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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

127 related articles for article (PubMed ID: 36150821)

  • 1. Best Practice for Clinical Somatic Variant Interpretation and Reporting.
    Schubert J; Wu J; Li MM; Cao K
    Clin Lab Med; 2022 Sep; 42(3):423-434. PubMed ID: 36150821
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Assessments of Somatic Variant Classification Using the Association for Molecular Pathology/American Society of Clinical Oncology/College of American Pathologists Guidelines: A Report from the Association for Molecular Pathology.
    Li MM; Cottrell CE; Pullambhatla M; Roy S; Temple-Smolkin RL; Turner SA; Wang K; Zhou Y; Vnencak-Jones CL
    J Mol Diagn; 2023 Feb; 25(2):69-86. PubMed ID: 36503149
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Standards and Guidelines for the Interpretation and Reporting of Sequence Variants in Cancer: A Joint Consensus Recommendation of the Association for Molecular Pathology, American Society of Clinical Oncology, and College of American Pathologists.
    Li MM; Datto M; Duncavage EJ; Kulkarni S; Lindeman NI; Roy S; Tsimberidou AM; Vnencak-Jones CL; Wolff DJ; Younes A; Nikiforova MN
    J Mol Diagn; 2017 Jan; 19(1):4-23. PubMed ID: 27993330
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Variant Interpretation for Cancer (VIC): a computational tool for assessing clinical impacts of somatic variants.
    He MM; Li Q; Yan M; Cao H; Hu Y; He KY; Cao K; Li MM; Wang K
    Genome Med; 2019 Aug; 11(1):53. PubMed ID: 31443733
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Multi-Institutional Evaluation of Interrater Agreement of Variant Classification Based on the 2017 Association for Molecular Pathology, American Society of Clinical Oncology, and College of American Pathologists Standards and Guidelines for the Interpretation and Reporting of Sequence Variants in Cancer.
    Sirohi D; Schmidt RL; Aisner DL; Behdad A; Betz BL; Brown N; Coleman JF; Corless CL; Deftereos G; Ewalt MD; Fernandes H; Hsiao SJ; Mansukhani MM; Murray SS; Niu N; Ritterhouse LL; Suarez CJ; Tafe LJ; Thorson JA; Segal JP; Furtado LV
    J Mol Diagn; 2020 Feb; 22(2):284-293. PubMed ID: 31837433
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity): Joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consortium (CGC), and Variant Interpretation for Cancer Consortium (VICC).
    Horak P; Griffith M; Danos AM; Pitel BA; Madhavan S; Liu X; Chow C; Williams H; Carmody L; Barrow-Laing L; Rieke D; Kreutzfeldt S; Stenzinger A; Tamborero D; Benary M; Rajagopal PS; Ida CM; Lesmana H; Satgunaseelan L; Merker JD; Tolstorukov MY; Campregher PV; Warner JL; Rao S; Natesan M; Shen H; Venstrom J; Roy S; Tao K; Kanagal-Shamanna R; Xu X; Ritter DI; Pagel K; Krysiak K; Dubuc A; Akkari YM; Li XS; Lee J; King I; Raca G; Wagner AH; Li MM; Plon SE; Kulkarni S; Griffith OL; Chakravarty D; Sonkin D
    Genet Med; 2022 May; 24(5):986-998. PubMed ID: 35101336
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinically actionable cancer somatic variants (CACSV): a tumor interpreted dataset for analytical workflows.
    Sobahy TM; Tashkandi G; Bahussain D; Al-Harbi R
    BMC Med Genomics; 2022 Apr; 15(1):95. PubMed ID: 35468810
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Standards and Guidelines for Validating Next-Generation Sequencing Bioinformatics Pipelines: A Joint Recommendation of the Association for Molecular Pathology and the College of American Pathologists.
    Roy S; Coldren C; Karunamurthy A; Kip NS; Klee EW; Lincoln SE; Leon A; Pullambhatla M; Temple-Smolkin RL; Voelkerding KV; Wang C; Carter AB
    J Mol Diagn; 2018 Jan; 20(1):4-27. PubMed ID: 29154853
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The current state of clinical interpretation of sequence variants.
    Hoskinson DC; Dubuc AM; Mason-Suares H
    Curr Opin Genet Dev; 2017 Feb; 42():33-39. PubMed ID: 28157586
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Tailoring the American College of Medical Genetics and Genomics and the Association for Molecular Pathology Guidelines for the Interpretation of Sequenced Variants in the
    Muiño-Mosquera L; Steijns F; Audenaert T; Meerschaut I; De Paepe A; Steyaert W; Symoens S; Coucke P; Callewaert B; Renard M; De Backer J
    Circ Genom Precis Med; 2018 Jun; 11(6):e002039. PubMed ID: 29875124
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Standardized decision support in next generation sequencing reports of somatic cancer variants.
    Dienstmann R; Dong F; Borger D; Dias-Santagata D; Ellisen LW; Le LP; Iafrate AJ
    Mol Oncol; 2014 Jul; 8(5):859-73. PubMed ID: 24768039
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Variant Classification Concordance using the ACMG-AMP Variant Interpretation Guidelines across Nine Genomic Implementation Research Studies.
    Amendola LM; Muenzen K; Biesecker LG; Bowling KM; Cooper GM; Dorschner MO; Driscoll C; Foreman AKM; Golden-Grant K; Greally JM; Hindorff L; Kanavy D; Jobanputra V; Johnston JJ; Kenny EE; McNulty S; Murali P; Ou J; Powell BC; Rehm HL; Rolf B; Roman TS; Van Ziffle J; Guha S; Abhyankar A; Crosslin D; Venner E; Yuan B; Zouk H; ; Jarvik GP
    Am J Hum Genet; 2020 Nov; 107(5):932-941. PubMed ID: 33108757
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A Canadian guideline on the use of next-generation sequencing in oncology.
    Yip S; Christofides A; Banerji S; Downes MR; Izevbaye I; Lo B; MacMillan A; McCuaig J; Stockley T; Yousef GM; Spatz A
    Curr Oncol; 2019 Apr; 26(2):e241-e254. PubMed ID: 31043833
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Bioinformatics workflows for clinical applications in precision oncology.
    Jäger N
    Semin Cancer Biol; 2022 Sep; 84():103-112. PubMed ID: 33476720
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Tiered Somatic Variant Classification Adoption Has Increased Worldwide With Some Practice Differences Based on Location and Institutional Setting.
    Bruehl FK; Kim AS; Li MM; Lindeman NI; Moncur JT; Souers RJ; Vasalos P; Voelkerding KV; Xian RR; Surrey LF
    Arch Pathol Lab Med; 2022 Jul; 146(7):822-832. PubMed ID: 34979564
    [TBL] [Abstract][Full Text] [Related]  

