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 *

552 related articles for article (PubMed ID: 31172278)

  • 21. Putting genome-wide sequencing in neonates into perspective.
    van der Sluijs PJ; Aten E; Barge-Schaapveld DQCM; Bijlsma EK; Bökenkamp-Gramann R; Donker Kaat L; van Doorn R; van de Putte DF; van Haeringen A; Ten Harkel ADJ; Hilhorst-Hofstee Y; Hoffer MJV; den Hollander NS; van Ierland Y; Koopmans M; Kriek M; Moghadasi S; Nibbeling EAR; Peeters-Scholte CMPCD; Potjer TP; van Rij M; Ruivenkamp CAL; Rutten JW; Steggerda SJ; Suerink M; Tan RNGB; van der Tuin K; Visser R; van der Werf-'t Lam AS; Williams M; Witlox R; Santen GWE
    Genet Med; 2019 May; 21(5):1074-1082. PubMed ID: 30287924
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Multicenter Consensus Approach to Evaluation of Neonatal Hypotonia in the Genomic Era: A Review.
    Morton SU; Christodoulou J; Costain G; Muntoni F; Wakeling E; Wojcik MH; French CE; Szuto A; Dowling JJ; Cohn RD; Raymond FL; Darras BT; Williams DA; Lunke S; Stark Z; Rowitch DH; Agrawal PB
    JAMA Neurol; 2022 Apr; 79(4):405-413. PubMed ID: 35254387
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Targeted gene panel sequencing for the rapid diagnosis of acutely ill infants.
    Brunelli L; Jenkins SM; Gudgeon JM; Bleyl SB; Miller CE; Tvrdik T; Dames SA; Ostrander B; Daboub JAF; Zielinski BA; Zinkhan EK; Underhill HR; Wilson T; Bonkowsky JL; Yost CC; Botto LD; Jenkins J; Pysher TJ; Bayrak-Toydemir P; Mao R
    Mol Genet Genomic Med; 2019 Jul; 7(7):e00796. PubMed ID: 31192527
    [TBL] [Abstract][Full Text] [Related]  

  • 24. The Role of Genome Sequencing in Neonatal Intensive Care Units.
    Kingsmore SF; Cole FS
    Annu Rev Genomics Hum Genet; 2022 Aug; 23():427-448. PubMed ID: 35676073
    [TBL] [Abstract][Full Text] [Related]  

