Evidence map›Paper›PMID 28271036›Full record

ArticleMolecular metabolism2017

Functional and clinical relevance of novel and known

Dennis Löffler, Susanne Behrendt, John W M Creemers, Jürgen Klammt, Gabriela Aust, Juraj Stanik, Wieland Kiess, Peter Kovacs, Antje Körner

Open access · goldAbstract read
In one paragraph

Article in Molecular metabolism, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

23 citing papers in PubMed, 47 citations in OpenAlex.

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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

9 authors at 5 institutions in 3 countries.

Dennis LöfflerCenter for Pediatric Research Leipzig, University Hospital for Children & Adolescents, University of Leipzig, Leipzig, Germany; Integrated Research and Treatment Center (IFB) Adiposity Diseases, Medical Faculty, University of Leipzig, Leipzig, Germany.
Susanne BehrendtCenter for Pediatric Research Leipzig, University Hospital for Children & Adolescents, University of Leipzig, Leipzig, Germany; Integrated Research and Treatment Center (IFB) Adiposity Diseases, Medical Faculty, University of Leipzig, Leipzig, Germany.
John W M CreemersDepartment of Human Genetics, University of Leuven, Leuven, Belgium.
Jürgen KlammtCenter for Pediatric Research Leipzig, University Hospital for Children & Adolescents, University of Leipzig, Leipzig, Germany.
Gabriela AustResearch Laboratories of the Department of Surgery, University of Leipzig, Leipzig, Germany.
Juraj StanikCenter for Pediatric Research Leipzig, University Hospital for Children & Adolescents, University of Leipzig, Leipzig, Germany; First Department of Pediatrics, Medical Faculty at Comenius University, Bratislava, Slovakia; DIABGENE Laboratory, Institute of Experimental Endocrinology, Biomedical Research Center SAS, Bratislava, Slovakia.
Wieland KiessCenter for Pediatric Research Leipzig, University Hospital for Children & Adolescents, University of Leipzig, Leipzig, Germany.
Peter KovacsIntegrated Research and Treatment Center (IFB) Adiposity Diseases, Medical Faculty, University of Leipzig, Leipzig, Germany.
Antje KörnerCenter for Pediatric Research Leipzig, University Hospital for Children & Adolescents, University of Leipzig, Leipzig, Germany; Integrated Research and Treatment Center (IFB) Adiposity Diseases, Medical Faculty, University of Leipzig, Leipzig, Germany. Electronic address: antje.koerner@medizin.uni-leipzig.de.
Leipzig University · DEUniversity Hospital Leipzig · DEIFB Adiposity Diseases · DEInstitute of Experimental Endocrinology of the Slovak Academy of Sciences · SKKU Leuven · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveVariants in

resultsIn 52 obese children selected for elevated proinsulin levels and/or impaired glucose tolerance, we found eight known variants and two novel heterozygous variants (c.1095 + 1G > A and p.S24C) by sequencing the

conclusionsWe identified and functionally characterized two rare novel

Indexed as

AdolescentBlood GlucoseChildFemaleGenetic Predisposition to DiseaseGenotypeGlucoseGlucose IntoleranceHumansInsulinMalePediatric ObesityPolymorphism, Single NucleotideProprotein Convertase 1Blood GlucoseGlucoseInsulinPCSK1 protein, humanProprotein Convertase 1ChildrenObesityPC1/3PCSK1Prohormone convertase 1/3

Identifiers

PMID28271036
PMCPMC5323889
OpenAlexW2559747420

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.