Autori: Cuturilo Goran
| Naslov | Inherited variants in CHD3 demonstrate variable expressivity in Snijders Blok-Campeau syndrome (Meeting Abstract) |
| Autori | Van der Spek Jet ... Cuturilo Goran ... (broj koautora 33) |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2022), vol. 30 br. SUPPL 1, Suppl. 1, str. 234-234 |
| Ispravka | Web of Science Elečas Rang časopisa Citati: Web of Science |
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| Naslov | What are key parameters for obtaining the most likely clinical diagnosis from the wide phenotypic spectrum of skeletal dysplasia in patients with previously identified disease-causing gene variant (Meeting Abstract) |
| Autori | Mijovic Marija Bukva Bojan  Ruml-Stojanovic Jelena Miletic Aleksandra Bosankic Brankica Petrovic Hristina Cuturilo Goran
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| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2022), vol. 30 br. SUPPL 1, Suppl. 1, str. 181-181 |
| Ispravka | Web of Science Elečas Rang časopisa Citati: Web of Science |
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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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| Naslov | Skeletal dysplasia in the era of genomic testing: first experience of a single genetic outpatient clinic from Serbia (Meeting Abstract) |
| Autori | Mijovic Marija Ruml-Stojanovic Jelena Miletic Aleksandra Bosankic Brankica Janeski Hristina Peterlin Borut Maver Ales Cuturilo Goran |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2020), vol. 28 br. SUPPL 1, Suppl. 1, str. 831-831 |
| Ispravka | Web of Science Elečas Rang časopisa Citati: Web of Science |
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| Naslov | Recurrent congenital microcephaly: a case report (Meeting Abstract) |
| Autori | Komnenic-Radovanovic Milica Novakovic Ivana V Cuturilo Goran Ruml-Stojanovic Jelena Petrovic Bojana Kontic-Vucinic Olivera
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| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2020), vol. 28 br. SUPPL 1, Suppl. 1, str. 801-802 |
| Ispravka | Web of Science Elečas Rang časopisa Citati: Web of Science |
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| Naslov | The role of A2ML1 variants in Noonan syndrome remains unverified (Meeting Abstract) |
| Autori | Brinkmann Julia ... Cuturilo Goran ... (broj koautora 24) |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2020), vol. 28 br. SUPPL 1, Suppl. 1, str. 479-479 |
| Ispravka | Web of Science Elečas Rang časopisa Citati: Web of Science |
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