The genetics of intracranial aneurysms

scientific article

The genetics of intracranial aneurysms is …
instance of (P31):
review articleQ7318358
scholarly articleQ13442814

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P356DOI10.1007/S10038-006-0407-4
P698PubMed publication ID16736093
P5875ResearchGate publication ID7046963

P2093author name stringIturo Inoue
Boris Krischek
P2860cites workRisk Factors for Subarachnoid Hemorrhage: An Updated Systematic Review of Epidemiological StudiesQ22306374
Multiple Rare Alleles Contribute to Low Plasma Levels of HDL CholesterolQ22337068
Mapping a Mendelian form of intracranial aneurysm to 1p34.3-p36.13Q24530733
Search for intracranial aneurysm susceptibility gene(s) using Finnish familiesQ24799061
The Familial Intracranial Aneurysm (FIA) study protocolQ24801697
Unruptured intracranial aneurysms: prospective data have arrivedQ30812293
Lack of association between endoglin intron 7 insertion polymorphism and intracranial aneurysms in a white population: evidence of racial/ethnic differencesQ31028420
Collagen organization in the branching region of human brain arteriesQ32038470
The detection and management of unruptured intracranial aneurysmsQ33179583
Tissue inhibitor of metalloproteinases-1, -2, and -3 polymorphisms in a white population with intracranial aneurysmsQ33194728
Intracranial aneurysms in Finnish families: confirmation of linkage and refinement of the interval to chromosome 19q13.3.Q33911043
Genomewide-linkage and haplotype-association studies map intracranial aneurysm to chromosome 7q11Q34020559
Electrothrombosis of saccular aneurysms via endovascular approach. Part 2: Preliminary clinical experienceQ34114645
Mutation detection of PKD1 identifies a novel mutation common to three families with aneurysms and/or very-early-onset diseaseQ34146291
Association between heritable connective tissue disorders and intracranial aneurysmsQ34154210
Advances in the genetics of cerebrovascular disease and strokeQ34242566
Follow-up of intracranial aneurysms in autosomal-dominant polycystic kidney diseaseQ34313894
The ACE I allele is associated with increased risk for ruptured intracranial aneurysmsQ35435193
The pathobiology of aortic aneurysmsQ35688072
Risk of rupture associated with intact cerebral aneurysms in the Japanese population: a systematic review of the literature from Japan.Q36116304
Etiology of intracranial berry aneurysmsQ38626835
The incidence and treatment of asymptomatic, unruptured cerebral aneurysmsQ39405841
Absence of linkage of familial intracranial aneurysms to 7q11 in highly aggregated Japanese familiesQ39644766
II genotype of the angiotensin-converting enzyme gene increases the risk for subarachnoid hemorrhage from ruptured aneurysmQ39686013
Bifurcation geometry and the presence of cerebral artery aneurysmsQ39689916
Association of polymorphisms and haplotypes in the elastin gene in Dutch patients with sporadic aneurysmal subarachnoid hemorrhage.Q39691614
Alpha1-antichymotrypsin gene (SERPINA3) A/T polymorphism as a risk factor for aneurysmal subarachnoid hemorrhageQ39708092
Neurovascular manifestations of heritable connective tissue disorders. A reviewQ40741519
Importance of management of unruptured cerebral aneurysmsQ40893990
Morphometric analysis of reticular and elastin fibers in the cerebral arteries of patients with intracranial aneurysmsQ41233977
Prevalence and risk of rupture of intracranial aneurysms: a systematic reviewQ41691486
The presence of tandem endothelial nitric oxide synthase gene polymorphisms identifying brain aneurysms more prone to ruptureQ42651906
Interleukin 1beta-511 C/T polymorphism and risk of aneurysmal subarachnoid haemorrhageQ42718511
Subarachnoid haemorrhage in first and second degree relatives of patients with subarachnoid haemorrhageQ42872719
Aneurysmal subarachnoid hemorrhage in Izumo City and Shimane Prefecture of Japan. IncidenceQ43454719
Association of positional and functional candidate genes FGF1, FBN2, and LOX on 5q31 with intracranial aneurysmQ44443622
Polymorphisms of the NADPH oxidase P22PHOX gene in a Caucasian population with intracranial aneurysmsQ44586639
Prevalence of intracranial saccular aneurysms in a Japanese community based on a consecutive autopsy series during a 30-year observation period. The Hisayama studyQ44780472
Mutations in the lysyl oxidase gene not associated with intracranial aneurysm in central European familiesQ44992602
The Risk of Subarachnoid and Intracerebral Hemorrhages in Blacks as Compared with WhitesQ46388332
Deficiencies in estrogen-mediated regulation of cerebrovascular homeostasis may contribute to an increased risk of cerebral aneurysm pathogenesis and rupture in menopausal and postmenopausal womenQ46852644
Extended single nucleotide polymorphism and haplotype analysis of the elastin gene in Caucasians with intracranial aneurysms provides evidence for racially/ethnically based differencesQ47288577
