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Results: 1 to 20 of 125

Cited In for PubMed (Select 17519398)


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. doi: 10.2174/1389202916666150303232520.


Detection of critical congenital heart defects: Review of contributions from prenatal and newborn screening.

Olney RS, Ailes EC, Sontag MK.

Semin Perinatol. 2015 Apr;39(3):230-7. doi: 10.1053/j.semperi.2015.03.007.


c.620C>T mutation in GATA4 is associated with congenital heart disease in South India.

Mattapally S, Nizamuddin S, Murthy KS, Thangaraj K, Banerjee SK.

BMC Med Genet. 2015 Feb 18;16:7. doi: 10.1186/s12881-015-0152-7.


Secundum atrial septal defect in adults: a practical review and recent developments.

Kuijpers JM, Mulder BJ, Bouma BJ.

Neth Heart J. 2015 Apr;23(4):205-11. doi: 10.1007/s12471-015-0663-z.


Unraveling the association between mRNA expressions and mutant phenotypes in a genome-wide assessment of mice.

Liao BY, Weng MP.

Proc Natl Acad Sci U S A. 2015 Apr 14;112(15):4707-12. doi: 10.1073/pnas.1415046112. Epub 2015 Mar 30.


Association between 5, 10-methylenetetrahydrofolate reductase (MTHFR) polymorphisms and congenital heart disease: A meta-analysis.

Wang W, Hou Z, Wang C, Wei C, Li Y, Jiang L.

Meta Gene. 2013 Oct 28;1:109-25. doi: 10.1016/j.mgene.2013.09.009. eCollection 2013 Dec.


MATR3 disruption in human and mouse associated with bicuspid aortic valve, aortic coarctation and patent ductus arteriosus.

Quintero-Rivera F, Xi QJ, Keppler-Noreuil KM, Lee JH, Higgins AW, Anchan RM, Roberts AE, Seong IS, Fan X, Lage K, Lu LY, Tao J, Hu X, Berezney R, Gelb BD, Kamp A, Moskowitz IP, Lacro RV, Lu W, Morton CC, Gusella JF, Maas RL.

Hum Mol Genet. 2015 Apr 15;24(8):2375-89. doi: 10.1093/hmg/ddv004. Epub 2015 Jan 7.


Ethnical variations in the incidence of congenital heart defects in gorgan, northern iran: a single-center study.

Nikyar B, Sedehi M, Qorbani M, Nikyar A, Golalipour MJ.

J Tehran Heart Cent. 2014 Jan 12;9(1):9-14.


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 17;15:1127. doi: 10.1186/1471-2164-15-1127.


Current Practice and Utility of Chromosome Microarray Analysis in Infants Undergoing Cardiac Surgery.

Buckley JR, Kavarana MN, Chowdhury SM, Scheurer MA.

Congenit Heart Dis. 2015 May;10(3):E131-8. doi: 10.1111/chd.12241. Epub 2014 Dec 14.


Congenital heart disease: the crossroads of genetics, epigenetics and environment.

Vecoli C, Pulignani S, Foffa I, Andreassi MG.

Curr Genomics. 2014 Oct;15(5):390-9. doi: 10.2174/1389202915666140716175634.


Quantitative proteomic analysis of serum from pregnant women carrying a fetus with conotruncal heart defect using isobaric tags for relative and absolute quantitation (iTRAQ) labeling.

Zhang Y, Kang Y, Zhou Q, Zhou J, Wang H, Jin H, Liu X, Ma D, Li X.

PLoS One. 2014 Nov 13;9(11):e111645. doi: 10.1371/journal.pone.0111645. eCollection 2014.


Investigation of copy number variation in children with conotruncal heart defects.

Campos CM, Zanardo EA, Dutra RL, Kulikowski LD, Kim CA.

Arq Bras Cardiol. 2015 Jan;104(1):24-31. doi: 10.5935/abc.20140169. Epub 2014 Nov 11. English, Portuguese.


Maternal lifestyle factors in pregnancy and congenital heart defects in offspring: review of the current evidence.

Feng Y, Yu D, Yang L, Da M, Wang Z, Lin Y, Ni B, Wang S, Mo X.

Ital J Pediatr. 2014 Nov 11;40:85. doi: 10.1186/s13052-014-0085-3.


Periostin Expression is Altered in Aortic Valves in Smad6 Mutant Mice.

Sugi Y, Kern MJ, Markwald RR, Burnside JL.

J Neonatal Biol. 2012 Jan 21;1. pii: 4692.


Epidemiology of Cardiovascular Malformations among Newborns in Monchegorsk (North-West Russia): a Register-Based Study.

Postoev VA, Talykova LV, Vaktskjold A.

J Public Health Res. 2014 Aug 4;3(2):270. doi: 10.4081/jphr.2014.270. eCollection 2014 Jul 2.


Association of aminoacyl-tRNA synthetases gene polymorphisms with the risk of congenital heart disease in the Chinese Han population.

Da M, Feng Y, Xu J, Hu Y, Lin Y, Ni B, Qian B, Hu Z, Mo X.

PLoS One. 2014 Oct 13;9(10):e110072. doi: 10.1371/journal.pone.0110072. eCollection 2014.


Maternal parity and the risk of congenital heart defects in offspring: a dose-response meta-analysis of epidemiological observational studies.

Feng Y, Yu D, Chen T, Liu J, Tong X, Yang L, Da M, Shen S, Fan C, Wang S, Mo X.

PLoS One. 2014 Oct 8;9(10):e108944. doi: 10.1371/journal.pone.0108944. eCollection 2014.


Maternal obesity and tobacco use modify the impact of genetic variants on the occurrence of conotruncal heart defects.

Tang X, Nick TG, Cleves MA, Erickson SW, Li M, Li J, MacLeod SL, Hobbs CA.

PLoS One. 2014 Oct 2;9(9):e108903. doi: 10.1371/journal.pone.0108903. eCollection 2014.

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