Autori: Maver Ales
| Naslov | Increased burden of rare variants in GWAS associated genes in familial multiple sclerosis (Meeting Abstract) |
| Autori | Turk Aleksander Maver Ales Juvan Peter Drulovic Jelena S Mesaros Sarlota T Novakovic Ivana V Cizmarevic Nada S Ristic Smiljana Matic Ivana S Peterlin Borut |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2025), vol. 33 br. , Suppl. 1, str. 1046-1046 |
| Ispravka | ISI/Web of Science Elečas Rang časopisa |
| Naslov | Biallelic RFC1 expansions as a rare cause of familial and early onset Parkinson's disease in the Slavic population (Meeting Abstract) |
| Autori | Kovanda Anja Susmelj Lara Lukezic Tadeja Maver Ales Racki Valentino Vuletic Vladimira Svetel Marina V Novakovic Ivana V Peterlin Borut |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2025), vol. 33 br. , Suppl. 1, str. 797-798 |
| Ispravka | ISI/Web of Science Elečas Rang časopisa |
| Naslov | Clinical application of whole exome sequencing in the diagnosis of men with severely impaired spermatogenesis (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 Buretic-Tomljanovic Alena Peterlin Borut |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2025), vol. 33 br. , Suppl. 1, str. 570-570 |
| Ispravka | ISI/Web of Science Elečas Rang časopisa |
| Naslov | Discovery of PHB1 as a novel candidate gene in dominant optic atrophy (Meeting Abstract) |
| Autori | Volk Marija Trost Nusa Visnjar Tanja Maver Ales Vidmar Martina Jarc Fakin Ana Petrovic-Pajic Sanja Hawlina Marko Peterlin Borut |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2025), vol. 33 br. , Suppl. 1, str. 93-93 |
| Ispravka | ISI/Web of Science Elečas Rang časopisa |
| Naslov | The role of DNA mismatch repair mutS/mutL homolog genes in spermatogenesis and male infertility: a systematic review and cohort study (Review) |
| 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 Buretic-Tomljanovic Alena Peterlin Borut |
| Info | REPRODUCTIVE BIOLOGY AND ENDOCRINOLOGY, (2025), vol. 23 br. 1, str. - |
| Projekat | Slovenian Research and Innovation Agency [P3-0326] |
| 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 Severe Idiopathic Male Infertility (Article) |
| 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 | WORLD JOURNAL OF MENS HEALTH, (2025), vol. 43 br. 4, str. 908-917 |
| Projekat | Slovenian Research and Innovation Agency [P3-0326] |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science |
| Naslov | Biallelic RFC1 Expansions Are a Rare Cause of Early-Onset and Familial Parkinson's Disease (Editorial Material; Early Access) |
| Autori | Kovanda Anja Susmelj Lara Jaklic Helena Lukezic Tadeja Maver Ales Petrovic Igor N Dragasevic-Miskovic Natasa T Svetel Marina V Racki Valentino Vuletic Vladimira Novakovic Ivana V Peterlin Borut |
| Info | CLINICAL GENETICS, (2025), vol. br. , str. - |
| Projekat | Slovenian Research and Innovation Agency (ARIS) [P3-0326, J3-4517] |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: |
| Naslov | Increased burden of rare variants in GWAS associated genes in familial multiple sclerosis (Article) |
| Autori | Turk Aleksander Maver Ales Juvan Peter Drulovic Jelena S Mesaros Sarlota T Novakovic Ivana V Starcevic-Cizmarevic Nada Ristic Smiljana Stankovic-Matic Ivana Peterlin Borut |
| Info | SCIENTIFIC REPORTS, (2025), vol. 15 br. 1, str. - |
| Projekat | Slovenian Research Agency [P3-0326, P4-0220] |
| 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 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 |
| Info | WORLD JOURNAL OF MENS HEALTH, (2025), vol. br. , str. - |
| Projekat | Slovenian Research and Inno-vation Agency [P3-0326] |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: |
| 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 |
