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IBROSpeakerSupport grant for the 22q11.2 Deletion Syndrome Symposium

It is our great pleasure to share that dr Danijela Stanisavljević Ninković, a member of STREAMLINE team, has been awarded an #IBROSpeakerSupport grant for the 22q11.2 Deletion Syndrome Symposium!

The International Brain Research Organization (IBRO) is the global association of neuroscience societies established in 1961 that aims to promote and support neuroscience around the world through training, education, research, outreach and engagement activities, and the publication of two journals, Neuroscience and IBRO Neuroscience Reports.

The 22q11.2 Deletion Syndrome Symposium offers a unique opportunity for parents and children affected by the condition to connect, share experiences, and gain valuable insights. Participants will benefit from the knowledge of leading specialists in Serbia and across Europe, who will present the latest advancements in research, diagnostics, and management of 22q11.2 Deletion Syndrome, including its associated risks for neurodevelopmental disorders.
We have carefully selected speakers with extensive expertise, ensuring a comprehensive and engaging program. This event also serves to strengthen the connections established during the STREAMLINE project, and we are deeply grateful to IBRO for supporting this initiative.
Details about registration will be announced soon. Stay tuned for updates about the Symposium, which will take place on November 22, 2025.

STREAMLINE Symposium „22q Awareness Day“

On Friday, November 22th, the third Symposium entitled “22q Awareness Day ” was organized within the STREAMLINE project. We gathered around researchers, doctors, parents and children living with 22q11 deletion syndrome. This was another wonderful meeting with the hope that it will grow into a tradition.
The Symposium started with Dr. Danijela Drakulić who presented STREAMLINE projects activities. Her opening speech was followed by from representatives of National organization for rare diseases of Serbia (NORBS) and “22q ex YU”, Stefan Živković and Vesna Vujičić, who talked about the current activities of their associations. At the end of opening speech Ana Knežević (President of inclusive center “Here’s a hand” (Evo ruka)) said that her message is that we should help to parents and children living with 22q11 deletion syndrome.
STREAMLINE team members spent this wonderful evening with parents and children living with 22q11 deletion syndrome, enjoying in good talk and music. This was a great opportunity to better understand the life of people with 22q11.2 deletion syndrome and their daily struggles, but also to become familiar with their way of thinking and their many talents. Perhaps the most important thing is that this Symposium enabled parents who share the same problems to exchange experiences, to broaden perspectives, and create new contacts.

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STREAMLINE for Students

Choosing a professional path is one of the most frequent problems students have in career counseling. Therefore, on November 8th, as part of the “Find out first-hand” program, the Center for Career Development and Student Counseling of the University of Belgrade and the Institute for Molecular Genetics and Genetic Engineering (IMGGI) of the University of Belgrade, organized a visit for final year students from the different faculties of natural sciences, University of Belgrade. Students had the opportunity to become more familiar with IMGGI, projects, and career planning possibilities. Dr Mina Perić described students how it is to work with human induced pluripotent cells technology, an exciting new era for the fields of stem cell biology and regenerative medicine, as well as disease modeling and drug discovery.

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22q Awareness Day

November 22nd is the International 22q11 Day, with initiative to increase awareness about 22q11.2 deletion syndrome (22q11.2DS) by wearing a red wardrobe and lighting several buildings in red around the Europe.
22q11.2DS is a genetic disorder caused by a heterozygous microdeletion of region q11.2 of chromosome 22. It is the most common microdeletion syndrome in humans with an estimated incidence of approximately 1/4000 per live births. After Down syndrome, 22q11.2 deletion syndrome is the second most common cause of developmental delay and congenital heart diseases. The spectrum of clinical manifestations in patients with this syndrome is very variable, even within the same family. Approximately, 25% of patients with 22q11.2DS develop schizophrenia. Intellectual disability is detected in approximately 45% of patients with 22q11.2DS, while Autism Spectrum Disorder is seen in 14-50% of cases. It accounts for approximately 2.4% of people with developmental disabilities and approximately 10% to 15% of people with Tetralogy of Fallot (a type of heart defect). Males and females of all ethnic backgrounds are affected in equal numbers.

