Mutations in SCN3A cause early infantile epileptic encephalopathy T Zaman, I Helbig, IB Božović, SD DeBrosse, AC Bergqvist, K Wallis, ... Annals of neurology 83 (4), 703-717, 2018 | 93 | 2018 |
Down syndrome: parental origin, recombination, and maternal age J Vraneković, IB Božović, Z Grubić, J Wagner, D Pavlinić, S Dahoun, ... Genetic testing and molecular biomarkers 16 (1), 70-73, 2012 | 46 | 2012 |
MTHFR C677T and A1298C polymorphisms as a risk factor for congenital heart defects in Down syndrome I Babić Božović, J Vraneković, N StarčevićČizmarević, ... Pediatrics international 53 (4), 546-550, 2011 | 40 | 2011 |
Altered LINE-1 methylation in mothers of children with Down syndrome I Babić Božović, A Stanković, M Živković, J Vraneković, M Kapović, ... PLoS One 10 (5), e0127423, 2015 | 39 | 2015 |
Pregnant women’s attitudes toward amniocentesis before receiving Down syndrome screening results B Brajenović-Milić, I Babić, S Ristić, J Vraneković, G Brumini, M Kapović Women's Health Issues 18 (2), 79-84, 2008 | 28 | 2008 |
Functional inference of methylenetetrahydrofolate reductase gene polymorphisms on enzyme stability as a potential risk factor for Down syndrome in Croatia J Vraneković, I Babić Božović, N Starčević Čizmarević, ... Disease markers 28 (5), 293-298, 2010 | 27 | 2010 |
Prenatal diagnosis of complete trisomy 19q I Babić, B Brajenović‐Milić, O Petrović, E Mustać, M Kapović Prenatal Diagnosis: Published in Affiliation With the International Society …, 2007 | 11 | 2007 |
Folati i folna kiselina: dosadašnje spoznaje I Babić Božović, J Vraneković Medicina Fluminensis: Medicina Fluminensis 50 (2), 169-175, 2014 | 9 | 2014 |
Use of cerebrospinal fluid biomarker analysis for improving Alzheimer's disease diagnosis in a non-specialized setting M Malnar, M Kosiček, R Bene, I Petek Tarnik, S Pavelin, I Babić, ... Acta Neurobiol Exp 72 (3), 264-271, 2012 | 9 | 2012 |
Diagnostic yield of exome sequencing in myopathies: Experience of a Slovenian tertiary centre I Babić Božović, A Maver, L Leonardis, M Meznaric, D Osredkar, ... PloS one 16 (6), e0252953, 2021 | 8 | 2021 |
Severe psychomotor retardation in a boy with a small supernumerary marker chromosome 19p J Vraneković, B Brajenović-Milić, Z Modrušan-Mozetić, I Babić, M Kapović Cytogenetic and Genome Research 121 (3-4), 298-301, 2008 | 8 | 2008 |
Maternal LINE-1 DNA methylation and congenital heart defects in down syndrome I Babić Božović, A Stanković, M Živković, J Vraneković, ... Frontiers in Genetics 10, 414994, 2019 | 7 | 2019 |
Methylenetetrahydrofolate reductase Dimer configuration as a risk factor for maternal meiosis i-derived trisomy 21 J Vraneković, I Babić Božović, I Bilić Čače, B Brajenović Milić Human heredity 85 (2), 61-65, 2021 | 5 | 2021 |
Folate and folic acid: current knowledge and gaps I Babić Božović, J Vraneković Medicina Fluminensis: Medicina Fluminensis 50 (2), 169-175, 2014 | 5 | 2014 |
Čimbenici rizika za javljanje intraventrikularnog krvarenja u prijevremeno rođene novorođenčadi u Jedinici novorođenačkog intenzivnog liječenja, Klinike za ginekologiju i … I Bilić Čače, A Milardović, I Babić Božović, M Kolak Medicina Fluminensis: Medicina Fluminensis 52 (4.), 515-526, 2016 | 3* | 2016 |
DNMT3B rs2424913 as a Risk Factor for Congenital Heart Defects in Down Syndrome D Majstorović, A Barišić, IB Božović, IB Čače, N Čače, M Štifanić, ... Genes 14 (3), 576, 2023 | 2 | 2023 |
Globalna DNA metilacija i trisomija 21 I Babić Božović University of Rijeka. Faculty of Medicine, 2013 | 2 | 2013 |
The Expanding Phenotypical Spectrum of WARS2-Related Disorder: Four Novel Cases with a Common Recurrent Variant MG Pauly, GC Korenke, SH Diaw, A Grözinger, A Cazurro-Gutiérrez, ... Genes 14 (4), 822, 2023 | 1 | 2023 |
LINE-1 DNA methylation and congenital heart defects in Down syndrome J Vranekovic, I Babic Bozovic, M Zivkovic, A Stankovic, B Brajenovic Milic Molecular and experimental biology in medicine 2 (1), 34-37, 2019 | 1 | 2019 |
Mitologemska izvorišta u Pričama iz davnine Ivane Brlić-Mažuranić. I Rukavina Rijec (Word) 15 (4), 2009 | 1 | 2009 |