Evidence map›Paper›PMID 26690531›Full record

ArticleJournal of genetics2015

Genetic screening of EXT1 and EXT2 in Cypriot families with hereditary multiple osteochondromas.

George A Tanteles, Michael Nicolaou, Vassos Neocleous, Christos Shammas, Maria A Loizidou, Angelos Alexandrou, Elena Ellina, Nasia Patsia, Carolina Sismani, Leonidas A Phylactou and 1 more

Open access · greenAbstract read
PubMed Publisher
In one paragraph

Article in Journal of genetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.5field-weighted citation impact, top 29% 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

7 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Benign tumors of the chest wall.Journal of thoracic disease · 2024
    Review
  3. Article
  4. Mutational Analysis ofBioMed research international · 2021
    Article
  5. Article
  6. Article
  7. Article
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

11 authors at 1 institution in 1 country.

George A TantelesDepartment of Clinical Genetics, The Cyprus Institute of Neurology and Genetics, Nicosia CY2370, Cyprus. gtanteles@cing.ac.cy.
Michael Nicolaou
Vassos Neocleous
Christos Shammas
Maria A Loizidou
Angelos Alexandrou
Elena Ellina
Nasia Patsia
Carolina Sismani
Leonidas A Phylactou
Violetta Christophidou-Anastasiadou
Cyprus Institute of Neurology and Genetics · CY

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

AdolescentAdultChild, PreschoolExostoses, Multiple HereditaryExostosin 1Exostosin 2FemaleGenetic TestingHumansMaleMiddle AgedN-AcetylglucosaminyltransferasesExostosin 1Exostosin 2N-Acetylglucosaminyltransferases

Identifiers

PMID26690531
OpenAlexW2218376176

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.