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NAR Cancer|May 6, 2026
Sensitive detection of somatic mutations in GC-rich cancer gene promotersMeifang Qi, Preshita Sanjay Dave, Nicole Francis, et al.NPJ Genomic Medicine|April 10, 2026
Clinical validation of a high-performance somatic exome sequencing assay: from target-enrichment strategy to variant callingJunko Tsuji, Micah Rickles-Young, Justin Abreu, et al.Nature Cancer|January 26, 2026
Genomic risk model to implement precision prostate cancer screening in clinical care: the ProGRESS studyJason L Vassy, Anna M Dornisch, Roshan Karunamuni, et al.American Journal of Human Genetics|March 24, 2026
The Electronic Medical Records and Genomics study: Design and analytic framework for assessing the impact of genome-informed risk assessmentsNita Limdi, T Mark Beasley, Josh Cortopassi, et al.Medrxiv : the Preprint Server for Health Sciences|June 19, 2023
Selection, optimization, and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse populationsNiall J Lennon, Leah C Kottyan, Christopher Kachulis, et al.Nature Medicine|February 20, 2024
Selection, optimization and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse US populationsNiall J Lennon, Leah C Kottyan, Christopher Kachulis, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 9, 2023
Returning integrated genomic risk and clinical recommendations: The eMERGE studyJodell E Linder, Aimee Allworth, Harris T Bland, et al.Pageof 1