These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
187 related articles for article (PubMed ID: 37347242)
1. 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 DT; Lee K; Abul-Husn NS; Amendola LM; Brothers K; Chung WK; Gollob MH; Gordon AS; Harrison SM; Hershberger RE; Klein TE; Richards CS; Stewart DR; Martin CL; Genet Med; 2023 Aug; 25(8):100866. PubMed ID: 37347242 [TBL] [Abstract][Full Text] [Related]
2. 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 DT; Lee K; Abul-Husn NS; Amendola LM; Brothers K; Chung WK; Gollob MH; Gordon AS; Harrison SM; Hershberger RE; Klein TE; Richards CS; Stewart DR; Martin CL; Genet Med; 2022 Jul; 24(7):1407-1414. PubMed ID: 35802134 [No Abstract] [Full Text] [Related]
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 DT; Lee K; Chung WK; Gordon AS; Herman GE; Klein TE; Stewart DR; Amendola LM; Adelman K; Bale SJ; Gollob MH; Harrison SM; Hershberger RE; McKelvey K; Richards CS; Vlangos CN; Watson MS; Martin CL; Genet Med; 2021 Aug; 23(8):1381-1390. PubMed ID: 34012068 [No Abstract] [Full Text] [Related]
4. 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 DT; Lee K; Gordon AS; Amendola LM; Adelman K; Bale SJ; Chung WK; Gollob MH; Harrison SM; Herman GE; Hershberger RE; Klein TE; McKelvey K; Richards CS; Vlangos CN; Stewart DR; Watson MS; Martin CL; Genet Med; 2021 Aug; 23(8):1391-1398. PubMed ID: 34012069 [No Abstract] [Full Text] [Related]
5. 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 KA; Zheng SL; Henry A; Josephs K; Edwards M; de Marvao A; Whiffin N; Roberts A; Lumbers TR; O'Regan DP; Ware JS Genet Med; 2022 Mar; 24(3):744-746. PubMed ID: 34906520 [No Abstract] [Full Text] [Related]
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 SS; Adelman K; Bale SJ; Chung WK; Eng C; Evans JP; Herman GE; Hufnagel SB; Klein TE; Korf BR; McKelvey KD; Ormond KE; Richards CS; Vlangos CN; Watson M; Martin CL; Miller DT Genet Med; 2017 Feb; 19(2):249-255. PubMed ID: 27854360 [TBL] [Abstract][Full Text] [Related]
7. The use of ACMG secondary findings recommendations for general population screening: a policy statement of the American College of Medical Genetics and Genomics (ACMG). ACMG Board of Directors Genet Med; 2019 Jul; 21(7):1467-1468. PubMed ID: 31019278 [No Abstract] [Full Text] [Related]
8. ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing. Green RC; Berg JS; Grody WW; Kalia SS; Korf BR; Martin CL; McGuire AL; Nussbaum RL; O'Daniel JM; Ormond KE; Rehm HL; Watson MS; Williams MS; Biesecker LG; Genet Med; 2013 Jul; 15(7):565-74. PubMed ID: 23788249 [TBL] [Abstract][Full Text] [Related]
9. Correction to: 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 DT; Lee K; Chung WK; Gordon AS; Herman GE; Klein TE; Stewart DR; Amendola LM; Adelman K; Bale SJ; Gollob MH; Harrison SM; Hershberger RE; McKelvey K; Richards CS; Vlangos CN; Watson MS; Martin CL; Genet Med; 2021 Aug; 23(8):1582-1584. PubMed ID: 34345026 [No Abstract] [Full Text] [Related]
10. Consideration of disease penetrance in the selection of secondary findings gene-disease pairs: A policy statement of the American College of Medical Genetics and Genomics (ACMG). Gordon AS; Lee K; Abul-Husn NS; Amendola LM; Brothers K; Chung WK; Gollob MH; Harrison SM; Hershberger RE; Richards CS; Stewart DR; Martin CL; Miller DT; Genet Med; 2024 Jul; 26(7):101142. PubMed ID: 38819344 [No Abstract] [Full Text] [Related]
