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 *

141 related articles for article (PubMed ID: 38521975)

  • 1. Diagnostic yield after next-generation sequencing in pediatric cardiovascular disease.
    Slavotinek AM; Thompson ML; Martin LJ; Gelb BD
    HGG Adv; 2024 Jul; 5(3):100286. PubMed ID: 38521975
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genetic Evaluation of Inpatient Neonatal and Infantile Congenital Heart Defects: New Findings and Review of the Literature.
    Helm BM; Landis BJ; Ware SM
    Genes (Basel); 2021 Aug; 12(8):. PubMed ID: 34440418
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetic testing practices in infants with congenital heart disease.
    Connor JA; Hinton RB; Miller EM; Sund KL; Ruschman JG; Ware SM
    Congenit Heart Dis; 2014; 9(2):158-67. PubMed ID: 23782710
    [TBL] [Abstract][Full Text] [Related]  

  • 4. COngenital heart disease and the Diagnostic yield with Exome sequencing (CODE) study: prospective cohort study and systematic review.
    Mone F; Eberhardt RY; Morris RK; Hurles ME; McMullan DJ; Maher ER; Lord J; Chitty LS; Giordano JL; Wapner RJ; Kilby MD;
    Ultrasound Obstet Gynecol; 2021 Jan; 57(1):43-51. PubMed ID: 32388881
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Utilization of Whole Exome Sequencing to Identify Causative Mutations in Familial Congenital Heart Disease.
    LaHaye S; Corsmeier D; Basu M; Bowman JL; Fitzgerald-Butt S; Zender G; Bosse K; McBride KL; White P; Garg V
    Circ Cardiovasc Genet; 2016 Aug; 9(4):320-9. PubMed ID: 27418595
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The Congenital Heart Disease Genetic Network Study: rationale, design, and early results.
    ; Gelb B; Brueckner M; Chung W; Goldmuntz E; Kaltman J; Kaski JP; Kim R; Kline J; Mercer-Rosa L; Porter G; Roberts A; Rosenberg E; Seiden H; Seidman C; Sleeper L; Tennstedt S; Kaltman J; Schramm C; Burns K; Pearson G; Rosenberg E
    Circ Res; 2013 Feb; 112(4):698-706. PubMed ID: 23410879
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Comprehensive evaluation of genetic variants using chromosomal microarray analysis and exome sequencing in fetuses with congenital heart defect.
    Qiao F; Wang Y; Zhang C; Zhou R; Wu Y; Wang C; Meng L; Mao P; Cheng Q; Luo C; Hu P; Xu Z
    Ultrasound Obstet Gynecol; 2021 Sep; 58(3):377-387. PubMed ID: 33142350
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinical utility of exome sequencing in infantile heart failure.
    Ritter A; Bedoukian E; Berger JH; Copenheaver D; Gray C; Krantz I; Izumi K; Juusola J; Leonard J; Lin K; Medne L; Santani A; Skraban C; Yang S; Ahrens-Nicklas RC
    Genet Med; 2020 Feb; 22(2):423-426. PubMed ID: 31527676
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic aetiology distribution of 398 foetuses with congenital heart disease in the prenatal setting.
    Yi T; Hao X; Sun H; Zhang Y; Han J; Gu X; Sun L; Liu X; Zhao Y; Guo Y; Zhou X; He Y
    ESC Heart Fail; 2023 Apr; 10(2):917-930. PubMed ID: 36478645
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Clinical application of targeted next-generation sequencing in fetuses with congenital heart defect.
    Hu P; Qiao F; Wang Y; Meng L; Ji X; Luo C; Xu T; Zhou R; Zhang J; Yu B; Wang L; Wang T; Pan Q; Ma D; Liang D; Xu Z
    Ultrasound Obstet Gynecol; 2018 Aug; 52(2):205-211. PubMed ID: 29536580
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Chromosome microarray testing for patients with congenital heart defects reveals novel disease causing loci and high diagnostic yield.
    Geng J; Picker J; Zheng Z; Zhang X; Wang J; Hisama F; Brown DW; Mullen MP; Harris D; Stoler J; Seman A; Miller DT; Fu Q; Roberts AE; Shen Y
    BMC Genomics; 2014 Dec; 15(1):1127. PubMed ID: 25516202
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. TAB2 variants cause cardiovascular heart disease, connective tissue disorder, and developmental delay.
    Hanson J; Brezavar D; Hughes S; Amudhavalli S; Fleming E; Zhou D; Alaimo JT; Bonnen PE
    Clin Genet; 2022 Feb; 101(2):214-220. PubMed ID: 34741306
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Focused Exome Sequencing Gives a High Diagnostic Yield in the Indian Subcontinent.
    Duraisamy AJ; Liu R; Sureshkumar S; Rose R; Jagannathan L; da Silva C; Coovadia A; Ramachander V; Chandrasekar S; Raja I; Sajnani M; Selvaraj SM; Narang B; Darvishi K; Bhayal AC; Katikala L; Guo F; Chen-Deutsch X; Balciuniene J; Ma Z; Nallamilli BRR; Bean L; Collins C; Hegde M
    J Mol Diagn; 2024 Jun; 26(6):510-519. PubMed ID: 38582400
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Utility of genetic evaluation in infants with congenital heart defects admitted to the cardiac intensive care unit.
    Ahrens-Nicklas RC; Khan S; Garbarini J; Woyciechowski S; D'Alessandro L; Zackai EH; Deardorff MA; Goldmuntz E
    Am J Med Genet A; 2016 Dec; 170(12):3090-3097. PubMed ID: 27605484
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Lessons from exome sequencing in prenatally diagnosed heart defects: A basis for prenatal testing.
    Westphal DS; Leszinski GS; Rieger-Fackeldey E; Graf E; Weirich G; Meitinger T; Ostermayer E; Oberhoffer R; Wagner M
    Clin Genet; 2019 May; 95(5):582-589. PubMed ID: 30868567
    [TBL] [Abstract][Full Text] [Related]  

