Andreja Zagorac

Maribor, Slovenia

Last Updated: 09/26/2026

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Found 12 publications

Case Report: Rare triple-line chromosome 9 mosaicism (47,XX,+del(9)(q13)/47,XX,+9/46,XX) associated with severe neurodevelopmental impairment and congenital anomalies.

Case Report: Rare triple-line chromosome 9 mosaicism (47,XX,+del(9)(q13)/47,XX,+9/46,XX) associated with severe neurodevelopmental impairment and congenital anomalies.

Journal: Frontiers in genetics

Published: December 17, 2025

Genome-wide copy-number analysis improves detection of pathogenic AZFc and autosomal variants in idiopathic non-obstructive azoospermia.

Genome-wide copy-number analysis improves detection of pathogenic AZFc and autosomal variants in idiopathic non-obstructive azoospermia.

Journal: Molecular cytogenetics

Published: December 02, 2025

Clinical Evaluation of Two Non-Invasive Genetic Tests for Detection and Monitoring of Urothelial Carcinoma: Validation of UroVysion and Xpert Bladder Cancer Detection Test.

Clinical Evaluation of Two Non-Invasive Genetic Tests for Detection and Monitoring of Urothelial Carcinoma: Validation of UroVysion and Xpert Bladder Cancer Detection Test.

Journal: Frontiers in genetics

Published: December 20, 2021

CNVs and Chromosomal Aneuploidy in Patients With Early-Onset Schizophrenia and Bipolar Disorder: Genotype-Phenotype Associations.

CNVs and Chromosomal Aneuploidy in Patients With Early-Onset Schizophrenia and Bipolar Disorder: Genotype-Phenotype Associations.

Journal: Frontiers in psychiatry

Published: September 14, 2020

Rare structural variants in the DOCK8 gene identified in a cohort of 439 patients with neurodevelopmental disorders.

Rare structural variants in the DOCK8 gene identified in a cohort of 439 patients with neurodevelopmental disorders.

Journal: Scientific reports

Published: April 04, 2018

Identification of genomic copy number variations associated with specific clinical features of head and neck cancer.

Identification of genomic copy number variations associated with specific clinical features of head and neck cancer.

Journal: Molecular cytogenetics

Published: November 16, 2017

A mosaic form of microphthalmia with linear skin defects.

A mosaic form of microphthalmia with linear skin defects.

Journal: BMC pediatrics

Published: August 29, 2017

TMPRSS2:ERG gene aberrations may provide insight into pT stage in prostate cancer.

TMPRSS2:ERG gene aberrations may provide insight into pT stage in prostate cancer.

Journal: BMC urology

Published: August 11, 2015

MTHFR C677T and A1298C Genotypes and Haplotypes in Slovenian Couples with Unexplained Infertility Problems and in Embryonic Tissues from Spontaneous Abortions.

MTHFR C677T and A1298C Genotypes and Haplotypes in Slovenian Couples with Unexplained Infertility Problems and in Embryonic Tissues from Spontaneous Abortions.

Journal: Balkan journal of medical genetics : BJMG

Published: November 23, 2013

An evaluation of SOX2 and hTERC gene amplifications as screening markers in oral and oropharyngeal squamous cell carcinomas.

An evaluation of SOX2 and hTERC gene amplifications as screening markers in oral and oropharyngeal squamous cell carcinomas.

Journal: Molecular cytogenetics

Published: September 25, 2013

Slovenian five-year experiences with rapid prenatal diagnosis of common chromosome aneuploidies using quantitative-fluorescence polymerase chain reaction.

Slovenian five-year experiences with rapid prenatal diagnosis of common chromosome aneuploidies using quantitative-fluorescence polymerase chain reaction.

Journal: Genetic testing and molecular biomarkers

Published: June 22, 2013

A coalescence of two syndromes in a girl with terminal deletion and inverted duplication of chromosome 5.

A coalescence of two syndromes in a girl with terminal deletion and inverted duplication of chromosome 5.

Journal: BMC medical genetics

Published: April 18, 2013

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Last Updated: 09/26/2026