A diagnosis is quite challenging for 22q11 individuals due to their extremely diverse range of symptoms. Actually, 50% of people with 22q11 never receive a diagnosis. However, early treatment of the symptoms can lessen their severity, thus a person with 22q11 can have a far better life if diagnosed early. Additionally, early diagnosis helps educators better adjusting the learning environment, health experts better modifying their treatments, and parents better preparing for the arrival of their kid. Increasing public knowledge will thus lead to earlier illness diagnosis and better treatment.

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Academician Milena Stevanović was awarded for her contribution to the development of molecular biology in Serbia by the Serbian Society for Molecular Biology (MolBioS)

Congratulations to Academician Milena Stevanović, who was awarded for her contribution to the development of molecular biology in Serbia by the Serbian Society for Molecular Biology (MolBioS). The award ceremony took place at the Serbian Academy of Sciences and Arts on October 8th. Prof. Dr. Gordana Matić highlighted Academician Milena Stevanović’s significant contributions to genetic engineering, human molecular genetics, elucidating molecular mechanisms of oncogenesis and neurogenesis, as well as disease modeling. Academician Milena Stevanović also made a great impact on the Faculty of Biology at the University of Belgrade through her dedication to student education. Prof. Dr. Gordana Matić also emphasized that Academician Milena Stevanović should be regarded as a symbol of molecular biology in Serbia.

Additionally, Prof. Dr. Goran Brajušković acknowledged Academician Milena Stevanović’s substantial contributions to the development and promotion of molecular biology in Serbia. At the conclusion, Academician Milena Stevanović shared her journey from her early days as a student, from her first SOX gene cloning to the first images of human induced pluripotent stem cells generated in Serbia, highlighting the beauty of molecular biology.

Academician Milena Stevanović considers her greatest success to be leaving a laboratory full of researchers capable of independently carrying on the research work.

STREAMLINE outreach at VII Congress of the Serbian Genetic Society

VII Congress of the Serbian Genetic Society was held from October 2nd to October 5th, 2024. at Zlatibor mountain of extraordinary beauty, and pleasant climate. This Congress covered many fields of genetics including molecular genetics and genomics, medical genetics and personalized medicine, population and evolutionary genetics, microbial genetics, breeding and genetic engineering, genotoxicology, new technologies, and others. This was a great opportunity to increase the visibility of the STREAMLINE Project and STREAMLINE hub among academic public. Accordingly, within the congress STREAMLINE team organized thematic workshop: “STREAMLINE hub for modelling disease and discovering molecular mechanisms of neurodevelopmental disorders”. The majority of attendees was Congress participants that had an opportunity to learn about the latest iPSCs-based approaches for studying neurodevelopmental disorders, as well as to join STREAMLINE hub.

As invited speaker, dr Danijela Drakulic, presented STREAMLINE outputs through lecture “Establishment of a model system for studying neurodevelopmental disorders using induced pluripotent stem cells derived from patients with 22q11.2 Deletion” within session Medical genetics. The main focused of the lecture was on STREAMLINE Exploratory Research Project and how far we have come in designing a new iPSCs-based tool for unveiling neuropathological mechanisms of human neurodevelopmental disorders.

During poster sesions, the youngest STREAMLINE team members Jovana Kostić and Ivana Simeunović presented their PhD topics in form of posters – “Patient-derived induced pluripotent stem cells with 22q11.2 microdeletion: a model system for investigating neurodevelopmental disorders” and “Characterization of induced pluripotent stem cells from patients with 22q11.2 Duplication Syndrome”, subsequently. Particularly, they briefly introduced the establishment of iPSCs from patients with 22q11.2 duplication and deletion syndrome as model systems for studying neurodevelopmental disorders.

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STREAMLINE at Netherlands School of Bioinformatics and Systems Biology

In the period from 23rd to 27th September, PhD students from STREAMLINE team Stefan Lazić, Jelena Pejić, Luka Bojić, Jovana Kostić and Ivana Simeunović attended the course Multi-Omics and Data Sciences in Complex Disease held at the University of Maastricht, the Netherlands. The course is organized by the Netherlands School of Bioinformatics and Systems Biology (BioSB), which focuses on knowledge exchange and training in these areas. 

