BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

178 related articles for article (PubMed ID: 37728764)

  • 1. Frequency of actionable secondary findings in 7472 Korean genomes derived from the National Project of Bio Big Data pilot study.
    Kim Y; Kim JM; Cho HW; Park HY; Park MH
    Hum Genet; 2023 Nov; 142(11):1561-1569. PubMed ID: 37728764
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Actionable secondary findings following exome sequencing of 836 non-obstructive azoospermia cases and their value in patient management.
    Kasak L; Lillepea K; Nagirnaja L; Aston KI; Schlegel PN; Gonçalves J; Carvalho F; Moreno-Mendoza D; Almstrup K; Eisenberg ML; Jarvi KA; O'Bryan MK; Lopes AM; Conrad DF; ; Punab M; Laan M
    Hum Reprod; 2022 Jun; 37(7):1652-1663. PubMed ID: 35535697
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Frequency and spectrum of actionable pathogenic secondary findings in 196 Korean exomes.
    Jang MA; Lee SH; Kim N; Ki CS
    Genet Med; 2015 Dec; 17(12):1007-11. PubMed ID: 25856671
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Actionable secondary findings in the 73 ACMG-recommended genes in 1559 Thai exomes.
    Chetruengchai W; Shotelersuk V
    J Hum Genet; 2022 Mar; 67(3):137-142. PubMed ID: 34621001
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Secondary genomic findings in the 2020 China Neonatal Genomes Project participants.
    Xiao H; Zhang JT; Dong XR; Lu YL; Wu BB; Wang HJ; Zhao ZY; Yang L; Zhou WH
    World J Pediatr; 2022 Oct; 18(10):687-694. PubMed ID: 35727495
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Frequency of genomic secondary findings among 21,915 eMERGE network participants.
    eMERGE Clinical Annotation Working Group
    Genet Med; 2020 Sep; 22(9):1470-1477. PubMed ID: 32546831
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Landscape of Secondary Findings in Chinese Population: A Practice of ACMG SF v3.0 List.
    Huang Y; Liu B; Shi J; Zhao S; Xu K; Sun L; Chen N; Tian W; Zhang J; Wu N
    J Pers Med; 2022 Sep; 12(9):. PubMed ID: 36143288
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The rate of secondary genomic findings in the Saudi population.
    Aloraini T; Alsubaie L; Alasker S; Al Muitiri A; Alswaid A; Eyiad W; Al Mutairi F; Ababneh F; Alfadhel M; Alfares A
    Am J Med Genet A; 2022 Jan; 188(1):83-88. PubMed ID: 34515413
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Physician-directed genetic screening to evaluate personal risk for medically actionable disorders: a large multi-center cohort study.
    Haverfield EV; Esplin ED; Aguilar SJ; Hatchell KE; Ormond KE; Hanson-Kahn A; Atwal PS; Macklin-Mantia S; Hines S; Sak CW; Tucker S; Bleyl SB; Hulick PJ; Gordon OK; Velsher L; Gu JYJ; Weissman SM; Kruisselbrink T; Abel C; Kettles M; Slavotinek A; Mendelsohn BA; Green RC; Aradhya S; Nussbaum RL
    BMC Med; 2021 Aug; 19(1):199. PubMed ID: 34404389
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The burden of pathogenic variants in clinically actionable genes in a founder population.
    Lynch MT; Maloney KA; Pollin TI; Streeten EA; Xu H; ; Shuldiner AR; Van Hout CV; Gonzaga-Jauregui C; Mitchell BD
    Am J Med Genet A; 2021 Nov; 185(11):3476-3484. PubMed ID: 34467620
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Actionable secondary findings in arrhythmogenic right ventricle cardiomyopathy genes: impact and challenge of genetic counseling.
    Abicht A; Schön U; Laner A; Holinski-Feder E; Diebold I
    Cardiovasc Diagn Ther; 2021 Apr; 11(2):637-649. PubMed ID: 33968641
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Identification of Medically Actionable Secondary Findings in the 1000 Genomes.
    Olfson E; Cottrell CE; Davidson NO; Gurnett CA; Heusel JW; Stitziel NO; Chen LS; Hartz S; Nagarajan R; Saccone NL; Bierut LJ
    PLoS One; 2015; 10(9):e0135193. PubMed ID: 26332594
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Actionable genomic variants in 6045 participants from the Qatar Genome Program.
    Elfatih A; Mifsud B; Syed N; Badii R; Mbarek H; Abbaszadeh F; ; Estivill X
    Hum Mutat; 2021 Aug; ():. PubMed ID: 34428338
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Secondary findings in a large Pakistani cohort tested with whole genome sequencing.
    Skrahin A; Cheema HA; Hussain M; Rana NN; Rehman KU; Kumar R; Oprea G; Ameziane N; Rolfs A; Skrahina V
    Life Sci Alliance; 2023 Mar; 6(3):. PubMed ID: 36635046
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Actionable Genotypes and Their Association with Life Span in Iceland.
    Jensson BO; Arnadottir GA; Katrinardottir H; Fridriksdottir R; Helgason H; Oddsson A; Sveinbjornsson G; Eggertsson HP; Halldorsson GH; Atlason BA; Jonsson H; Oskarsson GR; Sturluson A; Gudjonsson SA; Thorisson GA; Zink F; Moore KHS; Palsson G; Sigurdsson A; Jonasdottir A; Jonasdottir A; Magnusson MK; Helgadottir A; Steinthorsdottir V; Gudmundsson J; Stacey SN; Hilmarsson R; Olafsson I; Johannsson OT; Arnar DO; Saemundsdottir J; Magnusson OT; Masson G; Halldorsson BV; Helgason A; Stefansson H; Jonsdottir I; Holm H; Rafnar T; Thorsteinsdottir U; Gudbjartsson DF; Stefansson K; Sulem P
    N Engl J Med; 2023 Nov; 389(19):1741-1752. PubMed ID: 37937776
    [TBL] [Abstract][Full Text] [Related]  

  • 17. High-frequency actionable pathogenic exome variants in an average-risk cohort.
    Rego S; Dagan-Rosenfeld O; Zhou W; Sailani MR; Limcaoco P; Colbert E; Avina M; Wheeler J; Craig C; Salins D; Röst HL; Dunn J; McLaughlin T; Steinmetz LM; Bernstein JA; Snyder MP
    Cold Spring Harb Mol Case Stud; 2018 Dec; 4(6):. PubMed ID: 30487145
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A systematic literature review of disclosure practices and reported outcomes for medically actionable genomic secondary findings.
    Sapp JC; Facio FM; Cooper D; Lewis KL; Modlin E; van der Wees P; Biesecker LG
    Genet Med; 2021 Dec; 23(12):2260-2269. PubMed ID: 34433902
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Identification of a Novel BRCA1 Pathogenic Mutation in Korean Patients Following Reclassification of BRCA1 and BRCA2 Variants According to the ACMG Standards and Guidelines Using Relevant Ethnic Controls.
    Park JS; Nam EJ; Park HS; Han JW; Lee JY; Kim J; Kim TI; Lee ST
    Cancer Res Treat; 2017 Oct; 49(4):1012-1021. PubMed ID: 28111427
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.