Author

Alejandro Nieto-Patlán

Baylor College of MedicineORCID 0000-0002-8668-6853Unclaimed 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· 2 Approach:statistical model· 2 Research Focus:variant effect prediction· 2 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Abduarahman Almutairi· 1 shared Agustin Bernacchia· 1 shared Alice Y. K. ChaniD· 1 shared Anita Chacko· 1 shared Benjamin McLeaniD· 1 shared Bo YuaniD· 1 shared Brian Chung· 1 shared Britt A. JohnsoniD· 1 shared

Activity by Year

2022-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Abduarahman Almutairi

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2 papers

Recent·Most cited

The ClinGen Severe Combined Immunodeficiency Disease Variant Curation Expert Panel: Specifications for classification of variants in ADA, DCLRE1C, IL2RG, IL7R, JAK3, RAG1, and RAG2

Vanessa Cristina Jacovas, Michelle Zelnick, Shannon M. McNulty, Justyne E. Ross, Namrata Khurana, Xueyang Pan, Alejandro Nieto-Patlán, Shiloh Martin, Benjamin McLean, Marwa Elnagheeb, Morton Jerome Cowan, Jennifer M. Puck, M S Hershfield, James W. Verbsky, Jolan Eszter Walter, , Xinrui Shi

The paper develops SCID-specific variant classification guidelines by adapting ACMG/AMP criteria for seven SCID-related genes using expert review and a pilot variant set.

Genetics in Medicine · Oct 15, 2025Peer-reviewedGenetic & Genomic Medicine

COVID-19 relevant genetic variants confirmed in an admixed population

Tomas Texis, José Luis Cruz-Jaramilllo, Willebaldo García‐Muñoz, Lourdes Anzures-Cortés, Lorenza Haddad-Talancón, Sergio Sánchez‐García, María del Carmen Jiménez Martínez, Edgar Pérez‐Barragán, Alejandro Nieto-Patlán, José Darío Martínez‐Ezquerro, Kenneth Rubio-Carrasco, Mauricio Rodríguez‐Dorantes, Sergio Alberto Cortés-Ramírez, Gabriela Mellado‐Sánchez, Sonia Mayra Pérez‐Tapia, Vanessa González-Covarrubias

The paper confirms the presence of previously reported genetic variants associated with COVID-19 in an admixed population and identifies additional variants with significant allele frequency differences between patients and the general population.

medRxiv · Apr 15, 2022 · PreprintGenetic & Genomic Medicine