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Investigation of de novo mutations in a schizophrenia case-parent trio by induced pluripotent stem cell-based in vitro disease modeling: convergence of schizophrenia- and autism-related cellular phenotypes

Crossref DOI link: https://doi.org/10.1186/s13287-020-01980-5

Published Online: 2020-11-27

Published Print: 2020-12

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

Hathy, Edit

Szabó, Eszter

Varga, Nóra

Erdei, Zsuzsa

Tordai, Csongor

Czehlár, Boróka

Baradits, Máté

Jezsó, Bálint

Koller, Júlia

Nagy, László

Molnár, Mária Judit

Homolya, László

Nemoda, Zsófia

Apáti, Ágota

Réthelyi, János M. https://orcid.org/0000-0002-3641-012X
Funding

Funding for this research was provided by:

NKTH (SCHIZO-08, SCHIZO-08)

National Brain Research Program (KTIA_NAP_13-2014-0011, KTIA_NAP_13-1-2013-0001, 2017-1.2.1-NKP-2017-00002, 2017-1.2.1-NKP-2017-00002, 2017-1.2.1-NKP-2017-00002, 2017-1.2.1-NKP-2017-00002)

Emberi Eroforrások Minisztériuma (Neurology thematic programme)
License Information

Text and Data Mining valid from 2020-11-27

Version of Record valid from 2020-11-27
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Article History

Received: 23 September 2020

Accepted: 18 October 2020

First Online: 27 November 2020

Ethics approval and consent to participate

: The genetic analysis, generation of iPSC lines, and all downstream assays were approved by the Human Reproduction Committee of the Hungarian Health Science Council (ETT HRB). All participants gave written informed consent. All individuals (all family members) mentioned in the article gave consent to publish their personal data.

: The authors declare no competing financial or non-financial interests.

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