Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7422
Gene Symbol: VEGFA
VEGFA
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
0.100 AlteredExpression BEFREE Interestingly, all five VEGF family of proteins exhibited altered developmental expression patterns that could cause abnormal development. 28719137

2017

Entrez Id: 7422
Gene Symbol: VEGFA
VEGFA
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
0.100 Biomarker BEFREE Cavernous malformations are more likely to bleed or to increase in size during pregnancy, under the influence of female hormones and vascular growth factors such as vascular endothelial growth factor. 23979052

2013

Entrez Id: 7422
Gene Symbol: VEGFA
VEGFA
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
0.100 GeneticVariation BEFREE An overview of the association between congenital malformations and VEGF/NOTCH polymorphisms in humans will be discussed along with their potential mechanisms and processes as revealed by transgenic mouse models. 22683047

2012

Entrez Id: 7422
Gene Symbol: VEGFA
VEGFA
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
0.100 GeneticVariation BEFREE The present study suggests, for the first time to our knowledge, that VEGFA mutations may be associated with congenital LVOTO malformations. 20420808

2010

Entrez Id: 7422
Gene Symbol: VEGFA
VEGFA
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
0.100 GeneticVariation BEFREE We genotyped 771 CVM cases, of whom 595 had the outflow tract malformation Tetralogy of Fallot (TOF), and carried out TDT and case-control analyses using haplotype-tagging SNPs in VEGF. 19308252

2009

Entrez Id: 7422
Gene Symbol: VEGFA
VEGFA
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
0.100 Biomarker BEFREE Disturbed vascular endothelial growth factor (VEGF) production during early heart morphogenesis causes endocardial cushion malformation, which results in congenital heart disease (CHD). 16569553

2006

Entrez Id: 7422
Gene Symbol: VEGFA
VEGFA
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
0.100 GeneticVariation BEFREE NOGA-guided analysis of regional myocardial perfusion abnormalities treated with intramyocardial injections of plasmid encoding vascular endothelial growth factor A-165 in patients with chronic myocardial ischemia: subanalysis of the EUROINJECT-ONE multicenter double-blind randomized study. 16159809

2005

Entrez Id: 7422
Gene Symbol: VEGFA
VEGFA
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
0.100 Biomarker BEFREE Excessive VEGF stimulation may play a pivotal role in the initiation and development of brain vessel malformations in states of relative endoglin insufficiency in adulthood. 14747750

2004

Entrez Id: 7422
Gene Symbol: VEGFA
VEGFA
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
0.100 Biomarker BEFREE Such a model should be useful for uncovering the role of VEGF isoforms in the mechanisms of angiogenesis and for investigating intracerebral hemorrhage due to ischemic stroke or congenital malformations. 9342366

1997

Entrez Id: 7422
Gene Symbol: VEGFA
VEGFA
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
0.100 Biomarker BEFREE In order to study the role of angiogenesis in AVMs, we have analyzed the expression of the endothelial cell mitogen vascular endothelial growth factor (VEGF) and a novel endothelial cell-specific receptor tyrosine kinase, Tie, by in situ hybridization and immunohistochemistry in these malformations and surrounding brain tissue. 8939195

1996