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The Role of Iron and Iron Overload in Chronic Liver Disease

Medical science monitor, 2016-06, Vol.22, p.2144-2151

2016

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Association of circadian rhythm genes ARNTL/BMAL1 and CLOCK with multiple sclerosis

PloS one, 2018-01, Vol.13 (1), p.e0190601-e0190601

2018

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Identification of rare genetic variation of NLRP1 gene in familial multiple sclerosis

Scientific reports, 2017-06, Vol.7 (1), p.3715-8, Article 3715

2017

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Systematic review and meta-analysis of genetic association studies in idiopathic recurrent spontaneous abortion

Fertility and sterility, 2017-01, Vol.107 (1), p.150-159.e2

2017

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CCR5 Δ32 and CTLA-4 +49 A/G Gene Polymorphisms and Interferon-β Treatment Response in Croatian and Slovenian Multiple Sclerosis Patients

International journal of molecular sciences, 2024-07, Vol.25 (13), p.7412

2024

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The effects of microbiota abundance on symptom severity in Parkinson's disease: A systematic review

Frontiers in aging neuroscience, 2022-12, Vol.14, p.1020172-1020172

2022

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Refining the Global Phylogeny of Mitochondrial N1a, X, and HV2 Haplogroups Based on Rare Mitogenomes from Croatian Isolates

Genes, 2023-08, Vol.14 (8), p.1614

2023

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GiOPARK Project: The Genetic Study of Parkinson's Disease in the Croatian Population

Genes, 2024-02, Vol.15 (2), p.255

2024

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Altered LINE-1 Methylation in Mothers of Children with Down Syndrome

PloS one, 2015-05, Vol.10 (5), p.e0127423-e0127423

2015

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Could the CCR5-Δ32 Mutation be Protective in SARS-CoV-2 Infection?

Physiological research, 2021-12, Vol.70 (Suppl 2), p.S249-S252

2021

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Matrix metalloproteinases 1, 2, 3 and 9 functional single-nucleotide polymorphisms in idiopathic recurrent spontaneous abortion

Reproductive biomedicine online, 2012-05, Vol.24 (5), p.567-575

2012

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Insertion/deletion polymorphism in intron 16 of ACE gene in idiopathic recurrent spontaneous abortion: case-control study, systematic review and meta-analysis

Reproductive biomedicine online, 2016-02, Vol.32 (2), p.237-246

2016

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Functional single nucleotide polymorphisms of matrix metalloproteinase 7 and 12 genes in idiopathic recurrent spontaneous abortion

Journal of assisted reproduction and genetics, 2017-03, Vol.34 (3), p.365-371

2017

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Genetic variation in tissue inhibitors of metalloproteinases as a risk factor for idiopathic recurrent spontaneous abortion

Fertility and sterility, 2013-06, Vol.99 (7), p.1923-1929

2013

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The insertion/deletion polymorphism in the angiotensin-converting enzyme gene and nicotine dependence in schizophrenia patients

Journal of Neural Transmission, 2017-04, Vol.124 (4), p.511-518

2017

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The −2549 insertion/deletion polymorphism in the promoter region of the VEGFA gene in couples with idiopathic recurrent spontaneous abortion

Journal of assisted reproduction and genetics, 2015-12, Vol.32 (12), p.1789-1794

2015

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Y chromosome azoospermia factor region microdeletions are not associated with idiopathic recurrent spontaneous abortion in a Slovenian population: association study and literature review

Fertility and sterility, 2013-05, Vol.99 (6), p.1663-1667

2013

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Association between the ACE-I/D polymorphism and nicotine dependence amongst patients with lung cancer

Biomedical reports, 2020-12, Vol.13 (6), p.58-1

2020

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Angiotensin-converting enzyme insertion/deletion gene polymorphism in multiple sclerosis: a meta-analysis

Neurological sciences, 2016-12, Vol.37 (12), p.1955-1959

2016

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MMP-2 − 1575 G/A polymorphism modifies the onset of optic neuritis as a first presenting symptom in MS?

