmannORCID

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3 papers

Recent·Most cited

GeneticsThe American NaturalistPeer-reviewedAug 11, 2022

Close kin dyads indicate intergenerational dispersal and barriers

Thomas L. Schmidt, Samia Elfékih, Li‐Jun Cao…·Ary A. Hoffmann

This paper introduces a method to infer intergenerational dispersal and detect barriers using close kin dyads in mosquito populations, validated with genome-wide data from Aedes aegypti.

18 citations

ArabidopsisDNA methylation

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GeneticsParasites & VectorsPeer-reviewedJul 11, 2021

Voltage-sensitive sodium channel (Vssc) mutations associated with pyrethroid insecticide resistance in Aedes aegypti (L.) from Jeddah, Kingdom of Saudi Arabia - baseline information for a Wolbachia release program

Nancy M. Endersby‐Harshman, AboElgasim Ali, Basim Alhumrani…·Ary A. Hoffmann

This study identifies Vssc mutations associated with pyrethroid resistance in Ae. aegypti from Jeddah, providing baseline data for a Wolbachia release program.

16 citations

Arabidopsisstatistical model

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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.

76 citationstop 2%

humanwhole-exome sequencing

𝕏 PostBluesky