  • 25. The Impact of Rapid Exome Sequencing on Medical Management of Critically Ill Children.
    Freed AS; Clowes Candadai SV; Sikes MC; Thies J; Byers HM; Dines JN; Ndugga-Kabuye MK; Smith MB; Fogus K; Mefford HC; Lam C; Adam MP; Sun A; McGuire JK; DiGeronimo R; Dipple KM; Deutsch GH; Billimoria ZC; Bennett JT
    J Pediatr; 2020 Nov; 226():202-212.e1. PubMed ID: 32553838
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Rapid exome sequencing in critically ill children impacts acute and long-term management of patients and their families: A retrospective regional evaluation.
    McDermott H; Sherlaw-Sturrock C; Baptista J; Hartles-Spencer L; Naik S
    Eur J Med Genet; 2022 Sep; 65(9):104571. PubMed ID: 35842091
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Rapid exome sequencing as a first-tier test in neonates with suspected genetic disorder: results of a prospective multicenter clinical utility study in the Netherlands.
    Olde Keizer RACM; Marouane A; Kerstjens-Frederikse WS; Deden AC; Lichtenbelt KD; Jonckers T; Vervoorn M; Vreeburg M; Henneman L; de Vries LS; Sinke RJ; Pfundt R; Stevens SJC; Andriessen P; van Lingen RA; Nelen M; Scheffer H; Stemkens D; Oosterwijk C; van Amstel HKP; de Boode WP; van Zelst-Stams WAG; Frederix GWJ; Vissers LELM;
    Eur J Pediatr; 2023 Jun; 182(6):2683-2692. PubMed ID: 36997769
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. Critical Trio Exome Benefits In-Time Decision-Making for Pediatric Patients With Severe Illnesses.
    Wu ET; Hwu WL; Chien YH; Hsu C; Chen TF; Chen NQ; Chou HC; Tsao PN; Fan PC; Tsai IJ; Lin SP; Hsieh WS; Chang TM; Chen CN; Lee CH; Chou YY; Chiu PC; Tsai WH; Hsiung HC; Lai F; Lee NC
    Pediatr Crit Care Med; 2019 Nov; 20(11):1021-1026. PubMed ID: 31261230
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Diagnostic Utility of Whole Genome Sequencing After Negative Karyotyping/Chromosomal Microarray in Infants Born With Multiple Congenital Anomalies.
    Yang M; Kim JA; Jo HS; Park JH; Ahn SY; Sung SI; Park WS; Cho HW; Kim JM; Park MH; Park HY; Jang JH; Chang YS
    J Korean Med Sci; 2024 Sep; 39(36):e250. PubMed ID: 39315442
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Whole-Exome Sequencing and Whole-Genome Sequencing in Critically Ill Neonates Suspected to Have Single-Gene Disorders.
    Smith LD; Willig LK; Kingsmore SF
    Cold Spring Harb Perspect Med; 2015 Dec; 6(2):a023168. PubMed ID: 26684335
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test.
    Lionel AC; Costain G; Monfared N; Walker S; Reuter MS; Hosseini SM; Thiruvahindrapuram B; Merico D; Jobling R; Nalpathamkalam T; Pellecchia G; Sung WWL; Wang Z; Bikangaga P; Boelman C; Carter MT; Cordeiro D; Cytrynbaum C; Dell SD; Dhir P; Dowling JJ; Heon E; Hewson S; Hiraki L; Inbar-Feigenberg M; Klatt R; Kronick J; Laxer RM; Licht C; MacDonald H; Mercimek-Andrews S; Mendoza-Londono R; Piscione T; Schneider R; Schulze A; Silverman E; Siriwardena K; Snead OC; Sondheimer N; Sutherland J; Vincent A; Wasserman JD; Weksberg R; Shuman C; Carew C; Szego MJ; Hayeems RZ; Basran R; Stavropoulos DJ; Ray PN; Bowdin S; Meyn MS; Cohn RD; Scherer SW; Marshall CR
    Genet Med; 2018 Apr; 20(4):435-443. PubMed ID: 28771251
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Integrating rapid exome sequencing into NICU clinical care after a pilot research study.
    D'Gama AM; Del Rosario MC; Bresnahan MA; Yu TW; Wojcik MH; Agrawal PB
    NPJ Genom Med; 2022 Sep; 7(1):51. PubMed ID: 36064943
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Rapid exome sequencing in PICU patients with new-onset metabolic or neurological disorders.
    Carey AS; Schacht JP; Umandap C; Fasel D; Weng C; Cappell J; Chung WK; Kernie SG
    Pediatr Res; 2020 Nov; 88(5):761-768. PubMed ID: 32221475
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Phenotype-driven variant filtration strategy in exome sequencing toward a high diagnostic yield and identification of 85 novel variants in 400 patients with rare Mendelian disorders.
    Marinakis NM; Svingou M; Veltra D; Kekou K; Sofocleous C; Tilemis FN; Kosma K; Tsoutsou E; Fryssira H; Traeger-Synodinos J
    Am J Med Genet A; 2021 Aug; 185(8):2561-2571. PubMed ID: 34008892
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Rapid Paediatric Sequencing (RaPS): comprehensive real-life workflow for rapid diagnosis of critically ill children.
    Mestek-Boukhibar L; Clement E; Jones WD; Drury S; Ocaka L; Gagunashvili A; Le Quesne Stabej P; Bacchelli C; Jani N; Rahman S; Jenkins L; Hurst JA; Bitner-Glindzicz M; Peters M; Beales PL; Williams HJ
    J Med Genet; 2018 Nov; 55(11):721-728. PubMed ID: 30049826
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Laboratory investigations in genetic syndromes: examples of clinical approach in the neonatal unit.
    De Sanctis L; Giuffrè M
    Minerva Pediatr; 2010 Jun; 62(3 Suppl 1):193-5. PubMed ID: 21089740
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Genetic counseling in pediatric acute care: Reflections on ultra-rapid genomic diagnoses in neonates.
    Ayres S; Gallacher L; Stark Z; Brett GR
    J Genet Couns; 2019 Apr; 28(2):273-282. PubMed ID: 30663825
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Exome and Whole Genome Sequencing in the Neonatal Intensive Care Unit.
    Muriello M
    Clin Perinatol; 2022 Mar; 49(1):167-179. PubMed ID: 35209999
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Provision and availability of genomic medicine services in Level IV neonatal intensive care units.
    Wojcik MH; Callahan KP; Antoniou A; Del Rosario MC; Brunelli L; ElHassan NO; Gogcu S; Murthy K; Rumpel JA; Wambach JA; Suhrie K; Fishler K; Chaudhari BP
    Genet Med; 2023 Oct; 25(10):100926. PubMed ID: 37422715
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 28.