@ARTICLE{
author={Volk Marija,Maver Ales,Vidmar Martina Jarc,Trost Nusa,Visnjar Tanja,Fakin Ana,Kovac Lea,Habjan Maja Sustar,Malinar Lucija,Petrovic Pajic Sanja MI,Jerman Urska Dragin,Romih Rok,Hawlina Marko,Peterlin Borut},
year={2026},
title={Discovery of PHB1 as a Novel Candidate Gene in Dominant Optic Atrophy},
journal={CLINICAL GENETICS},
volume={},
number={},
pages={-},
document_type={Article; Early Access},
} 

@ARTICLE{
author={Turk Aleksander,Maver Ales,Juvan Peter,Drulovic Jelena S,Mesaros Sarlota T,Novakovic Ivana V,Cizmarevic Nada S,Ristic Smiljana,Matic Ivana S,Peterlin Borut},
year={2025},
title={Increased burden of rare variants in GWAS associated genes in familial multiple sclerosis},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={33},
number={},
pages={1046-1046},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Kovanda Anja,Susmelj Lara,Lukezic Tadeja,Maver Ales,Racki Valentino,Vuletic Vladimira,Svetel Marina V,Novakovic Ivana V,Peterlin Borut},
year={2025},
title={Biallelic RFC1 expansions as a rare cause of familial and early onset Parkinson's disease in the Slavic population},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={33},
number={},
pages={797-798},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={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},
year={2025},
title={Clinical application of whole exome sequencing in the diagnosis of men with severely impaired spermatogenesis},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={33},
number={},
pages={570-570},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Volk Marija,Trost Nusa,Visnjar Tanja,Maver Ales,Vidmar Martina Jarc,Fakin Ana,Petrovic-Pajic Sanja,Hawlina Marko,Peterlin Borut},
year={2025},
title={Discovery of PHB1 as a novel candidate gene in dominant optic atrophy},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={33},
number={},
pages={93-93},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={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},
year={2025},
title={The role of DNA mismatch repair mutS/mutL homolog genes in spermatogenesis and male infertility: a systematic review and cohort study},
journal={REPRODUCTIVE BIOLOGY AND ENDOCRINOLOGY},
volume={23},
number={1},
pages={-},
document_type={Review},
} 

@ARTICLE{
author={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},
year={2025},
title={Genetic Testing for Monogenic Forms of Male Infertility Contributes to the Clinical Diagnosis of Men with Severe Idiopathic Male Infertility},
journal={WORLD JOURNAL OF MENS HEALTH},
volume={43},
number={4},
pages={908-917},
document_type={Article},
} 

@ARTICLE{
author={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},
year={2025},
title={Biallelic RFC1 Expansions Are a Rare Cause of Early-Onset and Familial Parkinson's Disease},
journal={CLINICAL GENETICS},
volume={},
number={},
pages={-},
document_type={Editorial Material; Early Access},
} 

@ARTICLE{
author={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},
year={2025},
title={ACE gene and male infertility: a South Slavic case-control study and multi-omics data integration},
journal={SYSTEMS BIOLOGY IN REPRODUCTIVE MEDICINE},
volume={71},
number={1},
pages={524-537},
document_type={Article},
} 

@ARTICLE{
author={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},
year={2025},
title={Increased burden of rare variants in GWAS associated genes in familial multiple sclerosis},
journal={SCIENTIFIC REPORTS},
volume={15},
number={1},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={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},
year={2025},
title={Genetic Testing for Monogenic Forms of Male Infertility Contributes to the Clinical Diagnosis of Men with Severe Idiopathic Male Infertility},
journal={WORLD JOURNAL OF MENS HEALTH},
volume={},
number={},
pages={-},
document_type={Article; Early Access},
} 

