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 (vol 19, pg 249, 2016)

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Kalia, Sarah S.
Adelman, Kathy
Bale, Sherri J.
Chung, Wendy K.
Eng, Christine
Evans, James P.
Herman, Gail E.
Hufnagel, Sophia B.
Klein, Teri E.
Korf, Bruce R.
McKelvey, Kent D.
Ormond, Kelly E.
Richards, C. Sue
Vlangos, Christopher N.
Watson, Michael
Martin, Christa L.
Miller, David T.
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Q3 [遗传学];
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071007 ; 090102 ;
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页码:484 / 485
页数:2
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  • [1] 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
    Kalia, Sarah S.
    Adelman, Kathy
    Bale, Sherri J.
    Chung, Wendy K.
    Eng, Christine
    Evans, James P.
    Herman, Gail E.
    Hufnagel, Sophia B.
    Klein, Teri E.
    Korf, Bruce R.
    McKelvey, Kent D.
    Ormond, Kelly E.
    Richards, C. Sue
    Vlangos, Christopher N.
    Watson, Michael
    Martin, Christa L.
    Miller, David T.
    [J]. GENETICS IN MEDICINE, 2017, 19 (02) : 249 - 255
  • [2] Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2021 update: a policy statement of the American College of Medical Genetics and Genomics (ACMG)
    Miller, David T.
    Lee, Kristy
    Gordon, Adam S.
    Amendola, Laura M.
    Adelman, Kathy
    Bale, Sherri J.
    Chung, Wendy K.
    Gollob, Michael H.
    Harrison, Steven M.
    Herman, Gail E.
    Hershberger, Ray E.
    Klein, Teri E.
    McKelvey, Kent
    Richards, C. Sue
    Vlangos, Christopher N.
    Stewart, Douglas R.
    Watson, Michael S.
    Martin, Christa Lese
    [J]. GENETICS IN MEDICINE, 2021, 23 (08) : 1391 - 1398
  • [3] 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)
    Miller, David T.
    Lee, Kristy
    Chung, Wendy K.
    Gordon, Adam S.
    Herman, Gail E.
    Klein, Teri E.
    Stewart, Douglas R.
    Amendola, Laura M.
    Adelman, Kathy
    Bale, Sherri J.
    Gollob, Michael H.
    Harrison, Steven M.
    Hershberger, Ray E.
    McKelvey, Kent
    Richards, C. Sue
    Vlangos, Christopher N.
    Watson, Michael S.
    Martin, Christa Lese
    [J]. GENETICS IN MEDICINE, 2021, 23 (08) : 1381 - 1390
  • [4] 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)
    Miller, David T.
    Lee, Kristy
    Abul-Husn, Noura S.
    Amendola, Laura M.
    Brothers, Kyle
    Chung, Wendy K.
    Gollob, Michael H.
    Gordon, Adam S.
    Harrison, Steven M.
    Hershberger, Ray E.
    Klein, Teri E.
    Richards, C. Sue
    Stewart, Douglas R.
    Martin, C. L.
    [J]. GENETICS IN MEDICINE, 2023, 25 (08)
  • [5] 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)
    Miller, David T.
    Lee, Kristy
    Abul-Husn, Noura S.
    Amendla, Laura M.
    Brothers, Kyle
    Chung, Wendy K.
    Gollob, Michael H.
    Gordon, Adam S.
    Harrison, Steven M.
    Hershberger, Ray E.
    Klein, Teri E.
    Richards, Carolyn Sue
    Stewart, Douglas R.
    Martin, Christa Lese
    [J]. GENETICS IN MEDICINE, 2022, 24 (07) : 1407 - 1414
  • [6] Correspondence on "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)" by Miller et al
    McGurk, Kathryn A.
    Zheng, Sean L.
    Henry, Albert
    Josephs, Katherine
    Edwards, Matthew
    de Marvao, Antonio
    Whiffin, Nicola
    Roberts, Angharad
    Lumbers, Thomas R.
    O'Regan, Declan P.
    Ware, James S.
    [J]. GENETICS IN MEDICINE, 2022, 24 (03) : 744 - 746
  • [7] Correspondence on "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)" by Miller et al Response
    Gollob, Michael H.
    Hershberger, Ray E.
    Gordon, Adam S.
    Harrison, Steven M.
    Lee, Kristy
    Martin, Christa Lese
    Miller, David T.
    [J]. GENETICS IN MEDICINE, 2022, 24 (03) : 747 - 748
  • [8] The use of ACMG secondary findings recommendations for general population screening: a policy statement of the American College of Medical Genetics and Genomics (ACMG)
    Watson, Michael
    [J]. GENETICS IN MEDICINE, 2019, 21 (07) : 1467 - 1468
  • [9] Response to "The use of ACMG secondary findings recommendations for general population screening: a policy statement of the American College of Medical Genetics and Genomics (ACMG)"
    Nussbaum, Robert L.
    Haverfield, Eden
    Esplin, Edward D.
    Aradhya, Swaroop
    [J]. GENETICS IN MEDICINE, 2019, 21 (12) : 2836 - 2837
  • [10] ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing (vol 15, pg 565, 2013)
    Green, Robert C.
    Berg, Jonathan S.
    Grody, Wayne W.
    Kalia, Sarah S.
    Korf, Bruce R.
    Martin, Christa L.
    McGuire, Amy L.
    Nussbaum, Robert L.
    O'Daniel, Julianne M.
    Ormond, Kelly E.
    Rehm, Heidi L.
    Watson, Michael S.
    Williams, Marc S.
    Biesecker, Leslie G.
    [J]. GENETICS IN MEDICINE, 2017, 19 (05) : 606 - 606