Autori: Maver Ales
| Naslov | Genetic Testing for Monogenic Forms of Male Infertility Contributes to the Clinical Diagnosis of Men with Severe Idiopathic Male Infertility (Article; Early Access) |
| 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
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| Info | WORLD JOURNAL OF MENS HEALTH, (2025), vol. br. , str. - |
| Projekat | Slovenian Research and Inno-vation Agency [P3-0326] |
| Ispravka | Web of Science Članak Elečas Rang časopisa Citati: |
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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 (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 | Web of Science 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 (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 | Web of Science Elečas Rang časopisa |
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| 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
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| Info | GENES, (2024), vol. 15 br. 11, str. - |
| Ispravka | Web of Science Članak Elečas Rang časopisa |
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| 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
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| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2024), vol. 32 br. , Suppl. 1, str. 356-357 |
| Projekat | Slovenian Research Agency [P3-0326] |
| Ispravka | Web of Science Elečas Rang časopisa |
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| 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
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| Info | BALKAN JOURNAL OF MEDICAL GENETICS, (2023), vol. 26 br. 2, str. 59-64 |
| 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 | 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 | Web of Science Članak Elečas Rang časopisa |
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| 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
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| Info | BALKAN JOURNAL OF MEDICAL GENETICS, (2023), vol. 26 br. 1, str. 63-67 |
| Ispravka | Web of Science Članak Elečas Rang časopisa |
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| 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
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| Info | GENETIKA-BELGRADE, (2022), vol. 54 br. 3, str. 1351-1364 |
| Projekat | Serbian Ministry of education, science, and technological development [175090, 175091, 200] |
| Ispravka | Web of Science Članak Elečas Rang časopisa |
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