11. The ACMG SF v3.0 gene list increases returnable variant detection by 22% when compared with v2.0 in the ClinSeq cohort. Johnston JJ; Brennan ML; Radenbaugh B; Yoo SJ; Hernandez SM; ; Lewis KL; Katz AE; Manolio TA; Biesecker LG Genet Med; 2022 Mar; 24(3):736-743. PubMed ID: 34906458 [TBL] [Abstract][Full Text] [Related]
12. Frequency and management of medically actionable incidental findings from genome and exome sequencing data: a systematic review. Elfatih A; Mohammed I; Abdelrahman D; Mifsud B Physiol Genomics; 2021 Sep; 53(9):373-384. PubMed ID: 34250816 [TBL] [Abstract][Full Text] [Related]
13. Misattributed parentage as an unanticipated finding during exome/genome sequencing: current clinical laboratory practices and an opportunity for standardization. Eno C; Bayrak-Toydemir P; Bean L; Braxton A; Chao EC; El-Khechen D; Esplin ED; Friedman B; Hagman KDF; Hambuch T; Hernandez A; Juusola J; Londre G; Machado J; Mao R; Mighion L; Rehm HL; Ward P; Deignan JL Genet Med; 2019 Apr; 21(4):861-866. PubMed ID: 30214068 [TBL] [Abstract][Full Text] [Related]
14. Points to consider when assessing relationships (or suspecting misattributed relationships) during family-based clinical genomic testing: a statement of the American College of Medical Genetics and Genomics (ACMG). Deignan JL; Chao E; Gannon JL; Greely HT; Hagman KDF; Mao R; Topper S; Genet Med; 2020 Aug; 22(8):1285-1287. PubMed ID: 32404921 [No Abstract] [Full Text] [Related]
15. The use of fetal exome sequencing in prenatal diagnosis: a points to consider document of the American College of Medical Genetics and Genomics (ACMG). Monaghan KG; Leach NT; Pekarek D; Prasad P; Rose NC; Genet Med; 2020 Apr; 22(4):675-680. PubMed ID: 31911674 [No Abstract] [Full Text] [Related]
16. Return of non-ACMG recommended incidental genetic findings to pediatric patients: considerations and opportunities from experiences in genomic sequencing. Bowling KM; Thompson ML; Kelly MA; Scollon S; Slavotinek AM; Powell BC; Kirmse BM; Hendon LG; Brothers KB; Korf BR; Cooper GM; Greally JM; Hurst ACE Genome Med; 2022 Nov; 14(1):131. PubMed ID: 36414972 [TBL] [Abstract][Full Text] [Related]
17. Points to consider for reporting of germline variation in patients undergoing tumor testing: a statement of the American College of Medical Genetics and Genomics (ACMG). Li MM; Chao E; Esplin ED; Miller DT; Nathanson KL; Plon SE; Scheuner MT; Stewart DR; Genet Med; 2020 Jul; 22(7):1142-1148. PubMed ID: 32321997 [No Abstract] [Full Text] [Related]
18. Points to consider in the practice of postmortem genetic testing: A statement of the American College of Medical Genetics and Genomics (ACMG). Deignan JL; De Castro M; Horner VL; Johnston T; Macaya D; Maleszewski JJ; Reddi HV; Tayeh MK; Genet Med; 2023 May; 25(5):100017. PubMed ID: 36799919 [No Abstract] [Full Text] [Related]
19. Understanding variations in secondary findings reporting practices across U.S. genome sequencing laboratories. Ackerman SL; Koenig BA AJOB Empir Bioeth; 2018; 9(1):48-57. PubMed ID: 29131714 [TBL] [Abstract][Full Text] [Related]
20. Incidental detection of acquired variants in germline genetic and genomic testing: a points to consider statement of the American College of Medical Genetics and Genomics (ACMG). Chao EC; Astbury C; Deignan JL; Pronold M; Reddi HV; Weitzel JN; Genet Med; 2021 Jul; 23(7):1179-1184. PubMed ID: 33864022 [No Abstract] [Full Text] [Related] [Next] [New Search]