BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

318 related articles for article (PubMed ID: 32850417)

  • 1. Tumor Testing for Somatic and Germline
    Peixoto A; Pinto P; Guerra J; Pinheiro M; Santos C; Pinto C; Santos R; Escudeiro C; Bartosch C; Canário R; Barbosa A; Gouveia A; Petiz A; Abreu MH; Sousa S; Pereira D; Silva J; Teixeira MR
    Front Oncol; 2020; 10():1318. PubMed ID: 32850417
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The detection of germline and somatic BRCA1/2 genetic variants through parallel testing of patients with high-grade serous ovarian cancer: a national retrospective audit.
    Frugtniet B; Morgan S; Murray A; Palmer-Smith S; White R; Jones R; Hanna L; Fuller C; Hudson E; Mullard A; Quinton AE
    BJOG; 2022 Feb; 129(3):433-442. PubMed ID: 34657373
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Differential Sensitivity of Germline and Somatic
    Vendrell JA; Ban IO; Solassol I; Audran P; Cabello-Aguilar S; Topart D; Lindet-Bourgeois C; Colombo PE; Legouffe E; D'Hondt V; Fabbro M; Solassol J
    Int J Mol Sci; 2023 Sep; 24(18):. PubMed ID: 37762485
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Germline and somatic variants in ovarian carcinoma: A next-generation sequencing (NGS) analysis.
    Andrikopoulou A; Zografos E; Apostolidou K; Kyriazoglou A; Papatheodoridi AM; Kaparelou M; Koutsoukos K; Liontos M; Dimopoulos MA; Zagouri F
    Front Oncol; 2022; 12():1030786. PubMed ID: 36531003
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutation Patterns in Portuguese Families with Hereditary Breast and Ovarian Cancer Syndrome.
    Vicente R; Alpuim Costa D; Vitorino M; Mendes AD; Santos C; Fontes-Sousa M
    Cancers (Basel); 2022 Sep; 14(19):. PubMed ID: 36230639
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Globally Rare
    Oosthuizen J; Kotze MJ; Van Der Merwe N; Myburgh EJ; Bester P; van der Merwe NC
    Front Oncol; 2020; 10():619469. PubMed ID: 33643918
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Routine Plasma-Based Genotyping to Comprehensively Detect Germline, Somatic, and Reversion
    Vidula N; Rich TA; Sartor O; Yen J; Hardin A; Nance T; Lilly MB; Nezami MA; Patel SP; Carneiro BA; Fan AC; Brufsky AM; Parker BA; Bridges BB; Agarwal N; Maughan BL; Raymond VM; Fairclough SR; Lanman RB; Bardia A; Cristofanilli M
    Clin Cancer Res; 2020 Jun; 26(11):2546-2555. PubMed ID: 32034076
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Gene Panel Tumor Testing in Ovarian Cancer Patients Significantly Increases the Yield of Clinically Actionable Germline Variants beyond
    Barbosa A; Pinto P; Peixoto A; Guerra J; Pinto C; Santos C; Pinheiro M; Escudeiro C; Bartosch C; Silva J; Teixeira MR
    Cancers (Basel); 2020 Sep; 12(10):. PubMed ID: 33008098
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Implementation of next-generation sequencing for molecular diagnosis of hereditary breast and ovarian cancer highlights its genetic heterogeneity.
    Pinto P; Paulo P; Santos C; Rocha P; Pinto C; Veiga I; Pinheiro M; Peixoto A; Teixeira MR
    Breast Cancer Res Treat; 2016 Sep; 159(2):245-56. PubMed ID: 27553368
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Examining the Diagnostic Yield of Tumour Testing and Qualifying Germline Concordance for Hereditary Cancer Variants in Patients with High-Grade Serous Carcinoma.
    Goebel EA; Kerkhof J; Dzyubak O; McLachlin CM; McGee J; Sadikovic B
    Genes (Basel); 2022 Aug; 13(8):. PubMed ID: 36011309
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Deleterious somatic variants in 473 consecutive individuals with ovarian cancer: results of the observational AGO-TR1 study (NCT02222883).
    Hauke J; Hahnen E; Schneider S; Reuss A; Richters L; Kommoss S; Heimbach A; Marmé F; Schmidt S; Prieske K; Gevensleben H; Burges A; Borde J; De Gregorio N; Nürnberg P; El-Balat A; Thiele H; Hilpert F; Altmüller J; Meier W; Dietrich D; Kimmig R; Schoemig-Markiefka B; Kast K; Braicu E; Baumann K; Jackisch C; Park-Simon TW; Ernst C; Hanker L; Pfisterer J; Schnelzer A; du Bois A; Schmutzler RK; Harter P
    J Med Genet; 2019 Sep; 56(9):574-580. PubMed ID: 30979843
    [TBL] [Abstract][Full Text] [Related]  

