Autori: Cuturilo Goran
| Naslov | Autistic Traits and Cognitive Dysfunctions in Children with Patogenic Copy Number Variants: a Pilot Study from Serbia (Meeting Abstract) |
| Autori | Mihaljevic Marina M Pejovic-Milovancevic Milica M Janeski Hristina Mandic-Maravic Vanja B Grujicic Roberto Drakulic Danijela D Stevanovic Milena J Cuturilo Goran |
| Info | EUROPEAN NEUROPSYCHOPHARMACOLOGY, (2019), vol. 29 br. , Suppl. 4, str. 1278-1279 |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science |
| Naslov | Activating Mutations of RRAS2 Are a Rare Cause of Noonan Syndrome (Article) |
| Autori | Capri Yline ... Cuturilo Goran ... (broj koautora 33) |
| Info | AMERICAN JOURNAL OF HUMAN GENETICS, (2019), vol. 104 br. 6, str. 1223-1232 |
| Projekat | ERN-ITHACA networking; E-Rare (NSEuroNet) [ERARE15-pp-063, 01GM1602B, 01GM1602A]; AIRC [IG21614]; Ministero della Salute; German Federal Ministry of Education and Research -BMBF (German Network for RASopathy Research "GeNeRARe") [01GM1519D, 01GM1902C, 01G |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
| Naslov | A novel CTNNB1 mutation in a patient with teratoma and multiple malformations - expansion of the phenotypic spectrum and possible new gene for Currarino phenotype (Meeting Abstract) |
| Autori | Mijovic Marija Miletic Aleksandra Ruml-Stojanovic Jelena Peterlin Borut Maver Ales Borlja Nikola Dimitrijevic Brankica Lukic M Cuturilo Goran |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2018), vol. 26 br. , Suppl. S, str. 465-465 |
| Ispravka | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science |
| Naslov | Recessive DNAH9 Loss-of-Function Mutations Cause Laterality Defects and Subtle Respiratory Ciliary-Beating Defects (Article) |
| Autori | Loges Niki T ... Cuturilo Goran ... (broj koautora 27) |
| Info | AMERICAN JOURNAL OF HUMAN GENETICS, (2018), vol. 103 br. 6, str. 995-1008 |
| Projekat | Deutsche Forschungsgemeinschaft (DFG) [OM6/7, OM6/8, OM6/10, CRC1140 KIDGEM, KFO 326, OL450/1, HJ7/1-1]; IZKF Muenster [Om2/009/12, Om/015/16]; European Union seventh FP [305404]; "Innovative Medical Research'' of the University of Muenster Medical School |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
| Naslov | Phenotype and genotype of 87 patients with Mowat-Wilson syndrome and recommendations for care (Article) |
| Autori | Ivanovski Ivan P Djuric Olivera S ... Cuturilo Goran ... Kuburovic Vladimir ... (broj koautora 80) |
| Info | GENETICS IN MEDICINE, (2018), vol. 20 br. 9, str. 965-975 |
| Projekat | Telethon Italy [14131, GTB12001]; Associazione Italiana Mowat Wilson ONLUS (AIMW) [GTB12001] |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
| Naslov | PITX2 deficiency and associated human disease: insights from the zebrafish model (Article) |
| Autori | Hendee Kathryn E Sorokina Elena A Muheisen Sanaa S Reis Linda M Tyler Rebecca C Markovic Vujica D Cuturilo Goran Link Brian A Semina Elena V |
| Info | HUMAN MOLECULAR GENETICS, (2018), vol. 27 br. 10, str. 1675-1695 |
| Projekat | National Institutes of Health (NIH) - USA [EY015518]; Children's Research Institute Foundation at Children's Hospital of Wisconsin; NEIUnited States Department of Health & Hum |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
| Naslov | Diagnostic exome sequencing of syndromic epilepsy patients in clinical practice (Article) |
| Autori | Tumiene B Maver Ales Writzl Karin Hodzic A Cuturilo Goran Kuzmanic-Samija Radenka Culic V Peterlin Borut |
| Info | CLINICAL GENETICS, (2018), vol. 93 br. 5, str. 1057-1062 |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
| Naslov | Comprehensive use of extended exome analysis improves diagnostic yield in rare disease: a retrospective survey in 1,059 cases (Article) |
| Autori | Bergant Gaber Maver Ales Lovrecic Luca Cuturilo Goran Hodzic Alenka Peterlin Borut |
| Info | GENETICS IN MEDICINE, (2018), vol. 20 br. 3, str. 303-312 |
| Projekat | Slovenian Research Agency [P3-0326] |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
| Naslov | The novel RAF1 mutation p.(Gly361Ala) located outside the kinase domain of the CR3 region in two patients with Noonan syndrome, including one with a rare brain tumor (Article) |
| Autori | Harms Frederike L Alawi Malik Amor David J Tan Tiong Y Cuturilo Goran Lissewski Christina Brinkmann Julia Schanze Denny Kutsche Kerstin Zenker Martin |
| Info | AMERICAN JOURNAL OF MEDICAL GENETICS PART A, (2018), vol. 176 br. 2, str. 470-476 |
| Projekat | BMBF [01GM1519A, 01GM1519E]; Deutsche Forschungsgemeinschaft [KU 1240/9-1, ZE 524/10-1] |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
| Naslov | The Impact of 22q11.2 Microdeletion on Cardiac Surgery Postoperative Outcome (Article) |
| Autori | Cuturilo Goran Drakulic Danijela D Jovanovic Ida V Ilic Slobodan G Kalanj Jasna Vulicevic Irena Raus Misela V Skoric Dejan Mijovic Marija Medjo Biljana P Rsovac Snezana Stevanovic Milena J |
| Info | PEDIATRIC CARDIOLOGY, (2017), vol. 38 br. 8, str. 1680-1685 |
| Projekat | Ministry of Education, Science and Technological Development, Republic of Serbia [173051] |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
