Identification of molecular signatures and pathways involved in Rett syndrome using a multi-omics approach.

Journal Information

Full Title: Hum Genomics

Abbreviation: Hum Genomics

Country: Unknown

Publisher: Unknown

Language: N/A

Publication Details

Subject Category: Genetics

Available in Europe PMC: Yes

Available in PMC: Yes

PDF Available: No

Transparency Score
3/6
50.0% Transparent
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Evidence found in paper:

"Declarations Ethics approval and consent to participateAll individuals included or their legal guardians provided written informed consent before evaluation. The study was approved by the ethical committee of the Fundació Sant Joan de Déu (#PIC-219–20). The research conformed to the principles of the Declaration of Helsinki. Consent for publicationAll individuals included or their legal guardians provided written consent to share pseudonymised patient data and analysis data. Competing interestsThe authors declare that they have no competing interests. Competing interests The authors declare that they have no competing interests."

Evidence found in paper:

"Funding This research was funded with a grant from the Spanish Ministry of Health (Instituto de Salud Carlos III/FEDER, PI20/00389), the parent association ‘Síndrome duplicación MECP2: Miradas que hablan’ (PFNR0085), funding from Muévete por los que no Pueden (PCP/00282), the doctoral grant FI from the Government of Catalonia (Secretaria d’Universitats I Recerca) and the European Social Fund (2020 FI-B 00888) to Ainhoa Pascual-Alonso, and the FPU (Formación del Profesorado Universitario) doctoral grant from the Spanish Ministry of Science, Innovation and Universities (FPU18/02152) to Clara Xiol."

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Open Access
Paper is freely available to read
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Tool: rtransparent

OST Version: N/A

Last Updated: Aug 05, 2025