Matrix metalloproteinase-9 coding sequence single-nucleotide polymorphisms in caucasians with intracranial aneurysmsQ47297689
Influence of endothelial nitric oxide synthase T-786C single nucleotide polymorphism on aneurysm sizeQ47394828
Endothelial nitric oxide synthase T-786C single nucleotide polymorphism: a putative genetic marker differentiating small versus large ruptured intracranial aneurysmsQ47425827
Elastin Polymorphism Haplotype and Intracranial Aneurysms Are Not Associated in Central EuropeQ47980217
Has there been a decline in subarachnoid hemorrhage mortality?Q50558701
Incidence and prognosis of subarachnoid hemorrhage in a Japanese rural community.Q50559522
Natural history of unruptured intracranial aneurysms: risks for aneurysm formation, growth, and rupture.Q50708947
A study of inbreeding and kinship in intracranial aneurysms in the Saguenay Lac-Saint-Jean region (Quebec, Canada).Q51004946
The pathogenesis of cerebral aneurysms.Q51225582
Lack of an association between the angiotensin-converting enzyme insertion/deletion polymorphism and intracranial aneurysms in a Caucasian population in the United States.Q51843633
Endoglin is not a major susceptibility gene for intracranial aneurysm among Japanese.Q52015938
Occult intracranial aneurysms in polycystic kidney disease: screening with MR angiography.Q52883196
Is there any evidence for linkage on chromosome 17cen in affected Japanese sib-pairs with an intracranial aneurysm?Q53631952
Endoglin gene insertion polymorphism not associated with aneurysmal subarachnoid hemorrhage.Q53860715
Update on genetic evidence for rupture-prone compared with rupture-resistant intracranial saccular aneurysms.Q53875184
A DNA sequence polymorphism in the endoglin gene is not associated with intracranial aneurysm or aneurysmal subarachnoid hemorrhage.Q54657320
Polymorphism of the heme oxygenase-1 gene and cerebral aneurysmsQ57243053
Familial intracranial aneurysmsQ57784004
Examination of ELN as a Candidate Gene in the Utah Intracranial Aneurysm PedigreesQ59548778
Confirmation of chromosome 7q11 locus for predisposition to intracranial aneurysmQ59548803
'Medial defects' in the prenatal human cerebral arteries: an electron microscopic studyQ71042776
Genotypic variations of type III collagen in patients with cerebral aneurysmsQ71469328
Familial aneurysmal subarachnoid hemorrhage: a community-based studyQ72038040
[Cerebellar infarcts that require differentiation from tumors: diagnosis with MRI]Q72379314
Subarachnoid hemorrhage and family history. A population-based case-control studyQ72526382
Clinical analysis of incidentally discovered unruptured aneurysmsQ72628501
Exclusion of mutations in the gene for type III collagen (COL3A1) as a common cause of intracranial aneurysms or cervical artery dissections: results from sequence analysis of the coding sequences of type III collagen from 55 unrelated patientsQ72643554
Inflammation and intracranial aneurysmsQ73152826
Recurrence of intracranial aneurysms in autosomal-dominant polycystic kidney diseaseQ73215823
Functional polymorphism in the matrix metalloproteinase-9 promoter as a potential risk factor for intracranial aneurysmQ73230342
Type III collagen deficiency in a family with intracranial aneurysmsQ73552305
Unruptured intracranial aneurysms: natural history, clinical outcome, and risks of surgical and endovascular treatmentQ73681953
Genetic evaluation of lipoprotein(a) in intracranial aneurysm diseaseQ74145786
Polymorphisms in matrix metalloproteinase-1, -3, -9, and -12 genes in relation to subarachnoid hemorrhageQ74485860
Ultrastructural connective tissue aberrations in patients with intracranial aneurysmsQ74743027
Increased expression of phosphorylated c-Jun amino-terminal kinase and phosphorylated c-Jun in human cerebral aneurysms: role of the c-Jun amino-terminal kinase/c-Jun pathway in apoptosis of vascular wallsQ74794806
Collagen type I alpha2 (COL1A2) is the susceptible gene for intracranial aneurysmsQ75319587
Polymorphism of the endoglin gene in patients with intracranial saccular aneurysmsQ77386719
Asymptomatic familial cerebral aneurysmsQ77390912
Angiotensin I-converting enzyme gene polymorphism in intracranial saccular aneurysm individualsQ77454471
Type III collagen deficiency in saccular intracranial aneurysms. Defect in gene regulation?Q78095050
Genome-wide linkage in a large Dutch consanguineous family maps a locus for intracranial aneurysms to chromosome 2p13Q80496932
Absence of alpha-1 antitrypsin deficiency alleles (S and Z) in Japanese and Korean patients with aneurysmal subarachnoid hemorrhageQ80968098
Genome-wide scan for Japanese familial intracranial aneurysms: linkage to several chromosomal regionsQ81072729
P433issue7
P304page(s)587-594
P577publication date2006-05-31
P1433published inJournal of Human GeneticsQ6295302
P1476titleThe genetics of intracranial aneurysms
P478volume51

