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 *

205 related articles for article (PubMed ID: 35961607)

  • 21. [Epidemiology and genetics of congenital heart diseases and cardiomyopathies in children].
    Bonnet D
    Rev Prat; 2006 Mar; 56(6):599-604. PubMed ID: 16705916
    [TBL] [Abstract][Full Text] [Related]  

  • 22. An update on the molecular diagnosis of congenital heart disease: focus on loss-of-function mutations.
    Li YJ; Yang YQ
    Expert Rev Mol Diagn; 2017 Apr; 17(4):393-401. PubMed ID: 28274167
    [TBL] [Abstract][Full Text] [Related]  

  • 23. How do we define congenital heart defects for scientific studies?
    Garne E; Olsen MS; Johnsen SP; Hjortdal V; Andersen HØ; Nissen H; Søndergaard L; Videbaek J;
    Congenit Heart Dis; 2012; 7(1):46-9. PubMed ID: 22010848
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Appropriate Use of Genetic Testing in Congenital Heart Disease Patients.
    Ito S; Chapman KA; Kisling M; John AS
    Curr Cardiol Rep; 2017 Mar; 19(3):24. PubMed ID: 28224467
    [TBL] [Abstract][Full Text] [Related]  

  • 25. The genetics of isolated congenital heart disease.
    Nees SN; Chung WK
    Am J Med Genet C Semin Med Genet; 2020 Mar; 184(1):97-106. PubMed ID: 31876989
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A Comprehensive Clinical Genetics Approach to Critical Congenital Heart Disease in Infancy.
    Shikany AR; Landis BJ; Parrott A; Miller EM; Coyan A; Walters L; Hinton RB; Goldenberg P; Ware SM
    J Pediatr; 2020 Dec; 227():231-238.e14. PubMed ID: 32717230
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Genetics of congenital heart disease: the contribution of the noncoding regulatory genome.
    Postma AV; Bezzina CR; Christoffels VM
    J Hum Genet; 2016 Jan; 61(1):13-9. PubMed ID: 26223183
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Genetic characterisation of 22q11.2 variations and prevalence in patients with congenital heart disease.
    Hou HT; Chen HX; Wang XL; Yuan C; Yang Q; Liu ZG; He GW
    Arch Dis Child; 2020 Apr; 105(4):367-374. PubMed ID: 31666243
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Genetics of congenital heart disease: the glass half empty.
    Fahed AC; Gelb BD; Seidman JG; Seidman CE
    Circ Res; 2013 Feb; 112(4):707-20. PubMed ID: 23410880
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Changing prevalence of severe congenital heart disease: Results from the National Register for Congenital Heart Defects in Germany.
    Pfitzer C; Helm PC; Ferentzi H; Rosenthal LM; Bauer UMM; Berger F; Schmitt KRL
    Congenit Heart Dis; 2017 Dec; 12(6):787-793. PubMed ID: 28719142
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Syndromic Hirschsprung's disease and associated congenital heart disease: a systematic review.
    Duess JW; Puri P
    Pediatr Surg Int; 2015 Aug; 31(8):781-5. PubMed ID: 26156879
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The prevalence of adult congenital heart disease, results from a systematic review and evidence based calculation.
    van der Bom T; Bouma BJ; Meijboom FJ; Zwinderman AH; Mulder BJ
    Am Heart J; 2012 Oct; 164(4):568-75. PubMed ID: 23067916
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Integration of Large-Scale Genomic Data Sources With Evolutionary History Reveals Novel Genetic Loci for Congenital Heart Disease.
    Fotiou E; Williams S; Martin-Geary A; Robertson DL; Tenin G; Hentges KE; Keavney B
    Circ Genom Precis Med; 2019 Oct; 12(10):442-451. PubMed ID: 31613678
    [TBL] [Abstract][Full Text] [Related]  

  • 34. PharmGKB, an Integrated Resource of Pharmacogenomic Knowledge.
    Gong L; Whirl-Carrillo M; Klein TE
    Curr Protoc; 2021 Aug; 1(8):e226. PubMed ID: 34387941
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Copy number variant analysis for syndromic congenital heart disease in the Chinese population.
    Li P; Chen W; Li M; Zhao Z; Feng Z; Gao H; Suo M; Xu Z; Tian G; Wu F; Wei S; Huang G
    Hum Genomics; 2022 Oct; 16(1):51. PubMed ID: 36316717
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Identification of Novel Congenital Heart Disease Candidate Genes Using Chromosome Microarray.
    Shanshen E; Rosenberg J; Van Bergen AH
    Pediatr Cardiol; 2018 Jan; 39(1):148-159. PubMed ID: 28993849
    [TBL] [Abstract][Full Text] [Related]  

  • 37. The birth prevalence, severity, and temporal trends of congenital heart disease in the middle-income country: A population-based study.
    Mat Bah MN; Sapian MH; Jamil MT; Abdullah N; Alias EY; Zahari N
    Congenit Heart Dis; 2018 Nov; 13(6):1012-1027. PubMed ID: 30289622
    [TBL] [Abstract][Full Text] [Related]  

  • 38. New Insights into the Impact of Genome-Wide Copy Number Variations on Complex Congenital Heart Disease in Saudi Arabia.
    Dasouki MJ; Wakil SM; Al-Harazi O; Alkorashy M; Muiya NP; Andres E; Hagos S; Aldusery H; Dzimiri N; Colak D
    OMICS; 2020 Jan; 24(1):16-28. PubMed ID: 31855513
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Systems genetics analysis identifies calcium-signaling defects as novel cause of congenital heart disease.
    Izarzugaza JMG; Ellesøe SG; Doganli C; Ehlers NS; Dalgaard MD; Audain E; Dombrowsky G; Banasik K; Sifrim A; Wilsdon A; Thienpont B; Breckpot J; Gewillig M; ; Brook JD; Hitz MP; Larsen LA; Brunak S
    Genome Med; 2020 Aug; 12(1):76. PubMed ID: 32859249
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [The competence network for congenital heart defects. Networking instead of isolated efforts for optimized research and care].
    Bauer U; Niggemeyer E; Lange PE
    Med Klin (Munich); 2006 Sep; 101(9):753-8. PubMed ID: 16977402
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.