Ass.prof. Jadranka Vraneković
Ass.prof. Jadranka Vraneković
Department of medical biology and genetics, School of Medicine, University of Rijeka
Potvrđena adresa e-pošte na medri.uniri.hr
NaslovCitiranoGodina
MTHFR C677T and A1298C polymorphisms as a risk factor for congenital heart defects in Down syndrome
IB Božović, J Vraneković, N StarčevićČizmarević, V Mahulja‐Stamenković, ...
Pediatrics International 53 (4), 546-550, 2011
252011
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
222012
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
222008
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
182010
BanI polymorphism of cytosolic phospholipase A2 gene is associated with age at onset in male patients with schizophrenia and schizoaffective disorder
S Nadalin, G Rubeša, J Giacometti, M Vulin, D Tomljanović, J Vraneković, ...
Prostaglandins, Leukotrienes and Essential Fatty Acids 78 (6), 351-360, 2008
172008
Altered LINE-1 methylation in mothers of children with Down syndrome
IB Božović, A Stanković, M Živković, J Vraneković, M Kapović, ...
PloS one 10 (5), e0127423, 2015
152015
Maternal serum screening for Down syndrome: a survey of pregnant women’s views
J Paravić, B Brajenović-Milić, D Tišlarić, M Kapović, V Jurcan, S Milotti
Public Health Genomics 2 (2-3), 109-112, 1999
131999
Screening for Down’s syndrome and neural tube defect in Croatia
B Brajenović-Milić, D Tišlarić, J Bačić, J Paravić, A Slivar, M Kapovic, ...
Fetal diagnosis and therapy 13 (6), 367-371, 1998
111998
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
82008
HFE mutations and transferrin C1/C2 polymorphism among Croatian patients with schizophrenia and schizoaffective disorder
A Buretić-Tomljanović, J Vraneković, G Rubeša, S Jonovska, ...
Molecular biology reports 39 (3), 2253-2258, 2012
42012
HFE mutations and transferrin C1/C2 polymorphism among Croatian patients with schizophrenia and schizoaffective disorder
A Buretić-Tomljanović, J Vraneković, G Rubeša, S Jonovska, ...
Molecular biology reports 39 (3), 2253-2258, 2012
42012
Prenatalna dijagnostika–naša iskustva
B Brajenović-Milić, J Vraneković, A Frković, O Petrović, D Pavešić, ...
Medicina 42 (41), 276-280, 2004
42004
Folati i folna kiselina: dosadašnje spoznaje
I Babić Božović, J Vraneković
Medicina Fluminensis: Medicina Fluminensis 50 (2), 169-175, 2014
32014
Folate and folic acid: current knowledge and gaps
I Babić Božović, J Vraneković
Medicina Fluminensis: Medicina Fluminensis 50 (2), 169-175, 2014
32014
Identification of supernumerary marker chromosome derived from chromosome 19p
J Vraneković, B Brajenović-Milić, M Kapović
Hrvatski kongres iz humane genetike (4; 2007), 2007
12007
Maternal LINE 1 DNA Methylation and Congenital Heart Defects in Down Syndrome
I Babić-Božović, A Stankovic, M Živković, J Vraneković, ...
Frontiers in Genetics 10, 41, 2019
2019
Maternal LINE-1 DNA Methylation and Congenital Heart Defects in Down Syndrome
IB Božović, A Stanković, M Živković, J Vraneković, ...
Frontiers in Genetics 10, 2019
2019
Marker chromosome-challenge in prenatal diagnostics: report of cases
A Barišić, J Vraneković, BB Ivana, BM Bojana
Dani humane genetike prof. dr. sc. Ljiljana Zergollern Čupak, 2018
2018
LINE-1 methylation in mothers of children with DS and CHD
IB Božović, A Stanković, M Živković, J Vraneković, B Brajenović-Milić
VI. Hrvatski kongres humane genetike, 2015
2015
Maternal MTHFR C677T polymorphism: a risk factor for meiotic I nondisjunction of chromosome 21
J Vraneković, IB Božović, G Brumini, M Katunarić, B Brajenović-Milić
10th European Cytogenetics Conference, 2015
2015
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