Discover Community Create You

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

Population-based assessment of familial inheritance and neurologic comorbidities among patients with an isolated atrial septal defect.

Congenital heart disease - 1 Jan 2000

Steenblik Matthew H, Mineau Geraldine P, Pimentel Richard, Michaels Andrew D

Abstract excerpt

BACKGROUND: Interatrial shunts, caused by either atrial septal defect (ASD) or patent foramen ovale, have been reported to have a familial association. We sought to examine the familial risk of isolated interatrial shunt and explore associated comorbidities of stroke, transient ischemic attack (TIA), and migraine using a population database. METHODS: The Utah Population Database is linked to inpatient and...

Read the complete abstract on PubMed

Topics

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

Share to Cerebrovascular Disorders
Share to Comorbidity

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Databases, Factual

Share to Heart Septal Defects, Atrial

Share to Ischemic Attack, Transient

Share to Migraine Disorders

Share to Siblings

Share to Stroke

Source

Identifiers

PMID: 19925540
DOI: 10.1111/j.1747-0803.2009.00340.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Population-based assessment of familial inheritance and neurologic comorbidities among patients with an isolated atrial septal defect.PMID 19925540Read ↗

Association of a Family History of Atrial Fibrillation With Incidence and Outcomes of Atrial Fibrillation: A Population-Based Family Cohort Study.Semantic proximity Read ↗

Risk of Stroke in Patients With Atrial Fibrillation Is Associated With Stroke in Siblings: A Nationwide Study.Semantic proximity Read ↗

Association Between Family History and Early-Onset Atrial Fibrillation Across Racial and Ethnic Groups.Semantic proximity Read ↗

Risk Factors for Syncope Associated With Multigenerational Relatives With a History of Syncope.Semantic proximity Read ↗

Family history of stroke and cardiovascular diseases in early-onset cryptogenic ischaemic stroke.Semantic proximity Read ↗

Genetic Epidemiology of Spontaneous Subarachnoid HemorrhageSemantic proximity Read ↗

Variants in the FLT4 and HYDIN genes are related to the susceptibility of atrial septal defects in southwest Han people of ChinaSemantic proximity Read ↗

The association between interatrial shunt and subtypes of migraine: a Mendelian randomization study.Semantic proximity Read ↗

Association between the European GWAS-identified susceptibility locus at chromosome 4p16 and the risk of atrial septal defect: a case-control study in Southwest China and a meta-analysis.Semantic proximity Read ↗

Clinical and genetic investigation of atrial septal defect with atrioventricular conduction defect in a large consanguineous Tunisian family.Semantic proximity Read ↗

Familial clustering and subsequent incidence of atrial fibrillation among first-degree relatives in Denmark.Semantic proximity Read ↗

Inheritance of persistent foramen ovale and atrial septal defects and the relation to familial migraine with auraSemantic proximity Read ↗

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