Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4846
Gene Symbol: NOS3
NOS3
0.680 Therapeutic phenotype RGD Of note, apelin treatment significantly ameliorated the symptoms of preeclampsia, improved the impaired endothelial nitric oxide synthase/nitric oxide signaling and attenuated activation of oxidative stress in RUPP rats. 29250138 2017
Entrez Id: 4846
Gene Symbol: NOS3
NOS3
0.680 GeneticVariation phenotype LHGDN The -786T/C polymorphism of the endothelial nitric oxide synthase gene in preeclampsia. 17382454 2008
Entrez Id: 4846
Gene Symbol: NOS3
NOS3
0.680 GeneticVariation phenotype LHGDN Polymorphisms in the endothelial nitric oxide synthase (eNOS) gene have been inconsistently associated with preeclampsia. 18855535 2008
Entrez Id: 4846
Gene Symbol: NOS3
NOS3
0.680 GeneticVariation phenotype LHGDN No association of the genetic polymorphisms of endothelial nitric oxide synthase, dimethylarginine dimethylaminohydrolase, and vascular endothelial growth factor with preeclampsia in Korean populations. 18251679 2008
Entrez Id: 4846
Gene Symbol: NOS3
NOS3
0.680 GeneticVariation phenotype LHGDN Similar to the findings in Western populations, polymorphisms in the eNOS gene may be protective against PE in a Chinese population, in contrast to the results in the Japanese population. 17636229 2007
Entrez Id: 4846
Gene Symbol: NOS3
NOS3
0.680 Biomarker phenotype LHGDN Endothelial nitric oxide synthase gene influences the risk of pre-eclampsia, the recurrence of negative pregnancy events, and the maternal-fetal flow. 16915032 2006
Entrez Id: 4846
Gene Symbol: NOS3
NOS3
0.680 GeneticVariation phenotype LHGDN Furthermore, in the pre-eclampsia patients who subsequently developed abruptio placentae, the eNOS GT genotype emerged as a major risk factor for the development of abruptio placentae (p<0.0001). 16059745 2005
Entrez Id: 4846
Gene Symbol: NOS3
NOS3
0.680 GeneticVariation phenotype LHGDN Polymorphisms in the endothelial NO synthase (eNOS) gene have been evaluated as risk factors for preeclampsia. 15364897 2004
Entrez Id: 4846
Gene Symbol: NOS3
NOS3
0.680 GeneticVariation phenotype LHGDN Frequency of the intron 4 polymorphism of NOS3 (designated allele A) among patients with preeclampsia compared with controls. 12044319 2001
Entrez Id: 4846
Gene Symbol: NOS3
NOS3
0.680 Biomarker phenotype CTD_human
Entrez Id: 4846
Gene Symbol: NOS3
NOS3
0.680 Biomarker phenotype HPO
Entrez Id: 219736
Gene Symbol: STOX1
STOX1
0.610 SusceptibilityMutation phenotype ORPHANET STOX1: Key player in trophoblast dysfunction underlying early onset preeclampsia with growth retardation. 21490791 2011
Entrez Id: 219736
Gene Symbol: STOX1
STOX1
0.610 AlteredExpression phenotype LHGDN In addition, they strongly suggest that anomalies in STOX1 expression are associated with the onset of preeclampsia, thus indicating that this gene should be the target of future studies. 19079545 2008
Entrez Id: 219736
Gene Symbol: STOX1
STOX1
0.610 Biomarker phenotype CTD_human
Entrez Id: 219736
Gene Symbol: STOX1
STOX1
0.610 Biomarker phenotype HPO
Entrez Id: 2321
Gene Symbol: FLT1
FLT1
0.600 Biomarker phenotype CTD_human This locus is near the FLT1 gene encoding Fms-like tyrosine kinase 1, providing biological support, as a placental isoform of this protein (sFlt-1) is implicated in the pathology of preeclampsia. 28628106 2017
Entrez Id: 2321
Gene Symbol: FLT1
FLT1
0.600 SusceptibilityMutation phenotype ORPHANET This locus is near the FLT1 gene encoding Fms-like tyrosine kinase 1, providing biological support, as a placental isoform of this protein (sFlt-1) is implicated in the pathology of preeclampsia. 28628106 2017
Entrez Id: 10699
Gene Symbol: CORIN
CORIN
0.600 SusceptibilityMutation phenotype ORPHANET Role of corin in trophoblast invasion and uterine spiral artery remodelling in pregnancy. 22437503 2012
Entrez Id: 2321
Gene Symbol: FLT1
FLT1
0.600 Biomarker phenotype LHGDN Prevalence of agonistic autoantibodies against the angiotensin II type 1 receptor and soluble fms-like tyrosine kinase 1 in a gestational age-matched case study. 19064815 2009
Entrez Id: 2321
Gene Symbol: FLT1
FLT1
0.600 Biomarker phenotype LHGDN First-trimester serum levels of soluble endoglin and soluble fms-like tyrosine kinase-1 as first-trimester markers for late-onset preeclampsia. 18771978 2008
Entrez Id: 2321
Gene Symbol: FLT1
FLT1
0.600 AlteredExpression phenotype LHGDN Apoptotic levels do not correlate with Flt1 in preeclampsia placentae and are not regulated by in vivo exposure to the antihypertensives clonidine and hydralazine. 19003637 2008
Entrez Id: 2321
Gene Symbol: FLT1
FLT1
0.600 AlteredExpression phenotype LHGDN However, an increased expression of ENG and FLT1 was detected by qRT-PCR in the PE + SGA group. 18330824 2008
Entrez Id: 2321
Gene Symbol: FLT1
FLT1
0.600 Biomarker phenotype LHGDN Cigarette smoke exposure and angiogenic factors in pregnancy and preeclampsia. 18566591 2008
Entrez Id: 2321
Gene Symbol: FLT1
FLT1
0.600 Biomarker phenotype LHGDN A longitudinal study of angiogenic (placental growth factor) and anti-angiogenic (soluble endoglin and soluble vascular endothelial growth factor receptor-1) factors in normal pregnancy and patients destined to develop preeclampsia and deliver a small for gestational age neonate. 18175241 2008
Entrez Id: 2321
Gene Symbol: FLT1
FLT1
0.600 Biomarker phenotype CTD_human Placental expression of ceruloplasmin in pregnancies complicated by severe preeclampsia. 18679377 2008