Evidence map›Paper›PMID 33036198›Full record

ArticleGenes2020

Jie Song, Katrin Hinderhofer, Lilian T Kaufmann, Nicola Benjamin, Christine Fischer, Ekkehard Grünig, Christina A Eichstaedt

Open access · goldAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Genes, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 33% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
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

7 authors at 2 institutions in 2 countries.

Jie SongLaboratory for Molecular Genetic Diagnostics, Institute of Human Genetics, Heidelberg University, Im Neuenheimer Feld 366, 69120 Heidelberg, Germany.
Katrin HinderhoferLaboratory for Molecular Genetic Diagnostics, Institute of Human Genetics, Heidelberg University, Im Neuenheimer Feld 366, 69120 Heidelberg, Germany.
Lilian T KaufmannLaboratory for Molecular Genetic Diagnostics, Institute of Human Genetics, Heidelberg University, Im Neuenheimer Feld 366, 69120 Heidelberg, Germany.
Nicola BenjaminCentre for Pulmonary Hypertension, Thoraxklinik gGmbH Heidelberg at Heidelberg University Hospital, Röntgenstrasse 1, 69126 Heidelberg, Germany.
Christine FischerLaboratory for Molecular Genetic Diagnostics, Institute of Human Genetics, Heidelberg University, Im Neuenheimer Feld 366, 69120 Heidelberg, Germany.
Ekkehard GrünigCentre for Pulmonary Hypertension, Thoraxklinik gGmbH Heidelberg at Heidelberg University Hospital, Röntgenstrasse 1, 69126 Heidelberg, Germany.
Christina A EichstaedtLaboratory for Molecular Genetic Diagnostics, Institute of Human Genetics, Heidelberg University, Im Neuenheimer Feld 366, 69120 Heidelberg, Germany.ORCID 0000-0001-7288-8297
Heidelberg University · DECentral South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pathogenic variants have been identified in 85% of heritable pulmonary arterial hypertension (PAH) patients. These variants were mainly located in the bone morphogenetic protein receptor 2 (

Indexed as

Gene Expression RegulationGenetic Predisposition to DiseaseMutationPromoter Regions, GeneticAdultBone Morphogenetic Protein Receptors, Type IIFemaleHumansMalePenetrancePulmonary Arterial HypertensionRetrospective StudiesBMPR2 protein, humanBone Morphogenetic Protein Receptors, Type IIBMPR2 promoterheritable pulmonary arterial hypertensionpathogenic variant

Identifiers

PMID33036198
PMCPMC7601247
OpenAlexW3091808625

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.