Detalhe da pesquisa
1.
Rare variants in NR2F2 cause congenital heart defects in humans.
Am J Hum Genet
; 94(4): 574-85, 2014 04 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-24702954
2.
Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot.
Hum Mol Genet
; 22(7): 1473-81, 2013 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23297363
3.
Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease.
Am J Hum Genet
; 91(3): 489-501, 2012 Sep 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-22939634
4.
Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls.
Hum Mol Genet
; 21(7): 1513-20, 2012 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22199024
5.
Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans.
Am J Hum Genet
; 98(3): 592, 2016 Mar 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-28863274
6.
Association between C677T polymorphism of methylene tetrahydrofolate reductase and congenital heart disease: meta-analysis of 7697 cases and 13,125 controls.
Circ Cardiovasc Genet
; 6(4): 347-53, 2013 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-23876493
7.
Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16.
Nat Genet
; 45(7): 822-4, 2013 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-23708191