Pronađeno: 1-7 / 7 radova

Autori: Harwood Adrian J

>> Filter: Samo Article i Review

Naslov Transcriptomic profiling of iPSC-derived astrocytes from patients with 22q11.2 deletion syndrome (Meeting Abstract)
Autori Simeunovic Ivana V  Kovacevic-Grujicic Natasa R  Peric Mina I  Petter Olena  Ehrhart Friederike  Kostic Jovana N  Lazic Stefan  Cuturilo Goran  De Nijs Laurence  Linden David EJ  Harwood Adrian J  Stevanovic Milena J  Drakulic Danijela D 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2025), vol. 33 br. , Suppl. 1, str. 431-431
Ispravka ISI/Web of Science   Elečas   Rang časopisa  
Naslov Establishment of a patient-derived induced pluripotent stem cells with 22q11.2 microdeletion: a model system for studying neurodevelopmental disorders (Meeting Abstract)
Autori Drakulic Danijela D  Kovacevic-Grujicic Natasa R  Peric Mina I  Petter Olena  Simeunovic Ivana V  Kostic Jovana N  Cuturilo Goran  Harwood Adrian J  Stevanovic Milena J 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2025), vol. 33 br. , Suppl. 1, str. 301-301
Ispravka ISI/Web of Science   Elečas   Rang časopisa  
Naslov Establishment and characterization of induced pluripotent stem cells from patients with 22q11.2 Duplication Syndrome (Meeting Abstract)
Autori Kovacevic-Grujicic Natasa R  Kostic Jovana N  Drakulic Danijela D  Peric Mina I  Simeunovic Ivana V  Cuturilo Goran  Petter Olena  Harwood Adrian J  Stevanovic Milena J 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2025), vol. 33 br. , Suppl. 1, str. 299-300
Ispravka ISI/Web of Science   Elečas   Rang časopisa  
Naslov Expression of miR-185 during neural differentiation of induced pluripotent stem cells from patients with 22q11.2 Deletion Syndrome (Meeting Abstract)
Autori Stanisavljevic-Ninkovic Danijela  Simeunovic Ivana V  Drakulic Danijela D  Kovacevic-Grujicic Natasa R  Peric Mina I  Kostic Jovana N  Cuturilo Goran  Petter Olena  Harwood Adrian J  Stevanovic Milena J 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2025), vol. 33 br. , Suppl. 1, str. 774-774
Ispravka ISI/Web of Science   Elečas   Rang časopisa  
Naslov "Mindds-Connect" - Federated Data Sharing Platform for Neurodevelopmental Disorders and Rare Genetic Mutations (Meeting Abstract)
Autori Mihaljevic Marina M  Huremagic Benjamin  Harwood Janet  Jorge Paola  Teles Natalia  Novakowska Beata  Vandeweyer Geert  Drakulic Danijela D  Van Amelsvoort Therese  Linden David  Straccia Marco  Vermeersch Joris  Harwood Adrian J 
Info EUROPEAN NEUROPSYCHOPHARMACOLOGY, (2023), vol. 75 br. , Suppl. 1, str. S132-S132
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa  
Naslov Rare Pathogenic Copy Number Variation in the 16p11.2 (BP4-BP5) Region Associated with Neurodevelopmental and Neuropsychiatric Disorders: A Review of the Literature (Review)
Autori Oliva-Teles Natalia  De Stefano Maria Chiara  Gallagher Louise  Rakic Severin  Jorge Paula  Cuturilo Goran  Markovska-Simoska Silvana  Borg Isabella  Wolstencroft Jeanne  Tumer Zeynep  Harwood Adrian J  Kodra Yllka  Skuse David 
Info INTERNATIONAL JOURNAL OF ENVIRONMENTAL RESEARCH AND PUBLIC HEALTH, (2020), vol. 17 br. 24, str. -
Projekat COST ACTIONEuropean Cooperation in Science and Technology (COST) [16210]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Copy number variants (CNVs): a powerful tool for iPSC-based modelling of ASD (Review)
Autori Drakulic Danijela D  Djurovic Srdjan  Syed Yasir Ahmed  Trattaro Sebastiano  Caporale Nicolo  Falk Anna  Ofir Rivka  Heine Vivi M  Chawner Samuel JRA  Rodriguez-Moreno Antonio  Van den Bree Marianne BM  Testa Giuseppe  Petrakis Spyros  Harwood Adrian J 
Info MOLECULAR AUTISM, (2020), vol. 11 br. 1, str. -
Projekat Ministry of Education, Science and Technological Development, Republic of Serbia [173051, 45103-68/2020-14/200042]; South-Eastern Norway Regional Health Authority [2018094]; Spanish "Agencia Estatal de Investigacion" [BFU2015-68655-P]; SSFSwedish Foundati
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Ispis zapisa u formatu:TXT | BibTeX