@ARTICLE{
author={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},
year={2024},
title={A novel splice-site FHOD3 founder variant is a common cause of hypertrophic cardiomyopathy in the population of the Balkans - a cohort study},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={32},
number={},
pages={1390-1390},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={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},
year={2024},
title={A novel splice-site FHOD3 founder variant is a common cause of hypertrophic cardiomyopathy in the population of the Balkans - a cohort study},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={32},
number={},
pages={1390-1390},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Devic-Pavlic Sanja,Sverko Roberta,Barisic Anita,Mladenic Tea,Vranekovic Jadranka,Stankovic Aleksandra D,Peterlin Ana,Peterlin Borut,Ostojic Sasa,Pereza Nina},
year={2024},
title={MTHFR Gene Polymorphisms and DNA Methylation in Idiopathic Spontaneous Preterm Birth},
journal={MEDICINA-LITHUANIA},
volume={60},
number={12},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={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},
year={2024},
title={Rare and Uncommon Gene Variants Associated with Familial Multiple Sclerosis: A Case-Control Study},
journal={MULTIPLE SCLEROSIS JOURNAL},
volume={30},
number={3},
pages={866-867},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Jovanovic Aleksa Lj,Pekmezovic Tatjana D,Mesaros Sarlota T,Novakovic Ivana V,Peterlin Borut,Veselinovic Nikola D,Tamas Olivera S,Ivanovic Jovana B,Maric Gorica D,Andabaka Marko M,Momcilovic Nikola,Drulovic Jelena S},
year={2024},
title={Earlier age of symptom onset in younger generation of familial cases of multiple sclerosis},
journal={NEUROLOGICAL SCIENCES},
volume={},
number={},
pages={-},
document_type={Article; Early Access},
} 

@ARTICLE{
author={Jovanovic Aleksa Lj,Pekmezovic Tatjana D,Mesaros Sarlota T,Novakovic Ivana V,Peterlin Borut,Veselinovic Nikola D,Tamas Olivera S,Ivanovic Jovana B,Maric Gorica D,Andabaka Marko M,Momcilovic Nikola,Drulovic Jelena S},
year={2024},
title={Exclusive breastfeeding may be a protective factor in individuals with familial multiple sclerosis. A population registry-based case-control study},
journal={MULTIPLE SCLEROSIS AND RELATED DISORDERS},
volume={82},
number={},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={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},
year={2024},
title={Genetic testing for monogenic forms of male infertility contributes to the clinical diagnosis of men with idiopathic severe male infertility},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={32},
number={},
pages={356-357},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={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,Mahdieh Nejat},
year={2023},
title={A novel splice-site <i>FHOD3</i> founder variant is a common cause of hypertrophic cardiomyopathy in the population of the Balkans-A cohort study},
journal={PLOS ONE},
volume={18},
number={12},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Petrovic Pajic Sanja MI,Habjan Maja Sustar,Brecelj Jelka,Fakin Ana,Volk Marija,Maver Ales,Jezernik Gregor,Peterlin Borut,Glavac Damjan,Hawlina Marko,Jarc-Vidmar Martina},
year={2023},
title={Leber Hereditary Optic Neuropathy in a Family of Carriers of MT-ND5 m.13042G>T (A236S) Novel Variant},
journal={JOURNAL OF NEURO-OPHTHALMOLOGY},
volume={43},
number={3},
pages={341-347},
document_type={Article},
} 

@ARTICLE{
author={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},
year={2022},
title={Analysis of "Clinical Exome" Panel in Serbian Patients with Cognitive Disorders},
journal={GENETIKA-BELGRADE},
volume={54},
number={3},
pages={1351-1364},
document_type={Article},
} 

@ARTICLE{
author={Sarajlija Adrijan,Armengol L,Maver Ales,Kitic Ivana,Prokic Dragan,Cehic Maja,Djuricic MS,Peterlin Borut},
year={2022},
title={A Novel Variant in the LIPA Gene Associated with Distinct Phenotype},
journal={BALKAN JOURNAL OF MEDICAL GENETICS},
volume={25},
number={1},
pages={93-99},
document_type={Article},
} 

