Evidence map›Paper›PMID 28623238›Full record

ArticleEMBO molecular medicine2017

A normal genetic variation modulates synaptic MMP-9 protein levels and the severity of schizophrenia symptoms.

Katarzyna Lepeta, Katarzyna J Purzycka, Katarzyna Pachulska-Wieczorek, Marina Mitjans, Martin Begemann, Behnam Vafadari, Krystian Bijata, Ryszard W Adamiak, Hannelore Ehrenreich, Magdalena Dziembowska and 1 more

Open access · goldAbstract read
In one paragraph

Article in EMBO molecular medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
4.4field-weighted citation impact, top 6% 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

22 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Article
  3. ALife science alliance · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Dysregulation of Synaptic Plasticity Markers in Schizophrenia.Indian journal of clinical biochemistry : IJCB · 2023
    Review
  9. Review
  10. Article
  11. Review
  12. Article
  13. Protein Translation and Psychiatric Disorders.The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry · 2020
    Review
  14. Variants inAnimals : an open access journal from MDPI · 2019
    Article
  15. MMPs in learning and memory and neuropsychiatric disorders.Cellular and molecular life sciences : CMLS · 2019
    Review
  16. Article
  17. Article
  18. Review
  19. Review
  20. 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 4 institutions in 2 countries.

Katarzyna LepetaDepartment of Molecular and Cellular Neurobiology, Nencki Institute of Experimental Biology, Polish Academy of Sciences, Warsaw, Poland.
Katarzyna J PurzyckaDepartment of RNA Structure and Function, Institute of Bioorganic Chemistry, Polish Academy of Sciences, Poznan, Poland‡.
Katarzyna Pachulska-WieczorekDepartment of RNA Structure and Function, Institute of Bioorganic Chemistry, Polish Academy of Sciences, Poznan, Poland‡.
Marina MitjansClinical Neuroscience, Max Planck Institute of Experimental Medicine, DFG Research Center for Nanoscale Microscopy and Molecular Physiology of the Brain (CNMPB), Göttingen, Germany.
Martin BegemannClinical Neuroscience, Max Planck Institute of Experimental Medicine, DFG Research Center for Nanoscale Microscopy and Molecular Physiology of the Brain (CNMPB), Göttingen, Germany.
Behnam VafadariDepartment of Molecular and Cellular Neurobiology, Nencki Institute of Experimental Biology, Polish Academy of Sciences, Warsaw, Poland.
Krystian BijataInstitute of Biochemistry and Biophysics, Polish Academy of Sciences, Laboratory of RNA Biology and Functional Genomics, Warsaw, Poland.
Ryszard W AdamiakDepartment of RNA Structure and Function, Institute of Bioorganic Chemistry, Polish Academy of Sciences, Poznan, Poland‡.
Hannelore EhrenreichClinical Neuroscience, Max Planck Institute of Experimental Medicine, DFG Research Center for Nanoscale Microscopy and Molecular Physiology of the Brain (CNMPB), Göttingen, Germany ehrenreich@em.mpg.de m.dziembowska@cent.uw.edu.pl l.kaczmarek@nencki.gov.pl.
Magdalena DziembowskaDepartment of Molecular and Cellular Neurobiology, Nencki Institute of Experimental Biology, Polish Academy of Sciences, Warsaw, Poland ehrenreich@em.mpg.de m.dziembowska@cent.uw.edu.pl l.kaczmarek@nencki.gov.pl.
Leszek KaczmarekDepartment of Molecular and Cellular Neurobiology, Nencki Institute of Experimental Biology, Polish Academy of Sciences, Warsaw, Poland ehrenreich@em.mpg.de m.dziembowska@cent.uw.edu.pl l.kaczmarek@nencki.gov.pl.ORCID 0000-0002-7207-3490
Instytut Biologii Doświadczalnej im. Marcelego Nenckiego · PLInstitute of Bioorganic Chemistry, Polish Academy of Sciences · PLNanoscale Microscopy and Molecular Physiology of the Brain Cluster of Excellence 171 — DFG Research Center 103 · DEInstitute of Biochemistry and Biophysics, Polish Academy of Sciences · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Matrix metalloproteinase 9 (MMP-9) has recently emerged as a molecule that contributes to pathological synaptic plasticity in schizophrenia, but explanation of the underlying mechanisms has been missing. In the present study, we performed a phenotype-based genetic association study (PGAS) in > 1,000 schizophrenia patients from the Göttingen Research Association for Schizophrenia (GRAS) data collection and found an association between the

Indexed as

Polymorphism, Single Nucleotide3' Untranslated RegionsAdolescentAdultAgedAnimalsCells, CulturedChronic DiseaseDisease Models, AnimalFemaleFragile X Messenger Ribonucleoprotein 1Genetic Association StudiesHumansMaleMatrix Metalloproteinase 9Mice3' Untranslated RegionsFMR1 protein, humanFragile X Messenger Ribonucleoprotein 1Matrix Metalloproteinase 9RNA, Messengerdendritic spine morphologyFragile X mental retardation proteinmatrix metalloproteinase 9phenotype‐based genetic association studysingle‐nucleotide polymorphism

Identifiers

PMID28623238
PMCPMC5538295
OpenAlexW2624795293

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.