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 *

384 related articles for article (PubMed ID: 29950170)

  • 21. Parents' attitudes toward pediatric genetic testing for common disease risk.
    Tercyak KP; Hensley Alford S; Emmons KM; Lipkus IM; Wilfond BS; McBride CM
    Pediatrics; 2011 May; 127(5):e1288-95. PubMed ID: 21502235
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Delivering genome sequencing for rapid genetic diagnosis in critically ill children: parent and professional views, experiences and challenges.
    Hill M; Hammond J; Lewis C; Mellis R; Clement E; Chitty LS
    Eur J Hum Genet; 2020 Nov; 28(11):1529-1540. PubMed ID: 32561901
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Parental preferences toward genomic sequencing for non-medically actionable conditions in children: a discrete-choice experiment.
    Lewis MA; Stine A; Paquin RS; Mansfield C; Wood D; Rini C; Roche MI; Powell CM; Berg JS; Bailey DB
    Genet Med; 2018 Feb; 20(2):181-189. PubMed ID: 28771249
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Application of a next-generation sequencing (NGS) panel in newborn screening efficiently identifies inborn disorders of neonates.
    Huang X; Wu D; Zhu L; Wang W; Yang R; Yang J; He Q; Zhu B; You Y; Xiao R; Zhao Z
    Orphanet J Rare Dis; 2022 Feb; 17(1):66. PubMed ID: 35193651
    [TBL] [Abstract][Full Text] [Related]  

  • 25. The Reproductive Journey in the Genomic Era: From Preconception to Childhood.
    Garcia-Herrero S; Simon B; Garcia-Planells J
    Genes (Basel); 2020 Dec; 11(12):. PubMed ID: 33352697
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Parental interest in genomic sequencing of newborns: enrollment experience from the BabySeq Project.
    Genetti CA; Schwartz TS; Robinson JO; VanNoy GE; Petersen D; Pereira S; Fayer S; Peoples HA; Agrawal PB; Betting WN; Holm IA; McGuire AL; Waisbren SE; Yu TW; Green RC; Beggs AH; Parad RB;
    Genet Med; 2019 Mar; 21(3):622-630. PubMed ID: 30209271
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Expanding the Australian Newborn Blood Spot Screening Program using genomic sequencing: do we want it and are we ready?
    White S; Mossfield T; Fleming J; Barlow-Stewart K; Ghedia S; Dickson R; Richards F; Bombard Y; Wiley V
    Eur J Hum Genet; 2023 Jun; 31(6):703-711. PubMed ID: 36935418
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Public views on participating in newborn screening using genome sequencing.
    Bombard Y; Miller FA; Hayeems RZ; Barg C; Cressman C; Carroll JC; Wilson BJ; Little J; Avard D; Painter-Main M; Allanson J; Giguere Y; Chakraborty P
    Eur J Hum Genet; 2014 Nov; 22(11):1248-54. PubMed ID: 24549052
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Methods and feasibility study for exome sequencing as a universal second-tier test in newborn screening.
    Ruiz-Schultz N; Sant D; Norcross S; Dansithong W; Hart K; Asay B; Little J; Chung K; Oakeson KF; Young EL; Eilbeck K; Rohrwasser A
    Genet Med; 2021 Apr; 23(4):767-776. PubMed ID: 33442025
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Second-Tier Next Generation Sequencing Integrated in Nationwide Newborn Screening Provides Rapid Molecular Diagnostics of Severe Combined Immunodeficiency.
    Strand J; Gul KA; Erichsen HC; Lundman E; Berge MC; Trømborg AK; Sørgjerd LK; Ytre-Arne M; Hogner S; Halsne R; Gaup HJ; Osnes LT; Kro GAB; Sorte HS; Mørkrid L; Rowe AD; Tangeraas T; Jørgensen JV; Alme C; Bjørndalen TEH; Rønnestad AE; Lang AM; Rootwelt T; Buechner J; Øverland T; Abrahamsen TG; Pettersen RD; Stray-Pedersen A
    Front Immunol; 2020; 11():1417. PubMed ID: 32754152
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Parents' Experiences of Receiving the Initial Positive Newborn Screening (NBS) Result for Cystic Fibrosis and Sickle Cell Disease.
    Chudleigh J; Buckingham S; Dignan J; O'Driscoll S; Johnson K; Rees D; Wyatt H; Metcalfe A
    J Genet Couns; 2016 Dec; 25(6):1215-1226. PubMed ID: 27098418
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Views of children and young adults about Whole Genome Sequencing in newborn screening: a qualitative study.
    Parfett M; Johnson F; Bennett R; Ulph F
    Eur J Hum Genet; 2024 Sep; 32(9):1159-1165. PubMed ID: 38898203
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. Considering consent: a structural equation modelling analysis of factors influencing decisional quality when accepting newborn screening.
    Nicholls SG; Southern KW
    J Inherit Metab Dis; 2014 Mar; 37(2):197-205. PubMed ID: 24043381
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Parents' Perspectives on Supporting Their Decision Making in Genome-Wide Sequencing.
    Li KC; Birch PH; Garrett BM; MacPhee M; Adam S; Friedman JM
    J Nurs Scholarsh; 2016 May; 48(3):265-75. PubMed ID: 27061758
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Personal utility of genomic sequencing for infants with congenital deafness.
    Tutty E; Amor DJ; Jarmolowicz A; Paton K; Downie L
    Am J Med Genet A; 2021 Dec; 185(12):3634-3643. PubMed ID: 34184819
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Information and consent for newborn screening: practices and attitudes of service providers.
    Kerruish NJ; Webster D; Dickson N
    J Med Ethics; 2008 Sep; 34(9):648-52. PubMed ID: 18757632
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Parental attitudes regarding newborn screening of PKU and DMD.
    Campbell E; Ross LF
    Am J Med Genet A; 2003 Jul; 120A(2):209-14. PubMed ID: 12833401
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A genome sequencing system for universal newborn screening, diagnosis, and precision medicine for severe genetic diseases.
    Kingsmore SF; Smith LD; Kunard CM; Bainbridge M; Batalov S; Benson W; Blincow E; Caylor S; Chambers C; Del Angel G; Dimmock DP; Ding Y; Ellsworth K; Feigenbaum A; Frise E; Green RC; Guidugli L; Hall KP; Hansen C; Hobbs CA; Kahn SD; Kiel M; Van Der Kraan L; Krilow C; Kwon YH; Madhavrao L; Le J; Lefebvre S; Mardach R; Mowrey WR; Oh D; Owen MJ; Powley G; Scharer G; Shelnutt S; Tokita M; Mehtalia SS; Oriol A; Papadopoulos S; Perry J; Rosales E; Sanford E; Schwartz S; Tran D; Reese MG; Wright M; Veeraraghavan N; Wigby K; Willis MJ; Wolen AR; Defay T
    Am J Hum Genet; 2022 Sep; 109(9):1605-1619. PubMed ID: 36007526
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Parents' views on accepting, declining, and expanding newborn bloodspot screening.
    van der Pal SM; Wins S; Klapwijk JE; van Dijk T; Kater-Kuipers A; van der Ploeg CPB; Jans SMPJ; Kemp S; Verschoof-Puite RK; van den Bosch LJM; Henneman L
    PLoS One; 2022; 17(8):e0272585. PubMed ID: 35980961
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 20.