@ARTICLE{
author={Petrovic Pajic Sanja MI,Jarc-Vidmar Martina,Fakin Ana,Sustar-Habjan Maja,Brecelj Jelka,Volk Marija,Maver Ales,Peterlin Borut,Hawlina Marko},
year={2022},
title={Case report: Long-term follow-up of two patients with LHON caused by DNAJC30:c.152G > A pathogenic variant-case series},
journal={FRONTIERS IN NEUROLOGY},
volume={13},
number={},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Petrovic Pajic Sanja MI,Lapajne Luka,Vratanar Bor,Fakin Ana,Jarc-Vidmar Martina,Sustar-Habjan Maja,Volk Marija,Maver Ales,Peterlin Borut,Hawlina Marko},
year={2022},
title={The Relative Preservation of the Central Retinal Layers in Leber Hereditary Optic Neuropathy},
journal={JOURNAL OF CLINICAL MEDICINE},
volume={11},
number={20},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={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},
year={2022},
title={Clinical Exome Sequencing in Serbian Patients with Movement Disorders - Single Centre Experience},
journal={GENETIKA-BELGRADE},
volume={54},
number={1},
pages={395-409},
document_type={Article},
} 

@ARTICLE{
author={Petrovic Pajic Sanja MI,Lapajne Luka,Fakin Ana,Jarc-Vidmar Martina,Glavac Damjan,Volk Marija,Maver Ales,Vratanar Bor,Stare Janez,Peterlin Borut,Hawlina Marko},
year={2022},
title={Relative preservation of central retinal layers in LHON in comparison to other optic neuropathies},
journal={INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE},
volume={63},
number={7},
pages={-},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Maver Ales,Kovanda Anja,Bergant Gaber,Teran Natasa,Vrecar Irena,Brankovic Marija,Jankovic Milena Z,Svetel Marina V,Kostic Vladimir S,Novakovic Ivana V,Racki Valentino,Vuletic Vladimira,Peterlin Borut},
year={2022},
title={Diagnostic yield of whole exome sequencing in early-onset and familial Parkinson's disease in the Balkans},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={30},
number={SUPPL 1},
pages={292-292},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Pereza Nina,Terzic Rifet,Plaseska-Karanfilska Dijana,Miljanovic Olivera,Novakovic Ivana V,Poslon Zeljka,Ostojic Sasa,Peterlin Borut},
year={2022},
title={Current State of Compulsory Basic and Clinical Courses in Genetics for Medical Students at Medical Faculties in Balkan Countries With Slavic Languages},
journal={FRONTIERS IN GENETICS},
volume={12},
number={},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Barisic Anita,Stankovic Aleksandra D,Stojkovic Ljiljana,Pereza Nina,Ostojic Sasa,Peterlin Ana,Peterlin Borut,Vranekovic Jadranka},
year={2022},
title={Maternal LINE-1 DNA Methylation in Early Spontaneous Preterm Birth},
journal={BIOLOGICAL RESEARCH FOR NURSING},
volume={24},
number={1},
pages={85-93},
document_type={Article},
} 

@ARTICLE{
author={Hodzic Alenka,Maver Ales,Plaseska-Karanfilska Dijana,Ristanovic Momcilo,Noveski Predrag,Zorn Branko,Terzic Marija,Kunej Tanja,Peterlin Borut},
year={2021},
title={De novo mutations in idiopathic male infertility-A pilot study},
journal={ANDROLOGY},
volume={9},
number={1},
pages={212-220},
document_type={Article},
} 

