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

被引：0

作者：

Gollob, Michael H. ^{[1
,2
]}

Hershberger, Ray E. ^{[3
,4
]}

Gordon, Adam S. ^{[5
,6
]}

Harrison, Steven M. ^{[7
]}

Lee, Kristy ^{[8
]}

Martin, Christa Lese ^{[9
]}

Miller, David T. ^{[10
]}

机构：

[1] Univ Toronto, Fac Med, Dept Med, Div Cardiol, Toronto, ON, Canada

[2] Univ Toronto, Temerty Fac Med, Dept Physiol, Toronto, ON, Canada

[3] Ohio State Univ, Coll Med, Dept Internal Med, Div Human Genet, Columbus, OH 43210 USA

[4] Ohio State Univ, Coll Med, Dept Internal Med, Div Cardiovasc Med, Columbus, OH 43210 USA

[5] Northwestern Univ, Dept Pharmacol, Feinberg Sch Med, Chicago, IL 60611 USA

[6] Northwestern Univ, Ctr Genet Med, Feinberg Sch Med, Chicago, IL 60611 USA

[7] Ambry Genet, Aliso Viejo, CA USA

[8] Univ North Carolina Chapel Hill, Sch Med, Dept Genet, Chapel Hill, NC USA

[9] Geisinger, Autism & Dev Med Inst, Danville, PA USA

[10] Boston Childrens Hosp, Div Genet & Genom, 300 Longwood Ave,Hunnewell 5, Boston, MA 02115 USA

来源：

GENETICS IN MEDICINE | 2022年 / 24卷 / 03期

关键词：

D O I：

10.1016/j.gim.2021.10.021

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：747 / 748

页数：2

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
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
[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] 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
[9] 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
[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)

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