Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Association between polymorphisms rs1333040 and rs7865618 of chromosome 9p21 and sporadic brain arteriovenous malformations.

Cerebrovascular diseases (Basel, Switzerland) - 1 Jan 2014

Sturiale Carmelo Lucio, Fontanella Marco Maria, Gatto Ilaria, Puca Alfredo, Giarretta Igor, D'Arrigo Sonia, Lofrese Giorgio, Rainero Innocenzo, Gallone Salvatore, Pinessi Lorenzo, Ducati Alessandro, Maira Giulio, Pola Roberto

Abstract excerpt

BACKGROUND: The chromosomal locus 9p21 is a novel genetic marker for a variety of cardiovascular and cerebrovascular diseases. In a recent study, we have demonstrated an association between the single nucleotide polymorphism (SNP) rs1333040C>T on chromosome 9p21 and sporadic brain arteriovenous malformations (BAVMs). Here, we extended our analysis to an additional SNP on chromosome 9p21 (rs7865618A>G) and...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Aged, 80 and over
Share to Child, Preschool

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosomes, Human, Pair 9

Share to Genetic Association Studies

Share to Intracranial Arteriovenous Malformations

Share to Polymorphism, Genetic

Share to Young Adult

Source

Identifiers

PMID: 24820060
DOI: 10.1159/000360752

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Association between polymorphisms rs1333040 and rs7865618 of chromosome 9p21 and sporadic brain arteriovenous malformations.PMID 24820060Read ↗

Association between the rs1333040 polymorphism on the chromosomal 9p21 locus and sporadic brain arteriovenous malformations.Semantic proximity Read ↗

Common variants on 9p21.3 are associated with brain arteriovenous malformations with accompanying arterial aneurysms.Semantic proximity Read ↗

Genome-wide association study of sporadic brain arteriovenous malformations.Semantic proximity Read ↗

Susceptibility loci for sporadic brain arteriovenous malformation; a replication study and meta-analysis.Semantic proximity Read ↗

Single nucleotide polymorphisms associated with sporadic brain arteriovenous malformations: where do we stand?Semantic proximity Read ↗

Exome-wide Analysis of De Novo and Rare Genetic Variants in Patients With Brain Arteriovenous Malformation.Semantic proximity Read ↗

Polymorphisms of the vascular endothelial growth factor A gene and susceptibility to sporadic brain arteriovenous malformation in a Chinese population.Semantic proximity Read ↗

Are there genetic influences on sporadic brain arteriovenous malformations?Semantic proximity Read ↗

The rs9509 polymorphism of MMP-9 is associated with risk of hemorrhage in brain arteriovenous malformations.Semantic proximity Read ↗

The rs522616 polymorphism in the matrix metalloproteinase-3 (MMP-3) gene is associated with sporadic brain arteriovenous malformation in a Chinese population.Semantic proximity Read ↗

High-Throughput Sequencing to Detect Novel Likely Gene-Disrupting Variants in Pathogenesis of Sporadic Brain Arteriovenous MalformationsSemantic proximity Read ↗

Confirmation of an association of single-nucleotide polymorphism rs1333040 on 9p21 with familial and sporadic intracranial aneurysms in Japanese patients.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.