Associated Papers
Rare damaging CCR2 variants are associated with lower lifetime cardiovascular risk.
Georgakis MK et al.
Genome Medicine, 2025
Rare damaging CCR2 variants are associated with lower lifetime cardiovascular risk.
Georgakis MK et al.
Medrxiv : the Preprint Server for Health Sciences, 2024
Identifying new potential genetic biomarkers for HELLP syndrome using massive parallel sequencing.
Jiménez KM et al.
Pregnancy Hypertension, 2020
Exploring the Molecular Aetiology of Preeclampsia by Massive Parallel Sequencing of DNA.
Laissue P et al.
Current Hypertension Reports, 2020
Genome sequencing elucidates Sardinian genetic architecture and augments association analyses for lipid and blood inflammatory markers.
Sidore C et al.
Nature Genetics, 2015
Select a paper to view details