Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2200
Gene Symbol: FBN1
FBN1
0.030 AlteredExpression disease BEFREE The value of plasma fibrillin-1 level in patients with spontaneous cerebral artery dissection. 29386281 2018
Entrez Id: 2200
Gene Symbol: FBN1
FBN1
0.030 Biomarker disease BEFREE We describe a three generation family with FBN1-related WMS whose cardiovascular manifestations include TAA and cervical artery dissection, thus expanding the cardiovascular phenotype of WMS. 28696036 2017
Entrez Id: 4524
Gene Symbol: MTHFR
MTHFR
0.030 GeneticVariation disease BEFREE We examined the possible association between the polymorphism of methylenetetrahydrofolate reductase (MTHFR)-C677T and the gene mutation in transforming growth factor beta receptor II (TGFBR2) in a cohort of CCAD patients. 27017342 2016
Entrez Id: 4524
Gene Symbol: MTHFR
MTHFR
0.030 GeneticVariation disease BEFREE We examined the association between different polymorphisms frequently found in young patients with cryptogenic stroke [methylenetetrahydrofolate reductase (MTHFR) C677T, factor II (prothrombin) G20210A, factor V G1691A (Leiden), nitric oxide synthase 3 (NOS3) intron 4 VNTR, and apolipoprotein E (APOE) epsilon4 gene] in patients with a cerebral infarct caused by spontaneous cervical artery dissection. 20446941 2010
Entrez Id: 4524
Gene Symbol: MTHFR
MTHFR
0.030 Biomarker disease BEFREE Migraine may act as mediator in the methylenetetrahydrofolate reductase-ischemic stroke pathway with a more prominent effect in the subgroup of patients with spontaneous artery dissection. 17962595 2007
Entrez Id: 2200
Gene Symbol: FBN1
FBN1
0.030 GeneticVariation disease BEFREE Mutations in fibrillin 1 are the cause of dissecting aneurysm leading to rupture of the ascending aorta. 10885576 2000
Entrez Id: 4318
Gene Symbol: MMP9
MMP9
0.020 AlteredExpression disease BEFREE Local IL-1β might participate in the formation of aortic DA through the upregulation of MMP-2 and MMP-9 and the breakage of elastin fibres, which finally weakens the biomechanical properties of the aortic wall. 30169834 2019
Entrez Id: 348
Gene Symbol: APOE
APOE
0.020 Biomarker disease BEFREE As the activity of OCG in dissecting aneurysms is not clear, we tested the hypothesis that OCG contributes to angiotensin II (Ang II)-induced dissecting aneurysm (Ang II-induced AAA) in apolipoprotein E knockout mice. 29685509 2018
Entrez Id: 348
Gene Symbol: APOE
APOE
0.020 GeneticVariation disease BEFREE We examined the association between different polymorphisms frequently found in young patients with cryptogenic stroke [methylenetetrahydrofolate reductase (MTHFR) C677T, factor II (prothrombin) G20210A, factor V G1691A (Leiden), nitric oxide synthase 3 (NOS3) intron 4 VNTR, and apolipoprotein E (APOE) epsilon4 gene] in patients with a cerebral infarct caused by spontaneous cervical artery dissection. 20446941 2010
Entrez Id: 4318
Gene Symbol: MMP9
MMP9
0.020 GeneticVariation disease BEFREE MMP-9 polymorphisms are not associated with spontaneous cervical artery dissection. 14963289 2004
Entrez Id: 3553
Gene Symbol: IL1B
IL1B
0.010 Biomarker disease BEFREE Local IL-1β might participate in the formation of aortic DA through the upregulation of MMP-2 and MMP-9 and the breakage of elastin fibres, which finally weakens the biomechanical properties of the aortic wall. 30169834 2019
Entrez Id: 4313
Gene Symbol: MMP2
MMP2
0.010 AlteredExpression disease BEFREE Local IL-1β might participate in the formation of aortic DA through the upregulation of MMP-2 and MMP-9 and the breakage of elastin fibres, which finally weakens the biomechanical properties of the aortic wall. 30169834 2019
Entrez Id: 100616496
Gene Symbol: ERVW-4
ERVW-4
0.010 Biomarker disease BEFREE High incidence and clinical characteristics of fibromuscular dysplasia in patients with spontaneous cervical artery dissection: The ARCADIA-POL study. 30739593 2019
Entrez Id: 410
Gene Symbol: ARSA
ARSA
0.010 Biomarker disease BEFREE In addition, artery dissection was highly associated with combined ASA and unilateral PSA infarctions and long segments of SCI (all p < 0.05). 31092838 2019
Entrez Id: 2006
Gene Symbol: ELN
ELN
0.010 Biomarker disease BEFREE Victoria blue staining confirmed the formation of the DA and the reduction of elastin content after induction by BAPN. 30169834 2019
Entrez Id: 5972
Gene Symbol: REN
REN
0.010 GeneticVariation disease BEFREE Our report offers evidence that mutations in the REN gene could have pathogenic role in arterial dissection. 31371142 2019
Entrez Id: 959
Gene Symbol: CD40LG
CD40LG
0.010 Biomarker disease BEFREE Deficiency of (hematopoietic) CD40L protects against dissecting aneurysm formation and reduces the incidence of fatal rupture. 29519940 2018
Entrez Id: 6513
Gene Symbol: SLC2A1
SLC2A1
0.010 Biomarker disease BEFREE We queried our database for all patients treated with PED for dissecting aneurysms of the V4 segment. 28962011 2018
Entrez Id: 4948
Gene Symbol: OCA2
OCA2
0.010 Biomarker disease BEFREE We queried our database for all patients treated with PED for dissecting aneurysms of the V4 segment. 28962011 2018
Entrez Id: 8682
Gene Symbol: PEA15
PEA15
0.010 Biomarker disease BEFREE We queried our database for all patients treated with PED for dissecting aneurysms of the V4 segment. 28962011 2018
Entrez Id: 64115
Gene Symbol: VSIR
VSIR
0.010 Biomarker disease BEFREE We describe that 3D fat-saturated T1 VISTA was helpful for the diagnosis and follow-up in our case of cervicocephalic artery dissection complicated with progressive ischemic stroke. 28538402 2017
Entrez Id: 59
Gene Symbol: ACTA2
ACTA2
0.010 GeneticVariation disease BEFREE We present a young woman whose ACTA2 mutation was ascertained during pregnancy because of her father's history of dissecting aneurysms. 29202781 2017
Entrez Id: 84221
Gene Symbol: SPATC1L
SPATC1L
0.010 GeneticVariation disease BEFREE EGFLAM and SPATC1L may thus be susceptibility loci for true aortic aneurysm and RNASE13 may be such a locus for dissecting aneurysm in Japanese individuals. 28339009 2017
Entrez Id: 440163
Gene Symbol: RNASE13
RNASE13
0.010 GeneticVariation disease BEFREE EGFLAM and SPATC1L may thus be susceptibility loci for true aortic aneurysm and RNASE13 may be such a locus for dissecting aneurysm in Japanese individuals. 28339009 2017
Entrez Id: 4846
Gene Symbol: NOS3
NOS3
0.010 GeneticVariation disease BEFREE We examined the association between different polymorphisms frequently found in young patients with cryptogenic stroke [methylenetetrahydrofolate reductase (MTHFR) C677T, factor II (prothrombin) G20210A, factor V G1691A (Leiden), nitric oxide synthase 3 (NOS3) intron 4 VNTR, and apolipoprotein E (APOE) epsilon4 gene] in patients with a cerebral infarct caused by spontaneous cervical artery dissection. 20446941 2010