Evidence map›Paper›PMID 35272364›Full record

ArticleThrombosis and haemostasis2022

Integrated GWAS and Gene Expression Suggest ORM1 as a Potential Regulator of Plasma Levels of Cell-Free DNA and Thrombosis Risk.

Sonia Lopez, Angel Martinez-Perez, Alba Rodriguez-Rius, Ana Viñuela, Andrew A Brown, Laura Martin-Fernandez, Noelia Vilalta, Marc Arús, Nikolaos I Panousis, Alfonso Buil and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Thrombosis and haemostasis, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.9field-weighted citation impact, top 28% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 6 institutions in 5 countries.

Sonia LopezGenomics of Complex Diseases Unit, Research Institute Hospital de la Santa Creu i Sant Pau, IIB Sant Pau, Barcelona, Spain.ORCID 0000-0002-5023-5153
Angel Martinez-PerezGenomics of Complex Diseases Unit, Research Institute Hospital de la Santa Creu i Sant Pau, IIB Sant Pau, Barcelona, Spain.ORCID 0000-0002-5934-1454
Alba Rodriguez-RiusGenomics of Complex Diseases Unit, Research Institute Hospital de la Santa Creu i Sant Pau, IIB Sant Pau, Barcelona, Spain.
Ana ViñuelaBiosciences Institute, Faculty of Medicine, Newcastle University, Newcastle Upon Tyne, United Kingdom.
Andrew A BrownPopulation Health and Genomics, University of Dundee, Dundee, Scotland, United Kingdom.
Laura Martin-FernandezGenomics of Complex Diseases Unit, Research Institute Hospital de la Santa Creu i Sant Pau, IIB Sant Pau, Barcelona, Spain.
Noelia VilaltaHaemostasis and Thrombosis Unit, Department of Hematology, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
Marc ArúsHaemostasis and Thrombosis Unit, Department of Hematology, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
Nikolaos I PanousisWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, South Cambridgeshire, United Kingdom.
Alfonso BuilInstitute of Biological Psychiatry, Mental Health Sct. Hans Hospital, Roskilde, Denmark.
Maria Sabater-LlealGenomics of Complex Diseases Unit, Research Institute Hospital de la Santa Creu i Sant Pau, IIB Sant Pau, Barcelona, Spain.
Juan Carlos SoutoHaemostasis and Thrombosis Unit, Department of Hematology, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
Emmanouil T DermitzakisDepartment of Genetic Medicine and Development, University of Geneva, Geneva, Switzerland.
Jose Manuel SoriaGenomics of Complex Diseases Unit, Research Institute Hospital de la Santa Creu i Sant Pau, IIB Sant Pau, Barcelona, Spain.
Hospital de Sant Pau · ESUniversity of Geneva · CHNewcastle University · GBSankt Hans Hospital · DKUniversitat Autònoma de Barcelona · ESUniversity of Dundee · GB

Funding

CP17/00142 Miguel Servet contract from the ISCIIIFI2017B_00673 Agència de Gestió d'ajuts Universitaris i de RecercaPI14/00582 Instituto de Salud Carlos III and Fondo de Investigación Sanitaria (ISCIII-FIS)PI17/00059 Instituto de Salud Carlos III and Fondo de Investigación Sanitaria (ISCIII-FIS)SGR 1736, J.M.S Grupo Consolidado Generalitat de Catalunya
6 · The paper itself

Abstract

Plasma cell-free DNA (cfDNA) is a surrogate marker of neutrophil extracellular traps (NETs) that contribute to immunothrombosis. There is growing interest about the mechanisms underlying NET formation and elevated cfDNA, but little is known about the factors involved. We aimed to identify genes involved in the regulation of cfDNA levels using data from the Genetic Analysis of Idiopathic Thrombophilia (GAIT-2) Project.Imputed genotypes, whole blood RNA-Seq data, and plasma cfDNA quantification were available for 935 of the GAIT-2 participants from 35 families with idiopathic thrombophilia. We performed heritability and GWAS analysis for cfDNA. The heritability of cfDNA was 0.26 (

Indexed as

Cell-Free Nucleic AcidsOrosomucoidThrombosisGene ExpressionGenome-Wide Association StudyHumansThrombophiliaCell-Free Nucleic AcidsORM1 protein, humanOrosomucoid

Identifiers

PMID35272364
PMCPMC9251712
OpenAlexW4220761785

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.