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Autori: Peterlin Borut

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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 Web of Science   Članak   Elečas   Rang časopisa  
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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 Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science  
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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]
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Naslov ACE gene and male infertility: a South Slavic case-control study and multi-omics data integration (Article)
Autori Kunej Tanja Podgrajsek Rebeka Jaklic Helena Hodzic Alenka Stimpfel Martin Miljanovic Olivera Ristanovic Momcilo Novakovic Ivana V  Plaseska-Karanfilska Dijana Noveski Predrag Ostojic Sasa Buretic-Tomljanovic Alena Grskovic Antun Peterlin Borut 
Info SYSTEMS BIOLOGY IN REPRODUCTIVE MEDICINE, (2025), vol. 71 br. 1, str. 524-537
Projekat Slovenian Research and Innovation Agency [P3-0326, P4-0220]
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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]
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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]
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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]
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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 Pusenjak Marusa Skrjanec 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]
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Naslov MTHFR Gene Polymorphisms and DNA Methylation in Idiopathic Spontaneous Preterm Birth (Article)
Autori Devic-Pavlic Sanja Sverko Roberta Barisic Anita Mladenic Tea Vranekovic Jadranka Stankovic Aleksandra D  Peterlin Ana Peterlin Borut Ostojic Sasa Pereza Nina 
Info MEDICINA-LITHUANIA, (2024), vol. 60 br. 12, str. -
Projekat University of Rijeka, Croatia; [uniri-iskusni-biomed-23-195]
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Naslov Rare and Uncommon Gene Variants Associated with Familial Multiple Sclerosis: A Case-Control Study (Meeting Abstract)
Autori Jovanovic Aleksa Lj  Turk Aleksander Novakovic Ivana V  Mesaros Sarlota T Veselinovic Nikola D Tamas Olivera S Maric Gorica D  Andabaka Marko M Momcilovic Nikola Pekmezovic Tatjana D  Peterlin Borut Drulovic Jelena S  
Info MULTIPLE SCLEROSIS JOURNAL, (2024), vol. 30 br. 3, Suppl. S, str. 866-867
Projekat Ministry of Science, Technological development and Innovation of the Republic of Serbia [200110]
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