Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2492
Gene Symbol: FSHR
FSHR
0.800 GeneticVariation disease BEFREE The paper focuses on the recent identification of mutations in the FSH receptor gene that display an increased sensitivity to hCG and are responsible for the development of spontaneous OHSS occurring during pregnancy. 16034183 2005
Entrez Id: 2492
Gene Symbol: FSHR
FSHR
0.800 GeneticVariation disease BEFREE We conclude that the FSH receptor genotype did not play a significant role in the risk of iatrogenic OHSS in this cohort. 15950638 2005
Entrez Id: 2492
Gene Symbol: FSHR
FSHR
0.800 GeneticVariation disease LHGDN We conclude that the FSH receptor genotype did not play a significant role in the risk of iatrogenic OHSS in this cohort. 15950638 2005
Entrez Id: 2492
Gene Symbol: FSHR
FSHR
0.800 GeneticVariation disease BEFREE The recent identification of mutations in the FSH receptor gene, which display an increased sensitivity to hCG and are responsible for the development of spontaneous ovarian hyperstimulation syndrome (OHSS), provides for the first time the molecular basis for the physiopathology of spontaneous OHSS. 14998941 2004
Entrez Id: 2492
Gene Symbol: FSHR
FSHR
0.800 Biomarker disease BEFREE Together with the two previous studies, this report shows that inappropriate stimulation of the FSHr by hCG is a cause of spontaneous OHSS. 15080154 2004
Entrez Id: 2492
Gene Symbol: FSHR
FSHR
0.800 GeneticVariation disease LHGDN The recent identification of mutations in the FSH receptor gene, which display an increased sensitivity to hCG and are responsible for the development of spontaneous ovarian hyperstimulation syndrome (OHSS), provides for the first time the molecular basis for the physiopathology of spontaneous OHSS. 14998941 2004
Entrez Id: 2492
Gene Symbol: FSHR
FSHR
0.800 GeneticVariation disease LHGDN In a second phase, we studied FSHr allele frequencies according to the severity of OHSS. 15579795 2004
Entrez Id: 2492
Gene Symbol: FSHR
FSHR
0.800 Biomarker disease BEFREE Together with the two previous studies, this report shows that inappropriate stimulation of the FSHr by hCG is a cause of spontaneous OHSS. 15001619 2004
Entrez Id: 2492
Gene Symbol: FSHR
FSHR
0.800 GeneticVariation disease BEFREE In a second phase, we studied FSHr allele frequencies according to the severity of OHSS. 15579795 2004
Entrez Id: 2492
Gene Symbol: FSHR
FSHR
0.800 GeneticVariation disease UNIPROT Together with the two previous studies, this report shows that inappropriate stimulation of the FSHr by hCG is a cause of spontaneous OHSS. 15080154 2004
Entrez Id: 2492
Gene Symbol: FSHR
FSHR
0.800 GeneticVariation disease UNIPROT Ovarian hyperstimulation syndrome due to a mutation in the follicle-stimulating hormone receptor. 12930928 2003
Entrez Id: 2492
Gene Symbol: FSHR
FSHR
0.800 GeneticVariation disease UNIPROT A chorionic gonadotropin-sensitive mutation in the follicle-stimulating hormone receptor as a cause of familial gestational spontaneous ovarian hyperstimulation syndrome. 12930927 2003
Entrez Id: 2492
Gene Symbol: FSHR
FSHR
0.800 CausalMutation disease CLINVAR
Entrez Id: 2492
Gene Symbol: FSHR
FSHR
0.800 Biomarker disease CTD_human
Entrez Id: 10062
Gene Symbol: NR1H3
NR1H3
0.200 Biomarker disease MGD Nogo-B receptor deficiency increases liver X receptor alpha nuclear translocation and hepatic lipogenesis through an adenosine monophosphate-activated protein kinase alpha-dependent pathway. 27480224 2016
Entrez Id: 1813
Gene Symbol: DRD2
DRD2
0.200 Therapeutic disease RGD Dopamine receptor 2 activation inhibits ovarian vascular endothelial growth factor secretion in an ovarian hyperstimulation syndrome (OHSS) animal model: implications for treatment of OHSS with dopamine receptor 2 agonists. 25217874 2014
Entrez Id: 10062
Gene Symbol: NR1H3
NR1H3
0.200 Biomarker disease MGD Absence of nuclear receptors for oxysterols liver X receptor induces ovarian hyperstimulation syndrome in mice. 19325005 2009
Entrez Id: 10062
Gene Symbol: NR1H3
NR1H3
0.200 Biomarker disease MGD Multiple roles of the nuclear receptors for oxysterols liver X receptor to maintain male fertility. 17341595 2007
Entrez Id: 10062
Gene Symbol: NR1H3
NR1H3
0.200 Biomarker disease MGD Reciprocal regulation of inflammation and lipid metabolism by liver X receptors. 12524534 2003
Entrez Id: 10062
Gene Symbol: NR1H3
NR1H3
0.200 Biomarker disease MGD Cholesterol and bile acid metabolism are impaired in mice lacking the nuclear oxysterol receptor LXR alpha. 9630215 1998
Entrez Id: 7422
Gene Symbol: VEGFA
VEGFA
0.100 AlteredExpression disease BEFREE VEGF and EGR-1 levels were assessed, and binary logistic regression analysis was applied to predict associations between clinical variables and OHSS. 31004220 2019
Entrez Id: 6046
Gene Symbol: BRD2
BRD2
0.100 GeneticVariation disease BEFREE Among women at high risk for developing severe OHSS who are triggered with a standard dose (0.2 mg) of the GnRH agonist triptorelin, women with BMI 25 kg/m<sup>2</sup> or greater had significantly fewer mature oocytes, required a higher total dose of recombinant FSH compared with women with BMI less than 25 kg/m<sup>2</sup>. 31839394 2019
Entrez Id: 7422
Gene Symbol: VEGFA
VEGFA
0.100 AlteredExpression disease BEFREE Although ovarian angiogenesis was significantly inhibited, rapamycin could not decrease the elevated levels of vascular endothelial growth factor, IL-6 and IL-11 in OHSS ovaries. 31329230 2019
Entrez Id: 7422
Gene Symbol: VEGFA
VEGFA
0.100 Biomarker disease BEFREE Twenty-one subjects were evaluated.There was no significant difference between patients with OHSS and control subjects with respect to VEGF, TNFα, CRP, inhibin A and inhibin B. 31122524 2019
Entrez Id: 7422
Gene Symbol: VEGFA
VEGFA
0.100 Biomarker disease BEFREE Studies proved that cabergoline administration blocks the increase in vascular permeability via dephosphorylation of VEGF receptors and hence can be used as prophylactic agent against OHSS. 31133458 2019