Evidence map›Paper›PMID 34615878›Full record

ArticleNature communications2021

Author Correction: Rare genetic variants affecting urine metabolite levels link population variation to inborn errors of metabolism.

Yurong Cheng, Pascal Schlosser, Johannes Hertel, Peggy Sekula, Peter J Oefner, Ute Spiekerkoetter, Johanna Mielke, Daniel F Freitag, Miriam Schmidts, GCKD Investigators and 5 more

Abstract readPublished Erratum
PubMed Full text at PMC Publisher
In one paragraph

Article in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors.

Yurong ChengInstitute of Genetic Epidemiology, Faculty of Medicine and Medical Center, University of Freiburg, Freiburg, Germany.
Pascal SchlosserInstitute of Genetic Epidemiology, Faculty of Medicine and Medical Center, University of Freiburg, Freiburg, Germany.ORCID http://orcid.org/0000-0002-8460-0462
Johannes HertelSchool of Medicine, National University of Ireland, Galway, Galway, Ireland.
Peggy SekulaInstitute of Genetic Epidemiology, Faculty of Medicine and Medical Center, University of Freiburg, Freiburg, Germany.ORCID http://orcid.org/0000-0003-2263-447X
Peter J OefnerInstitute of Functional Genomics, University of Regensburg, Regensburg, Germany.
Ute SpiekerkoetterDepartment of General Pediatrics and Adolescent Medicine, Medical Center and Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Johanna MielkeDivision Pharmaceuticals, Open Innovation & Digital Technologies, Bayer AG, Wuppertal, Germany.
Daniel F FreitagDivision Pharmaceuticals, Open Innovation & Digital Technologies, Bayer AG, Wuppertal, Germany.ORCID http://orcid.org/0000-0003-0857-8950
Miriam SchmidtsDepartment of General Pediatrics and Adolescent Medicine, Medical Center and Faculty of Medicine, University of Freiburg, Freiburg, Germany.ORCID http://orcid.org/0000-0002-1714-6749
GCKD Investigators
Florian KronenbergInstitute of Genetic Epidemiology, Department of Genetics and Pharmacology, Medical University of Innsbruck, Innsbruck, Austria.ORCID http://orcid.org/0000-0003-2229-1120
Kai-Uwe EckardtDepartment of Nephrology and Hypertension, University of Erlangen-Nürnberg, Erlangen, Germany.ORCID http://orcid.org/0000-0003-3823-0920
Ines ThieleSchool of Medicine, National University of Ireland, Galway, Galway, Ireland.
Yong LiInstitute of Genetic Epidemiology, Faculty of Medicine and Medical Center, University of Freiburg, Freiburg, Germany.ORCID http://orcid.org/0000-0003-2651-8791
Anna KöttgenInstitute of Genetic Epidemiology, Faculty of Medicine and Medical Center, University of Freiburg, Freiburg, Germany. anna.koettgen@uniklinik-freiburg.de.ORCID http://orcid.org/0000-0002-4671-3714

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID34615878
PMCPMC8494923

What OpenQuestion holds

Textmetadata
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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.