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

A replication study of genetic risk loci for ischemic stroke in a Dutch population: a case-control study.

Scientific reports - 22 Sept 2017

Hauer Allard J, Pulit Sara L, van den Berg Leonard H, de Bakker Paul I W, Veldink Jan H, Ruigrok Ynte M

Abstract excerpt

We aimed to replicate reported associations of 10 SNPs at eight distinct loci with overall ischemic stroke (IS) and its subtypes in an independent cohort of Dutch IS patients. We included 1,375 IS patients enrolled in a prospective multicenter hospital-based cohort in the Netherlands, and 1,533 population-level controls of Dutch descent. We tested these SNPs for association with overall IS and its subtypes (large...

Read the complete abstract on PubMed

Topics

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

Share to Age Factors
Share to Aged
Share to Brain Ischemia

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Case-Control Studies

Share to Genetic Loci

Share to Netherlands

Share to Sex Factors

Share to Stroke

Source

Open in PubMed Open full text

Identifiers

PMID: 28939865
DOI: 10.1038/s41598-017-07404-4
PMCID: PMC5610184

Genes

PITX2
ZFHX3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A replication study of genetic risk loci for ischemic stroke in a Dutch population: a case-control study.PMID 28939865Read ↗

Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies.Semantic proximity Read ↗

Identification of Novel Genetic Risk Variants Associated With Early-Onset Ischemic Stroke in Taiwan.Semantic proximity Read ↗

Low-frequency and common genetic variation in ischemic stroke: The METASTROKE collaboration.Semantic proximity Read ↗

Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes.Semantic proximity Read ↗

Identification of 20 novel loci associated to ischemic stroke. Epigenome-Wide Association StudySemantic proximity Read ↗

Genetic Risk Factors for Ischemic and Hemorrhagic Stroke.Semantic proximity Read ↗

Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project.Semantic proximity Read ↗

Association of GWAS-Supported Variants rs2200733 and rs6843082 on Chromosome 4q25 with Ischemic Stroke in the Southern Chinese Han Population.Semantic proximity Read ↗

Genetic heritability of ischemic stroke and the contribution of previously reported candidate gene and genomewide associations.Semantic proximity Read ↗

Common variants at 6p21.1 are associated with large artery atherosclerotic stroke.Semantic proximity Read ↗

Effect of PITX2 genetic variants on the susceptibility to stroke in the Chinese Han population.Semantic proximity Read ↗

Variants in the Atherogenic ALOX5AP, THBD, and KNG1 Genes Potentiate the Risk of Ischemic Stroke via a Genetic Main Effect and Epistatic Interactions in a Chinese Population.Semantic proximity Read ↗

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