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

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Identification of rare genetic variation of NLRP1 gene in familial multiple sclerosis von Maver, Ales, Lavtar, Polona, Ristić, Smiljana, Stopinšek, Sanja, Simčič, Saša, Hočevar, Keli, Sepčić, Juraj, Drulović, Jelena, Pekmezović, Tatjana, Novaković, Ivana, Alenka, Hodžić, Rudolf, Gorazd, Šega, Saša, Starčević-Čizmarević, Nada, Palandačić, Anja, Zamolo, Gordana, Kapović, Miljenko, Likar, Tina, Peterlin, Borut

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Association of circadian rhythm genes ARNTL/BMAL1 and CLOCK with multiple sclerosis von Lavtar, Polona, Rudolf, Gorazd, Maver, Aleš, Hodžić, Alenka, Starčević Čizmarević, Nada, Živković, Maja, Šega Jazbec, Saša, Klemenc Ketiš, Zalika, Kapović, Miljenko, Dinčić, Evica, Raičević, Ranko, Sepčić, Juraj, Lovrečić, Luca, Stanković, Aleksandra, Ristić, Smiljana, Peterlin, Borut

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

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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 von Nekić, Jasna, Stanković Matić, Ivana, Rački, Valentino, Janko Labinac, Dolores, Vuletić, Vladimira, Kapović, Miljenko, Ristić, Smiljana, Peterlin, Borut, Starčević Čizmarević, Nada

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The effects of microbiota abundance on symptom severity in Parkinson's disease: A systematic review von Papić, Eliša, Rački, Valentino, Hero, Mario, Tomić, Zoran, Starčević-Čižmarević, Nada, Kovanda, Anja, Kapović, Miljenko, Hauser, Goran, Peterlin, Borut, Vuletić, Vladimira

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Altered LINE-1 Methylation in Mothers of Children with Down Syndrome von Babic Bozovic, Ivana, Kapovic, Miljenko, Brajenovic-Milic, Bojana, Vranekovic, Jadranka, Zivkovic, Maja, Stankovic, Aleksandra

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Could the CCR5-Δ32 Mutation be Protective in SARS-CoV-2 Infection? von Eizmarevic, Nada Starcevic, Kapovic, Miljenko, Roncevic, Dobrica, Ristic, Smiljana

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Matrix metalloproteinases 1, 2, 3 and 9 functional single-nucleotide polymorphisms in idiopathic recurrent spontaneous abortion von Pereza, Nina, Ostojić, Saša, Volk, Marija, Kapović, Miljenko, Peterlin, Borut

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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 von Pereza, Nina, Ostojić, Saša, Zdravčević, Matea, Volk, Marija, Kapović, Miljenko, Peterlin, Borut

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Refining the Global Phylogeny of Mitochondrial N1a, X, and HV2 Haplogroups Based on Rare Mitogenomes from Croatian Isolates von Havaš Auguštin, Dubravka, Šarac, Jelena, Reidla, Maere, Tamm, Erika, Grahovac, Blaženka, Kapović, Miljenko, Novokmet, Natalija, Rudan, Pavao, Missoni, Saša, Marjanović, Damir, Korolija, Marina

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GiOPARK Project: The Genetic Study of Parkinson's Disease in the Croatian Population von Rački, Valentino, Bergant, Gaber, Papić, Eliša, Kovanda, Anja, Hero, Mario, Rožmarić, Gloria, Starčević Čizmarević, Nada, Ristić, Smiljana, Ostojić, Saša, Kapović, Miljenko, Maver, Aleš, Peterlin, Borut, Vuletić, Vladimira

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

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Genetic variation in tissue inhibitors of metalloproteinases as a risk factor for idiopathic recurrent spontaneous abortion von Pereza, Nina, M.D, Volk, Marija, M.D, Zrakić, Nikolina, Kapović, Miljenko, M.D., Ph.D, Peterlin, Borut, M.D., Ph.D, Ostojić, Saša, M.D., Ph.D

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

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

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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... von Pereza, Nina, M.D, Črnjar, Ksenija, M.D, Buretić-Tomljanović, Alena, Ph.D, Volk, Marija, M.D, Kapović, Miljenko, M.D., Ph.D, Peterlin, Borut, M.D., Ph.D, Ostojić, Saša, M.D., Ph.D

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

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

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MMP-2 −1575G/A polymorphism modifies the onset of optic neuritis as a first presenting symptom in MS? von Gašparović, Iva, Čizmarević, Nada Starčević, Lovrečić, Luca, Perković, Olivio, Lavtar, Polona, Sepčić, Juraj, Jazbec, Saša Šega, Kapović, Miljenko, Peterlin, Borut, Ristić, Smiljana

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