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Potential of Gentiana lutea for the Treatment of Obesity-associated Diseases

Current pharmaceutical design, 2019-01, Vol.25 (18), p.2071

2019

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Non-Coding RNAs in Preeclampsia-Molecular Mechanisms and Diagnostic Potential

International journal of molecular sciences, 2021-09, Vol.22 (19), p.10652

2021

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Telomere fragility in radiology workers occupationally exposed to low doses of ionising radiation

Arhiv za higijenu rada i toksikologiju, 2022-04, Vol.73 (1), p.23-30

2022

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Expanding the phenotypic spectrum of MPDZ gene variants: A case report with prenatally detected Dandy–Walker malformation and single ventricle heart

Prenatal diagnosis, 2024-07, Vol.44 (8), p.1008-1011

2024

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Placenta-specific plasma miR518b is a potential biomarker for preeclampsia

Clinical biochemistry, 2020-05, Vol.79, p.28-33

2020

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Optimization of the method for isolation of epithelial cells from the non-glandular part of the rat stomach for flow cytometry

Veterinarski arhiv, 2020-09, Vol.90 (5), p.517-525

2020

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Prenatal ultrasonographic manifestations of partial trisomy 12q(12q24.2→qter) and partial monosomy 2q (2q37.3→qter)

Vojnosanitetski pregled, 2020, Vol.77 (7), p.754-757

2020

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First molecular-cytogenetic characterization of Fanconi anemia fragile sites in primary lymphocytes of FA-D2 patients in different stages of the disease

Molecular cytogenetics, 2016-09, Vol.9 (1), p.70-70, Article 70

2016

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Genotyping Fanconi anemia patients from Serbia reveals three novel FANCD2 variants

Genetika (Beograd), 2017, Vol.49 (2), p.559-572

2017

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Substitution rate and natural selection in parvovirus B19

Scientific reports, 2016-10, Vol.6 (1), p.35759-35759, Article 35759

2016

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Prevalence of FA-D2 Rare Complementation Group of Fanconi Anemia in Serbia

Indian journal of pediatrics, 2014-03, Vol.81 (3), p.260-265

2014

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Metoidioplasty

Urologic clinics of North America, 2019-11, Vol.46 (4), p.555-566

2019

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Lomljivost telomera u bolničkih radnika profesionalno izloženih niskim dozama ionizirajućega zračenja

Arhiv za higijenu rada i toksikologiju, 2022-03, Vol.73 (1), p.23

2022

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Small supernumerary marker chromosomes in prenatal diagnosis-molecular characterization and clinical outcomes

Frontiers in genetics, 2024-01, Vol.14, p.1326985-1326985

2024

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Isolated Male Epispadias Repair: Long-Term Outcomes

Life (Basel, Switzerland), 2024-04, Vol.14 (4), p.446

2024

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Prenatal diagnosis of Pallister–Killian syndrome in young woman: ultrasound indicators and confirmation by FISH

Archives of gynecology and obstetrics, 2009-03, Vol.279 (3), p.377-379

2009

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Enhanced frequency of sister chromatid exchanges induced by diepoxybutane is specific characteristic of Fanconi anemia cellular phenotype

Genetika (Beograd), 2013, Vol.45 (2), p.393-403

2013

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Autism spectrum disorder and Coffin–Siris syndrome—Case report

Frontiers in psychiatry, 2023-08, Vol.14

2023

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Biological Effects of Echinacea Purpurea on Human Blood Cells

Arhiv za higijenu rada i toksikologiju, 2009-06, Vol.60 (2), p.165-172

2009

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Combined presence of coagulation factor XIII V34L and plasminogen activator inhibitor 1 4G/5G gene polymorphisms significantly contribute to recurrent pregnancy loss in Serbian population

Journal of medical biochemistry, 2020-01, Vol.39 (2), p.199-207

2020

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Corrigendum to “Placenta-specific plasma miR518b is a potential biomarker for preeclampsia” [Clin. Biochem. 79 (2020) 28–33]

Clinical biochemistry, 2020-11, Vol.85, p.57-57

2020

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A maternal deletion upstream of the imprint control region 2 in 11p15 causes loss of methylation and familial Beckwith-Wiedemann syndrome

European journal of human genetics : EJHG, 2016-08, Vol.24 (9), p.1280-1286

2016

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Psychosexual Functioning Outcome Testing after Hypospadias Repair

Healthcare (Basel), 2020-02, Vol.8 (1), p.32

2020

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Fanconi Anemia Is Characterized by Delayed Repair Kinetics of DNA Double-Strand Breaks

The Tohoku Journal of Experimental Medicine, 2010, Vol.221(1), pp.69-76

2010

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Potential of Gentiana lutea for the Treatment of Obesity-associated Diseases

Non-Coding RNAs in Preeclampsia-Molecular Mechanisms and Diagnostic Potential

Telomere fragility in radiology workers occupationally exposed to low doses of ionising radiation

Expanding the phenotypic spectrum of MPDZ gene variants: A case report with prenatally detected Dandy–Walker malformation and single ventricle heart

Placenta-specific plasma miR518b is a potential biomarker for preeclampsia

Combined NGS Approaches Identify Mutations in the Intraflagellar Transport Gene IFT140 in Skeletal Ciliopathies with Early Progressive Kidney Disease

Optimization of the method for isolation of epithelial cells from the non-glandular part of the rat stomach for flow cytometry

Prenatal ultrasonographic manifestations of partial trisomy 12q(12q24.2→qter) and partial monosomy 2q (2q37.3→qter)

First molecular-cytogenetic characterization of Fanconi anemia fragile sites in primary lymphocytes of FA-D2 patients in different stages of the disease

Genotyping Fanconi anemia patients from Serbia reveals three novel FANCD2 variants

Substitution rate and natural selection in parvovirus B19

Prevalence of FA-D2 Rare Complementation Group of Fanconi Anemia in Serbia

Metoidioplasty

Lomljivost telomera u bolničkih radnika profesionalno izloženih niskim dozama ionizirajućega zračenja

Small supernumerary marker chromosomes in prenatal diagnosis-molecular characterization and clinical outcomes

Isolated Male Epispadias Repair: Long-Term Outcomes

Prenatal diagnosis of Pallister–Killian syndrome in young woman: ultrasound indicators and confirmation by FISH

Enhanced frequency of sister chromatid exchanges induced by diepoxybutane is specific characteristic of Fanconi anemia cellular phenotype

Autism spectrum disorder and Coffin–Siris syndrome—Case report

Biological Effects of Echinacea Purpurea on Human Blood Cells

Combined presence of coagulation factor XIII V34L and plasminogen activator inhibitor 1 4G/5G gene polymorphisms significantly contribute to recurrent pregnancy loss in Serbian population

Corrigendum to “Placenta-specific plasma miR518b is a potential biomarker for preeclampsia” [Clin. Biochem. 79 (2020) 28–33]

A maternal deletion upstream of the imprint control region 2 in 11p15 causes loss of methylation and familial Beckwith-Wiedemann syndrome

Psychosexual Functioning Outcome Testing after Hypospadias Repair

Fanconi Anemia Is Characterized by Delayed Repair Kinetics of DNA Double-Strand Breaks

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