@ARTICLE{
author={Mijovic Marija,Ruml-Stojanovic Jelena,Miletic Aleksandra,Bosankic Brankica,Janeski Hristina,Peterlin Borut,Maver Ales,Cuturilo Goran},
year={2020},
title={Skeletal dysplasia in the era of genomic testing: first experience of a single genetic outpatient clinic from Serbia},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={28},
number={SUPPL 1},
pages={831-831},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Petrovic Pajic Sanja MI,Jarc-Vidmar Martina,Fakin Ana,Sustar Maja,Brecelj Jelka,Lapajne Luka,Volk Marija,Maver Ales,Peterlin Borut,Hawlina Marko},
year={2020},
title={Phenotype and genotype spectrum of patients with a bilateral optic neuropathy in population of Slovenia},
journal={INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE},
volume={61},
number={7},
pages={-},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Ruml-Stojanovic Jelena,Miletic Aleksandra,Peterlin Borut,Maver Ales,Mijovic Marija,Borlja Nikola,Dimitrijevic Brankica,Soldatovic Ivan A,Cuturilo Goran},
year={2020},
title={Diagnostic and Clinical Utility of Clinical Exome Sequencing in Children With Moderate and Severe Global Developmental Delay / Intellectual Disability},
journal={JOURNAL OF CHILD NEUROLOGY},
volume={35},
number={2},
pages={116-131},
document_type={Article},
} 

@ARTICLE{
author={Joksic Ivana D,Cuturilo Goran,Jurisic Aleksandar I,Djuricic Slavisa M,Peterlin Borut,Mijovic Marija,Karadzov-Orlic Natasa T,Egic Amira,Milovanovic Zagorka M},
year={2019},
title={Otopalatodigital Syndrome Type I: Novel Characteristics and Prenatal Manifestations in Two Siblings},
journal={BALKAN JOURNAL OF MEDICAL GENETICS},
volume={22},
number={2},
pages={83-87},
document_type={Article},
} 

@ARTICLE{
author={Maver Ales,Cuturilo Goran,Stojanovic Ruml J,Peterlin Borut},
year={2019},
title={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},
journal={BALKAN JOURNAL OF MEDICAL GENETICS},
volume={22},
number={2},
pages={65-68},
document_type={Article},
} 

@ARTICLE{
author={Maver Ales,Cuturilo Goran,Kovanda Anja,Miletic Aleksandra,Peterlin Borut},
year={2019},
title={Rare missense TUBGCP5 gene variant in a patient with primary microcephaly},
journal={EUROPEAN JOURNAL OF MEDICAL GENETICS},
volume={62},
number={12},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Ruml-Stojanovic Jelena,Mijovic Marija,Miletic Aleksandra,Dimitrijevic Brankica,Peterlin Borut,Maver Ales,Cuturilo Goran},
year={2019},
title={Novel mosaic CREBBP mutation in a patient with overlapping clinical features of Rubinstein-Taybi syndrome and Floating-Harbor syndrome},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={27},
number={},
pages={945-945},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Mijovic Marija,Miletic Aleksandra,Dimitrijevic Brankica,Peterlin Borut,Maver Ales,Ruml-Stojanovic Jelena,Zivanovic M,Cuturilo Goran},
year={2019},
title={Exome sequencing in disclosing causes of unexpected death in child - single genetic center experience},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={27},
number={},
pages={164-164},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Hodzic Alenka,Maver Ales,Zorn Branko,Plaseska-Karanfilska Dijana,Ristanovic Momcilo,Novakovic Ivana V,Peterlin Borut},
year={2019},
title={De novo mutations in idiopathic male infertility},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={27},
number={},
pages={16-17},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Peterlin Borut,Vidmar Lovro,Drulovic Jelena S,Sepcic Juraj,Novakovic Ivana V,Ristic Smiljana,Sega-Jazbec Sasa,Maver Ales},
year={2019},
title={Increased burden of ultra-rare genetic variants in the inflammasome regulatory genes in patients with multiple sclerosis},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={26},
number={},
pages={885-885},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Vidmar Lovro,Mayer Ales,Drulovic Jelena S,Sepcic Juraj,Novakovic Ivana V,Ristic Smiljana,Sega Sasa,Peterlin Borut},
year={2019},
title={Multiple Sclerosis patients carry an increased burden of exceedingly rare genetic variants in the inflammasome regulatory genes},
journal={SCIENTIFIC REPORTS},
volume={9},
number={},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Mijovic Marija,Miletic Aleksandra,Ruml-Stojanovic Jelena,Peterlin Borut,Maver Ales,Borlja Nikola,Dimitrijevic Brankica,Lukic M,Cuturilo Goran},
year={2018},
title={A novel CTNNB1 mutation in a patient with teratoma and multiple malformations - expansion of the phenotypic spectrum and possible new gene for Currarino phenotype},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={26},
number={},
pages={465-465},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Peterlin AM,Maver Ales,Hodzic A,Sega Sasa,Drulovic Jelena S,Novakovic Ivana V,Pekmezovic Tatjana D,Ristic S,Kapovic Miljenko,Peterlin Borut},
year={2018},
title={The burden of rare genetic variants in genes involved in tumor necrosis factor (TNF) signalling pathway in multiple sclerosis (MS)},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={26},
number={},
pages={400-400},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Hocevar Keli,Peterlin Ana,Mitrovic-Jovanovic Ana,Bozovic Aleksandra,Ristanovic Momcilo,Tul Natasa,Peterlin Borut},
year={2018},
title={Association between angiotensin-converting enzyme gene insertion/deletion polymorphism and susceptibility to preterm birth: A case-control study and meta-analysis},
journal={EUROPEAN JOURNAL OF OBSTETRICS & GYNECOLOGY AND REPRODUCTIVE BIOLOGY},
volume={231},
number={},
pages={122-128},
document_type={Article},
} 

