Autori: Peterlin Borut
| 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 | Otopalatodigital Syndrome Type I: Novel Characteristics and Prenatal Manifestations in Two Siblings (Article) |
| Autori | Joksic Ivana D Cuturilo Goran Jurisic Aleksandar I Djuricic Slavisa M Peterlin Borut Mijovic Marija Karadzov-Orlic Natasa T Egic Amira Milovanovic Zagorka M |
| Info | BALKAN JOURNAL OF MEDICAL GENETICS, (2019), vol. 22 br. 2, str. 83-87 |
| 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 | 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 | 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 | 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 |
| Naslov | Genetic variation in leptin and leptin receptor genes as a risk factor for idiopathic male infertility (Article) |
| Autori | Hodzic Alenka Ristanovic Momcilo Zorn Branko Tulic Cane Dz Maver Ales Novakovic Ivana V Plaseska-Karanfilska Dijana Peterlin Borut |
| Info | ANDROLOGY, (2017), vol. 5 br. 1, str. 70-74 |
| Projekat | Slovenian Research Agency [P3-0326] |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
