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 *

181 related articles for article (PubMed ID: 37794437)

  • 21. Current Trends in Genetics and Neonatal Care.
    Uveges MK; Holm IA
    Adv Neonatal Care; 2021 Dec; 21(6):473-481. PubMed ID: 33538495
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Folic acid supplementation and malaria susceptibility and severity among people taking antifolate antimalarial drugs in endemic areas.
    Crider K; Williams J; Qi YP; Gutman J; Yeung L; Mai C; Finkelstain J; Mehta S; Pons-Duran C; Menéndez C; Moraleda C; Rogers L; Daniels K; Green P
    Cochrane Database Syst Rev; 2022 Feb; 2(2022):. PubMed ID: 36321557
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Precision medicine in rare diseases: What is next?
    Tesi B; Boileau C; Boycott KM; Canaud G; Caulfield M; Choukair D; Hill S; Spielmann M; Wedell A; Wirta V; Nordgren A; Lindstrand A
    J Intern Med; 2023 Oct; 294(4):397-412. PubMed ID: 37211972
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A framework to start the debate on neonatal screening policies in the EU: an Expert Opinion Document.
    Cornel MC; Rigter T; Weinreich SS; Burgard P; Hoffmann GF; Lindner M; Gerard Loeber J; Rupp K; Taruscio D; Vittozzi L
    Eur J Hum Genet; 2014 Jan; 22(1):12-7. PubMed ID: 23652378
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Meeting Patients' Right to the Correct Diagnosis: Ongoing International Initiatives on Undiagnosed Rare Diseases and Ethical and Social Issues.
    Gainotti S; Mascalzoni D; Bros-Facer V; Petrini C; Floridia G; Roos M; Salvatore M; Taruscio D
    Int J Environ Res Public Health; 2018 Sep; 15(10):. PubMed ID: 30248891
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Newborn screening conditions: What we know, what we do not know, and how we will know it.
    Levy HL
    Genet Med; 2010 Dec; 12(12 Suppl):S213-4. PubMed ID: 21150366
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Challenges in the diagnosis and discovery of rare genetic disorders using contemporary sequencing technologies.
    Seaby EG; Ennis S
    Brief Funct Genomics; 2020 Jul; 19(4):243-258. PubMed ID: 32393978
    [TBL] [Abstract][Full Text] [Related]  

  • 28. USE OF GENOME DATA IN NEWBORNS AS A STARTING POINT FOR LIFE-LONG PRECISION MEDICINE.
    Brenner SE; Kingsmore S; Mooney SD; Nussbaum R; Puck J
    Pac Symp Biocomput; 2016; 21():568-75. PubMed ID: 26776219
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Massively Parallel Sequencing for Rare Genetic Disorders: Potential and Pitfalls.
    McInerney-Leo AM; Duncan EL
    Front Endocrinol (Lausanne); 2020; 11():628946. PubMed ID: 33679611
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Genomic newborn screening: Are we entering a new era of screening?
    Spiekerkoetter U; Bick D; Scott R; Hopkins H; Krones T; Gross ES; Bonham JR
    J Inherit Metab Dis; 2023 Sep; 46(5):778-795. PubMed ID: 37403863
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Availability of Genetic Tests in Public Health Services in Brazil: Data from the Brazilian Rare Diseases Network.
    de Oliveira BM; Neiva MB; Carvalho I; Schwartz IVD; Alves D; Felix TM;
    Public Health Genomics; 2023; 26(1):145-158. PubMed ID: 37356424
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Newborn Sequencing in Genomic Medicine and Public Health.
    Berg JS; Agrawal PB; Bailey DB; Beggs AH; Brenner SE; Brower AM; Cakici JA; Ceyhan-Birsoy O; Chan K; Chen F; Currier RJ; Dukhovny D; Green RC; Harris-Wai J; Holm IA; Iglesias B; Joseph G; Kingsmore SF; Koenig BA; Kwok PY; Lantos J; Leeder SJ; Lewis MA; McGuire AL; Milko LV; Mooney SD; Parad RB; Pereira S; Petrikin J; Powell BC; Powell CM; Puck JM; Rehm HL; Risch N; Roche M; Shieh JT; Veeraraghavan N; Watson MS; Willig L; Yu TW; Urv T; Wise AL
    Pediatrics; 2017 Feb; 139(2):. PubMed ID: 28096516
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Next-Generation Sequencing: The Translational Medicine Approach from "Bench to Bedside to Population".
    Beigh MM
    Medicines (Basel); 2016 Jun; 3(2):. PubMed ID: 28930123
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Solving patients with rare diseases through programmatic reanalysis of genome-phenome data.
    Matalonga L; Hernández-Ferrer C; Piscia D; ; Schüle R; Synofzik M; Töpf A; Vissers LELM; de Voer R; ; ; ; ; Tonda R; Laurie S; Fernandez-Callejo M; Picó D; Garcia-Linares C; Papakonstantinou A; Corvó A; Joshi R; Diez H; Gut I; Hoischen A; Graessner H; Beltran S;
    Eur J Hum Genet; 2021 Sep; 29(9):1337-1347. PubMed ID: 34075210
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Advancing Understanding of Inequities in Rare Disease Genomics.
    Serrano JG; O'Leary M; VanNoy GE; Mangilog BE; Holm IA; Fraiman YS; Rehm HL; O'Donnell-Luria A; Wojcik MH
    Clin Ther; 2023 Aug; 45(8):745-753. PubMed ID: 37517917
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Ethical issues with newborn screening in the genomics era.
    Tarini BA; Goldenberg AJ
    Annu Rev Genomics Hum Genet; 2012; 13():381-93. PubMed ID: 22559326
    [TBL] [Abstract][Full Text] [Related]  

  • 37. RD-Connect, NeurOmics and EURenOmics: collaborative European initiative for rare diseases.
    Lochmüller H; Badowska DM; Thompson R; Knoers NV; Aartsma-Rus A; Gut I; Wood L; Harmuth T; Durudas A; Graessner H; Schaefer F; Riess O; ; ;
    Eur J Hum Genet; 2018 Jun; 26(6):778-785. PubMed ID: 29487416
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Next-generation sequencing for diagnosis of rare diseases in the neonatal intensive care unit.
    Daoud H; Luco SM; Li R; Bareke E; Beaulieu C; Jarinova O; Carson N; Nikkel SM; Graham GE; Richer J; Armour C; Bulman DE; Chakraborty P; Geraghty M; Lines MA; Lacaze-Masmonteil T; Majewski J; Boycott KM; Dyment DA
    CMAJ; 2016 Aug; 188(11):E254-E260. PubMed ID: 27241786
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Implementation of a genomic medicine multi-disciplinary team approach for rare disease in the clinical setting: a prospective exome sequencing case series.
    Taylor J; Craft J; Blair E; Wordsworth S; Beeson D; Chandratre S; Cossins J; Lester T; Németh AH; Ormondroyd E; Patel SY; Pagnamenta AT; Taylor JC; Thomson KL; Watkins H; Wilkie AOM; Knight JC
    Genome Med; 2019 Jul; 11(1):46. PubMed ID: 31345272
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Genome Sequencing for Newborn Screening-An Effective Approach for Tackling Rare Diseases.
    Jiang S; Wang H; Gu Y
    JAMA Netw Open; 2023 Sep; 6(9):e2331141. PubMed ID: 37656463
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.