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Autori: Peterlin Borut

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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 Web of Science   Elečas   Rang časopisa   Citati: Web of Science  
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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 Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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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 Web of Science   Elečas   Rang časopisa   Citati: Web of Science  
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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 Web of Science   Elečas   Rang časopisa   Citati: Web of Science  
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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 Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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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 Web of Science   Elečas   Rang časopisa   Citati: Web of Science  
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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 Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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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 Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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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 Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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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 Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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