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 *

271 related articles for article (PubMed ID: 20012542)

  • 1. Molecular genetics of congenital atrial septal defects.
    Posch MG; Perrot A; Berger F; Ozcelik C
    Clin Res Cardiol; 2010 Mar; 99(3):137-47. PubMed ID: 20012542
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Cardiac alpha-myosin (MYH6) is the predominant sarcomeric disease gene for familial atrial septal defects.
    Posch MG; Waldmuller S; Müller M; Scheffold T; Fournier D; Andrade-Navarro MA; De Geeter B; Guillaumont S; Dauphin C; Yousseff D; Schmitt KR; Perrot A; Berger F; Hetzer R; Bouvagnet P; Özcelik C
    PLoS One; 2011; 6(12):e28872. PubMed ID: 22194935
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A gain-of-function TBX20 mutation causes congenital atrial septal defects, patent foramen ovale and cardiac valve defects.
    Posch MG; Gramlich M; Sunde M; Schmitt KR; Lee SH; Richter S; Kersten A; Perrot A; Panek AN; Al Khatib IH; Nemer G; Mégarbané A; Dietz R; Stiller B; Berger F; Harvey RP; Ozcelik C
    J Med Genet; 2010 Apr; 47(4):230-5. PubMed ID: 19762328
    [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. Severity and recurrence risk of congenital heart defects exemplified by atrial septal defect secundum.
    Gold RJ; Rose V; Yau Y
    Clin Genet; 1987 Sep; 32(3):148-55. PubMed ID: 3621660
    [TBL] [Abstract][Full Text] [Related]  

  • 6. PITX2c loss-of-function mutations responsible for congenital atrial septal defects.
    Yuan F; Zhao L; Wang J; Zhang W; Li X; Qiu XB; Li RG; Xu YJ; Xu L; Qu XK; Fang WY; Yang YQ
    Int J Med Sci; 2013; 10(10):1422-9. PubMed ID: 23983605
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Clinical and molecular characterisation of Holt-Oram syndrome focusing on cardiac manifestations.
    Jhang WK; Lee BH; Kim GH; Lee JO; Yoo HW
    Cardiol Young; 2015 Aug; 25(6):1093-8. PubMed ID: 25216260
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mutational spectrum in the cardiac transcription factor gene NKX2.5 (CSX) associated with congenital heart disease.
    Stallmeyer B; Fenge H; Nowak-Göttl U; Schulze-Bahr E
    Clin Genet; 2010 Dec; 78(6):533-40. PubMed ID: 20456451
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Familial recurrence of congenital heart disease in patients with ostium secundum atrial septal defect.
    Caputo S; Capozzi G; Russo MG; Esposito T; Martina L; Cardaropoli D; Ricci C; Argiento P; Pacileo G; Calabrò R
    Eur Heart J; 2005 Oct; 26(20):2179-84. PubMed ID: 15980033
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A novel variant in TBX20 (p.D176N) identified by whole-exome sequencing in combination with a congenital heart disease related gene filter is associated with familial atrial septal defect.
    Liu JJ; Fan LL; Chen JL; Tan ZP; Yang YF
    J Zhejiang Univ Sci B; 2014 Sep; 15(9):830-7. PubMed ID: 25183037
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Alpha-cardiac myosin heavy chain (MYH6) mutations affecting myofibril formation are associated with congenital heart defects.
    Granados-Riveron JT; Ghosh TK; Pope M; Bu'Lock F; Thornborough C; Eason J; Kirk EP; Fatkin D; Feneley MP; Harvey RP; Armour JA; David Brook J
    Hum Mol Genet; 2010 Oct; 19(20):4007-16. PubMed ID: 20656787
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Bridging the gap between anatomy and molecular genetics for an improved understanding of congenital heart disease.
    Reamon-Buettner SM; Spanel-Borowski K; Borlak J
    Ann Anat; 2006 May; 188(3):213-20. PubMed ID: 16711160
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Congenital heart diseases and their association with the variant distribution features on susceptibility genes.
    Su W; Zhu P; Wang R; Wu Q; Wang M; Zhang X; Mei L; Tang J; Kumar M; Wang X; Su L; Dong N
    Clin Genet; 2017 Mar; 91(3):349-354. PubMed ID: 27426723
    [TBL] [Abstract][Full Text] [Related]  

  • 14. R25C mutation in the NKX2.5 gene in Italian patients affected with non-syndromic and syndromic congenital heart disease.
    Beffagna G; Cecchetto A; Dal Bianco L; Lorenzon A; Angelini A; Padalino M; Vida V; Bhattacharya S; Stellin G; Rampazzo A; Daliento L
    J Cardiovasc Med (Hagerstown); 2013 Aug; 14(8):582-6. PubMed ID: 22964646
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16.
    Cordell HJ; Bentham J; Topf A; Zelenika D; Heath S; Mamasoula C; Cosgrove C; Blue G; Granados-Riveron J; Setchfield K; Thornborough C; Breckpot J; Soemedi R; Martin R; Rahman TJ; Hall D; van Engelen K; Moorman AF; Zwinderman AH; Barnett P; Koopmann TT; Adriaens ME; Varro A; George AL; dos Remedios C; Bishopric NH; Bezzina CR; O'Sullivan J; Gewillig M; Bu'Lock FA; Winlaw D; Bhattacharya S; Devriendt K; Brook JD; Mulder BJ; Mital S; Postma AV; Lathrop GM; Farrall M; Goodship JA; Keavney BD
    Nat Genet; 2013 Jul; 45(7):822-4. PubMed ID: 23708191
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Congenital heart defects in molecularly proven Kabuki syndrome patients.
    Digilio MC; Gnazzo M; Lepri F; Dentici ML; Pisaneschi E; Baban A; Passarelli C; Capolino R; Angioni A; Novelli A; Marino B; Dallapiccola B
    Am J Med Genet A; 2017 Nov; 173(11):2912-2922. PubMed ID: 28884922
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genome-wide association studies highlight novel risk loci for septal defects and left-sided congenital heart defects.
    Broberg M; Ampuja M; Jones S; Ojala T; Rahkonen O; Kivelä R; Priest J; ; Palotie A; Ollila HM; Helle E
    BMC Genomics; 2024 Mar; 25(1):256. PubMed ID: 38454350
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Consanguineous marriage and congenital heart defects: a case-control study in the neonatal period.
    Yunis K; Mumtaz G; Bitar F; Chamseddine F; Kassar M; Rashkidi J; Makhoul G; Tamim H
    Am J Med Genet A; 2006 Jul; 140(14):1524-30. PubMed ID: 16763961
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cardiac homeobox gene NKX2-5 mutations and congenital heart disease: associations with atrial septal defect and hypoplastic left heart syndrome.
    Elliott DA; Kirk EP; Yeoh T; Chandar S; McKenzie F; Taylor P; Grossfeld P; Fatkin D; Jones O; Hayes P; Feneley M; Harvey RP
    J Am Coll Cardiol; 2003 Jun; 41(11):2072-6. PubMed ID: 12798584
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Replication of the 4p16 susceptibility locus in congenital heart disease in Han Chinese populations.
    Zhao B; Lin Y; Xu J; Ni B; Da M; Ding C; Hu Y; Zhang K; Yang S; Wang X; Yu S; Chen Y; Mo X; Liu J; Shen H; Sha J; Ma H
    PLoS One; 2014; 9(9):e107411. PubMed ID: 25215500
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.