Olivera Miljanovic

Podgorica, Montenegro

Last Updated: 09/26/2026

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Found 13 publications

ACE gene and male infertility: a South Slavic case-control study and multi-omics data integration.

ACE gene and male infertility: a South Slavic case-control study and multi-omics data integration.

Journal: Systems biology in reproductive medicine

Published: October 08, 2025

Toward clinical application of whole-exome sequencing in the diagnosis of men with severely impaired spermatogenesis.

Toward clinical application of whole-exome sequencing in the diagnosis of men with severely impaired spermatogenesis.

Journal: Fertility and sterility

Published: July 27, 2025

The role of DNA mismatch repair mutS/mutL homolog genes in spermatogenesis and male infertility: a systematic review and cohort study.

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 : RB&E

Published: April 15, 2025

Value of Optical Genome Mapping (OGM) for Diagnostics of Rare Diseases: A Family Case Report.

Value of Optical Genome Mapping (OGM) for Diagnostics of Rare Diseases: A Family Case Report.

Journal: Balkan journal of medical genetics : BJMG

Published: March 12, 2025

F5 6665A>G Polymorphism Is Associated with Increased Risk of Venous Thromboembolism in Females.

F5 6665A>G Polymorphism Is Associated with Increased Risk of Venous Thromboembolism in Females.

Journal: International journal of molecular sciences

Published: December 27, 2024

Genetic Testing for Monogenic Forms of Male Infertility Contributes to the Clinical Diagnosis of Men with Severe Idiopathic Male Infertility.

Genetic Testing for Monogenic Forms of Male Infertility Contributes to the Clinical Diagnosis of Men with Severe Idiopathic Male Infertility.

Journal: The world journal of men's health

Published: June 14, 2024

A novel splice-site FHOD3 founder variant is a common cause of hypertrophic cardiomyopathy in the population of the Balkans-A cohort study.

A novel splice-site FHOD3 founder variant is a common cause of hypertrophic cardiomyopathy in the population of the Balkans-A cohort study.

Journal: PloS one

Published: July 13, 2023

Association of ATG16L1 rs2241880 and TP53 rs1042522 with characteristics and course of diffuse large B-cell lymphoma.

Association of ATG16L1 rs2241880 and TP53 rs1042522 with characteristics and course of diffuse large B-cell lymphoma.

Journal: Pathology, research and practice

Published: May 25, 2022

Maternal MTHFR 677C>T, 1298A>C gene polymorphisms and risk of offspring aneuploidy.

Maternal MTHFR 677C>T, 1298A>C gene polymorphisms and risk of offspring aneuploidy.

Journal: Prenatal diagnosis

Published: February 10, 2022

Polymorphisms of ACE and thrombophilic genes: risk for recurrent pregnancy loss.

Polymorphisms of ACE and thrombophilic genes: risk for recurrent pregnancy loss.

Journal: Journal of clinical pathology

Published: November 17, 2021

Current State of Compulsory Basic and Clinical Courses in Genetics for Medical Students at Medical Faculties in Balkan Countries With Slavic Languages.

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

Published: October 12, 2021

Association of cytokine gene polymorphisms and risk factors with otitis media proneness in children.

Association of cytokine gene polymorphisms and risk factors with otitis media proneness in children.

Journal: European journal of pediatrics

Published: December 09, 2015

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Last Updated: 09/26/2026