Author

Hasan Alkhairo

Gladstone InstitutesORCID 0009-0007-9905-8358Unclaimed 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 Research Focus:GWAS / association mapping· 2 Assay:GWAS summary statistics· 2 Research Focus:fine-mapping· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Catherine TcheandjieuiD· 2 shared Kruthika Raman IyeriD· 2 shared Philip S. TsaoiD· 2 shared Pik Fang KhoiD· 2 shared Africa-Wits INDEPTH (AWI-Gen)· 1 shared Alicia Huerta‐ChagoyaiD· 1 shared Anita ThapariD· 1 shared Arthur Jeremy WillseyiD· 1 shared

Activity by Year

2022-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 22 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Catherine TcheandjieuORCID

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3 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintJan 3, 2026

Locus 9p21.3 CAD Risk Across Diverse Populations: LD and Allelic Heterogeneity Explain Variation Across Ancestries and Reduced Replication in Africans

Hasan Alkhairo, Satoshi Koyama, Kruthika Raman Iyer…·Catherine Tcheandjieu

The paper investigates why the 9p21.3 CAD risk locus fails to replicate in African ancestry cohorts, finding ancestry-specific LD and haplotype diversity explain the lack of association.

DOI 10.64898/2026.01.02.25343215

humanGWAS summary statistics

𝕏 PostBluesky

Genetic & Genomic MedicineJACC Basic to Translational SciencePeer-reviewedOct 31, 2025

Mendelian randomization suggests a causal link between glycemic traits and thoracic aortic structures and diseases

Tselmen Daria, Kruthika Raman Iyer, Hasan Alkhairo…·Catherine Tcheandjieu

This study uses Mendelian randomization to show that higher glycemic traits are inversely associated with thoracic aortic diameters and reduced risk of aneurysm and dissection.

1 citation

humanGWAS summary statistics

𝕏 PostBluesky

Genetic & Genomic MedicinemedRxivPreprintSep 22, 2022

Rare Maternally Inherited Coding Variants on Chromosome X Carry Predominantly Male Risk in Autism, Tourette Syndrome, and Attention-deficit/Hyperactivity Disorder

Sheng Wang, Belinda Lei Wang, Vanessa Drury…·Arthur Jeremy Willsey

1 citation

humanwhole-exome sequencing

𝕏 PostBluesky