Evidence map›Paper›PMID 25529856›Full record

ArticleJournal of molecular neuroscience : MN2015

Genetic variability testing of neurodevelopmental genes in schizophrenic patients.

Tea Terzić, Matej Kastelic, Vita Dolžan, Blanka Kores Plesničar

Abstract read
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In one paragraph

Article in Journal of molecular neuroscience : MN, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 2 pooled it
1.1field-weighted citation impact, top 23% 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

15 citing papers in PubMed, 2 syntheses or guidelines pooled it, 20 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Review
  5. Review
  6. Article
  7. Association ofHealth science reports · 2024
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  11. Association Study ofJournal of personalized medicine · 2023
    Article
  12. Article
  13. Article
  14. Theranostic Biomarkers for Schizophrenia.International journal of molecular sciences · 2017
    Review
  15. 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 at 2 institutions in 1 country.

Tea TerzićUniversity Psychiatric Clinic Ljubljana, Studenec 48, 1260, Ljubljana, Slovenia.
Matej Kastelic
Vita Dolžan
Blanka Kores Plesničar
University of Ljubljana · SIUniversity Psychiatric Hospital · SI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study investigated the associations between single nucleotide polymorphisms in the neurodevelopmental Disrupted In Schizophrenia 1 (DISC1 ), neuregulin 1 (NRG1), brain-derived neurotrophic factor (BDNF) and NOTCH4 genes and the clinical symptoms and the occurrence of treatment-resistant schizophrenia in the Slovenian population. We included 138 schizophrenia patients, divided into treatment-responsive and treatment-resistant group and 94 healthy blood donors. All subjects were genotyped for eight polymorphisms (DISC1 rs6675281, DISC1 rs821616, NRG1 rs3735781, NRG1 rs3735782, NRG1 rs10503929, NRG1 rs3924999, BDNF rs6265, NOTCH rs367398) and investigated for associations with clinical variables. NOTCH4 rs367398 AA/AG was significantly associated with worse Positive and Negative Syndrome Scale (PANSS) and Clinical Global Impression (CGI) score. NOTCH4 rs367398 was not statistically significantly associated with the occurrence of treatment-resistant schizophrenia after the correction for multiple testing. Our data indicate that NOTCH4 polymorphism can influence clinical symptoms in Slovenian patients with schizophrenia.

Indexed as

Polymorphism, Single NucleotideAdultBrain-Derived Neurotrophic FactorCase-Control StudiesFemaleHumansMaleMiddle AgedNerve Tissue ProteinsNeuregulin-1Proto-Oncogene ProteinsReceptor, Notch4Receptors, NotchSchizophreniaBDNF protein, humanBrain-Derived Neurotrophic FactorDISC1 protein, humanNerve Tissue ProteinsNeuregulin-1NOTCH4 protein, humanNRG1 protein, humanProto-Oncogene ProteinsReceptor, Notch4Receptors, Notch

Identifiers

PMID25529856
OpenAlexW2028034898

What OpenQuestion holds

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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.