Journal of neuroimmunology, 2015-09, Vol.286, p.13-15

2015

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MMP-2 −1575G/A polymorphism modifies the onset of optic neuritis as a first presenting symptom in MS?

Journal of neuroimmunology, 2015-09, Vol.286, p.13-15

2015

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Cornelia de Lange syndrome caused by heterozygous deletions of chromosome 8q24: Comments on the article by Pereza et al. [2012]

American journal of medical genetics. Part A, 2015-06, Vol.167A (6), p.1426-1427

2015

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Human Y-specific STR haplotypes in the Western Croatian population sample

Forensic science international, 2005-05, Vol.149 (2), p.257-261

2005

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Epidemiology of multiple sclerosis in western Herzegovina

Clinical neurology and neurosurgery, 2007-11, Vol.109 (9), p.779-783

2007

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Genetic heritage of Croatians in the Southeastern European gene pool-Y chromosome analysis of the Croatian continental and Island population

American journal of human biology, 2016-11, Vol.28 (6), p.837-845

2016

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The Role of Iron and Iron Overload in Chronic Liver Disease

Association of circadian rhythm genes ARNTL/BMAL1 and CLOCK with multiple sclerosis

Identification of rare genetic variation of NLRP1 gene in familial multiple sclerosis

Systematic review and meta-analysis of genetic association studies in idiopathic recurrent spontaneous abortion

CCR5 Δ32 and CTLA-4 +49 A/G Gene Polymorphisms and Interferon-β Treatment Response in Croatian and Slovenian Multiple Sclerosis Patients

The effects of microbiota abundance on symptom severity in Parkinson's disease: A systematic review

Refining the Global Phylogeny of Mitochondrial N1a, X, and HV2 Haplogroups Based on Rare Mitogenomes from Croatian Isolates

GiOPARK Project: The Genetic Study of Parkinson's Disease in the Croatian Population

Altered LINE-1 Methylation in Mothers of Children with Down Syndrome

Could the CCR5-Δ32 Mutation be Protective in SARS-CoV-2 Infection?

Matrix metalloproteinases 1, 2, 3 and 9 functional single-nucleotide polymorphisms in idiopathic recurrent spontaneous abortion

Insertion/deletion polymorphism in intron 16 of ACE gene in idiopathic recurrent spontaneous abortion: case-control study, systematic review and meta-analysis

Functional single nucleotide polymorphisms of matrix metalloproteinase 7 and 12 genes in idiopathic recurrent spontaneous abortion

Genetic variation in tissue inhibitors of metalloproteinases as a risk factor for idiopathic recurrent spontaneous abortion

The insertion/deletion polymorphism in the angiotensin-converting enzyme gene and nicotine dependence in schizophrenia patients

The −2549 insertion/deletion polymorphism in the promoter region of the VEGFA gene in couples with idiopathic recurrent spontaneous abortion

Y chromosome azoospermia factor region microdeletions are not associated with idiopathic recurrent spontaneous abortion in a Slovenian population: association study and literature review

Association between the ACE-I/D polymorphism and nicotine dependence amongst patients with lung cancer

Angiotensin-converting enzyme insertion/deletion gene polymorphism in multiple sclerosis: a meta-analysis

MMP-2 − 1575 G/A polymorphism modifies the onset of optic neuritis as a first presenting symptom in MS?

MMP-2 −1575G/A polymorphism modifies the onset of optic neuritis as a first presenting symptom in MS?

Cornelia de Lange syndrome caused by heterozygous deletions of chromosome 8q24: Comments on the article by Pereza et al. [2012]

Human Y-specific STR haplotypes in the Western Croatian population sample

Epidemiology of multiple sclerosis in western Herzegovina

Genetic heritage of Croatians in the Southeastern European gene pool-Y chromosome analysis of the Croatian continental and Island population

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