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 *

322 related articles for article (PubMed ID: 29962246)

  • 1. Next-generation sequencing and the impact on prenatal diagnosis.
    Mellis R; Chandler N; Chitty LS
    Expert Rev Mol Diagn; 2018 Aug; 18(8):689-699. PubMed ID: 29962246
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Beyond screening for chromosomal abnormalities: Advances in non-invasive diagnosis of single gene disorders and fetal exome sequencing.
    Hayward J; Chitty LS
    Semin Fetal Neonatal Med; 2018 Apr; 23(2):94-101. PubMed ID: 29305293
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Update on the use of exome sequencing in the diagnosis of fetal abnormalities.
    Ferretti L; Mellis R; Chitty LS
    Eur J Med Genet; 2019 Aug; 62(8):103663. PubMed ID: 31085342
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prenatal Diagnosis Innovation: Genome Sequencing of Maternal Plasma.
    Wong FC; Lo YM
    Annu Rev Med; 2016; 67():419-32. PubMed ID: 26473414
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The potential diagnostic yield of whole exome sequencing in pregnancies complicated by fetal ultrasound anomalies.
    Diderich KEM; Romijn K; Joosten M; Govaerts LCP; Polak M; Bruggenwirth HT; Wilke M; van Slegtenhorst MA; van Bever Y; Brooks AS; Mancini GMS; van de Laar IMBH; Kromosoeto JNR; Knapen MFCM; Go ATJI; Van Opstal D; Hoefsloot LH; Galjaard RH; Srebniak MI
    Acta Obstet Gynecol Scand; 2021 Jun; 100(6):1106-1115. PubMed ID: 33249554
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Non-invasive prenatal testing using massively parallel sequencing of maternal plasma DNA: from molecular karyotyping to fetal whole-genome sequencing.
    Lo YM
    Reprod Biomed Online; 2013 Dec; 27(6):593-8. PubMed ID: 24140310
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The importance of pre- and post-test counseling for prenatal cell-free DNA screening for common fetal aneuploidies.
    Stefanovic V
    Expert Rev Mol Diagn; 2019 Mar; 19(3):201-215. PubMed ID: 30657716
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Maternal Plasma DNA and RNA Sequencing for Prenatal Testing.
    Tamminga S; van Maarle M; Henneman L; Oudejans CB; Cornel MC; Sistermans EA
    Adv Clin Chem; 2016; 74():63-102. PubMed ID: 27117661
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The current and future impact of genome-wide sequencing on fetal precision medicine.
    Sabbagh R; Van den Veyver IB
    Hum Genet; 2020 Sep; 139(9):1121-1130. PubMed ID: 31754893
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Detection of 46, XY Disorder of Sex Development (DSD) Based on Plasma Cell-Free DNA and Targeted Next-Generation Sequencing.
    De Falco L; Piscopo C; D'Angelo R; Evangelista E; Suero T; Sirica R; Ruggiero R; Savarese G; Di Carlo A; Furino G; Scarpato C; Fico A
    Genes (Basel); 2021 Nov; 12(12):. PubMed ID: 34946839
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clinical utility of exome sequencing in the prenatal diagnosis of congenital anomalies: A Review.
    Mone F; Quinlan-Jones E; Kilby MD
    Eur J Obstet Gynecol Reprod Biol; 2018 Dec; 231():19-24. PubMed ID: 30317140
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Exploring the clinical utility of exome sequencing/Mono, Duo, Trio in prenatal testing: a retrospective study in a tertiary care centre in South India.
    Ilangovan H; Elangovan J; Danda S; Beck MM; Navaneethan P; Athiyarath R
    J Perinat Med; 2024 Jun; 52(5):520-529. PubMed ID: 38709224
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Improving Single-Nucleotide Polymorphism-Based Fetal Fraction Estimation of Maternal Plasma Circulating Cell-Free DNA Using Bayesian Hierarchical Models.
    Larson NB; Wang C; Na J; Rowsey RA; Highsmith WE; Hoppman NL; Kocher JP; Klee EW
    J Comput Biol; 2018 Sep; 25(9):1040-1049. PubMed ID: 29932737
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Non invasive prenatal testing (NIPT) for common aneuploidies and beyond.
    Alberry MS; Aziz E; Ahmed SR; Abdel-Fattah S
    Eur J Obstet Gynecol Reprod Biol; 2021 Mar; 258():424-429. PubMed ID: 33550217
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Guidelines for NGS procedures applied to prenatal diagnosis by the Spanish Society of Gynecology and Obstetrics and the Spanish Association of Prenatal Diagnosis.
    Abulí A; Antolín E; Borrell A; Garcia-Hoyos M; García Santiago F; Gómez Manjón I; Maíz N; González González C; Rodríguez-Revenga L; Valenzuena Palafoll I; Suela J
    J Med Genet; 2024 Jul; 61(8):727-733. PubMed ID: 38834294
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Whole Exome Sequencing: Applications in Prenatal Genetics.
    Jelin AC; Vora N
    Obstet Gynecol Clin North Am; 2018 Mar; 45(1):69-81. PubMed ID: 29428287
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Rapid prenatal diagnosis using targeted exome sequencing: a cohort study to assess feasibility and potential impact on prenatal counseling and pregnancy management.
    Chandler N; Best S; Hayward J; Faravelli F; Mansour S; Kivuva E; Tapon D; Male A; DeVile C; Chitty LS
    Genet Med; 2018 Nov; 20(11):1430-1437. PubMed ID: 29595812
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Noninvasive prenatal testing.
    Lo JO; Cori D F; Norton ME; Caughey AB
    Obstet Gynecol Surv; 2014 Feb; 69(2):89-99. PubMed ID: 25112487
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Next-generation sequencing and prenatal 'omics: advanced diagnostics and new insights into human development.
    Vora NL; Hui L
    Genet Med; 2018 Aug; 20(8):791-799. PubMed ID: 30032162
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The importance of determining the limit of detection of non-invasive prenatal testing methods.
    Fiorentino F; Bono S; Pizzuti F; Mariano M; Polverari A; Duca S; Sessa M; Baldi M; Diano L; Spinella F
    Prenat Diagn; 2016 Apr; 36(4):304-11. PubMed ID: 26815144
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 17.