Skip to Main Content
ADVERTISEMENT
SCROLL TO CONTINUE WITH CONTENT



Property Value
Status
Version
Ad File
Disable Ads Flag
Environment
Moat Init
Moat Ready
Contextual Ready
Contextual URL
Contextual Initial Segments
Contextual Used Segments
AdUnit
SubAdUnit
Custom Targeting
Ad Events
Invalid Ad Sizes
Advertisement
Close
  • Home
  • Articles and Issues
    • Back
    • Current Issue
    • Articles in Press
    • List of Issues
  • Collections
  • GenePod
  • For Authors
    • Back
    • Author Information
    • Permissions
    • Researcher Academy 
    • Submit A Manuscript 
  • Journal Info
    • Back
    • About the Journal
    • Contact Information
    • Editorial Board
  • 2023 Media Kit
  • Subscribe
  • Submit Your Manuscript 
Advanced searchSave search

Please enter a term before submitting your search.

Ok
  • ACMG Homepage         Submit
  • Log in
  • Register
  • Log in
    • ACMG Homepage         Submit
    • Log in
  • Subscribe
Skip menu
    x

    Filter:

    Filters applied

    • ACMG Statements and Guidelines
    • Chung, Wendy KRemove Chung, Wendy K filter
    • Klein, Teri ERemove Klein, Teri E filter
    Clear all

    Article Type

    • Research Article2
    • Editorial1

    Publication Date

    • Last Year1
    • Last 2 Years2
    • Last 5 Years2
    Please choose a date range between 2017 and 2022.

    Author

    • Miller, David T3
    • Adelman, Kathy2
    • Amendola, Laura M2
    • Bale, Sherri J2
    • Gollob, Michael H2
    • Gordon, Adam S2
    • Harrison, Steven M2
    • Herman, Gail E2
    • Hershberger, Ray E2
    • Lee, Kristy2
    • Martin, Christa Lese2
    • Richards, C Sue2
    • Stewart, Douglas R2
    • Vlangos, Christopher N2
    • Abul-Husn, Noura S1
    • Brothers, Kyle1
    • Eng, Christine1
    • Evans, James P1
    • Hufnagel, Sophia B1
    • Kalia, Sarah S1
    • Korf, Bruce R1
    • Martin, Christa L1
    • McKelvey, Kent1

    Journal

    • Genetics in Medicine3

    Keyword

    • Exome sequencing1
    • exome sequencing1
    • genetic testing1
    • Genome sequencing1
    • genome sequencing1
    • Incidental findings1
    • incidental findings1
    • Secondary findings1
    • secondary findings1

    ACMG Statements and Guidelines

    These online statements and guidelines are definitive and may be cited using the digital object identifier (DOI). These recommendations are designed primarily as an educational resource for medical geneticists and other healthcare providers to help them provide quality medical genetics services; they should not be considered inclusive of all proper procedures and tests or exclusive of other procedures and tests that are reasonably directed to obtaining the same results. Please refer to the leading disclaimer in each document for more information.

    3 Results
    Subscribe to collection
    • Export
      • PDF
      • Citation

    Please select at least one article in order to proceed.

    Ok
    FilterHide Filter
    • ACMG Statement

      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
      Vol. 24Issue 7p1407–1414Published online: June 17, 2022
      • David T. Miller
      • Kristy Lee
      • Noura S. Abul-Husn
      • Laura M. Amendola
      • Kyle Brothers
      • Wendy K. Chung
      • and others
      Cited in Scopus: 13
      • Preview Hide Preview
      • Download PDF
      • Export Citation
        The American College of Medical Genetics and Genomics (ACMG) previously published guidance for reporting secondary findings (SF) in the context of clinical exome and genome sequencing in 2013, 2017, and 2021.1-3 The ACMG Secondary Findings Working Group (SFWG) and Board of Directors (BOD) have agreed that the list of recommended genes should now be updated annually, but with an ongoing goal of maintaining this as a minimum list. Reporting of SF should be considered neither a replacement for indication-based diagnostic clinical genetic testing nor a form of population screening.
      • ACMG Statement
        Open Archive

        ACMG SF v3.0 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
        Vol. 23Issue 8p1381–1390Published in issue: August, 2021
        • David T. Miller
        • Kristy Lee
        • Wendy K. Chung
        • Adam S. Gordon
        • Gail E. Herman
        • Teri E. Klein
        • and others
        Cited in Scopus: 175
        • Preview Hide Preview
        • Download PDF
        • Export Citation
          A correction to this article is available online at https://doi.org/10.1038/s41436-021-01278-8 .
          ACMG SF v3.0 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)
        • ACMG Statement
          Open Archive

          Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics

          Genetics in Medicine
          Vol. 19Issue 2p249–255Published in issue: February, 2017
          • Sarah S. Kalia
          • Kathy Adelman
          • Sherri J. Bale
          • Wendy K. Chung
          • Christine Eng
          • James P. Evans
          • and others
          Cited in Scopus: 1117
          • Preview Hide Preview
          • Download PDF
          • Export Citation
            Disclaimer: These recommendations are designed primarily as an educational resource for medical geneticists and other healthcare providers to help them provide quality medical services. Adherence to these recommendations is completely voluntary and does not necessarily assure a successful medical outcome. These recommendations should not be considered inclusive of all proper procedures and tests or exclusive of other procedures and tests that are reasonably directed toward obtaining the same results.
            Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics
          Page 1 of 1

          Login to your account

          Show
          Forgot password?
          Don’t have an account?
          Create a Free Account

          If you don't remember your password, you can reset it by entering your email address and clicking the Reset Password button. You will then receive an email that contains a secure link for resetting your password

          If the address matches a valid account an email will be sent to __email__ with instructions for resetting your password

          Cancel
          • Home
          • Articles and Issues
          • Current Issue
          • Articles in Press
          • List of Issues
          • Collections
          • GenePod
          • For Authors
          • Permissions
          • Researcher Academy
          • Journal Info
          • About the Journal
          • Activate Online Access
          • ACMG Career Center
          • Advertise in Genetics in Medicine
          • Contact Information
          • Editorial Board
          • Reprints
          • New Content Alerts
          • 2023 Media Kit
          • Subscribe
          • More Periodicals
          • Find a Periodical
          • Go to Product Catalog
          We use cookies to help provide and enhance our service and tailor content. To update your cookie settings, please visit the for this site.
          Copyright © 2023 Elsevier Inc. except certain content provided by third parties. The content on this site is intended for healthcare professionals.

          • Privacy Policy  
          • Terms and Conditions  
          • Accessibility  
          • Help & Contact

          RELX