Evidence map›Paper›PMID 33832210›Full record

ArticleHaematologica2021

Heritability and association with distinct genetic loci of erythropoietin levels in the general population.

Tanguy Corre, Belen Ponte, Edward Pivin, Menno Pruijm, Daniel Ackermann, Georg Ehret, Katharina Spanaus, Murielle Bochud, Roland H Wenger

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

Article in Haematologica, 2021. 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 39% 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. Fount, fate, features, and function of renal erythropoietin-producing cells.Pflugers Archiv : European journal of physiology · 2022
    Review
  3. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 7 institutions in 3 countries.

Tanguy CorreCenter for Primary Care and Public Health (Unisanté), University of Lausanne, Lausanne, Switzerland; National Centre of Competence in Research "Kidney.CH", Switzerland; Department of Computational Biology, University of Lausanne, Lausanne.
Belen PonteNephrology Service, Department Medicine, Geneva University Hospital, Geneva.
Edward PivinCenter for Primary Care and Public Health (Unisanté), University of Lausanne, Lausanne.
Menno PruijmNephrology Service, University Hospital of Lausanne and University of Lausanne, Lausanne.
Daniel AckermannDepartment of Nephrology and Hypertension, Inselspital, Bern University Hospital, University of Bern, Bern.
Georg EhretCardiology, Department of Medicine, Geneva University Hospital, Geneva.
Katharina SpanausInstitute of Clinical Chemistry, University Hospital of Zurich, Zurich.
Murielle BochudCenter for Primary Care and Public Health (Unisanté), University of Lausanne, Lausanne, Switzerland; National Centre of Competence in Research "Kidney.CH".
Roland H WengerNational Centre of Competence in Research "Kidney.CH", Switzerland; Institute of Physiology, University of Zurich, Zurich. roland.wenger@access.uzh.ch.
Centre universitaire de médecine générale et santé publique, Lausanne · CHCzech Academy of Sciences, Institute of Physiology · CZGeneva College · USUniversity Hospital of Bern · CHUniversity Hospital of Lausanne · CHUniversity Hospital of Zurich · CHUniversity of Lausanne · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

ErythropoietinGenetic LociGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansPolymorphism, Single NucleotideErythropoietin

Identifiers

PMID33832210
PMCPMC8409065
OpenAlexW3151715450

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.