Genetic findings and health care utilization among individuals undergoing population genomic screening for actionable hereditary disorders

This publication has 39 references indexed in Scilit:

• Genomic Screening at a Single Health System
  JAMA Network Open, 2025
• Genetics Visit Uptake Among Individuals Receiving Clinically Actionable Genomic Screening Results
  JAMA Network Open, 2024
• Prospective, multi-site study of healthcare utilization after actionable monogenic findings from clinical sequencing
  The American Journal of Human Genetics, 2023
• Testing and Management of Iron Overload After Genetic Screening–Identified Hemochromatosis
  JAMA Network Open, 2023
• Influence of family history on penetrance of hereditary cancers in a population setting
  eClinicalMedicine, 2023
• ACMG SF v3.2 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG)
  Genetics in Medicine, 2023
• ACMG SF v3.1 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG)
  Genetics in Medicine, 2022
• Returning actionable genomic results in a research biobank: Analytic validity, clinical implementation, and resource utilization
  The American Journal of Human Genetics, 2021
• A Rigorous Interlaboratory Examination of the Need to Confirm Next-Generation Sequencing–Detected Variants with an Orthogonal Method in Clinical Genetic Testing
  The Journal of Molecular Diagnostics, 2019
• Exome Sequencing–Based Screening for BRCA1/2 Expected Pathogenic Variants Among Adult Biobank Participants
  JAMA Network Open, 2018