@ARTICLE{
author={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},
year={2018},
title={Genotype and phenotype characteristics of Leber hereditary optic neuropathy (LHON) patients in Slovenia},
journal={INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE},
volume={59},
number={9},
pages={-},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Hodzic Alenka,Lavtar Polona,Ristanovic Momcilo,Novakovic Ivana V,Dotlic Jelena R,Peterlin Borut},
year={2018},
title={Genetic variation in the CLOCK gene is associated with idiopathic recurrent spontaneous abortion},
journal={PLOS ONE},
volume={13},
number={5},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Tumiene B,Maver Ales,Writzl Karin,Hodzic A,Cuturilo Goran,Kuzmanic-Samija Radenka,Culic V,Peterlin Borut},
year={2018},
title={Diagnostic exome sequencing of syndromic epilepsy patients in clinical practice},
journal={CLINICAL GENETICS},
volume={93},
number={5},
pages={1057-1062},
document_type={Article},
} 

@ARTICLE{
author={Bergant Gaber,Maver Ales,Lovrecic Luca,Cuturilo Goran,Hodzic Alenka,Peterlin Borut},
year={2018},
title={Comprehensive use of extended exome analysis improves diagnostic yield in rare disease: a retrospective survey in 1,059 cases},
journal={GENETICS IN MEDICINE},
volume={20},
number={3},
pages={303-312},
document_type={Article},
} 

@ARTICLE{
author={Hodzic Alenka,Ristanovic Momcilo,Zorn Branko,Tulic Cane Dz,Maver Ales,Novakovic Ivana V,Plaseska-Karanfilska Dijana,Peterlin Borut},
year={2017},
title={Genetic variation in leptin and leptin receptor genes as a risk factor for idiopathic male infertility},
journal={ANDROLOGY},
volume={5},
number={1},
pages={70-74},
document_type={Article},
} 

