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Proteomics of azoospermia: Towards the discovery of reliable markers for non‐invasive diagnosis

Proteomics. Clinical applications, 2023-01, Vol.17 (1), p.e2200060-n/a

2023

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Association of TNF‐a (rs361525 and rs1800629) with susceptibility to cervical intraepithelial lesion and cervical carcinoma in women from Republic of North Macedonia

International journal of immunogenetics, 2020-12, Vol.47 (6), p.522-528

2020

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The spectrum of BRCA1 and BRCA2 pathogenic sequence variants in Middle Eastern, North African, and South European countries

Human mutation, 2019-11, Vol.40 (11), p.e1-e23

2019

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De novo mutations in idiopathic male infertility—A pilot study

Andrology (Oxford), 2021-01, Vol.9 (1), p.212-220

2021

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Severe digital malformations in a rare variant of fibrodysplasia ossificans progressiva

American journal of medical genetics. Part A, 2019-07, Vol.179 (7), p.1310-1314

2019

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Loss of Y Chromosome in Peripheral Blood of Colorectal and Prostate Cancer Patients

PloS one, 2016-01, Vol.11 (1), p.e0146264

2016

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High Incidence of CPLANE1 -Related Joubert Syndrome in the Products of Conceptions from Early Pregnancy Losses

Balkan medical journal, 2024-03, Vol.41 (2), p.97-104

2024

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Novel Founder Mutation in FANCA Gene (c.3446_3449dupCCCT) Among Romani Patients from the Balkan Region

Balkan medical journal, 2018-01, Vol.35 (1), p.108-111

2018

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Multilevel regression modeling for aneuploidy classification and physical separation of maternal cell contamination facilitates the QF-PCR based analysis of common fetal aneuploidies

PloS one, 2019-08, Vol.14 (8), p.e0221227-e0221227

2019

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HPV E6/E7 mRNA versus HPV DNA biomarker in cervical cancer screening of a group of Macedonian women

Journal of medical virology, 2015-09, Vol.87 (9), p.1578-1586

2015

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Mutational Spectrum and Genotype-phenotype Correlations in Neurofibromatosis Type 1 Patients from North Macedonia: Identification of Ten Novel NF1 Pathogenic Variants

Balkan medical journal, 2023-07, Vol.40 (4), p.252-261

2023

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MicroRNA Profiling in Patients with Upper Tract Urothelial Carcinoma Associated with Balkan Endemic Nephropathy

BioMed research international, 2016-01, Vol.2016, p.7450461-10

2016

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

Frontiers in genetics, 2022-01, Vol.12, p.793834-793834

2022

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SNaPshot assay for the detection of the most common CFTR mutations in infertile men

PloS one, 2014-11, Vol.9 (11), p.e112498

2014

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Autoimmune lymphoproliferative syndrome identified through reverse phenotyping

Central-European journal of immunology, 2022-01, Vol.47 (2), p.179-182

2022

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Renal Hypouricemia 1: Rare Disorder as Common Disease in Eastern Slovakia Roma Population

Biomedicines, 2021-11, Vol.9 (11), p.1607

2021

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Efficient detection of Mediterranean β-thalassemia mutations by multiplex single-nucleotide primer extension

PloS one, 2012-10, Vol.7 (10), p.e48167-e48167

2012

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Prevalence of hepatitis C virus genotypes in risk groups in the Republic of Macedonia: A 5 years survey

Journal of medical virology, 2013-12, Vol.85 (12), p.2072-2078

2013

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Human Genetic Diseases

2011

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Association Study of Single‐Nucleotide Polymorphisms in FASLG, JMJDIA, LOC203413, TEX15, BRDT, OR2W3, INSR, and TAS2R38 Genes With Male Infertility

Journal of andrology, 2012-07, Vol.33 (4), p.675-683

2012

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Molecular and histological characteristics of early triploid and partial molar pregnancies

Polish journal of pathology, 2017, Vol.68 (2), p.138-143

2017

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Genetic Causes of Male Infertility

Balkan journal of medical genetics, 2012-12, Vol.15 (Supplement), p.31-34

2012

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Hyponatremic dehydration and metabolic alkalosis as dominant manifestation in cystic fibrosis infants with mild phenotype - a case series

Srpski arhiv za celokupno lekarstvo, 2018-09, Vol.146 (9-10), p.581-583

2018

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National Reference Centre for Genomics and Proteomics — Macprogen

Balkan journal of medical genetics, 2012-12, Vol.15 (Supplement), p.9-12

Plaseska-Karanfilska, D

2012

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Influence of OASL gene polymorphisms on host response to interferon therapy in chronic hepatitis C virus patients

The eurobiotech journal, 2017-05, Vol.1 (2), p.117-125

2017

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Proteomics of azoospermia: Towards the discovery of reliable markers for non‐invasive diagnosis

Association of TNF‐a (rs361525 and rs1800629) with susceptibility to cervical intraepithelial lesion and cervical carcinoma in women from Republic of North Macedonia

The spectrum of BRCA1 and BRCA2 pathogenic sequence variants in Middle Eastern, North African, and South European countries

De novo mutations in idiopathic male infertility—A pilot study

Severe digital malformations in a rare variant of fibrodysplasia ossificans progressiva

Loss of Y Chromosome in Peripheral Blood of Colorectal and Prostate Cancer Patients

High Incidence of CPLANE1 -Related Joubert Syndrome in the Products of Conceptions from Early Pregnancy Losses

Novel Founder Mutation in FANCA Gene (c.3446_3449dupCCCT) Among Romani Patients from the Balkan Region

Multilevel regression modeling for aneuploidy classification and physical separation of maternal cell contamination facilitates the QF-PCR based analysis of common fetal aneuploidies

HPV E6/E7 mRNA versus HPV DNA biomarker in cervical cancer screening of a group of Macedonian women

Mutational Spectrum and Genotype-phenotype Correlations in Neurofibromatosis Type 1 Patients from North Macedonia: Identification of Ten Novel NF1 Pathogenic Variants

MicroRNA Profiling in Patients with Upper Tract Urothelial Carcinoma Associated with Balkan Endemic Nephropathy

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

SNaPshot assay for the detection of the most common CFTR mutations in infertile men

Autoimmune lymphoproliferative syndrome identified through reverse phenotyping

Renal Hypouricemia 1: Rare Disorder as Common Disease in Eastern Slovakia Roma Population

Efficient detection of Mediterranean β-thalassemia mutations by multiplex single-nucleotide primer extension

Prevalence of hepatitis C virus genotypes in risk groups in the Republic of Macedonia: A 5 years survey

Human Genetic Diseases

Association Study of Single‐Nucleotide Polymorphisms in FASLG, JMJDIA, LOC203413, TEX15, BRDT, OR2W3, INSR, and TAS2R38 Genes With Male Infertility

Molecular and histological characteristics of early triploid and partial molar pregnancies

Genetic Causes of Male Infertility

Hyponatremic dehydration and metabolic alkalosis as dominant manifestation in cystic fibrosis infants with mild phenotype - a case series

National Reference Centre for Genomics and Proteomics — Macprogen

Influence of OASL gene polymorphisms on host response to interferon therapy in chronic hepatitis C virus patients

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