  • 17. CACSV: a computational web-sever that provides classification for cancer somatic genetic variants from different tissues.
    AlKurabi N; AlGahtani A; Sobahy TM
    BMC Bioinformatics; 2023 Mar; 24(1):95. PubMed ID: 36922756
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Cancer Predisposition Sequencing Reporter (CPSR): A flexible variant report engine for high-throughput germline screening in cancer.
    Nakken S; Saveliev V; Hofmann O; Møller P; Myklebost O; Hovig E
    Int J Cancer; 2021 Dec; 149(11):1955-1960. PubMed ID: 34310709
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Guidelines for Validation of Next-Generation Sequencing-Based Oncology Panels: A Joint Consensus Recommendation of the Association for Molecular Pathology and College of American Pathologists.
    Jennings LJ; Arcila ME; Corless C; Kamel-Reid S; Lubin IM; Pfeifer J; Temple-Smolkin RL; Voelkerding KV; Nikiforova MN
    J Mol Diagn; 2017 May; 19(3):341-365. PubMed ID: 28341590
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Adapting ACMG/AMP sequence variant classification guidelines for single-gene copy number variants.
    Brandt T; Sack LM; Arjona D; Tan D; Mei H; Cui H; Gao H; Bean LJH; Ankala A; Del Gaudio D; Knight Johnson A; Vincent LM; Reavey C; Lai A; Richard G; Meck JM
    Genet Med; 2020 Feb; 22(2):336-344. PubMed ID: 31534211
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.