Evidence map›Paper›PMID 28132164›Full record

ArticleEndocrine2017

A novel MKRN3 nonsense mutation causing familial central precocious puberty.

Athanasios Christoforidis, Nicos Skordis, Pavlos Fanis, Meropi Dimitriadou, Maria Sevastidou, Marie M Phelan, Vassos Neocleous, Leonidas A Phylactou

Open access · greenAbstract readCase ReportsLetter
PubMed Publisher
In one paragraph

Article in Endocrine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

19 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Effect of Propolis on Precocious Puberty in Female RatsJournal of clinical research in pediatric endocrinology · 2022
    Article
  6. Methylation status of hypothalamicFrontiers in endocrinology · 2022
    Article
  7. Genetic causes of central precocious puberty.Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology · 2022
    Review
  8. Article
  9. Review
  10. Makorin RING finger protein 3 and central precocious puberty.Current opinion in endocrine and metabolic research · 2020
    Article
  11. Article
  12. Journal of the Endocrine Society · 2019
    Article
  13. Article
  14. Review
  15. Article
  16. Genetics of pubertal timing.Current opinion in pediatrics · 2018
    Review
  17. Hypothalamic epigenetics driving female puberty.Journal of neuroendocrinology · 2018
    Review
  18. Observational
  19. 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

8 authors at 4 institutions in 3 countries.

Athanasios Christoforidis1st Pediatric Department, Aristotle University of Thessaloniki, Thessaloniki, Greece. christoforidis@doctors.org.uk.
Nicos SkordisDivision of Pediatric Endocrinology, Paedi Center for specialized Pediatrics, Nicosia, Cyprus.
Pavlos FanisDepartment of Molecular Genetics, Function & Therapy, The Cyprus Institute of Neurology & Genetics, Nicosia, Cyprus.
Meropi Dimitriadou1st Pediatric Department, Aristotle University of Thessaloniki, Thessaloniki, Greece.
Maria SevastidouDepartment of Molecular Genetics, Function & Therapy, The Cyprus Institute of Neurology & Genetics, Nicosia, Cyprus.
Marie M PhelanNMR Center for Structural Biology, Institute of Integrative Biology, University of Liverpool, Liverpool, UK.
Vassos NeocleousDepartment of Molecular Genetics, Function & Therapy, The Cyprus Institute of Neurology & Genetics, Nicosia, Cyprus.
Leonidas A PhylactouDepartment of Molecular Genetics, Function & Therapy, The Cyprus Institute of Neurology & Genetics, Nicosia, Cyprus.
Cyprus Institute of Neurology and Genetics · CYAristotle University of Thessaloniki · GRUniversity of Liverpool · GBUniversity of Nicosia · CY

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Codon, NonsenseAmino Acid SubstitutionChildDNA Mutational AnalysisFathersFemaleHeterozygoteHumansPedigreePuberty, PrecociousRibonucleoproteinsSex DistributionSiblingsUbiquitin-Protein LigasesCodon, NonsenseMKRN3 protein, humanRibonucleoproteinsUbiquitin-Protein Ligases

Identifiers

PMID28132164
OpenAlexW2511919177

What OpenQuestion holds

Textmetadata
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.