  • 12. BRCA somatic and germline mutation detection in paraffin embedded ovarian cancers by next-generation sequencing.
    Mafficini A; Simbolo M; Parisi A; Rusev B; Luchini C; Cataldo I; Piazzola E; Sperandio N; Turri G; Franchi M; Tortora G; Bovo C; Lawlor RT; Scarpa A
    Oncotarget; 2016 Jan; 7(2):1076-83. PubMed ID: 26745875
    [TBL] [Abstract][Full Text] [Related]  

  • 13. BRCA1/2 NGS Somatic Testing in Clinical Practice: A Short Report.
    Pepe F; Pisapia P; Russo G; Nacchio M; Pallante P; Vigliar E; De Angelis C; Insabato L; Bellevicine C; De Placido S; Troncone G; Malapelle U
    Genes (Basel); 2021 Nov; 12(12):. PubMed ID: 34946865
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Detection of BRCA1 and BRCA2 germline mutations in Japanese population using next-generation sequencing.
    Hirotsu Y; Nakagomi H; Sakamoto I; Amemiya K; Mochizuki H; Omata M
    Mol Genet Genomic Med; 2015 Mar; 3(2):121-9. PubMed ID: 25802882
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Universal Tumor DNA BRCA1/2 Testing of Ovarian Cancer: Prescreening PARPi Treatment and Genetic Predisposition.
    Vos JR; Fakkert IE; de Hullu JA; van Altena AM; Sie AS; Ouchene H; Willems RW; Nagtegaal ID; Jongmans MCJ; Mensenkamp AR; Woldringh GH; Bulten J; Leter EM; Kets CM; Simons M; Ligtenberg MJL; Hoogerbrugge N;
    J Natl Cancer Inst; 2020 Feb; 112(2):161-169. PubMed ID: 31076742
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Novel BRCA1 and BRCA2 Tumor Test as Basis for Treatment Decisions and Referral for Genetic Counselling of Patients with Ovarian Carcinomas.
    Weren RD; Mensenkamp AR; Simons M; Eijkelenboom A; Sie AS; Ouchene H; van Asseldonk M; Gomez-Garcia EB; Blok MJ; de Hullu JA; Nelen MR; Hoischen A; Bulten J; Tops BB; Hoogerbrugge N; Ligtenberg MJ
    Hum Mutat; 2017 Feb; 38(2):226-235. PubMed ID: 27767231
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Evaluation of Homologous Recombination Deficiency in Ovarian Cancer.
    Ratnaparkhi R; Javellana M; Jewell A; Spoozak L
    Curr Treat Options Oncol; 2024 Feb; 25(2):237-260. PubMed ID: 38300479
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Next-generation sequencing based detection of
    Hua D; Tian Q; Wang X; Bei T; Cui L; Zhang B; Bao C; Bai Y; Zhao X; Yuan P
    Front Oncol; 2022; 12():898916. PubMed ID: 36147908
    [No Abstract]   [Full Text] [Related]  

  • 19. Clinical Impact of Somatic Variants in Homologous Recombination Repair-Related Genes in Ovarian High-Grade Serous Carcinoma.
    Choi MC; Hwang S; Kim S; Jung SG; Park H; Joo WD; Song SH; Lee C; Kim TH; Kang H; An HJ
    Cancer Res Treat; 2020 Apr; 52(2):634-644. PubMed ID: 32019284
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Frequency of BRCA1 and BRCA2 mutations in ovarian cancer patients in South-East Poland.
    Jasiewicz A; Rudnicka H; Kluźniak W; Gronwald W; Kluz T; Cybulski C; Jakubowska A; Lubiński J; Gronwald J
    Hered Cancer Clin Pract; 2022 Apr; 20(1):12. PubMed ID: 35382848
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.