Author

Radja Messai Badji

Qatar FoundationORCID 0000-0002-0512-3312Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Assay:whole-genome sequencing· 2 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Research Focus:genome assembly· 1 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1

Frequent Co-Authors

Chadi SaadiD· 3 shared Hamdi MbarekiD· 3 shared Said I. IsmailiD· 3 shared Wadha Al‐MuftahiD· 3 shared Asmaa A. Al ThaniiD· 2 shared Dima DarwishiD· 2 shared Fatima AlkuwariiD· 2 shared Heba YasiniD· 2 shared

Activity by Year

2021-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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Curved chords = mutual co-authorship

3 shared papersGenetic & Genomic Medicine

Chadi SaadORCID

Mutual co-authors in cluster

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3 papers

Recent·Most cited

Genetic & Genomic MedicineNature GeneticsPeer-reviewedMar 1, 2023

Multi-ancestry genome-wide association study improves resolution of genes, pathways and pleiotropy for lung function and chronic obstructive pulmonary disease

Nick R. G. Shrine, Abril G. Izquierdo, Jing Chen…·Data Management and Computing Infrastructure group

This study performs a multi-ancestry GWAS on lung function and COPD, identifying 559 genes and 29 pathways, and showing genetic risk scores are associated with COPD across ancestries.

200 citationstop 1%

humanGWAS summary statistics

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Genetic & Genomic MedicineHuman MutationPeer-reviewedFeb 2, 2022

Qatar Genome: Insights on Genomics from the Middle East

Hamdi Mbarek, Geethanjali Devadoss Gandhi, Senthil Selvaraj…·Asma Al-Thani

The Qatar Genome Program sequenced 6,045 individuals, identifying 88 million variants, including novel ones, and revealed genetic structure and disease-related markers in the Qatari population.

109 citationstop 1%

humanwhole-genome sequencing

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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

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