@ARTICLE{
author={Zivkovic Maja D,Starcevic-Cizmarevic Nada,Lovrecic Luca,Klupka-Saric Inge,Stankovic Aleksandra D,Gasparovic Iva,Lavtar Polona,Dincic Evica R,Stojkovic Ljiljana,Rudolf Gorazd,Sega-Jazbec Sasa,Perkovic Olivio,Sinanovic Osman,Sepcic Juraj,Kapovic Miljenko,Peterlin Borut,Ristic Smiljana},
year={2014},
title={The Role of TPA I/D and PAI-1 4G/5G Polymorphisms in Multiple Sclerosis},
journal={DISEASE MARKERS},
volume={},
number={},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Hodzic Alenka,Ristanovic Momcilo,Zorn Branko,Tulic Cane Dz,Maver Ales,Novakovic Ivana V,Peterlin Borut},
year={2013},
title={Genetic Variation in Circadian Rhythm Genes CLOCK and ARNTL as Risk Factor for Male Infertility},
journal={PLOS ONE},
volume={8},
number={3},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Lavtar Polona,Rudolf Gorazd,Maver Ales,Lovrecic Luca,Ristic Smiljana,Starcevic-Cizmarevic Nada,Kapovic Miljenko,Sepcic Juraj,Stankovic Aleksandra D,Zivkovic Maja D,Dincic Evica R,Raicevic Ranko,Jazbec Sega S,Klemenc-Ketis Z,Peterlin-Potisk K,Peterlin Borut},
year={2012},
title={Circadian rhythm genes and multiple sclerosis (MS)},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={19},
number={},
pages={346-346},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Stankovic Aleksandra D,Gasparovic Iva,Peterlin Borut,Klupka-Saric Inge,Zivkovic Maja D,Starcevic-Cizmarevic Nada,Lovrecic Luca,Sinanovic Osman,Dincic Evica R,Perkovic Olivio,Rudolf Gorazd,Vidovic M,Stojkovic Ljiljana,Lavtar Polona,Sehanovic A,Ristic Smiljana},
year={2011},
title={Angiotensin-converting enzyme I/D gene polymorphism in multiple sclerosis},
journal={MULTIPLE SCLEROSIS JOURNAL},
volume={17},
number={},
pages={S115-S115},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Stankovic Aleksandra D,Dincic Evica R,Ristic Smiljana,Lovrecic Luca,Starcevic-Cizmarevic Nada,Djuric Tamara M,Sepcic Juraj,Kapovic Miljenko,Raicevic Ranko,Peterlin Borut,Alavantic Dragan,Zivkovic Maja D},
year={2010},
title={Interleukin 7 receptor alpha polymorphism rs6897932 and susceptibility to multiple sclerosis in the Western Balkans},
journal={MULTIPLE SCLEROSIS},
volume={16},
number={5},
pages={533-536},
document_type={Article},
} 

@ARTICLE{
author={Rosser ZH,Zerjal T,Hurles ME,Adojaan M,Alavantic Dragan,Amorim A,Amos W,Armenteros M,Arroyo E,Barbujani G,Beckman G,Beckman L,Bertranpetit J,Bosch E,Bradley DG,Brede G,Cooper G,Corte-Real HBSM,de Knijff P,Decorte R,Dubrova YE,Evgrafov O,Gilissen A,Glisic Sanja S,Golge M,Hill EW,Jeziorowska A,Kalaydjieva L,Kayser Manfred,Kivisild T,Kravchenko SA,Krumina A,Kucinskas V,Lavinha J,Livshits LA,Malaspina P,Maria S,McElreavey K,Meitinger TA,Mikelsaar AV,Mitchell RJ,Nafa K,Nicholson J,Norby S,Pandya Akash,Parik J,Patsalis PC,Pereira L,Peterlin Borut,Pielberg G,Prata ML,Previdere C,Roewer L,Rootsi S,Rubinsztein DC,Saillard J,Santos FR,Stefanescu G,Sykes BC,Tolun A,Villems R,Tyler-Smith C,Jobling MA},
year={2000},
title={Y-chromosomal diversity in Europe is clinal and influenced primarily by geography, rather than by language},
journal={AMERICAN JOURNAL OF HUMAN GENETICS},
volume={67},
number={6},
pages={1526-1543},
document_type={Article},
}