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 *

219 related articles for article (PubMed ID: 29080241)

  • 1. Next generation sequencing in pediatric hepatology and liver transplantation.
    Nicastro E; D'Antiga L
    Liver Transpl; 2018 Feb; 24(2):282-293. PubMed ID: 29080241
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Diagnosis of monogenic liver diseases in childhood by next-generation sequencing.
    Stalke A; Skawran B; Auber B; Illig T; Schlegelberger B; Junge N; Goldschmidt I; Leiskau C; von Neuhoff N; Baumann U; Pfister ED
    Clin Genet; 2018 Mar; 93(3):665-670. PubMed ID: 28776642
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Combining Panel-Based Next-Generation Sequencing and Exome Sequencing for Genetic Liver Diseases.
    Chen CB; Hsu JS; Chen PL; Wu JF; Li HY; Liou BY; Chang MH; Ni YH; Hwu WL; Chien YH; Chou YY; Yang YJ; Lee NC; Chen HL
    J Pediatr; 2023 Jul; 258():113408. PubMed ID: 37019333
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Metabolic liver diseases presenting with neonatal cholestasis: at the crossroad between old and new paradigms.
    Moreira-Silva H; Maio I; Bandeira A; Gomes-Martins E; Santos-Silva E
    Eur J Pediatr; 2019 Apr; 178(4):515-523. PubMed ID: 30693370
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Diagnosis of genetic disorders in childhood with next-generation sequencing].
    Menyhárt O; Győrffy B; Szabó A
    Orv Hetil; 2022 Dec; 163(51):2027-2040. PubMed ID: 36528826
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Performance of Next-Generation Sequencing for the Detection of Microsatellite Instability in Colorectal Cancer With Deficient DNA Mismatch Repair.
    Ratovomanana T; Cohen R; Svrcek M; Renaud F; Cervera P; Siret A; Letourneur Q; Buhard O; Bourgoin P; Guillerm E; Dorard C; Nicolle R; Ayadi M; Touat M; Bielle F; Sanson M; Le Rouzic P; Buisine MP; Piessen G; Collura A; Fléjou JF; de Reyniès A; Coulet F; Ghiringhelli F; André T; Jonchère V; Duval A
    Gastroenterology; 2021 Sep; 161(3):814-826.e7. PubMed ID: 33992635
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Relevance of next generation sequencing (NGS) data re-analysis in the diagnosis of monogenic diseases leading to organ failure.
    Saglia C; Bracciamà V; Trotta L; Mioli F; Faini AC; Brach Del Prever GM; Kalantari S; Luca M; Romeo CM; Scolari C; Peruzzi L; Calvo PL; Mussa A; Fenoglio R; Roccatello D; Alberti C; Carli D; Amoroso A; Deaglio S; Vaisitti T
    BMC Med Genomics; 2023 Nov; 16(1):303. PubMed ID: 38012624
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Next generation sequencing (NGS)-based approach to diagnosing Algerian patients with suspected inborn errors of immunity (IEIs).
    Peng XP; Al-Ddafari MS; Caballero-Oteyza A; El Mezouar C; Mrovecova P; Dib SE; Massen Z; Smahi MC; Faiza A; Hassaïne RT; Lefranc G; Aribi M; Grimbacher B
    Clin Immunol; 2023 Nov; 256():109758. PubMed ID: 37678716
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Clinical utility in infants with suspected monogenic conditions through next-generation sequencing.
    Hong S; Wang L; Zhao D; Zhang Y; Chen Y; Tan J; Liang L; Zhu T
    Mol Genet Genomic Med; 2019 Jun; 7(6):e684. PubMed ID: 30968598
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The combination of whole-exome sequencing and copy number variation sequencing enables the diagnosis of rare neurological disorders.
    Jiao Q; Sun H; Zhang H; Wang R; Li S; Sun D; Yang XA; Jin Y
    Clin Genet; 2019 Aug; 96(2):140-150. PubMed ID: 30945278
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Challenges of genetic diagnosis of inborn errors of metabolism in a major tertiary care center in Lebanon.
    Salman DO; Mahfouz R; Bitar ER; Samaha J; Karam PE
    Front Genet; 2022; 13():1029947. PubMed ID: 36468010
    [No Abstract]   [Full Text] [Related]  

  • 12. A scoping study to explore the cost-effectiveness of next-generation sequencing compared with traditional genetic testing for the diagnosis of learning disabilities in children.
    Beale S; Sanderson D; Sanniti A; Dundar Y; Boland A
    Health Technol Assess; 2015 Jun; 19(46):1-90. PubMed ID: 26132578
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Diagnostic Yield of an Algorithm for Neonatal and Infantile Cholestasis Integrating Next-Generation Sequencing.
    Nicastro E; Di Giorgio A; Marchetti D; Barboni C; Cereda A; Iascone M; D'Antiga L
    J Pediatr; 2019 Aug; 211():54-62.e4. PubMed ID: 31160058
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Hepatology Genome Rounds: An interdisciplinary approach to integrate genomic data into clinical practice.
    Chung DH; Zheng M; Bale AE; Vilarinho S
    J Hepatol; 2023 Oct; 79(4):1065-1071. PubMed ID: 37011712
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The added value of WES reanalysis in the field of genetic diagnosis: lessons learned from 200 exomes in the Lebanese population.
    Jalkh N; Corbani S; Haidar Z; Hamdan N; Farah E; Abou Ghoch J; Ghosn R; Salem N; Fawaz A; Djambas Khayat C; Rajab M; Mourani C; Moukarzel A; Rassi S; Gerbaka B; Mansour H; Baassiri M; Dagher R; Breich D; Mégarbané A; Desvignes JP; Delague V; Mehawej C; Chouery E
    BMC Med Genomics; 2019 Jan; 12(1):11. PubMed ID: 30665423
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Exome sequencing covers >98% of mutations identified on targeted next generation sequencing panels.
    LaDuca H; Farwell KD; Vuong H; Lu HM; Mu W; Shahmirzadi L; Tang S; Chen J; Bhide S; Chao EC
    PLoS One; 2017; 12(2):e0170843. PubMed ID: 28152038
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Diagnostics of Primary Immunodeficiencies through Next-Generation Sequencing.
    Gallo V; Dotta L; Giardino G; Cirillo E; Lougaris V; D'Assante R; Prandini A; Consolini R; Farrow EG; Thiffault I; Saunders CJ; Leonardi A; Plebani A; Badolato R; Pignata C
    Front Immunol; 2016; 7():466. PubMed ID: 27872624
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Do second generation sequencing techniques identify documented genetic markers for neonatal diabetes mellitus?
    Ali Khan I
    Heliyon; 2021 Sep; 7(9):e07903. PubMed ID: 34584998
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Guideline for the Evaluation of Cholestatic Jaundice in Infants: Joint Recommendations of the North American Society for Pediatric Gastroenterology, Hepatology, and Nutrition and the European Society for Pediatric Gastroenterology, Hepatology, and Nutrition.
    Fawaz R; Baumann U; Ekong U; Fischler B; Hadzic N; Mack CL; McLin VA; Molleston JP; Neimark E; Ng VL; Karpen SJ
    J Pediatr Gastroenterol Nutr; 2017 Jan; 64(1):154-168. PubMed ID: 27429428
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.