review article | Q7318358 |
scholarly article | Q13442814 |
P2093 | author name string | Ituro Inoue | |
Boris Krischek | |||
P2860 | cites work | Risk Factors for Subarachnoid Hemorrhage: An Updated Systematic Review of Epidemiological Studies | Q22306374 |
Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol | Q22337068 | ||
Mapping a Mendelian form of intracranial aneurysm to 1p34.3-p36.13 | Q24530733 | ||
Search for intracranial aneurysm susceptibility gene(s) using Finnish families | Q24799061 | ||
The Familial Intracranial Aneurysm (FIA) study protocol | Q24801697 | ||
Unruptured intracranial aneurysms: prospective data have arrived | Q30812293 | ||
Lack of association between endoglin intron 7 insertion polymorphism and intracranial aneurysms in a white population: evidence of racial/ethnic differences | Q31028420 | ||
Collagen organization in the branching region of human brain arteries | Q32038470 | ||
The detection and management of unruptured intracranial aneurysms | Q33179583 | ||
Tissue inhibitor of metalloproteinases-1, -2, and -3 polymorphisms in a white population with intracranial aneurysms | Q33194728 | ||
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 7q11 | Q34020559 | ||
Electrothrombosis of saccular aneurysms via endovascular approach. Part 2: Preliminary clinical experience | Q34114645 | ||
Mutation detection of PKD1 identifies a novel mutation common to three families with aneurysms and/or very-early-onset disease | Q34146291 | ||
Association between heritable connective tissue disorders and intracranial aneurysms | Q34154210 | ||
Advances in the genetics of cerebrovascular disease and stroke | Q34242566 | ||
Follow-up of intracranial aneurysms in autosomal-dominant polycystic kidney disease | Q34313894 | ||
The ACE I allele is associated with increased risk for ruptured intracranial aneurysms | Q35435193 | ||
The pathobiology of aortic aneurysms | Q35688072 | ||
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 aneurysms | Q38626835 | ||
The incidence and treatment of asymptomatic, unruptured cerebral aneurysms | Q39405841 | ||
Absence of linkage of familial intracranial aneurysms to 7q11 in highly aggregated Japanese families | Q39644766 | ||
II genotype of the angiotensin-converting enzyme gene increases the risk for subarachnoid hemorrhage from ruptured aneurysm | Q39686013 | ||
Bifurcation geometry and the presence of cerebral artery aneurysms | Q39689916 | ||
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 hemorrhage | Q39708092 | ||
Neurovascular manifestations of heritable connective tissue disorders. A review | Q40741519 | ||
Importance of management of unruptured cerebral aneurysms | Q40893990 | ||
Morphometric analysis of reticular and elastin fibers in the cerebral arteries of patients with intracranial aneurysms | Q41233977 | ||
Prevalence and risk of rupture of intracranial aneurysms: a systematic review | Q41691486 | ||
The presence of tandem endothelial nitric oxide synthase gene polymorphisms identifying brain aneurysms more prone to rupture | Q42651906 | ||
Interleukin 1beta-511 C/T polymorphism and risk of aneurysmal subarachnoid haemorrhage | Q42718511 | ||
Subarachnoid haemorrhage in first and second degree relatives of patients with subarachnoid haemorrhage | Q42872719 | ||
Aneurysmal subarachnoid hemorrhage in Izumo City and Shimane Prefecture of Japan. Incidence | Q43454719 | ||
Association of positional and functional candidate genes FGF1, FBN2, and LOX on 5q31 with intracranial aneurysm | Q44443622 | ||
Polymorphisms of the NADPH oxidase P22PHOX gene in a Caucasian population with intracranial aneurysms | Q44586639 | ||
Prevalence of intracranial saccular aneurysms in a Japanese community based on a consecutive autopsy series during a 30-year observation period. The Hisayama study | Q44780472 | ||
Mutations in the lysyl oxidase gene not associated with intracranial aneurysm in central European families | Q44992602 | ||
The Risk of Subarachnoid and Intracerebral Hemorrhages in Blacks as Compared with Whites | Q46388332 | ||
Deficiencies in estrogen-mediated regulation of cerebrovascular homeostasis may contribute to an increased risk of cerebral aneurysm pathogenesis and rupture in menopausal and postmenopausal women | Q46852644 | ||
Extended single nucleotide polymorphism and haplotype analysis of the elastin gene in Caucasians with intracranial aneurysms provides evidence for racially/ethnically based differences | Q47288577 | ||
Matrix metalloproteinase-9 coding sequence single-nucleotide polymorphisms in caucasians with intracranial aneurysms | Q47297689 | ||
Influence of endothelial nitric oxide synthase T-786C single nucleotide polymorphism on aneurysm size | Q47394828 | ||
Endothelial nitric oxide synthase T-786C single nucleotide polymorphism: a putative genetic marker differentiating small versus large ruptured intracranial aneurysms | Q47425827 | ||
Elastin Polymorphism Haplotype and Intracranial Aneurysms Are Not Associated in Central Europe | Q47980217 | ||
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 aneurysms | Q57243053 | ||
Familial intracranial aneurysms | Q57784004 | ||
Examination of ELN as a Candidate Gene in the Utah Intracranial Aneurysm Pedigrees | Q59548778 | ||
Confirmation of chromosome 7q11 locus for predisposition to intracranial aneurysm | Q59548803 | ||
'Medial defects' in the prenatal human cerebral arteries: an electron microscopic study | Q71042776 | ||
Genotypic variations of type III collagen in patients with cerebral aneurysms | Q71469328 | ||
Familial aneurysmal subarachnoid hemorrhage: a community-based study | Q72038040 | ||