  • 17. High-Throughput Genomics Identify Novel
    Zodanu GKE; Hwang JH; Mehta Z; Sisniega C; Barsegian A; Kang X; Biniwale R; Si MS; Satou GM; Halnon N; Ucla Congenital Heart Defect BioCore Faculty ; Grody WW; Van Arsdell GS; Nelson SF; Touma M
    Int J Mol Sci; 2024 May; 25(10):. PubMed ID: 38791509
    [TBL] [Abstract][Full Text] [Related]  

  • 18. From genes to therapy: A comprehensive exploration of congenital heart disease through the lens of genetics and emerging technologies.
    Nawaz K; Alifah N; Hussain T; Hameed H; Ali H; Hamayun S; Mir A; Wahab A; Naeem M; Zakria M; Pakki E; Hasan N
    Curr Probl Cardiol; 2024 Sep; 49(9):102726. PubMed ID: 38944223
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Exome sequencing in multiplex families with left-sided cardiac defects has high yield for disease gene discovery.
    Gordon DM; Cunningham D; Zender G; Lawrence PJ; Penaloza JS; Lin H; Fitzgerald-Butt SM; Myers K; Duong T; Corsmeier DJ; Gaither JB; Kuck HC; Wijeratne S; Moreland B; Kelly BJ; ; Garg V; White P; McBride KL
    PLoS Genet; 2022 Jun; 18(6):e1010236. PubMed ID: 35737725
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Yield rate of chromosomal microarray analysis in fetuses with congenital heart defects.
    Turan S; Asoglu MR; Gabbay-Benziv R; Doyle L; Harman C; Turan OM
    Eur J Obstet Gynecol Reprod Biol; 2018 Feb; 221():172-176. PubMed ID: 29306563
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.