Evidence map›Paper›PMID 29632148›Full record

ArticleJournal of medical genetics2018

Elena Daniela Aflorei, Benjamin Klapholz, Chenghao Chen, Serban Radian, Anca Neluta Dragu, Nina Moderau, Chrisostomos Prodromou, Paulo S Ribeiro, Ralf Stanewsky, Márta Korbonits

Open access · hybridAbstract read
In one paragraph

Article in Journal of medical genetics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

13 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Frontiers in endocrinology · 2023
    Article
  7. Article
  8. Article
  9. Article
  10. Genetics of Acromegaly and Gigantism.Journal of clinical medicine · 2021
    Review
  11. Review
  12. Article
  13. Review
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

10 authors at 6 institutions in 6 countries.

Elena Daniela AfloreiCentre for Endocrinology, Barts and the London School of Medicine, Queen Mary University of London, London, UK.ORCID 0000-0002-7105-591X
Benjamin KlapholzDepartment of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK.
Chenghao ChenDepartment of Cell and Developmental Biology, Division of Biosciences, Faculty of Life Sciences, University College London, London, UK.
Serban RadianCentre for Endocrinology, Barts and the London School of Medicine, Queen Mary University of London, London, UK.
Anca Neluta DraguCentre for Endocrinology, Barts and the London School of Medicine, Queen Mary University of London, London, UK.
Nina ModerauProtein Dynamics and Cell Signalling Laboratory, Centre for Tumour Biology, Barts Cancer Institute, Queen Mary University of London, London, UK.
Chrisostomos ProdromouGenome Damage and Stability Centre, University of Sussex, Brighton, UK.
Paulo S RibeiroProtein Dynamics and Cell Signalling Laboratory, Centre for Tumour Biology, Barts Cancer Institute, Queen Mary University of London, London, UK.
Ralf StanewskyDepartment of Cell and Developmental Biology, Division of Biosciences, Faculty of Life Sciences, University College London, London, UK.
Márta KorbonitsCentre for Endocrinology, Barts and the London School of Medicine, Queen Mary University of London, London, UK.
Queen Mary University of London · GBCarol Davila University of Medicine and Pharmacy · ROUniversity College London · GBUniversity of Cambridge · GBUniversity of Münster · DEUniversity of Sussex · GB

Funding

Resource Component: Acquisition, maintenance and distribution of Drosophila stocksP40OD018537 · OD · TRUSTEES OF INDIANA UNIVERSITY · PI Annette L. Parks · 2014 to 2026
$13.5M
Medical Research Council MR/M018539/1NIH HHS P40 OD018537
6 · The paper itself

Abstract

backgroundHeterozygous germline loss-of-function mutations in the aryl hydrocarbon receptor-interacting protein gene (

objectiveTo develop an

methodsWe generated a null mutant of the

resultsWe found that human

conclusionOur

Indexed as

Genetic Association StudiesGenetic Predisposition to DiseaseMutation, MissenseAllelesAmino Acid SequenceAmino Acid SubstitutionAnimalsAnimals, Genetically ModifiedBiological AssayDrosophila melanogasterFemaleGene ExpressionGenetic TestingGenotypeHumansIntracellular Signaling Peptides and Proteinsaryl hydrocarbon receptor-interacting proteinIntracellular Signaling Peptides and ProteinsAIPdrosophila melanogasterFIPApathogenic genetic variantpituitary adenoma

Identifiers

PMID29632148
PMCPMC6073908
OpenAlexW2797286081

What OpenQuestion 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 OpenQuestion graph.