Evidence map›Paper›PMID 40362679›Full record

ArticleInternational journal of molecular sciences2025

Functional Analysis of Antipsychotics in Human iPSC-Based Neural Progenitor 2D and 3D Schizophrenia Models.

Kiara Gitta Farkas, Katalin Vincze, Csongor Tordai, Ece İlay Özgen, Derin Gürler, Vera Deli, Julianna Lilienberg, Zsuzsa Erdei, Balázs Sarkadi, János Miklós Réthelyi and 1 more

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Special Issue "Molecular Underpinnings of Schizophrenia Spectrum Disorders".International journal of molecular sciences · 2025
    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.

Kiara Gitta FarkasInstitute of Molecular Life Sciences, HUN-REN Research Centre for Natural Sciences, H-1117 Budapest, Hungary.ORCID 0009-0002-7533-5764
Katalin VinczeInstitute of Molecular Life Sciences, HUN-REN Research Centre for Natural Sciences, H-1117 Budapest, Hungary.
Csongor TordaiInstitute of Molecular Life Sciences, HUN-REN Research Centre for Natural Sciences, H-1117 Budapest, Hungary.ORCID 0000-0001-9770-997X
Ece İlay ÖzgenDepartment of Molecular Biology and Genetics, Bilkent University, 06800 Ankara, Turkey.
Derin GürlerDepartment of Molecular Biology and Genetics, Bilkent University, 06800 Ankara, Turkey.
Vera DeliInstitute of Molecular Life Sciences, HUN-REN Research Centre for Natural Sciences, H-1117 Budapest, Hungary.
Julianna LilienbergInstitute of Molecular Life Sciences, HUN-REN Research Centre for Natural Sciences, H-1117 Budapest, Hungary.
Zsuzsa ErdeiInstitute of Molecular Life Sciences, HUN-REN Research Centre for Natural Sciences, H-1117 Budapest, Hungary.ORCID 0009-0003-0537-7421
Balázs SarkadiInstitute of Molecular Life Sciences, HUN-REN Research Centre for Natural Sciences, H-1117 Budapest, Hungary.ORCID 0000-0003-0592-4539
János Miklós RéthelyiDepartment of Psychiatry and Psychotherapy, Semmelweis University, H-1083 Budapest, Hungary.
Ágota ApátiInstitute of Molecular Life Sciences, HUN-REN Research Centre for Natural Sciences, H-1117 Budapest, Hungary.ORCID 0000-0003-0380-8139

Funding

National Research, Development and Innovation Office 2024-1.1.1-KKV_FÓKUSZ-2024-00022National Research, Development and Innovation Office GINOP-2.1.1-15-2015-00369National Research, Development and Innovation Office Hungarian Scientific Research Fund (OTKA) K-128369National Research, Development and Innovation Office National Brain Research Program (NAP) 2017-1.2.1-NKP-2017-00002National Research, Development and Innovation Office TKP2021-EGA-25
6 · The paper itself

Abstract

Schizophrenia is a complex psychiatric disorder of complex etiology. Despite decades of antipsychotic drug development and treatment, the mechanisms underlying cellular drug effects remain incompletely understood. Induced pluripotent stem cell (iPSC)-based disease and pharmacological modelling offer new avenues for drug development. In this study, we explored the development of two- and three-dimensional neural progenitor cultures and the impact of different antipsychotics in a schizophrenia model. Four human iPSC lines, including two carrying a de novo

Indexed as

Antipsychotic AgentsInduced Pluripotent Stem CellsNeural Stem CellsSchizophreniaCell DifferentiationCell ProliferationHumansSpheroids, CellularAntipsychotic Agentsantipsychotic medicationcell adhesioninduced pluripotent stem cell-derived neural cellsschizophrenia modelthree-dimensional spheroid

Identifiers

PMID40362679
PMCPMC12072398

What OpenQuestion holds

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LicenceCC BY
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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.