Evidence map›Paper›PMID 24824131›Full record

ArticleEuropean journal of human genetics : EJHG2014

Clinical utility gene card for: 15q13.3 microdeletion syndrome.

Maria Tropeano, Joris Andrieux, Evangelos Vassos, David A Collier

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in European journal of human genetics : EJHG, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. 15q13.3 duplication in two patients with childhood-onset schizophrenia.American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics · 2016
    Article
  5. Article
  6. 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

4 authors.

Maria TropeanoMRC Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, King's College London, London, UK.
Joris AndrieuxInstitut de Génétique Médicale, CHRU de Lille, Lille, France.
Evangelos VassosMRC Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, King's College London, London, UK.
David A Collier1] MRC Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, King's College London, London, UK [2] Discovery Neuroscience Research, Eli Lilly and Company Ltd, Lilly Research Laboratories, Erl Wood Manor, Surrey, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

alpha7 Nicotinic Acetylcholine ReceptorCell Cycle ProteinsChromosome DeletionChromosome DisordersChromosomes, Human, Pair 15EndodeoxyribonucleasesExodeoxyribonucleasesGenetic TestingHumansIntellectual DisabilityKruppel-Like Transcription FactorsMultifunctional EnzymesPolymorphism, Single NucleotideRepressor ProteinsSeizuresalpha7 Nicotinic Acetylcholine ReceptorCell Cycle ProteinsChrna7 protein, humanEndodeoxyribonucleasesExodeoxyribonucleasesFAN1 protein, humanKLF13 protein, humanKruppel-Like Transcription FactorsMultifunctional EnzymesRepressor Proteins

Identifiers

PMID24824131
PMCPMC4200442

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.