Strengthening regional stem cells based research for advancement of multi modal innovative strategy for modelling neurodevelopmental disorders

Informations projet

STREAMLINE

N° de convention de subvention: 101060201

DOI

10.3030/101060201

Projet clôturé

Date de signature de la CE 15 Mai 2022

Date de début 1 Juillet 2022

Date de fin 30 Juin 2025

Financé au titre de

• Widening participation and spreading excellence

Coût total

€ 1 162 391,00

Contribution de l’UE

€ 1 162 391,00

Coordonné par

INSTITUT ZA MOLEKULARNU GENETIKU I GENETICKO INZENJERSTVO
Serbia

CORDIS fournit des liens vers les livrables publics et les publications des projets HORIZON.

Les liens vers les livrables et les publications des projets du 7e PC, ainsi que les liens vers certains types de résultats spécifiques tels que les jeux de données et les logiciels, sont récupérés dynamiquement sur OpenAIRE .

Livrables

Documents, reports (6)

Data Management Plan developed
Risk list created
Dissemination, exploitation and communication plan created

Report on dissemination exploitation and communication plan

First report on virtual trainings by experts from partner institutions

Report on virtual trainings by experts from partner institutions

Project management handbook developed
First report on short-term staff exchanges and workshops

Report on shortterm staff exchanges and workshops

Websites, patent fillings, videos etc. (1)

Launch of the Project's motto and logos and the Project's website

Launch of the Projects motto and logos and the Projects website

Publications

Conference proceedings (10)

PATIENT-DERIVED INDUCED PLURIPOTENT STEM CELLS WITH 22Q11.2 MICRODELETION: A MODEL SYSTEM FOR INVESTIGATING NEURODEVELOPMENTAL DISORDER

Auteurs: Simeunović, Ivana; Čuturilo, Goran; Kovačević-Grujičić, Nataša; Petter, Olena; Perić, Mina; Kostić, Jovana; Stanisavljević Ninković, Danijela; Harwood J., Adrian; Stevanović, Milena; Drakulić, Danijela
Publié dans: VII Congress of the serbian genetic society, 2024
Éditeur: Serbian Genetic Society

Analysis of cohort of patients with 22q11.2 deletion syndrome - a single-center experience from Serbia

Auteurs: Simeunović, Ivana; Drakulić, Danijela; Cuturilo, Goran; Kovačević-Grujičić, Nataša; Kostić, Jovana; Stevanović, Milena
Publié dans: 8th Congress of the Serbian Neuroscience Society, 2023
Éditeur: Serbian Neuroscience Society

Establishment of induced pluripotent stem cells from patients with 22q11.2 duplication syndrome as a model system for studying neurodevelopmental disorders

Auteurs: Kostić, Jovana; Drakulić, Danijela; Čuturilo, Goran; Petter, Olena; Perić, Mina; Simeunović, Ivana; Harwood J., Adrian; Stevanović, Milena; Kovačević-Grujičić, Nataša
Publié dans: CoMBoS2 – the Second Congress of Molecular Biologists of Serbia, Abstract Book – Trends in Molecular Biology, Special issue 06-08 October 2023, Belgrade, Serbia, 2023
Éditeur: Institute of Molecular Genetics and Genetic Engineering (IMGGE), University of Belgrade

STREAMLINE HUB: a high capacity hub for research of neurodevelopmental disorders in the Western Balkan region

Auteurs: Drakulić, Danijela; Petrakis, Spyros; Harwood, Adrian J.; Linden, David; Lazić, Andrijana; Kovačević-Grujičić, Nataša; Stevanović, Milena
Publié dans: Hemijska industrija (Chemical Industry), 2024
Éditeur: Association of Chemical Engineers of Serbia

Genomic and clinical findings in patients with 22q11.2 duplication syndrome

Auteurs: Kostić, Jovana; Drakulić, Danijela; Cuturilo, Goran; Kovačević-Grujičić, Nataša; Simeunović, Ivana; Stevanović, Milena
Publié dans: 8th Congress of the Serbian Neuroscience Society, 2023
Éditeur: Serbian Neuroscience Society

ESTABLISHMENT OF A MODEL SYSTEM FOR STUDYING NEURODEVELOPMENTAL DISORDERS USING INDUCED PLURIPOTENT STEM CELLS DERIVED FROM PATIENTS WITH 22Q11.2 DELETION SYNDROME

Auteurs: Drakulić, Danijela; Harwood, Adrian; Petrakis, Spyros; Linden, David; Stevanović, Milena
Publié dans: VII Congress of the serbian genetic society, 2024
Éditeur: Serbian Genetic Society

