Autori: Maver Ales
| 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 | De novo mutations in idiopathic male infertility-A pilot study (Article) |
| Autori | Hodzic Alenka Maver Ales Plaseska-Karanfilska Dijana Ristanovic Momcilo Noveski Predrag Zorn Branko Terzic Marija Kunej Tanja Peterlin Borut |
| Info | ANDROLOGY, (2021), vol. 9 br. 1, str. 212-220 |
| Projekat | Slovenian Research Agency - Slovenia [P3-0326]; Ministry of Education and Science of R. Macedonia [17-4523/1] |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
| Naslov | Diagnostic and Clinical Utility of Clinical Exome Sequencing in Children With Moderate and Severe Global Developmental Delay / Intellectual Disability (Article) |
| Autori | Ruml-Stojanovic Jelena Miletic Aleksandra Peterlin Borut Maver Ales Mijovic Marija Borlja Nikola Dimitrijevic Brankica Soldatovic Ivan A Cuturilo Goran |
| Info | JOURNAL OF CHILD NEUROLOGY, (2020), vol. 35 br. 2, str. 116-131 |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
| Naslov | Clinical Next Generation Sequencing Reveals An H3f3a Gene as a New Potential Gene Candidate for Microcephaly Associated with Severe Developmental Delay, Intellectual Disability and Growth Retardation (Article) |
| Autori | Maver Ales Cuturilo Goran Stojanovic Ruml J Peterlin Borut |
| Info | BALKAN JOURNAL OF MEDICAL GENETICS, (2019), vol. 22 br. 2, str. 65-68 |
| Projekat | Slovenian Research Agency - Slovenia [J3-8205, J3-9280, P3-0326] |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
| Naslov | Rare missense TUBGCP5 gene variant in a patient with primary microcephaly (Article) |
| Autori | Maver Ales Cuturilo Goran Kovanda Anja Miletic Aleksandra Peterlin Borut |
| Info | EUROPEAN JOURNAL OF MEDICAL GENETICS, (2019), vol. 62 br. 12, str. - |
| Projekat | ARRS research programme [P3-0326, J3-8205, J3-5506] |
| 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 |
