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 *

133 related articles for article (PubMed ID: 38205742)

  • 21. A cost-effectiveness analysis of genomic sequencing in a prospective versus historical cohort of complex pediatric patients.
    Yeung A; Tan NB; Tan TY; Stark Z; Brown N; Hunter MF; Delatycki M; Stutterd C; Savarirayan R; Mcgillivray G; Stapleton R; Kumble S; Downie L; Regan M; Lunke S; Chong B; Phelan D; Brett GR; Jarmolowicz A; Prawer Y; Valente G; Smagarinsky Y; Martyn M; McEwan C; Goranitis I; Gaff C; White SM
    Genet Med; 2020 Dec; 22(12):1986-1993. PubMed ID: 32773771
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Systematic evidence-based review: outcomes from exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability.
    Malinowski J; Miller DT; Demmer L; Gannon J; Pereira EM; Schroeder MC; Scheuner MT; Tsai AC; Hickey SE; Shen J;
    Genet Med; 2020 Jun; 22(6):986-1004. PubMed ID: 32203227
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Evaluation of the feasibility, diagnostic yield, and clinical utility of rapid genome sequencing in infantile epilepsy (Gene-STEPS): an international, multicentre, pilot cohort study.
    D'Gama AM; Mulhern S; Sheidley BR; Boodhoo F; Buts S; Chandler NJ; Cobb J; Curtis M; Higginbotham EJ; Holland J; Khan T; Koh J; Liang NSY; McRae L; Nesbitt SE; Oby BT; Paternoster B; Patton A; Rose G; Scotchman E; Valentine R; Wiltrout KN; ; ; Hayeems RZ; Jain P; Lunke S; Marshall CR; Rockowitz S; Sebire NJ; Stark Z; White SM; Chitty LS; Cross JH; Scheffer IE; Chau V; Costain G; Poduri A; Howell KB; McTague A
    Lancet Neurol; 2023 Sep; 22(9):812-825. PubMed ID: 37596007
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Systematic evaluation of genome sequencing for the diagnostic assessment of autism spectrum disorder and fetal structural anomalies.
    Lowther C; Valkanas E; Giordano JL; Wang HZ; Currall BB; O'Keefe K; Pierce-Hoffman E; Kurtas NE; Whelan CW; Hao SP; Weisburd B; Jalili V; Fu J; Wong I; Collins RL; Zhao X; Austin-Tse CA; Evangelista E; Lemire G; Aggarwal VS; Lucente D; Gauthier LD; Tolonen C; Sahakian N; Stevens C; An JY; Dong S; Norton ME; MacKenzie TC; Devlin B; Gilmore K; Powell BC; Brandt A; Vetrini F; DiVito M; Sanders SJ; MacArthur DG; Hodge JC; O'Donnell-Luria A; Rehm HL; Vora NL; Levy B; Brand H; Wapner RJ; Talkowski ME
    Am J Hum Genet; 2023 Sep; 110(9):1454-1469. PubMed ID: 37595579
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Genome-Wide Sequencing Modalities for Children with Unexplained Global Developmental Delay and Intellectual Disabilities-A Narrative Review.
    Ko MH; Chen HJ
    Children (Basel); 2023 Mar; 10(3):. PubMed ID: 36980059
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Cost-Effectiveness of Targeted Exome Analysis as a Diagnostic Test in Glomerular Diseases.
    Jayasinghe K; Wu Y; Stark Z; Kerr PG; Mallett AJ; Gaff C; Martyn M; Goranitis I; Quinlan C
    Kidney Int Rep; 2021 Nov; 6(11):2850-2861. PubMed ID: 34805637
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Retrospective analysis supports algorithm as efficient diagnostic approach to treatable intellectual developmental disabilities.
    Sayson B; Popurs MA; Lafek M; Berkow R; Stockler-Ipsiroglu S; van Karnebeek CD
    Mol Genet Metab; 2015 May; 115(1):1-9. PubMed ID: 25801009
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Real-world patient-level cost-effectiveness analysis of omalizumab in patients with severe allergic asthma treated in four major medical centers in Turkey.
