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

被引:17
|
作者
McGurk, Kathryn A. [1 ]
Zheng, Sean L. [1 ,2 ]
Henry, Albert [3 ,4 ]
Josephs, Katherine [1 ]
Edwards, Matthew [2 ]
de Marvao, Antonio [5 ]
Whiffin, Nicola [6 ]
Roberts, Angharad [1 ,2 ]
Lumbers, Thomas R. [3 ,4 ,7 ]
O'Regan, Declan P. [5 ]
Ware, James S. [1 ,2 ,5 ]
机构
[1] Imperial Coll London, Natl Heart & Lung Inst, Fac Med, London, England
[2] Guys & St Thomas NHS Fdn Trust, Royal Brompton & Harefield Hosp, London, England
[3] UCL, British Heart Fdn Res Accelerator, London, England
[4] UCL, Inst Hlth Informat, London, England
[5] Imperial Coll London, MRC London Inst Med Sci, London, England
[6] Univ Oxford, Nuffield Dept Med, Wellcome Ctr Human Genet, Oxford, England
[7] Barts Hlth NHS Trust, St Bartholomews Hosp, Barts Heart Ctr, London, England
关键词
D O I
10.1016/j.gim.2021.10.020
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:744 / 746
页数:3
相关论文
共 20 条
  • [1] 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
  • [2] 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
  • [3] 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)
  • [4] 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
  • [5] 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
  • [6] 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
  • [7] 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)
    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 (04) : 484 - 485
  • [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] Correspondence on " Clinical utility of polygenic risk scores for embryo selection: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG)" " by Grebe et al
    Widen, Erik
    Lello, Louis
    Eccles, Jennifer
    Marin, Diego
    Treff, Nathan R.
    [J]. GENETICS IN MEDICINE, 2024, 26 (08)