@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={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={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={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,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={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={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={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={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={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={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={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},
}