Author

Rafael Zubirán

Instituto Nacional de Ciencias Médicas y Nutrición Salvador ZubiránORCID 0000-0003-4274-3585Unclaimed 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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Research Focus:GWAS / association mapping· 1 Organism:human· 1 Approach:statistical model· 1 Assay:whole-exome sequencing· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Alexander G. IoannidisiD· 1 shared Alexandro J. MartagóniD· 1 shared Arturo López PinedaiD· 1 shared Babak MoatamediD· 1 shared Carlos D. BustamanteiD· 1 shared Consuelo D. Quinto-CortésiD· 1 shared Daniel Elías-LópeziD· 1 shared Daniel Mas MontserratiD· 1 shared

Activity by Year

2025-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Alexander G. IoannidisORCID

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1 paper

Recent·Most cited

Genetic & Genomic MedicineHuman GenomicsPeer-reviewedNov 24, 2025

Analysis of a deeply-phenotyped familial hypercholesterolemia cohort from Mexico shows a role for both rare and common alleles across known dyslipidemia genes and reveals structural variation in a novel locus.

Nicholas Katsanis, Niki Mourtzi, Consuelo D. Quinto-Cortés…·Carlos D. Bustamante

The paper analyzes a Mexican FH cohort to show rare and common alleles in FH genes and a novel locus contribute to disease risk, with replication in UK Biobank.

1 citation

humanwhole-exome sequencing

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