Autori: Maver Ales
| Naslov | A novel splice-site FHOD3 founder variant is a common cause of hypertrophic cardiomyopathy in the population of the Balkans - a cohort study (Meeting Abstract) |
| 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 |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2024), vol. 32 br. , Suppl. 2, str. 1390-1390 |
| Projekat | [P3-0326] |
| Ispravka | ISI/Web of Science Elečas Rang časopisa |
| Naslov | A novel splice-site FHOD3 founder variant is a common cause of hypertrophic cardiomyopathy in the population of the Balkans - a cohort study (Meeting Abstract) |
| Autori | Vodnjov Nina Toplisek Janez Maver Ales Cuturilo Goran Jaklic Helena Teran Natasa Visnjar Tanja Pusenjak Marusa Skrjanec Hodzic Alenka Miljanovic Olivera Peterlin Borut Writzl Karin |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2024), vol. 32 br. , Suppl. 2, str. 1390-1390 |
| Projekat | [P3-0326] |
| Ispravka | ISI/Web of Science Elečas Rang časopisa |
| Naslov | Noonan Syndrome: Relation of Genotype to Cardiovascular Phenotype-A Multi-Center Retrospective Study (Article) |
| Autori | Ilic Nikola A Krasic Stasa D Maric Nina Gasic Vladimir V Krstic Jovana Cvetkovic Dimitrije Miljkovic Vesna Zec Boris Maver Ales Vukomanovic Vladislav A Sarajlija Adrijan |
| Info | GENES, (2024), vol. 15 br. 11, str. - |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa |
| Naslov | Genetic testing for monogenic forms of male infertility contributes to the clinical diagnosis of men with idiopathic severe male infertility (Meeting Abstract) |
| Autori | Podgrajsek Rebeka Hodzic Alenka Maver Ales Stimpfel Martin Andjelic Aleksander Miljanovic Olivera Ristanovic Momcilo Novakovic Ivana V Plaseska-Karanfilska Dijana Noveski Predrag Ostojic Sasa Grskovic Antun Buretic-Tomljanovic Alena Peterlin Borut |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2024), vol. 32 br. , Suppl. 1, str. 356-357 |
| Projekat | Slovenian Research Agency [P3-0326] |
| Ispravka | ISI/Web of Science Elečas Rang časopisa |
| Naslov | Expanding the Phenotypic Spectrum: Chronic Kidney Disease in a Patient with Combined Oxidative Phosphorylation Defect 21 (Article) |
| Autori | Paripovic Aleksandra Maver Ales Stajic Natasa Putnik Jovana Ostojic Slavica B Alimpic Biljana Ilic Nina Sarajlija Adrijan |
| Info | BALKAN JOURNAL OF MEDICAL GENETICS, (2023), vol. 26 br. 2, str. 59-64 |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa |
| 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 | Sensorineural Hearing Loss in a Child with Succinic Semialdehyde Dehydrogenase Deficiency (Article) |
| Autori | Parezanovic M Ilic Nina Ostojic Slavica B Stevanovic Galina B Jecmenica Jovana R Maver Ales Sarajlija Adrijan |
| Info | BALKAN JOURNAL OF MEDICAL GENETICS, (2023), vol. 26 br. 1, str. 63-67 |
| 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 |
