Nada Starčević Čizmarević

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

Aleš Maver, Polona Lavtar, Smiljana Ristič et al. · Scientific Reports · 2017 · 65 citations · Full text

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

Polona Lavtar, Goražd Rudolf, Aleš Maver et al. · PLoS ONE · 2018 · 51 citations · Full text

Genetics, Genetic Epidemiology, Neurological Progress +17

<i>MTHFR</i> C677T and A1298C polymorphisms as a risk factor for congenital heart defects in Down syndrome

Ivana Babič Božović, Jadranka Vraneković, Nada Starčević Čizmarević et al. · Pediatrics International · 2010 · 26 citations

Mutations in the hemochromatosis gene (HFE) and multiple sclerosis

Smiljana Ristič, Luca Lovrečić, Bojana Brajenović‐Milić et al. · Neuroscience Letters · 2005 · 26 citations

Genetic Disorder, Medicine, Genetics +5

Tumor Necrosis Factor-α-308 Gene Polymorphism in Croatian and Slovenian Multiple Sclerosis Patients

Smiljana Ristič, Luca Lovrečić, Nada Starčević Čizmarević et al. · European Neurology · 2007 · 23 citations