Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1636
Gene Symbol: ACE
ACE
0.310 GeneticVariation phenotype LHGDN DD genotype of ACE gene is a risk factor for intracerebral hemorrhage. 15277638 2004
Entrez Id: 2155
Gene Symbol: F7
F7
0.310 GeneticVariation phenotype LHGDN Polymorphisms in the coagulation factor VII gene and risk of primary intracerebral hemorrhage. 17880564 2007
Entrez Id: 351
Gene Symbol: APP
APP
0.130 GeneticVariation phenotype LHGDN [Recurrent intraparenchimal haemorrhages in a patient with cerebral amyloidotic angiopathy: description of one autopsy case]. 16789686 2006
Entrez Id: 351
Gene Symbol: APP
APP
0.130 GeneticVariation phenotype LHGDN A novel AbetaPP mutation exclusively associated with cerebral amyloid angiopathy. 16178030 2005
Entrez Id: 101928137
Gene Symbol: LINC02444
LINC02444
0.100 GeneticVariation phenotype GWASDB Meta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhage. 24656865 2014
Entrez Id: 100527963
Gene Symbol: PMF1-BGLAP
PMF1-BGLAP
0.100 GeneticVariation phenotype GWASCAT Meta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhage. 24656865 2014
Entrez Id: 100527963
Gene Symbol: PMF1-BGLAP
PMF1-BGLAP
0.100 GeneticVariation phenotype GWASDB Meta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhage. 24656865 2014
Entrez Id: 29780
Gene Symbol: PARVB
PARVB
0.100 GeneticVariation phenotype GWASCAT 17p12 Influences Hematoma Volume and Outcome in Spontaneous Intracerebral Hemorrhage. 29915124 2018
Entrez Id: 11243
Gene Symbol: PMF1
PMF1
0.100 GeneticVariation phenotype GWASCAT Meta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhage. 24656865 2014
Entrez Id: 9673
Gene Symbol: SLC25A44
SLC25A44
0.100 GeneticVariation phenotype GWASDB Meta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhage. 24656865 2014
Entrez Id: 11243
Gene Symbol: PMF1
PMF1
0.100 GeneticVariation phenotype GWASDB Meta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhage. 24656865 2014
Entrez Id: 348
Gene Symbol: APOE
APOE
0.040 GeneticVariation phenotype LHGDN Conflicting reports in the literature exist with regard to the association of apolipoprotein E (apo E) alleles and lobar intracerebral hemorrhage (ICH). 16100021 2005
Entrez Id: 348
Gene Symbol: APOE
APOE
0.040 GeneticVariation phenotype LHGDN The apolipoprotein E (APOE) polymorphism is an established risk factor for intracerebral hemorrhage (ICH) that is related to cerebral amyloid angiopathy in the white population. 18256366 2008
Entrez Id: 12
Gene Symbol: SERPINA3
SERPINA3
0.020 GeneticVariation phenotype LHGDN SERPINA3 polymorphism is not associated with primary intracerebral hemorrhage in a Polish population. 16424370 2006
Entrez Id: 12
Gene Symbol: SERPINA3
SERPINA3
0.020 GeneticVariation phenotype LHGDN Alpha-1 antichymotrypsin gene signal peptide a/t polymorphism and primary intracerebral hemorrhage. 18408372 2008
Entrez Id: 4524
Gene Symbol: MTHFR
MTHFR
0.010 GeneticVariation phenotype LHGDN We investigated relationships between polymorphisms in the methylenetetrahydrofolate reductase (MTHFR) gene, and plasma levels of HCY and folate in patients of Mongolian races who suffered from cerebral ischemia (CI, n = 42) or cerebral hemorrhage (CH, n = 20) and in the 24 age-matched controls. 15829163 2005
Entrez Id: 338
Gene Symbol: APOB
APOB
0.010 GeneticVariation phenotype LHGDN [Positive association of apolipoprotein B gene C7673T polymorphism with cerebral hemorrhage with family history]. 18393233 2008
Entrez Id: 2099
Gene Symbol: ESR1
ESR1
0.010 GeneticVariation phenotype LHGDN Since hypertension and atherosclerosis are major mechanisms in stroke development, we hypothesized that genetic variants of the ER alpha gene (ESR1) are determinants of future ischemic stroke or intracerebral hemorrhage (ICH). 17971628 2007
Entrez Id: 81027
Gene Symbol: TUBB1
TUBB1
0.010 GeneticVariation phenotype LHGDN We evaluated the role of the TUBB1 Q43P polymorphism and its synergism with other polymorphisms in the risk of developing subarachnoid (SAH) and intracerebral hemorrhage (ICH). 17488662 2007
Entrez Id: 350
Gene Symbol: APOH
APOH
0.010 GeneticVariation phenotype LHGDN We studied polymorphisms of the ApoH gene by the polymerase chain reaction-single strand conformation polymorphism technique and DNA sequencing in 140 PICH patients and 100 healthy control subjects. 14707422 2004
Entrez Id: 5327
Gene Symbol: PLAT
PLAT
0.500 Biomarker phenotype CTD_human Symptomatic intracerebral hemorrhage and recanalization after IV rt-PA: a multicenter study. 18753474 2008
Entrez Id: 5327
Gene Symbol: PLAT
PLAT
0.500 Biomarker phenotype CTD_human Essential role of endogenous tissue plasminogen activator through matrix metalloproteinase 9 induction and expression on heparin-produced cerebral hemorrhage after cerebral ischemia in mice. 14630814 2004
Entrez Id: 5327
Gene Symbol: PLAT
PLAT
0.500 Biomarker phenotype CTD_human Early stroke treatment associated with better outcome: the NINDS rt-PA stroke study. 11113218 2000
Entrez Id: 5327
Gene Symbol: PLAT
PLAT
0.500 Biomarker phenotype CTD_human Assessment of suitability of thrombolysis in middle cerebral artery infarction: a proof of concept study of a stereologically-based technique. 17690543 2007
Entrez Id: 2321
Gene Symbol: FLT1
FLT1
0.500 Biomarker phenotype CTD_human Cerebral angiogenesis after collagenase-induced intracerebral hemorrhage in rats. 17888890 2007