BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

142 related articles for article (PubMed ID: 29291004)

  • 1. Whole exome sequencing identifies novel mutation in eight Chinese children with isolated tetralogy of Fallot.
    Liu L; Wang HD; Cui CY; Qin YY; Fan TB; Peng BT; Zhang LZ; Wang CZ
    Oncotarget; 2017 Dec; 8(63):106976-106988. PubMed ID: 29291004
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot.
    Page DJ; Miossec MJ; Williams SG; Monaghan RM; Fotiou E; Cordell HJ; Sutcliffe L; Topf A; Bourgey M; Bourque G; Eveleigh R; Dunwoodie SL; Winlaw DS; Bhattacharya S; Breckpot J; Devriendt K; Gewillig M; Brook JD; Setchfield KJ; Bu'Lock FA; O'Sullivan J; Stuart G; Bezzina CR; Mulder BJM; Postma AV; Bentham JR; Baron M; Bhaskar SS; Black GC; Newman WG; Hentges KE; Lathrop GM; Santibanez-Koref M; Keavney BD
    Circ Res; 2019 Feb; 124(4):553-563. PubMed ID: 30582441
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Whole exome sequencing identifies novel inherited genetic variants in tetralogy of Fallot.
    Pan Y; Liu M; Zhang S; Mei H; Wu J
    J Thorac Dis; 2022 Aug; 14(8):3008-3015. PubMed ID: 36071769
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Whole-exome sequencing revealed novel genetic alterations in patients with tetralogy of Fallot.
    Pan Y; Liu M; Zhang S; Mei H; Wu J
    Transl Pediatr; 2023 Oct; 12(10):1835-1841. PubMed ID: 37969115
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Case Report: Tetralogy of Fallot in a Chinese Family Caused by a Novel Missense Variant of
    Wang J; Wang C; Xie H; Feng X; Wei L; Wang B; Li T; Pi M; Gong L
    Front Cardiovasc Med; 2022; 9():863650. PubMed ID: 35872890
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A Targeted, Next-Generation Genetic Sequencing Study on Tetralogy of Fallot, Combined With Cleft Lip and Palate.
    Liu L; Bu H; Yang Y; Tan Z; Zhang F; Hu S; Zhao T
    J Craniofac Surg; 2017 Jun; 28(4):e351-e355. PubMed ID: 28230599
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Whole-Exome Sequencing Reveals a Novel Mutation of FLNA Gene in an Iranian Family with Nonsyndromic Tetralogy of Fallot.
    Kalayinia S; Maleki M; Mahdavi M; Mahdieh N
    Lab Med; 2021 Nov; 52(6):614-618. PubMed ID: 33942857
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Family-based whole-genome sequencing identifies compound heterozygous protein-coding and noncoding mutations in tetralogy of Fallot.
    Wang Y; Jiang T; Tang P; Wu Y; Jiang Z; Dai J; Gu Y; Xu J; Da M; Ma H; Jin G; Mo X; Li Q; Wang X; Hu Z
    Gene; 2020 May; 741():144555. PubMed ID: 32165302
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Sequencing of a Chinese tetralogy of Fallot cohort reveals clustering mutations in myogenic heart progenitors.
    Tang CSM; Mononen M; Lam WY; Jin SC; Zhuang X; Garcia-Barcelo MM; Lin Q; Yang Y; Sahara M; Eroglu E; Chien KR; Hong H; Tam PKH; Gruber PJ
    JCI Insight; 2022 Jan; 7(2):. PubMed ID: 34905512
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Tetralogy of Fallot and Hypoplastic Left Heart Syndrome - Complex Clinical Phenotypes Meet Complex Genetic Networks.
    Lahm H; Schön P; Doppler S; Dreßen M; Cleuziou J; Deutsch MA; Ewert P; Lange R; Krane M
    Curr Genomics; 2015 Jun; 16(3):141-58. PubMed ID: 26069455
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Outlier-based identification of copy number variations using targeted resequencing in a small cohort of patients with Tetralogy of Fallot.
    Bansal V; Dorn C; Grunert M; Klaassen S; Hetzer R; Berger F; Sperling SR
    PLoS One; 2014; 9(1):e85375. PubMed ID: 24400131
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Peritoneal dialysis in an adult patient with tetralogy of Fallot diagnosed with incomplete Alagille syndrome.
    Ponikowska M; Pollak A; Kotwica-Strzalek E; Brodowska-Kania D; Mosakowska M; Ploski R; Niemczyk S
    BMC Med Genet; 2020 Oct; 21(1):195. PubMed ID: 33008311
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Loss of function in
    Kruszka P; Tanpaiboon P; Neas K; Crosby K; Berger SI; Martinez AF; Addissie YA; Pongprot Y; Sittiwangkul R; Silvilairat S; Makonkawkeyoon K; Yu L; Wynn J; Bennett JT; Mefford HC; Reynolds WT; Liu X; Mommersteeg MTM; Chung WK; Lo CW; Muenke M
    J Med Genet; 2017 Dec; 54(12):825-829. PubMed ID: 28592524
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Identification of a de novo LRP1 mutation in a Saudi family with Tetralogy of Fallot.
    Alrayes N; Mallah BA; Issa NM; Banaganapalli B; Ahmad Shaik N; Nasser KK; Alshehri BA; Bhuiyan ZA; Bdier AY; Al-Aama JY
    Gene; 2023 Jan; 851():146909. PubMed ID: 36162527
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mutations in genes related to myocyte contraction and ventricular septum development in non-syndromic tetralogy of Fallot.
    Harvey DC; Verma R; Sedaghat B; Hjelm BE; Morton SU; Seidman JG; Kumar SR
    Front Cardiovasc Med; 2023; 10():1249605. PubMed ID: 37840956
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Joint analysis of functionally related genes yields further candidates associated with Tetralogy of Fallot.
    Chelu A; Williams SG; Keavney BD; Talavera D
    J Hum Genet; 2022 Oct; 67(10):613-615. PubMed ID: 35718831
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Role of fibrillin-1 genetic mutations and polymorphism in aortic dilatation in patients undergoing intracardiac repair of tetralogy of Fallot.
    Chowdhury UK; Mishra AK; Balakrishnan P; Sharma S; Kabra M; Ray R; Kalaivani M; Gupta R; Govindappa RM; Subramaniam GK
    J Thorac Cardiovasc Surg; 2008 Sep; 136(3):757-66, 766.e1-10. PubMed ID: 18805282
    [TBL] [Abstract][Full Text] [Related]  

  • 19. San Luis Valley recombinant chromosome 8 and tetralogy of Fallot: a review of chromosome 8 anomalies and congenital heart disease.
    Gelb BD; Towbin JA; McCabe ER; Sujansky E
    Am J Med Genet; 1991 Sep; 40(4):471-6. PubMed ID: 1746613
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The aortic arch in tetralogy of Fallot: types of branching and clinical implications.
    Prabhu S; Kasturi S; Mehra S; Tiwari R; Joshi A; John C; Karl TR
    Cardiol Young; 2020 Aug; 30(8):1144-1150. PubMed ID: 32638692
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.