Publications by authors named "Miljenko Kapovic"

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Microbial diversity in drug-naïve Parkinson's disease patients.
Eliša Papić, Valentino Rački, Mario Hero, Ana Nyasha Zimani, Mojca Čižek Sajko

PLoS One· September 2025

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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.
Jasna Nekić, Ivana Stanković Matić, Valentino Rački, Dolores Janko Labinac, Vladimira Vuletić

Int J Mol Sci· July 2024

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GiOPARK Project: The Genetic Study of Parkinson's Disease in the Croatian Population.
Valentino Rački, Gaber Bergant, Eliša Papić, Anja Kovanda, Mario Hero

Genes (Basel)· February 2024

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Refining the Global Phylogeny of Mitochondrial N1a, X, and HV2 Haplogroups Based on Rare Mitogenomes from Croatian Isolates.
Dubravka Havaš Auguštin, Jelena Šarac, Maere Reidla, Erika Tamm, Blaženka Grahovac

Genes (Basel)· August 2023

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The effects of microbiota abundance on symptom severity in Parkinson's disease: A systematic review.
Eliša Papić, Valentino Rački, Mario Hero, Zoran Tomić, Nada Starčević-Čižmarević

Front Aging Neurosci· December 2022

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Association between the ACE-I/D polymorphism and nicotine dependence amongst patients with lung cancer.
Sergej Nadalin, Veljko Flego, Sanja Dević Pavlić, Darian Volarić, Anđelka Radojčić Badovinac

Biomed Rep· December 2020

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Association of circadian rhythm genes ARNTL/BMAL1 and CLOCK with multiple sclerosis.
Polona Lavtar, Gorazd Rudolf, Aleš Maver, Alenka Hodžić, Nada Starčević Čizmarević

PLoS One· February 2018

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Angiotensin-converting enzyme insertion/deletion gene polymorphism and interferon-β treatment response in multiple sclerosis patients: a preliminary report.
Smiljana Ristić, Nada Starčević Čizmarević, Polona Lavtar, Luca Lovrečić, Olivio Perković

Pharmacogenet Genomics· June 2017

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Identification of rare genetic variation of NLRP1 gene in familial multiple sclerosis.
Ales Maver, Polona Lavtar, Smiljana Ristić, Sanja Stopinšek, Saša Simčič

Sci Rep· June 2017

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The insertion/deletion polymorphism in the angiotensin-converting enzyme gene and nicotine dependence in schizophrenia patients.
Sergej Nadalin, Smiljana Ristić, Jelena Rebić, Vesna Šendula Jengić, Miljenko Kapović

J Neural Transm (Vienna)· April 2017

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Functional single nucleotide polymorphisms of matrix metalloproteinase 7 and 12 genes in idiopathic recurrent spontaneous abortion.
Anita Barišić, Nina Pereza, Alenka Hodžić, Miljenko Kapović, Borut Peterlin

J Assist Reprod Genet· March 2017

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Systematic review and meta-analysis of genetic association studies in idiopathic recurrent spontaneous abortion.
Nina Pereza, Saša Ostojić, Miljenko Kapović, Borut Peterlin

Fertil Steril· January 2017

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The lack of association between angiotensin-converting enzyme gene insertion/deletion polymorphism and nicotine dependence in multiple sclerosis.
Sergej Nadalin, Alena Buretić-Tomljanović, Polona Lavtar, Nada Starčević Čizmarević, Alenka Hodžić

Brain Behav· January 2017

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Angiotensin-converting enzyme insertion/deletion gene polymorphism in multiple sclerosis: a meta-analysis.
Smiljana Ristić, Nada Starčević Čizmarević, Juraj Sepčić, Miljenko Kapović, Borut Peterlin

Neurol Sci· December 2016

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Genetic heritage of Croatians in the Southeastern European gene pool-Y chromosome analysis of the Croatian continental and Island population.
Jelena Šarac, Tena Šarić, Dubravka Havaš Auguštin, Natalija Novokmet, Nenad Vekarić

Am J Hum Biol· November 2016

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The Role of Iron and Iron Overload in Chronic Liver Disease.
Sandra Milic, Ivana Mikolasevic, Lidija Orlic, Edita Devcic, Nada Starcevic-Cizmarevic, Miljenko Kapovic

Med Sci Monit· June 2016

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Altered LINE-1 Methylation in Mothers of Children with Down Syndrome.
Ivana Babić Božović, Aleksandra Stanković, Maja Živković, Jadranka Vraneković, Miljenko Kapović

PLoS One· April 2016

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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.
Nina Pereza, Saša Ostojić, Matea Zdravčević, Marija Volk, Miljenko Kapović

Reprod Biomed Online· February 2016

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The -2549 insertion/deletion polymorphism in the promoter region of the VEGFA gene in couples with idiopathic recurrent spontaneous abortion.
Nina Pereza, Saša Ostojić, Anamarija Smirčić, Alenka Hodžić, Miljenko Kapović

J Assist Reprod Genet· December 2015

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MMP-2 -1575G/A polymorphism modifies the onset of optic neuritis as a first presenting symptom in MS?
Iva Gašparović, Nada Starčević Čizmarević, Luca Lovrečić, Olivio Perković, Polona Lavtar

J Neuroimmunol· September 2015

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Functional polymorphisms of matrix metalloproteinases 1 and 9 genes in women with spontaneous preterm birth.
Nina Pereza, Ivana Pleša, Ana Peterlin, Žiga Jan, Nataša Tul

Dis Markers· July 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].
Nina Pereza, Srećko Severinski, Saša Ostojić, Marija Volk, Aleš Maver

Am J Med Genet A· June 2015

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The role of TPA I/D and PAI-1 4G/5G polymorphisms in multiple sclerosis.
Maja Zivković, Nada Starčević Čizmarević, Luca Lovrečić, Inge Klupka-Sarić, Aleksandra Stanković

Dis Markers· January 2015

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Perception of stress, depression, hypertension and myocardial infarction as predictors of adherence to hypertension drug treatment.
Aleksandar Ljubotina, Vladimir Mićović, Miljenko Kapović, Maja Ljubotina, Branislava Popović

Coll Antropol· December 2014

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Tumor necrosis factor-alpha gene promoter -308 and -238 polymorphisms in patients with lung cancer as a second primary tumor.
Veljko Flego, Smiljana Ristić, Sanja Dević Pavlić, Dubravka Matanić Lender, Ljiljana Bulat-Kardum

Med Sci Monit· October 2013

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