Pharmacogenomics of Multiple Sclerosis: A Systematic Review

por Hočevar, Keli, Ristić, Smiljana, Peterlin, Borut
Publicado 2019

Does the CCR5-Δ32 mutation explain the variable coronavirus-2019 pandemic statistics in Europe?

por Starčević Čizmarević, Nada, Tota, Marin, Ristić, Smiljana
Publicado 2020

In reply:

por Starčević Čizmarević, Nada, Tota, Marin, Ristić, Smiljana
Publicado 2021

ACE I/D polymorphism and epidemiological findings for COVID-19: One year after the pandemic outbreak in Europe

por Ristić, Smiljana, Pavlić, Sanja Dević, Nadalin, Sergej, Čizmarević, Nada Starčević
Publicado 2021

Multiple Sclerosis patients carry an increased burden of exceedingly rare genetic variants in the inflammasome regulatory genes

por Vidmar, Lovro, Maver, Ales, Drulović, Jelena, Sepčić, Juraj, Novaković, Ivana, Ristič, Smiljana, Šega, Saša, Peterlin, Borut
Publicado 2019

Could angiotensin-converting enzyme 1 I/D polymorphism be a modificator of COVID-19 response in different populations, diseases, and/or conditions?

por Dević Pavlić, Sanja, Nadalin, Sergej, Starčević Čizmarević, Nada, Buretić-Tomljanović, Alena, Radojčić Badovinac, Anđelka, Ristić, Smiljana
Publicado 2020

The Role of Iron and Iron Overload in Chronic Liver Disease

por Milic, Sandra, Mikolasevic, Ivana, Orlic, Lidija, Devcic, Edita, Starcevic-Cizmarevic, Nada, Stimac, Davor, Kapovic, Miljenko, Ristic, Smiljana
Publicado 2016

Risk of Upper Gastrointestinal Bleeding and Gastroduodenal Ulcers in Persons With Schizophrenia: A Danish Cohort Study

por Cotton, Cary C., Farkas, Dóra K., Foskett, Nadia, Sørensen, Henrik T., Milosavljevic-Ristic, Smiljana, Balas, Bogdan, Ehrenstein, Vera
Publicado 2019

Tumor necrosis factor-alpha gene promoter -308 and -238 polymorphisms in patients with lung cancer as a second primary tumor

por Flego, Veljko, Ristić, Smiljana, Pavlić, Sanja Dević, Lender, Dubravka Matanić, Bulat-Kardum, Ljiljana, Kapović, Miljenko, Badovinac, Andjelka Radojčić
Publicado 2013

Association between Insertion-Deletion Polymorphism of the Angiotensin-Converting Enzyme Gene and Treatment Response to Antipsychotic Medications: A Study of Antipsychotic-Naïve Fi...

por Nadalin, Sergej, Dević Pavlić, Sanja, Peitl, Vjekoslav, Karlović, Dalibor, Zatković, Lena, Ristić, Smiljana, Buretić-Tomljanović, Alena, Jakovac, Hrvoje
Publicado 2022

The Influence of Hemochromatosis Gene (HFE) Mutations on SARS-CoV-2 Susceptibility and COVID-19 Severity

por Ristić, Smiljana, Milić, Sandra, Tatalović, Tanja, Bilobrk, Matea, Rončević, Dobrica, Ćurko-Cofek, Božena, Barac-Latas, Vesna, Čizmarević, Nada Starčević
Publicado 2023

Low frequency of HFE gene mutations in Croatian patients suspected of having hereditary hemochromatosis

por Milić, Sandra, Ristić, Smiljana, Starčević-Čizmarević, Nada, Brajenović-Milić, Bojana, Crnić-Martinović, Marija, Kapović, Miljenko, Peterlin, Borut, Štimac, Davor
Publicado 2011

Functional Inference of Methylenetetrahydrofolate Reductase Gene Polymorphisms on Enzyme Stability as a Potential Risk Factor for Down Syndrome in Croatia

por Vraneković, Jadranka, Babić Božović, Ivana, Starčević Čizmarević, Nada, Buretić-Tomljanović, Alena, Ristić, Smiljana, Petrović, Oleg, Kapović, Miljenko, Brajenović-Milić, Bojana
Publicado 2010

The lack of association between angiotensin‐converting enzyme gene insertion/deletion polymorphism and nicotine dependence in multiple sclerosis

por Nadalin, Sergej, Buretić‐Tomljanović, Alena, Lavtar, Polona, Starčević Čizmarević, Nada, Hodžić, Alenka, Sepčić, Juraj, Kapović, Miljenko, Peterlin, Borut, Ristić, Smiljana
Publicado 2016

Gantenerumab reduces amyloid-β plaques in patients with prodromal to moderate Alzheimer’s disease: a PET substudy interim analysis

por Klein, Gregory, Delmar, Paul, Voyle, Nicola, Rehal, Sunita, Hofmann, Carsten, Abi-Saab, Danielle, Andjelkovic, Mirjana, Ristic, Smiljana, Wang, Guoqiao, Bateman, Randall, Kerchner, Geoffrey A., Baudler, Monika, Fontoura, Paulo, Doody, Rachelle
Publicado 2019

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

por 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
Publicado 2018

The Role of TPA I/D and PAI-1 4G/5G Polymorphisms in Multiple Sclerosis

por Živković, Maja, Starčević Čizmarević, Nada, Lovrečić, Luca, Klupka-Sarić, Inge, Stanković, Aleksandra, Gašparović, Iva, Lavtar, Polona, Dinčić, Evica, Stojković, Ljiljana, Rudolf, Gorazd, Šega Jazbec, Saša, Perković, Olivio, Sinanović, Osman, Sepčić, Juraj, Kapović, Miljenko, Peterlin, Borut, Ristić, Smiljana
Publicado 2014

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

por 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
Publicado 2017

Comparison of Pittsburgh compound B and florbetapir in cross-sectional and longitudinal studies

por Su, Yi, Flores, Shaney, Wang, Guoqiao, Hornbeck, Russ C., Speidel, Benjamin, Joseph-Mathurin, Nelly, Vlassenko, Andrei G., Gordon, Brian A., Koeppe, Robert A., Klunk, William E., Jack, Clifford R., Farlow, Martin R., Salloway, Stephen, Snider, Barbara J., Berman, Sarah B., Roberson, Erik D., Brosch, Jared, Jimenez-Velazques, Ivonne, van Dyck, Christopher H., Galasko, Douglas, Yuan, Shauna H., Jayadev, Suman, Honig, Lawrence S., Gauthier, Serge, Hsiung, Ging-Yuek R., Masellis, Mario, Brooks, William S., Fulham, Michael, Clarnette, Roger, Masters, Colin L., Wallon, David, Hannequin, Didier, Dubois, Bruno, Pariente, Jeremie, Sanchez-Valle, Raquel, Mummery, Catherine, Ringman, John M., Bottlaender, Michel, Klein, Gregory, Milosavljevic-Ristic, Smiljana, McDade, Eric, Xiong, Chengjie, Morris, John C., Bateman, Randall J., Benzinger, Tammie L.S.
Publicado 2019