Autori: Peterlin Borut
| Naslov | De novo mutations in idiopathic male infertility (Meeting Abstract) |
| Autori | Hodzic Alenka Maver Ales Zorn Branko Plaseska-Karanfilska Dijana Ristanovic Momcilo Novakovic Ivana V Peterlin Borut |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2019), vol. 27 br. , Suppl. 1, str. 16-17 |
| Ispravka | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
| Naslov | Increased burden of ultra-rare genetic variants in the inflammasome regulatory genes in patients with multiple sclerosis (Meeting Abstract) |
| Autori | Peterlin Borut Vidmar Lovro Drulovic Jelena S Sepcic Juraj Novakovic Ivana V Ristic Smiljana Sega-Jazbec Sasa Maver Ales |
| Info | EUROPEAN JOURNAL OF NEUROLOGY, (2019), vol. 26 br. , Suppl. 1, str. 885-885 |
| Projekat | Slovenian Research Agency |
| Ispravka | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science |
| Naslov | Multiple Sclerosis patients carry an increased burden of exceedingly rare genetic variants in the inflammasome regulatory genes (Article) |
| Autori | Vidmar Lovro Mayer Ales Drulovic Jelena S Sepcic Juraj Novakovic Ivana V Ristic Smiljana Sega Sasa Peterlin Borut |
| Info | SCIENTIFIC REPORTS, (2019), vol. 9 br. , str. - |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
| Naslov | A novel CTNNB1 mutation in a patient with teratoma and multiple malformations - expansion of the phenotypic spectrum and possible new gene for Currarino phenotype (Meeting Abstract) |
| Autori | Mijovic Marija Miletic Aleksandra Ruml-Stojanovic Jelena Peterlin Borut Maver Ales Borlja Nikola Dimitrijevic Brankica Lukic M Cuturilo Goran |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2018), vol. 26 br. , Suppl. S, str. 465-465 |
| Ispravka | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science |
| Naslov | The burden of rare genetic variants in genes involved in tumor necrosis factor (TNF) signalling pathway in multiple sclerosis (MS) (Meeting Abstract) |
| Autori | Peterlin AM Maver Ales Hodzic A Sega Sasa Drulovic Jelena S Novakovic Ivana V Pekmezovic Tatjana D Ristic S Kapovic Miljenko Peterlin Borut |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2018), vol. 26 br. , Suppl. S, str. 400-400 |
| Ispravka | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science |
| Naslov | Association between angiotensin-converting enzyme gene insertion/deletion polymorphism and susceptibility to preterm birth: A case-control study and meta-analysis (Article) |
| Autori | Hocevar Keli Peterlin Ana Mitrovic-Jovanovic Ana Bozovic Aleksandra Ristanovic Momcilo Tul Natasa Peterlin Borut |
| Info | EUROPEAN JOURNAL OF OBSTETRICS & GYNECOLOGY AND REPRODUCTIVE BIOLOGY, (2018), vol. 231 br. , str. 122-128 |
| Projekat | Slovenian Research Agency [P3-0326] |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
| Naslov | Genotype and phenotype characteristics of Leber hereditary optic neuropathy (LHON) patients in Slovenia (Meeting Abstract) |
| Autori | Petrovic Pajic Sanja MI Jarc-Vidmar Martina Fakin Ana Sustar Maja Brecelj Jelka Lapajne Luka Glavac Damjan Tajnik Mojca Peterlin Borut Volk Marija Maver Ales Hawlina Marko |
| Info | INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, (2018), vol. 59 br. 9, str. - |
| Ispravka | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science |
| Naslov | Genetic variation in the CLOCK gene is associated with idiopathic recurrent spontaneous abortion (Article) |
| Autori | Hodzic Alenka Lavtar Polona Ristanovic Momcilo Novakovic Ivana V Dotlic Jelena R Peterlin Borut |
| Info | PLOS ONE, (2018), vol. 13 br. 5, str. - |
| Projekat | Slovenian Research Agency [P3-0326] |
| 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 |
| Naslov | Comprehensive use of extended exome analysis improves diagnostic yield in rare disease: a retrospective survey in 1,059 cases (Article) |
| Autori | Bergant Gaber Maver Ales Lovrecic Luca Cuturilo Goran Hodzic Alenka Peterlin Borut |
| Info | GENETICS IN MEDICINE, (2018), vol. 20 br. 3, str. 303-312 |
| Projekat | Slovenian Research Agency [P3-0326] |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
