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

Redefining common and rare HTRA1 variants as risk factors for polyvascular disease.

Nature cardiovascular research - 1 Jun 2024

Debette Stéphanie, Ihara Masafumi

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Genetic Predisposition to Disease
Share to High-Temperature Requirement A Serine Peptidase 1
Share to Phenotype
Share to Polymorphism, Single Nucleotide

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Risk Assessment

Share to Risk Factors

Source

Identifiers

PMID: 39196235
DOI: 10.1038/s44161-024-00492-2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Redefining common and rare HTRA1 variants as risk factors for polyvascular disease.PMID 39196235Read ↗

Genetically proxied HTRA1 protease activity and circulating levels independently predict risk of ischemic stroke and coronary artery disease.Semantic proximity Read ↗

Genetically proxied HTRA1 protease activity and circulating levels independently predict risk of ischemic stroke and coronary artery diseaseSemantic proximity Read ↗

Human NPY gene variants in cardiovascular and metabolic diseases.Semantic proximity Read ↗

Meta-Analysis of the Association Between the rs228570 Vitamin D Receptor Gene Polymorphism and Arterial Hypertension Risk.Semantic proximity Read ↗

Novel nonsynonymous variants associated with blood pressure control in response to antihypertensives and their impact on cardiovascular outcomes.Semantic proximity Read ↗

Rare Variants in HTRA1, SGTB, and RBM12 Confer Risk of Atherosclerotic Cardiovascular Disease Independent of Traditional Cardiovascular Risk Factors.Semantic proximity Read ↗

Cerebral small vessel disease caused by a novel heterozygous mutation in HTRA1.Semantic proximity Read ↗

A genome-wide association study of treated A1C: a genetic needle in an environmental haystack?Semantic proximity Read ↗

Human thromboxane A2 receptor genetic variants: in silico, in vitro and "in platelet" analysis.Semantic proximity Read ↗

A missense <i>HTRA1</i> mutation expands CARASIL syndrome to the Caucasian populationSemantic proximity Read ↗

ACTN1 variants associated with thrombocytopenia.Semantic proximity Read ↗

Genetic variation in ABCA1 and risk of cardiovascular disease.Semantic proximity Read ↗

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