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cites work (P2860)
Q51234648A 54-year-old man with 12 intracranial aneurysms and familial subarachnoid hemorrhage: case report.
Q37601496A Review of the Genetics of Intracranial Berry Aneurysms and Implications for Genetic Counseling
Q85075384A rare association of ruptured left middle cerebral artery aneurysm and dextrocardia with situs inversus totalis
Q34228630Anesthetic management of patients with intracranial aneurysms.
Q92023931Aneurysm Formation, Growth, and Rupture: The Biology and Physics of Cerebral Aneurysms
Q42101613Association of Versican (VCAN) gene polymorphisms rs251124 and rs2287926 (G428D), with intracranial aneurysm.
Q28649596Cerebral aneurysms: formation, progression, and developmental chronology
Q38369977Collagen Type I Alpha 2 (COL1A2) Polymorphism Contributes to Intracranial Aneurysm Susceptibility: A Meta-Analysis.
Q46108176Endovascular Biopsy: In Vivo Cerebral Aneurysm Endothelial Cell Sampling and Gene Expression Analysis
Q34971540From GWAS to the clinic: risk factors for intracranial aneurysms
Q92350487Gene Expression in Intracranial Aneurysms-Comparison Analysis of Aneurysmal Walls and Extracranial Arteries with Real-Time Polymerase Chain Reaction and Immunohistochemistry
Q37027180Genetic risk factors for intracranial aneurysms: a meta-analysis in more than 116,000 individuals
Q84543448Genome-wide association study to identify genetic variants present in Japanese patients harboring intracranial aneurysms
Q36111357Interactions of miR-34b/c and TP53 polymorphisms on the risk of intracranial aneurysm
Q40080487Knowledge environments representing molecular entities for the virtual physiological human
Q86034429Lack of association of lysyl oxidase (LOX) gene polymorphisms with intracranial aneurysm in a south Indian population
Q37277240Molecular genetics of human intracranial aneurysms
Q34281117Nature versus Nurture: Death of a Dogma, and the Road Ahead
Q36514339OSIRISv1.2: a named entity recognition system for sequence variants of genes in biomedical literature
Q36920195Physical factors effecting cerebral aneurysm pathophysiology
Q39286785RNF213 Is Associated with Intracranial Aneurysms in the French-Canadian Population
Q89574610Rare and Low-Frequency Variant of ARHGEF17 Is Associated With Intracranial Aneurysms
Q89574589Rho Guanine Nucleotide Exchange Factor ARHGEF17 Is a Risk Gene for Intracranial Aneurysms
Q38200573Smooth muscle cells and the formation, degeneration, and rupture of saccular intracranial aneurysm wall--a review of current pathophysiological knowledge
Q55043122Systematic screening of lysyl oxidase-like (LOXL) family genes demonstrates that LOXL2 is a susceptibility gene to intracranial aneurysms.
Q92862825The Association between Genes Polymorphisms of Heparan Sulfate Proteoglycan 2 (HSPG2) and Chondroitin Sulfate Proteoglycan 2 (CSPG2) and Intracranial Aneurysm Susceptibility: A Meta-Analysis
Q38131014The genetics of vascular complications in autosomal dominant polycystic kidney disease (ADPKD).
Q37126431The influence of genetics on intracranial aneurysm formation and rupture: current knowledge and its possible impact on future treatment.
Q38560064Treatment of Intracranial Aneurysms: Clipping Versus Coiling.

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