Autori: Peterlin Borut
| 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 | ISI/Web of Science Članak Elečas Rang časopisa |
| Naslov | Leber Hereditary Optic Neuropathy in a Family of Carriers of MT-ND5 m.13042G>T (A236S) Novel Variant (Article) |
| Autori | Petrovic Pajic Sanja MI Habjan Maja Sustar Brecelj Jelka Fakin Ana Volk Marija Maver Ales Jezernik Gregor Peterlin Borut Glavac Damjan Hawlina Marko Jarc-Vidmar Martina |
| Info | JOURNAL OF NEURO-OPHTHALMOLOGY, (2023), vol. 43 br. 3, str. 341-347 |
| Projekat | Slovenian Research Agency (ARRS Program) [P3-0333, P3-0427] |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa |
| Naslov | Analysis of "Clinical Exome" Panel in Serbian Patients with Cognitive Disorders (Article) |
| Autori | Brankovic Marija Stefanova Elka D Mandic Gorana B Marjanovic Ana Dobricic Valerija S Maver Ales Bergant Gaber Stevic Zorica D Jankovic Milena Z Novakovic Ivana V Peterlin Borut Kostic Vladimir K |
| Info | GENETIKA-BELGRADE, (2022), vol. 54 br. 3, str. 1351-1364 |
| Projekat | Serbian Ministry of education, science, and technological development [175090, 175091, 200] |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa |
| Naslov | A Novel Variant in the LIPA Gene Associated with Distinct Phenotype (Article) |
| Autori | Sarajlija Adrijan Armengol L Maver Ales Kitic Ivana Prokic Dragan Cehic Maja Djuricic MS Peterlin Borut |
| Info | BALKAN JOURNAL OF MEDICAL GENETICS, (2022), vol. 25 br. 1, str. 93-99 |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa |
| Naslov | Case report: Long-term follow-up of two patients with LHON caused by DNAJC30:c.152G > A pathogenic variant-case series (Article) |
| Autori | Petrovic Pajic Sanja MI Jarc-Vidmar Martina Fakin Ana Sustar-Habjan Maja Brecelj Jelka Volk Marija Maver Ales Peterlin Borut Hawlina Marko |
| Info | FRONTIERS IN NEUROLOGY, (2022), vol. 13 br. , str. - |
| Projekat | Slovenian Research Agency; [P3-0333] |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science |
| Naslov | The Relative Preservation of the Central Retinal Layers in Leber Hereditary Optic Neuropathy (Article) |
| Autori | Petrovic Pajic Sanja MI Lapajne Luka Vratanar Bor Fakin Ana Jarc-Vidmar Martina Sustar-Habjan Maja Volk Marija Maver Ales Peterlin Borut Hawlina Marko |
| Info | JOURNAL OF CLINICAL MEDICINE, (2022), vol. 11 br. 20, str. - |
| Projekat | Slovenian Research Agency [P3-0333] |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
| Naslov | Clinical Exome Sequencing in Serbian Patients with Movement Disorders - Single Centre Experience (Article) |
| Autori | Brankovic Marija Dragasevic Natasa T Dobricic Valerija S Maver Ales Bergant Gaber Petrovic Igor N Peric Stojan Z Marjanovic Ana Jankovic Milena Z Jancic Jasna B Novakovic Ivana V Peterlin Borut Svetel Marina V Kostic Vladimir K |
| Info | GENETIKA-BELGRADE, (2022), vol. 54 br. 1, str. 395-409 |
| Projekat | Serbian Ministry of education, science, and technological development [175090, 175091] |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
| Naslov | Relative preservation of central retinal layers in LHON in comparison to other optic neuropathies (Meeting Abstract) |
| Autori | Petrovic Pajic Sanja MI Lapajne Luka Fakin Ana Jarc-Vidmar Martina Glavac Damjan Volk Marija Maver Ales Vratanar Bor Stare Janez Peterlin Borut Hawlina Marko |
| Info | INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, (2022), vol. 63 br. 7, str. - |
| Ispravka | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science |
| Naslov | Diagnostic yield of whole exome sequencing in early-onset and familial Parkinson's disease in the Balkans (Meeting Abstract) |
| Autori | Maver Ales Kovanda Anja Bergant Gaber Teran Natasa Vrecar Irena Brankovic Marija Jankovic Milena Z Svetel Marina V Kostic Vladimir S Novakovic Ivana V Racki Valentino Vuletic Vladimira Peterlin Borut |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2022), vol. 30 br. SUPPL 1, Suppl. 1, str. 292-292 |
| Ispravka | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science |
| Naslov | Current State of Compulsory Basic and Clinical Courses in Genetics for Medical Students at Medical Faculties in Balkan Countries With Slavic Languages (Article) |
| Autori | Pereza Nina Terzic Rifet Plaseska-Karanfilska Dijana Miljanovic Olivera Novakovic Ivana V Poslon Zeljka Ostojic Sasa Peterlin Borut |
| Info | FRONTIERS IN GENETICS, (2022), vol. 12 br. , str. - |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa |
