BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

139 related articles for article (PubMed ID: 35767006)

  • 1. Challenges of variant reinterpretation: Opinions of stakeholders and need for guidelines.
    Berger SM; Appelbaum PS; Siegel K; Wynn J; Saami AM; Brokamp E; O'Connor BC; Hamid R; Martin DM; Chung WK
    Genet Med; 2022 Sep; 24(9):1878-1887. PubMed ID: 35767006
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Reinterpretation, reclassification, and its downstream effects: challenges for clinical laboratory geneticists.
    El Mecky J; Johansson L; Plantinga M; Fenwick A; Lucassen A; Dijkhuizen T; van der Hout A; Lyle K; van Langen I
    BMC Med Genomics; 2019 Nov; 12(1):170. PubMed ID: 31779608
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Reinterpretation of sequence variants: one diagnostic laboratory's experience, and the need for standard guidelines.
    Chisholm C; Daoud H; Ghani M; Mettler G; McGowan-Jordan J; Sinclair-Bourque L; Smith A; Jarinova O
    Genet Med; 2018 Mar; 20(3):365-368. PubMed ID: 29240080
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Management of amended variant classification laboratory reports by genetic counselors in the United States and Canada: An exploratory study.
    Richardson B; Fitzgerald-Butt SM; Spoonamore KG; Wetherill L; Helm BM; Breman AM
    J Genet Couns; 2022 Apr; 31(2):479-488. PubMed ID: 34570930
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Reclassification of clinically-detected sequence variants: Framework for genetic clinicians and clinical scientists by CanVIG-UK (Cancer Variant Interpretation Group UK).
    Loong L; Garrett A; Allen S; Choi S; Durkie M; Callaway A; Drummond J; Burghel GJ; Robinson R; Torr B; Berry IR; Wallace AJ; Eccles DM; Ellard S; Baple E; Evans DG; Woodward ER; Kulkarni A; Lalloo F; Tischkowitz M; Lucassen A; Hanson H; Turnbull C;
    Genet Med; 2022 Sep; 24(9):1867-1877. PubMed ID: 35657381
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Analysis of VUS reporting, variant reinterpretation and recontact policies in clinical genomic sequencing consent forms.
    Vears DF; Niemiec E; Howard HC; Borry P
    Eur J Hum Genet; 2018 Dec; 26(12):1743-1751. PubMed ID: 30143804
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Is there a duty to reinterpret genetic data? The ethical dimensions.
    Appelbaum PS; Parens E; Berger SM; Chung WK; Burke W
    Genet Med; 2020 Mar; 22(3):633-639. PubMed ID: 31616070
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinical Utility of Reinterpreting Previously Reported Genomic Epilepsy Test Results for Pediatric Patients.
    SoRelle JA; Thodeson DM; Arnold S; Gotway G; Park JY
    JAMA Pediatr; 2019 Jan; 173(1):e182302. PubMed ID: 30398534
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Assessing management practices for variants of uncertain significance among genetic counselors in pediatrics.
    Cheung C; Berger SM; Ross M; Kramer T; Li Y; Andrews C; Dergham KR; Spitz E; Florido ME; Ahimaz P
    J Genet Couns; 2024 Jan; ():. PubMed ID: 38217320
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Offering preimplantation genetic testing for monogenic disorders (PGT-M) for conditions with reduced penetrance or variants of uncertain significance: Ethical insight from U.S. laboratory genetic counselors.
    Porto A; Gaber Caffrey R; Crowley-Matoka M; Spencer S; Li M; Propst L
    J Genet Couns; 2022 Feb; 31(1):261-268. PubMed ID: 34347921
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clinical Cardiovascular Genetic Counselors Take a Leading Role in Team-based Variant Classification.
    Reuter C; Grove ME; Orland K; Spoonamore K; Caleshu C
    J Genet Couns; 2018 Aug; 27(4):751-760. PubMed ID: 29234989
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Variant Reinterpretation in Survivors of Cardiac Arrest With Preserved Ejection Fraction (the Cardiac Arrest Survivors With Preserved Ejection Fraction Registry) by Clinicians and Clinical Commercial Laboratories.
    Davies B; Bartels K; Hathaway J; Xu F; Roberts JD; Tadros R; Green MS; Healey JS; Simpson CS; Sanatani S; Steinberg C; Gardner M; Angaran P; Talajic M; Hamilton R; Arbour L; Seifer C; Fournier A; Joza J; Krahn AD; Lehman A; Laksman ZWM
    Circ Genom Precis Med; 2021 Jun; 14(3):e003235. PubMed ID: 33960826
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The future of Cochrane Neonatal.
    Soll RF; Ovelman C; McGuire W
    Early Hum Dev; 2020 Nov; 150():105191. PubMed ID: 33036834
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinical and laboratory genetic counselor attitudes on the reporting of variants of uncertain significance for multigene cancer panels.
    Chang EY; Solomon I; Culver JO; Gorman N; Comeaux JG; Lerman C; Quinn EA; Ekstein T
    J Genet Couns; 2023 Jun; 32(3):706-716. PubMed ID: 36747331
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Retrospective reinterpretation and reclassification of BRCA1/2 variants from Chinese population.
    Li D; Shi Y; Li A; Cao D; Su H; Yang H; Zhi Q; Yang Y; Lan Z; Zhou T; You X; Hu G
    Breast Cancer; 2020 Nov; 27(6):1158-1167. PubMed ID: 32566972
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Managing Variant Interpretation Discrepancies in Hereditary Cancer: Clinical Practice, Concerns, and Desired Resources.
    Zirkelbach E; Hashmi S; Ramdaney A; Dunnington L; Ashfaq M; Nugent EK; Wilson K
    J Genet Couns; 2018 Aug; 27(4):761-769. PubMed ID: 29260485
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetic variants with discordant classifications: An assessment of genetic counselor attitudes and practices.
    Lahiri S; Reys B; Wunder J; Pirzadeh-Miller S
    J Genet Couns; 2023 Feb; 32(1):100-110. PubMed ID: 35978490
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Is there a duty to routinely reinterpret genomic variant classifications?
    Watts G; Newson AJ
    J Med Ethics; 2023 Nov; 49(12):808-814. PubMed ID: 37208157
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Challenges in genetic testing: clinician variant interpretation processes and the impact on clinical care.
    Berrios C; Hurley EA; Willig L; Thiffault I; Saunders C; Pastinen T; Goggin K; Farrow E
    Genet Med; 2021 Dec; 23(12):2289-2299. PubMed ID: 34257423
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The Somatic Curation and Interpretation Across Laboratories (SOCIAL) project-current state of solid-tumour variant interpretation for molecular pathology in Canada.
    Spence T; Sukhai MA; Kamel-Reid S; Stockley TL
    Curr Oncol; 2019 Dec; 26(6):353-360. PubMed ID: 31896933
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.