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American Journal of Human Genetics|February 18, 2025
Distinct explanations underlie gene-environment interactions in the UK BiobankArun Durvasula, Alkes L PriceAmerican Journal of Human Genetics|October 29, 2024
Homozygous variants in WDR83OS lead to a neurodevelopmental disorder with hypercholanemiaScott Barish, Sheng-Jia Lin, Reza Maroofian, et al.American Journal of Human Genetics|November 20, 2024
Employing effective recruitment and retention strategies to engage a diverse pediatric population in genomics researchMichelle A Ramos, Katherine E Bonini, Laura Scarimbolo, et al.American Journal of Human Genetics|November 19, 2024
The PRIMED Consortium: Reducing disparities in polygenic risk assessmentIftikhar J Kullo, Matthew P Conomos, Sarah C Nelson, et al.American Journal of Human Genetics|November 19, 2024
Toward trustable use of machine learning models of variant effects in the clinicMafalda Dias, Rose Orenbuch, Debora S Marks, et al.American Journal of Human Genetics|November 30, 2024
Leveraging diverse genomic data to guide equitable carrier screening: Insights from gnomAD v.4.1.0Matthew J Schmitz, Aryan Bashar, Vishal Soman, et al.American Journal of Human Genetics|March 12, 2025
The contribution of coding variants to the heritability of multiple cancer types using UK Biobank whole-exome sequencing dataNaomi Wilcox, Jonathan P Tyrer, Joe Dennis, et al.American Journal of Human Genetics|March 8, 2025
Data-driven insights to inform splice-altering variant assessmentPatricia J Sullivan, Julian M W Quinn, Pamela Ajuyah, et al.American Journal of Human Genetics|March 15, 2025
Actionable genetic variants in 4,198 Scottish participants from the Orkney and Shetland founder populations and implementation of return of resultsShona M Kerr, Lucija Klaric, Marisa D Muckian, et al.American Journal of Human Genetics|March 13, 2025
Artificial variables help to avoid over-clustering in single-cell RNA sequencingAlan DenAdel, Michelle L Ramseier, Andrew W Navia, et al.Pageof 979