[Cerebellar infarcts that require differentiation from tumors: diagnosis with MRI] | Q72379314 | ||
Subarachnoid hemorrhage and family history. A population-based case-control study | Q72526382 | ||
Clinical analysis of incidentally discovered unruptured aneurysms | Q72628501 | ||
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 patients | Q72643554 | ||
Inflammation and intracranial aneurysms | Q73152826 | ||
Recurrence of intracranial aneurysms in autosomal-dominant polycystic kidney disease | Q73215823 | ||
Functional polymorphism in the matrix metalloproteinase-9 promoter as a potential risk factor for intracranial aneurysm | Q73230342 | ||
Type III collagen deficiency in a family with intracranial aneurysms | Q73552305 | ||
Unruptured intracranial aneurysms: natural history, clinical outcome, and risks of surgical and endovascular treatment | Q73681953 | ||
Genetic evaluation of lipoprotein(a) in intracranial aneurysm disease | Q74145786 | ||
Polymorphisms in matrix metalloproteinase-1, -3, -9, and -12 genes in relation to subarachnoid hemorrhage | Q74485860 | ||
Ultrastructural connective tissue aberrations in patients with intracranial aneurysms | Q74743027 | ||
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 walls | Q74794806 | ||
Collagen type I alpha2 (COL1A2) is the susceptible gene for intracranial aneurysms | Q75319587 | ||
Polymorphism of the endoglin gene in patients with intracranial saccular aneurysms | Q77386719 | ||
Asymptomatic familial cerebral aneurysms | Q77390912 | ||
Angiotensin I-converting enzyme gene polymorphism in intracranial saccular aneurysm individuals | Q77454471 | ||
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 2p13 | Q80496932 | ||
Absence of alpha-1 antitrypsin deficiency alleles (S and Z) in Japanese and Korean patients with aneurysmal subarachnoid hemorrhage | Q80968098 | ||
Genome-wide scan for Japanese familial intracranial aneurysms: linkage to several chromosomal regions | Q81072729 | ||
P433 | issue | 7 | |
P304 | page(s) | 587-594 | |
P577 | publication date | 2006-05-31 | |
P1433 | published in | Journal of Human Genetics | Q6295302 |
P1476 | title | The genetics of intracranial aneurysms | |
P478 | volume | 51 |
Q51234648 | A 54-year-old man with 12 intracranial aneurysms and familial subarachnoid hemorrhage: case report. |
Q37601496 | A Review of the Genetics of Intracranial Berry Aneurysms and Implications for Genetic Counseling |
Q85075384 | A rare association of ruptured left middle cerebral artery aneurysm and dextrocardia with situs inversus totalis |
Q34228630 | Anesthetic management of patients with intracranial aneurysms. |
Q92023931 | Aneurysm Formation, Growth, and Rupture: The Biology and Physics of Cerebral Aneurysms |
Q42101613 | Association of Versican (VCAN) gene polymorphisms rs251124 and rs2287926 (G428D), with intracranial aneurysm. |
Q28649596 | Cerebral aneurysms: formation, progression, and developmental chronology |
Q38369977 | Collagen Type I Alpha 2 (COL1A2) Polymorphism Contributes to Intracranial Aneurysm Susceptibility: A Meta-Analysis. |
Q46108176 | Endovascular Biopsy: In Vivo Cerebral Aneurysm Endothelial Cell Sampling and Gene Expression Analysis |
Q34971540 | From GWAS to the clinic: risk factors for intracranial aneurysms |
Q92350487 | Gene Expression in Intracranial Aneurysms-Comparison Analysis of Aneurysmal Walls and Extracranial Arteries with Real-Time Polymerase Chain Reaction and Immunohistochemistry |
Q37027180 | Genetic risk factors for intracranial aneurysms: a meta-analysis in more than 116,000 individuals |
Q84543448 | Genome-wide association study to identify genetic variants present in Japanese patients harboring intracranial aneurysms |
Q36111357 | Interactions of miR-34b/c and TP53 polymorphisms on the risk of intracranial aneurysm |
Q40080487 | Knowledge environments representing molecular entities for the virtual physiological human |
Q86034429 | Lack of association of lysyl oxidase (LOX) gene polymorphisms with intracranial aneurysm in a south Indian population |
Q37277240 | Molecular genetics of human intracranial aneurysms |
Q34281117 | Nature versus Nurture: Death of a Dogma, and the Road Ahead |
Q36514339 | OSIRISv1.2: a named entity recognition system for sequence variants of genes in biomedical literature |
Q36920195 | Physical factors effecting cerebral aneurysm pathophysiology |
Q39286785 | RNF213 Is Associated with Intracranial Aneurysms in the French-Canadian Population |
Q89574610 | Rare and Low-Frequency Variant of ARHGEF17 Is Associated With Intracranial Aneurysms |
Q89574589 | Rho Guanine Nucleotide Exchange Factor ARHGEF17 Is a Risk Gene for Intracranial Aneurysms |
Q38200573 | Smooth muscle cells and the formation, degeneration, and rupture of saccular intracranial aneurysm wall--a review of current pathophysiological knowledge |
Q55043122 | Systematic screening of lysyl oxidase-like (LOXL) family genes demonstrates that LOXL2 is a susceptibility gene to intracranial aneurysms. |
Q92862825 | The Association between Genes Polymorphisms of Heparan Sulfate Proteoglycan 2 (HSPG2) and Chondroitin Sulfate Proteoglycan 2 (CSPG2) and Intracranial Aneurysm Susceptibility: A Meta-Analysis |
Q38131014 | The genetics of vascular complications in autosomal dominant polycystic kidney disease (ADPKD). |
Q37126431 | The influence of genetics on intracranial aneurysm formation and rupture: current knowledge and its possible impact on future treatment. |
Q38560064 | Treatment of Intracranial Aneurysms: Clipping Versus Coiling. |
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