During their stay in the Netherlands, they had the opportunity to hear more about current developments in the field of epigenomics, epigenome wide association studies (EWAS), as well as to apply the knowledge in practice on examples. In addition, the topics of the course were related to the design of studies in molecular epidemiology, machine learning, but also the integration of different types of data. Participants also had the opportunity to talk to experts in these fields about their experiments and analysis of their own data.

Thanks again to organizers from Netherlands School of Bioinformatics and Systems Biology from Maastricht for this great opportunity.

STREAMLINE hub for modelling diseases and discovering molecular mechanisms of neurodevelopmental disorders

It is our great pleasure to announce the thematic workshop “STREAMLINE hub for modelling diseases and discovering molecular mechanisms of neurodevelopmental disorders” at the VII Congress of the Serbian Genetic Society that will be held at Zlatibor from October 2nd to October 5th, 2024.

On the second day of the Congress, Thursday October 3rd, we will organize the thematic workshop dedicated to the latest iPSCs-based approaches for studying neurodevelopmental disorders.

Also, within the Congress dr Danijela Drakulic will give the lecture “Establishment of a model system for studying neurodevelopmental disorders using induced pluripotent stem cells derived from patients with 22q11.2 Deletion” and Ivana Simeunovic and Jovana Kostic will have poster presentations titled “Patient-derived induced pluripotent stem cells with 22q11.2 microdeletion: a model system for investigating neurodevelopmental disorders” and “Characterization of induced pluripotent stem cells from patients with 22q11.2 Duplication Syndrome”, subsequently.

 

Here you can find more information and scientific program of the VII Congress of the Serbian Genetic Society:

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13th Biennial International 22q11.2 Scientific Meeting

From July 16 to 18, 2024, Dr. Danijela Drakulic, Dr.Mina Peric, and Dr.Natasa Kovacevic Grujicic from IMGGE and Dr. Goran Cuturilo, University Children’s Hospital, Belgrade, attended the 13th Biennial International 22q11.2 Scientific Meeting at Praia D’El Rey Golf and Beach Resort, Obidos, Portugal.

Danijela gave a presentation „Generation of Induced Pluripotent Stem Cells Carrying 22q11.2 CNVs as a Model System for Studying Neurodevelopmental Disorders” in Session TRANSITION, TRANSCRIPTION, AND iPSCS, and Goran attended Session COORDINATION, INTERVENTIONS, AND OUTCOMES with presentation “An Overview of 22q11.2 Diagnostic and Research Facilities in the Countries of The Western Balkan Region”.

Also, we have organized workshop where members of the STREAMLINE project, Danijela Drakulic, Adrian Harwood, and Janet Harwood, and STREAMLINE Advisory Board member, Goran Cuturilo, presented the project and current results.

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STREAMLINE Summer School “Identification of key genes and novel drug targets for neurodevelopmental disorders”

The second STREAMLINE school dedicated to the latest research methodologies and approaches for Identification of key genes and novel drug targets for neurodevelopmental disorders was held from 4th to 6th of June at the Centre for Research and Technology Hellas (CERTH) in Thessaloniki, Greece. This Summer School was organized by CERTH and Maastricht University and gathered 31 PhD students and 8 researchers from Serbia and Bosnia. During this three-days event the young researchers had an opportunity to learn, throughout lectures and hands on trainings, about current state-of-the-art methodologies for identification of key genes and novel drug targets for neurodevelopmental disorders. The attendees got guidelines, from the experts in the field, on the methods of GWAS and imaging genetics, epigenetics and methylation analysis, microRNA analysis, methods and algorithms for in silico screening, pathway modelling, drug-related databases, PRS calculation algorithms and cell-based assays for experimental validation of selected compounds. This Summer School offered an excellent environment for fruitful discussions and new connections. We hope that this experience will be beneficial for their career and for further scientific discoveries.

We owe a great appreciation to all participants and speakers, as well as to our host Dr. Spyros Petrakis from CERTH, Thessaloniki, Greece.