Interleukin 7 receptor alpha polymorphism rs6897932 and susceptibility to multiple sclerosis in the Western Balkans von Stanković, Aleksandra, Dinčić, Evica, Ristić, Smiljana, Lovrečić, Luca, Starčević Cizmarević, Nada, Djurić, Tamara, Sepčić, Juraj, Kapović, Miljenko, Raičević, Ranko, Peterlin, Borut, Alavantić, Dragan, Živković, Maja

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Functional inference of methylenetetrahydrofolate reductase gene polymorphisms on enzyme stability as a potential risk factor for Down syndrome in Croatia von Vraneković, Jadranka, Babić Bozović, Ivana, Starcević Cizmarević, Nada, Buretić-Tomljanović, Alena, Ristić, Smiljana, Petrović, Oleg, Kapović, Miljenko, Brajenović-Milić, Bojana

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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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ACE I/D polymorphism and epidemiological findings for COVID-19: One year after the pandemic outbreak in Europe von Ristić, Smiljana, Pavlić, Sanja Dević, Nadalin, Sergej, Čizmarević, Nada Starčević

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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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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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Applicability of clinical genetic testing for deep brain stimulation treatment in monogenic Parkinson’s disease and monogenic dystonia: a multidisciplinary team perspective von Rački, Valentino, Hero, Mario, Papić, Eliša, Rožmarić, Gloria, Čizmarević, Nada Starčević, Chudy, Darko, Peterlin, Borut, Vuletić, Vladimira

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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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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 inference of methylenetetrahydrofolate reductase gene polymorphisms on enzyme stability as a potential risk factor for Down syndrome in Croatia von Vraneković, Jadranka, Babić Bozović, Ivana, Starcević Cizmarević, Nada, Buretić-Tomljanović, Alena, Ristić, Smiljana, Petrović, Oleg, Kapović, Miljenko, Brajenović-Milić, Bojana

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Potential protective role of a NOD2 polymorphism in the susceptibility to multiple sclerosis is not associated with interferon therapy von Zeckanovic, Aida, Maver, Ales, Ristic, Smiljana, Cizmarevic, Nada Starcevic, Peterlin, Borut, Lovrecic, Luca

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Lack of association between C282Y and H63D polymorphisms in the hemochromatosis gene and risk of multiple sclerosis: A meta-analysis von Starčević Čizmarević, Nada, Ćurko-Cofek, Božena, Barac-Latas, Vesna, Peterlin, Borut, Ristić, Smiljana

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The Influence of Hemochromatosis Gene (HFE) Mutations on SARS-CoV-2 Susceptibility and COVID-19 Severity von Ristić, Smiljana, Milić, Sandra, Tatalović, Tanja, Bilobrk, Matea, Rončević, Dobrica, Ćurko-Cofek, Božena, Barac-Latas, Vesna, Čizmarević, Nada Starčević

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Could angiotensin-converting enzyme 1 I/D polymorphism be a modificator of COVID-19 response in different populations, diseases, and/or conditions? von Dević Pavlić, Sanja, Nadalin, Sergej, Starčević Čizmarević, Nada, Buretić-Tomljanović, Alena, Radojčić Badovinac, Anđelka, Ristić, Smiljana

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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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MTHFR C677T and A1298C polymorphisms as a risk factor for congenital heart defects in Down syndrome von Babic Bozovic, Ivana, Vranekovic, Jadranka, StarcevicCizmarevic, Nada, Mahulja-Stamenkovic, Vesna, Prpic, Igor, Brajenovic-Milic, Bojana

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Does the CCR5-Δ32 mutation explain the variable coronavirus-2019 pandemic statistics in Europe? von Starčević Čizmarević, Nad, Tota, Marin, Ristić, Smiljana

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The impact of hemochromatosis mutations and transferrin genotype on gonadotropin serum levels in infertile men von Buretić-Tomljanović, Alena, Ph.D, Vlastelić, Ivan, M.D., M.S, Radojčić Badovinac, Anđelka, M.D., Ph.D, Starčević-Čizmarević, Nada, M.S, Nadalin, Sergej, M.D, Ristić, Smiljana, Ph.D

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Frequency of CCR5 gene 32-basepair deletion in Croatian normal population von Ristić, Smiljana, Starcević Cizmarević, Nada, Brajenović-Milić, Bojana, Crnić-Martinović, Marija, Kapović, Miljenko

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Could the CCR5-Δ32 Mutation be Protective in SARS-CoV-2 Infection? von STARČEVIĆ ČIZMAREVIĆ, N, KAPOVIĆ, M, RONČEVIĆ, D, RISTIĆ, S

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