Evidence map›Paper›PMID 35682742›Full record

ArticleInternational journal of molecular sciences2022

An Integrated Multi-Omic Network Analysis Identifies Seizure-Associated Dysregulated Pathways in the GAERS Model of Absence Epilepsy.

Anna Harutyunyan, Debbie Chong, Rui Li, Anup D Shah, Zahra Ali, Cheng Huang, Christopher K Barlow, Piero Perucca, Terence J O'Brien, Nigel C Jones and 3 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 20% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

  1. Pooled it
  2. In-depth characterization of the CaScientific reports · 2026
    Article
  3. KArchiv der Pharmazie · 2026
    Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. 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

13 authors at 3 institutions in 1 country.

Anna HarutyunyanDepartment of Medicine, The Royal Melbourne Hospital, The University of Melbourne, Melbourne, VIC 3052, Australia.ORCID 0000-0002-6165-5639
Debbie ChongDepartment of Neuroscience, Central Clinical School, Monash University, Melbourne, VIC 3004, Australia.
Rui LiDepartment of Neuroscience, Central Clinical School, Monash University, Melbourne, VIC 3004, Australia.
Anup D ShahMonash Biomedical Proteomics Facility and Monash Biomedicine Discovery Institute, Monash University, Clayton, VIC 3800, Australia.
Zahra AliDepartment of Neuroscience, Central Clinical School, Monash University, Melbourne, VIC 3004, Australia.
Cheng HuangMonash Biomedical Proteomics Facility and Monash Biomedicine Discovery Institute, Monash University, Clayton, VIC 3800, Australia.
Christopher K BarlowMonash Biomedical Proteomics Facility and Monash Biomedicine Discovery Institute, Monash University, Clayton, VIC 3800, Australia.ORCID 0000-0001-9309-2829
Piero PeruccaDepartment of Neuroscience, Central Clinical School, Monash University, Melbourne, VIC 3004, Australia.
Terence J O'BrienDepartment of Medicine, The Royal Melbourne Hospital, The University of Melbourne, Melbourne, VIC 3052, Australia.
Nigel C JonesDepartment of Medicine, The Royal Melbourne Hospital, The University of Melbourne, Melbourne, VIC 3052, Australia.ORCID 0000-0002-1080-8439
Ralf B SchittenhelmMonash Biomedical Proteomics Facility and Monash Biomedicine Discovery Institute, Monash University, Clayton, VIC 3800, Australia.ORCID 0000-0001-8738-1878
Alison AndersonDepartment of Medicine, The Royal Melbourne Hospital, The University of Melbourne, Melbourne, VIC 3052, Australia.
Pablo M Casillas-EspinosaDepartment of Medicine, The Royal Melbourne Hospital, The University of Melbourne, Melbourne, VIC 3052, Australia.
Monash University · AUThe Royal Melbourne Hospital · AUThe University of Melbourne · AU

Funding

National Health and Medical Research Council APP1087172National Health and Medical Research Council APP1163708National Health and Medical Research Council APP1176426United States Department of Defense EP200022
6 · The paper itself

Abstract

Absence epilepsy syndromes are part of the genetic generalized epilepsies, the pathogenesis of which remains poorly understood, although a polygenic architecture is presumed. Current focus on single molecule or gene identification to elucidate epileptogenic drivers is unable to fully capture the complex dysfunctional interactions occurring at a genetic/proteomic/metabolomic level. Here, we employ a multi-omic, network-based approach to characterize the molecular signature associated with absence epilepsy-like phenotype seen in a well validated rat model of genetic generalized epilepsy with absence seizures. Electroencephalographic and behavioral data was collected from Genetic Absence Epilepsy Rats from Strasbourg (GAERS,

Indexed as

Epilepsy, AbsenceEpilepsy, GeneralizedAnimalsDisease Models, AnimalLysineProteomicsRatsSeizuresLysineabsence epilepsyALDH2GAERSGSTM1lysine degradationmetabolomicsproteomicsWGCNA

Identifiers

PMID35682742
PMCPMC9181682
OpenAlexW4281670309

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.