Application of principal component analysis (PCA) and analytical hierarchy process (AHP) in analysis of articulatory characteristics of phonemes of children with 22q11.2 Deletion Syndrome

Auteurs: Drakulić, Danijela; Rakonjac, Marijana; Cuturilo, Goran; Kovačević-Grujičić, Nataša; Kušić-Tišma, Jelena; Morić, Ivana; Zukić, Branka; Stevanović, Milena
Publié dans: 4th Belgrade Bioinformatics Conference, 2023
Éditeur: Institute of Molecular Genetics and Genetic Engineering, University of Belgrade

CHARACTERIZATION OF INDUCED PLURIPOTENT STEM CELLS FROM PATIENTS WITH 22Q11.2 DUPLICATION SYNDROME

Auteurs: Kostić, Jovana; Cuturilo, Goran; Drakulić, Danijela; Petter, Olena; Perić, Mina; Simeunović, Ivana; Stanisavljević Ninković, Danijela; Harwood J., Adrian; Stevanović, Milena; Kovačević-Grujicić, Nataša
Publié dans: VII Congress of the serbian genetic society, 2024
Éditeur: Serbian Genetic Society

22q11.2 Deletion syndrome as a tool for modelling and research of neurodevelopmental disorders

Auteurs: Lazić, Adrijana; Drakulić, Danijela; Kovačević-Grujičić, Nataša; Perić, Mina; Petrakis, Spyros; Linden, David; Harwood, Adrian; Stevanović, Milena
Publié dans: CoMBoS2 – the Second Congress of Molecular Biologists of Serbia, Abstract Book – Trends in Molecular Biology, Special issue 06-08 October 2023, Belgrade, Serbia, 2023
Éditeur: Institute of Molecular Genetics and Genetic Engineering (IMGGE), University of Belgrade

Generation of induced pluripotent stem cells derived from patients with 22q11.2 deletion syndrome as a tool for studying neurodevelopmental disorders

Auteurs: Simeunović, Ivana; Čuturilo, Goran; Kovačević-Grujičić, Nataša; Petter, Olena; Perić, Mina; Kostić, Jovana; Harwood J., Adrian; Stevanović, Milena; Drakulić, Danijela
Publié dans: CoMBoS2 – the Second Congress of Molecular Biologists of Serbia, Abstract Book – Trends in Molecular Biology, Special issue 06-08 October 2023, Belgrade, Serbia, 2023
Éditeur: Institute of Molecular Genetics and Genetic Engineering (IMGGE), University of Belgrade

Other (2)

Additional file 1 of Neural excitation/inhibition imbalance and neurodevelopmental pathology in human copy number variant syndromes: a systematic review

Auteurs: Sylvester, Amy L.; Hensenne, Eva; Ivanov, Dimo; Poser, Benedikt A.; Linden, David E. J.; van Amelsvoort, Thérèse; Vingerhoets, Claudia
Publié dans: 2025
Éditeur: BioMed Central Ltd
DOI: 10.6084/M9.FIGSHARE.29276451.V1

Neural excitation/inhibition imbalance and neurodevelopmental pathology in human copy number variant syndromes: a systematic review

Auteurs: Sylvester, Amy L.; Hensenne, Eva; Ivanov, Dimo; Poser, Benedikt A.; Linden, David E. J.; van Amelsvoort, Therese; Vingerhoets, Claudia
Publié dans: Journal of Neurodevelopmental Disorders, 2025
Éditeur: BioMed Central Ltd
DOI: 10.1186/S11689-025-09614-8

Peer reviewed articles (2)

Intranuclear inclusions of polyQ-expanded ATXN1 sequester RNA molecules

Auteurs: Ioannis Gkekas, Aimilia-Christina Vagiona, Nikolaos Pechlivanis, Georgia Kastrinaki, Katerina Pliatsika, Sebastian Iben, Konstantinos Xanthopoulos, Fotis E. Psomopoulos, Miguel A. Andrade-Navarro, Spyros Petrakis
Publié dans: Frontiers in Molecular Neuroscience, Numéro 16, 2023, ISSN 1662-5099
Éditeur: Frontiers Media SA
DOI: 10.3389/FNMOL.2023.1280546

Speech Sounds Production, Narrative Skills, and Verbal Memory of Children with 22q11.2 Microdeletion

Auteurs: Marijana Rakonjac, Goran Cuturilo, Natasa Kovacevic-Grujicic, Ivana Simeunovic, Jovana Kostic, Milena Stevanovic, Danijela Drakulic
Publié dans: Children, Numéro 11, 2024, ISSN 2227-9067
Éditeur: MDPI AG
DOI: 10.3390/children11040489