Autori: Cuturilo Goran
| Naslov | Brain malformations and seizures by impaired chaperonin function of TRiC (Article) |
| Autori | Kraft Florian ...  Cuturilo Goran ... (broj koautora 87)
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| Info | SCIENCE, (2024), vol. 386 br. 6721, str. 516-525 |
| Projekat | Children's Discovery Institute, St Louis Children's Hospital Foundation; Children's Discovery Institute, St Louis Children's Hospital Foundation; Children's Discovery Institute, St Louis Children's Hospital Foundation; Italian Ministry of Health [RCR-2022-23682289, PNRR-MR1-2022-12376811]; Italian Ministry of Health; Italian Ministry of Health; Canadian Institutes of Health Research (CIHR) from the Canada Foundation for Innovation [FDN-167281, ERT-174211, OR2-189333, CFI-JELF 38412]; Canadian Institutes of Health Research (CIHR) from the Canada Foundation for Innovation; Canadian Institutes of Health Research (CIHR) from the Canada Foundation for Innovation; Canada Research Chairs program (Canada Research Chair in Neuromuscular Genomics and Health) [950-232279]; Canada Research Chairs program (Canada Research Chair in Neuromuscular Genomics and Health); Canada Research Chairs program (Canada Research Chair in Neuromuscular Genomics and Health); European Commission [101080249]; European Commission; European Commission; Canada Research Coordinating Committee New Frontiers in Research Fund [NFRFG-2022-00033]; Canada Research Coordinating Committee New Frontiers in Research Fund; Canada Research Coordinating Committee New Frontiers in Research Fund; Government of Canada Canada First Research Excellence Fund (CFREF) [CFREF-2022-00007]; Government of Canada Canada First Research Excellence Fund (CFREF); Government of Canada Canada First Research Excellence Fund (CFREF); CIHR Postdoctoral fellowship; CIHR Postdoctoral fellowship; CIHR Postdoctoral fellowship; German Research Foundation [WO 2385/2-1]; German Research Foundation; German Research Foundation; Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) [WE 1406/16-1, WE 1406/17-1]; Deutsche Forschungsgemeinschaft (DFG, German Research Foundation); Deutsche Forschungsgemeinschaft (DFG, German Research Foundation); DFG [418081722, 433158657, 499059538, INST 222/1458-1 FUGG, KU 1587/6-1, KU 1587/9-1, KU 1587 |
| Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science |
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| Naslov | Speech Sounds Production, Narrative Skills, and Verbal Memory of Children with 22q11.2 Microdeletion (Article) |
| Autori | Rakonjac Marijana Cuturilo Goran Kovacevic-Grujicic Natasa R Simeunovic Ivana V Kostic Jovana N Stevanovic Milena J Drakulic Danijela D
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| Info | CHILDREN-BASEL, (2024), vol. 11 br. 4, str. - |
| Projekat | European Union's Horizon Europe Coordination and Support Actions Programme |
| Ispravka | Web of Science Članak Elečas Rang časopisa |
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| Naslov | A novel splice-site FHOD3 founder variant is a common cause of hypertrophic cardiomyopathy in the population of the Balkans-A cohort study (Article) |
| Autori | Vodnjov Nina Toplisek Janez Maver Ales Cuturilo Goran Jaklic Helena Teran Natasa Visnjar Tanja Skrjanec Pusenjak Marusa Hodzic Alenka Miljanovic Olivera Peterlin Borut Writzl Karin Mahdieh Nejat |
| Info | PLOS ONE, (2023), vol. 18 br. 12, str. - |
| Projekat | Slovenian Research and Innovation Agency [P3-0326] |
| Ispravka | Web of Science Članak Elečas Rang časopisa |
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| Naslov | Inherited variants in CHD3 show variable expressivity in Snijders Blok-Campeau syndrome (Article) |
| Autori | Van der Spek Jet ... Cuturilo Goran ... (broj koautora 46) |
| Info | GENETICS IN MEDICINE, (2022), vol. 24 br. 6, str. 1283-1296 |
| Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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| Naslov | The landscape of Mucopolysaccharidosis in Southern and Eastern European countries: a survey from 19 specialistic centers (Article) |
| Autori | Tylki-Szymanska Anna ... Cuturilo Goran Djordjevic Maja S ... (broj koautora 18) |
| Info | ORPHANET JOURNAL OF RARE DISEASES, (2022), vol. 17 br. 1, str. - |
| Projekat | BioMarin Pharmaceuticals Inc. |
| Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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| Naslov | Ring chromosome 20: a further contribution to the delineation of epileptic phenotype (Article) |
| Autori | Borkovic Milan P Cuturilo Goran Cerovac Natasa M
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| Info | VOJNOSANITETSKI PREGLED, (2022), vol. 79 br. 2, str. 196-200 |
| Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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| Naslov | Genetic evaluation of newborns with critical congenital heart defects admitted to the intensive care unit (Article) |
| Autori | Miletic Aleksandra Ruml-Stojanovic Jelena Parezanovic Vojislav M Rsovac Snezana Drakulic Danijela D Soldatovic Ivan A Mijovic Marija Bosankic Brankica Petrovic Hristina Borlja Nikola Milivojevic Milena C Marjanovic Ana Marjanovic Ana Cuturilo Goran
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| Info | EUROPEAN JOURNAL OF PEDIATRICS, (2021), vol. 180 br. 10, str. 3219-3227 |
| Projekat | Ministry of Education, Science and Technological Development, Republic of Serbia [451-03-68/2020-14/200042] |
| Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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| Naslov | A Genetics-First Approach to Dissecting the Heterogeneity of Autism: Phenotypic Comparison of Autism Risk Copy Number Variants (Article) |
| Autori | Chawner Samuel JRA ... Cuturilo Goran ... Mihaljevic Marina M ... Pejovic-Milovancevic Milica M ... (broj koautora 31)
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| Info | AMERICAN JOURNAL OF PSYCHIATRY, (2021), vol. 178 br. 1, str. 77-86 |
| Projekat | Baily Thomas Charitable Trust [2315/1]; Brain Canada Foundation; Canada Research Chair in Genetics of NeurodevelopmentalDisorders; Canadian Institutes of Health Research (CIHR) [400528/159734]; Health and Care Research |
| Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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| Naslov | The clinical significance ofA2ML1variants in Noonan syndrome has to be reconsidered (Article) |
| Autori | Brinkmann Julia ... Cuturilo Goran ... (broj koautora 25) |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2021), vol. 29 br. 3, str. 524-527 |
| Projekat | ERN-ITHACA networking; German Federal Ministry of Education and Research-BMBF (German Network for RASopathy Research "GeNeRARe") [FKZ: 01GM1519A]; German Federal Ministry of Education and Research-BMBF (European Joint Programme on Rare Diseases (NSEuroNet |
| Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science |
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| 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 | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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