    Tugay D; Top M; Aydin Ö; Bavbek S; Damadoğlu E; Öner Erkekol F; Koca Kalkan I; Kalyoncu AF; Karakaya G; Oğuzülgen IK; Türktaş H; Abraham I
    J Med Econ; 2023; 26(1):720-730. PubMed ID: 37129881
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Long-term economic impacts of exome sequencing for suspected monogenic disorders: diagnosis, management, and reproductive outcomes.
    Schofield D; Rynehart L; Shresthra R; White SM; Stark Z
    Genet Med; 2019 Nov; 21(11):2586-2593. PubMed ID: 31110331
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Case for genome sequencing in infants and children with rare, undiagnosed or genetic diseases.
    Bick D; Jones M; Taylor SL; Taft RJ; Belmont J
    J Med Genet; 2019 Dec; 56(12):783-791. PubMed ID: 31023718
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Exome sequencing as the first-tier test for pediatric respiratory diseases: A single-center study.
    Hao C; Guo R; Liu J; Hu X; Guo J; Yao Y; Zhao Z; Qi Z; Yin J; Chen L; Wang H; Xu B; Li W
    Hum Mutat; 2021 Jul; 42(7):891-900. PubMed ID: 33942430
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Molecular Diagnostic Yield of Exome Sequencing and Chromosomal Microarray in Short Stature: A Systematic Review and Meta-Analysis.
    Li Q; Chen Z; Wang J; Xu K; Fan X; Gong C; Wu Z; Zhang TJ; Wu N
    JAMA Pediatr; 2023 Nov; 177(11):1149-1157. PubMed ID: 37695591
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Exome and genome sequencing in a heterogeneous population of patients with rare disease: Identifying predictors of a diagnosis.
    Pucel J; Briere LC; Reuter C; Gochyyev P; ; LeBlanc K
    Genet Med; 2024 Jun; 26(6):101115. PubMed ID: 38436216
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Exome Sequencing for Prenatal Detection of Genetic Abnormalities in Fetal Ultrasound Anomalies: An Economic Evaluation.
    Kodabuckus SS; Quinlan-Jones E; McMullan DJ; Maher ER; Hurles ME; Barton PM; Kilby MD
    Fetal Diagn Ther; 2020; 47(7):554-564. PubMed ID: 31962312
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Cost-effectiveness of whole-exome sequencing in progressive neurological disorders of children.
    Aaltio J; Hyttinen V; Kortelainen M; Frederix GWJ; Lönnqvist T; Suomalainen A; Isohanni P
    Eur J Paediatr Neurol; 2022 Jan; 36():30-36. PubMed ID: 34852981
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Optimising Exome Prenatal Sequencing Services (EXPRESS): a study protocol to evaluate rapid prenatal exome sequencing in the NHS Genomic Medicine Service.
    Hill M; Ellard S; Fisher J; Fulop N; Knight M; Kroese M; Ledger J; Leeson-Beevers K; McEwan A; McMullan D; Mellis R; Morris S; Parker M; Tapon D; Baple E; Blackburn L; Choudry A; Lafarge C; McInnes-Dean H; Peter M; Ramakrishnan R; Roberts L; Searle B; Smith E; Walton H; Wynn SL; Han Wu W; Chitty LS
    NIHR Open Res; 2022; 2():10. PubMed ID: 35935673
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Limitations of exome sequencing in detecting rare and undiagnosed diseases.
    Burdick KJ; Cogan JD; Rives LC; Robertson AK; Koziura ME; Brokamp E; Duncan L; Hannig V; Pfotenhauer J; Vanzo R; Paul MS; Bican A; Morgan T; Duis J; Newman JH; Hamid R; Phillips JA;
    Am J Med Genet A; 2020 Jun; 182(6):1400-1406. PubMed ID: 32190976
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Exome/Genome-Wide Testing in Newborn Screening: A Proportionate Path Forward.
    Rahimzadeh V; Friedman JM; de Wert G; Knoppers BM
    Front Genet; 2022; 13():865400. PubMed ID: 35860465
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Genetic Counseling and Genome Sequencing in Pediatric Rare Disease.
    Elliott AM
    Cold Spring Harb Perspect Med; 2020 Mar; 10(3):. PubMed ID: 31501267
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 7.