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

Burden of rare exome sequence variants in PROC gene is associated with venous thromboembolism: a population‐based study

4 Nov 2019

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 Blood Coagulation and Thrombosis Mechanisms
Share to Genomics and Rare Diseases
Share to Protease and Inhibitor Mechanisms

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 31680443
DOI: 10.1111/jth.14676

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Burden of rare exome sequence variants in PROC gene is associated with venous thromboembolism: a population‐based studyPMID 31680443Read ↗

Digenic Inheritance of PROC and SERPINC1 Mutations Contributes to Multiple Sites Venous Thrombosis.Semantic proximity Read ↗

Whole-exome sequencing of 14 389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factors.Semantic proximity Read ↗

What is currently known about the genetics of venous thromboembolism at the dawn of next generation sequencing technologies.Semantic proximity Read ↗

Thrombotic Risk Determined by Protein C Receptor (PROCR) Variants among Middle-Aged and Older Adults: A Population-Based Cohort StudySemantic proximity Read ↗

Exploring genetic drivers of unexplained venous thromboembolism through whole-exome sequencing.Semantic proximity Read ↗

Whole Genome Analysis of Venous Thromboembolism: the Trans-Omics for Precision Medicine Program.Semantic proximity Read ↗

A large-scale exome array analysis of venous thromboembolism.Semantic proximity Read ↗

Whole-exome sequencing in evaluation of patients with venous thromboembolismSemantic proximity Read ↗

Whole Exome Sequencing Identifies genetic variants in Chinese Han pregnant women with Venous thromboembolism-a case control studySemantic proximity Read ↗

Venous thromboembolic disease genetics: from variants to function.Semantic proximity Read ↗

Human genetics implicate thromboembolism in the pathogenesis of long COVID in individuals of European ancestrySemantic proximity Read ↗

Whole-exome sequencing identifies rare variants in STAB2 associated with venous thromboembolic disease.Semantic proximity Read ↗

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