Alenka Hodzic

Ljubljana, Slovenia

Last Updated: 09/26/2026

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Found 29 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

Second Case of Gonadal Mosaicism and a Novel Nonsense NR2F1 Gene Variant as the Cause of Bosch-Boonstra-Schaaf Optic Atrophy Syndrome.

Second Case of Gonadal Mosaicism and a Novel Nonsense NR2F1 Gene Variant as the Cause of Bosch-Boonstra-Schaaf Optic Atrophy Syndrome.

Journal: Clinical genetics

Published: July 18, 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

Insight into the complexity of male infertility: a multi-omics review.

Insight into the complexity of male infertility: a multi-omics review.

Journal: Systems biology in reproductive medicine

Published: March 22, 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

Transcriptomic signatures for human male infertility.

Transcriptomic signatures for human male infertility.

Journal: Frontiers in molecular biosciences

Published: May 22, 2023

Case Report: Non-ossifying fibromas with pathologic fractures in a patient with NONO-associated X-linked syndromic intellectual developmental disorder.

Case Report: Non-ossifying fibromas with pathologic fractures in a patient with NONO-associated X-linked syndromic intellectual developmental disorder.

Journal: Frontiers in genetics

Published: February 15, 2023

De novo mutations in idiopathic male infertility-A pilot study.

De novo mutations in idiopathic male infertility-A pilot study.

Journal: Andrology

Published: March 01, 2020

Genetic variation in the maternal vitamin D receptor FokI gene as a risk factor for recurrent pregnancy loss.

Genetic variation in the maternal vitamin D receptor FokI gene as a risk factor for recurrent pregnancy loss.

Journal: The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians

Published: August 27, 2019

Showing 1-12 of 29

Last Updated: 09/26/2026