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

Projektinformationen

STREAMLINE

ID Finanzhilfevereinbarung: 101060201

DOI

10.3030/101060201

Projekt abgeschlossen

EK-Unterschriftsdatum 15 Mai 2022

Startdatum 1 Juli 2022

Enddatum 30 Juni 2025

Finanziert unter

• Widening participation and spreading excellence

Gesamtkosten

€ 1 162 391,00

EU-Beitrag

€ 1 162 391,00

Koordiniert durch

INSTITUT ZA MOLEKULARNU GENETIKU I GENETICKO INZENJERSTVO
Serbia

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Leistungen

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

Veröffentlichungen

Conference proceedings (10)

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

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

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

Autoren: Simeunović, Ivana; Drakulić, Danijela; Cuturilo, Goran; Kovačević-Grujičić, Nataša; Kostić, Jovana; Stevanović, Milena
Veröffentlicht in: 8th Congress of the Serbian Neuroscience Society, 2023
Herausgeber: Serbian Neuroscience Society

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

Autoren: Kostić, Jovana; Drakulić, Danijela; Čuturilo, Goran; Petter, Olena; Perić, Mina; Simeunović, Ivana; Harwood J., Adrian; Stevanović, Milena; Kovačević-Grujičić, Nataša
Veröffentlicht in: CoMBoS2 – the Second Congress of Molecular Biologists of Serbia, Abstract Book – Trends in Molecular Biology, Special issue 06-08 October 2023, Belgrade, Serbia, 2023
Herausgeber: 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

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

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

Autoren: Kostić, Jovana; Drakulić, Danijela; Cuturilo, Goran; Kovačević-Grujičić, Nataša; Simeunović, Ivana; Stevanović, Milena
Veröffentlicht in: 8th Congress of the Serbian Neuroscience Society, 2023
Herausgeber: 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

Autoren: Drakulić, Danijela; Harwood, Adrian; Petrakis, Spyros; Linden, David; Stevanović, Milena
Veröffentlicht in: VII Congress of the serbian genetic society, 2024
Herausgeber: 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

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

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

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

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

Autoren: Lazić, Adrijana; Drakulić, Danijela; Kovačević-Grujičić, Nataša; Perić, Mina; Petrakis, Spyros; Linden, David; Harwood, Adrian; Stevanović, Milena
Veröffentlicht in: CoMBoS2 – the Second Congress of Molecular Biologists of Serbia, Abstract Book – Trends in Molecular Biology, Special issue 06-08 October 2023, Belgrade, Serbia, 2023
Herausgeber: 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

Autoren: Simeunović, Ivana; Čuturilo, Goran; Kovačević-Grujičić, Nataša; Petter, Olena; Perić, Mina; Kostić, Jovana; Harwood J., Adrian; Stevanović, Milena; Drakulić, Danijela
Veröffentlicht in: CoMBoS2 – the Second Congress of Molecular Biologists of Serbia, Abstract Book – Trends in Molecular Biology, Special issue 06-08 October 2023, Belgrade, Serbia, 2023
Herausgeber: 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

Autoren: Sylvester, Amy L.; Hensenne, Eva; Ivanov, Dimo; Poser, Benedikt A.; Linden, David E. J.; van Amelsvoort, Thérèse; Vingerhoets, Claudia
Veröffentlicht in: 2025
Herausgeber: 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

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

Peer reviewed articles (2)

Intranuclear inclusions of polyQ-expanded ATXN1 sequester RNA molecules

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

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

Autoren: Marijana Rakonjac, Goran Cuturilo, Natasa Kovacevic-Grujicic, Ivana Simeunovic, Jovana Kostic, Milena Stevanovic, Danijela Drakulic
Veröffentlicht in: Children, Ausgabe 11, 2024, ISSN 2227-9067
Herausgeber: MDPI AG
DOI: 10.3390/children11040489