Pregled po CROSBI profilu: Jadranka Vraneković (CROSBI Profil: 29422, MBZ: 270140)
Pronađeno 66 radova
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1.Majstorović, Dijana; Barišić, Anita; Vraneković, JadrankaDNMT3B rs2424913 as a risk factor for congenital heart defects in Down syndrome // 12th ISABS Conference on Forensic and Anthropologic Genetics and Mayo Clinic Lectures in Individualized Medicine
Dubrovnik, Hrvatska, 2022. str. 168-168 (poster, međunarodna recenzija, sažetak, znanstveni) -
2.Barišić, Anita; Ergović Ravančić, Maja; Majstorović, Dijana; Vraneković, JadrankaMicro and macronutrient profile in Down syndrome children and adolescents: systematic review and meta-analysis // 12th ISABS Conference on Forensic and Anthropologic Genetics and Mayo Clinic Lectures in Individualized Medicine
Dubrovnik, Hrvatska, 2022. str. 162-162 (poster, međunarodna recenzija, sažetak, znanstveni) -
3.(Clinical institute of genomic medicine, University Medical Centre Ljubljana, Ljubljana, Slovenia) Vraneković, Jadranka; Barišić, Anita; Majstorović, Dijana; Babić Božović, Ivana; Bilić Čače, Iva Brajenović Milić, BojanaDNA METHYLTRANSFERASE GENES AND CONGENITAL HEART DEFECTS IN DOWN SYNDROME // 13th European Cytogenomics Conference
Online Conference, 2021. str. 36-37 (poster, sažetak, znanstveni) -
4.Majstorović, Dijana; Barišić, Anita; Bilić–Čače Iva; Štifanić, Mauro; Vraneković, JadrankaFUNCTIONAL DNMT3B PROMOTER POLYMORPHISM (rs1569686) AND RISK FOR CONGENITAL HEART DEFECTS IN DOWN SYNDROME // 2nd Congress of Geneticists in Bosnia and Herzegovina
Sarajevo, 2021. str. 69-69 (poster, sažetak, ostalo) -
5.Brajenović - Milić, Bojana; Starčević Čizmarević, Nada; Vraneković, JadrankaPriručnik za vježbe iz predmeta Biologija / Brajenović - Milić, Bojana (ur.).
RIJEKA: Medicinski fakultet Sveučilišta u Rijeci, 2021 -
6.Majstorović, Dijana; Barišić, Anita; Štifanić, Mauro; Dobrača, Igor; Vraneković, JadrankaThe Importance of Genomic Literacy and Education in Nursing // Frontiers in Genetics, 12 (2021), 759950, 8 doi:10.3389/fgene.2021.759950 (međunarodna recenzija, kratko priopcenje, znanstveni)
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7.Šverko, Roberta; Dević Pavlić, Sanja; Barišić, Anita; Vraneković, Jadranka; Stanković, Aleksandra; Peterlin, Ana; Peterlin, Borut; Ostojić, Saša; Pereza, NinaMTHFR gene polymorphisms and DNA methylation in idiopathic spontaneous preterm birth // The 8th World Congress on Controversies in Preconception, Preimplantation and Prenatal Genetic Diagnosis
online conference, 2021. str. 1-1 (poster, međunarodna recenzija, sažetak, znanstveni) -
8.Mladenić, Tea; Dević Pavlić, Sanja; Barišić, Anita; Vraneković, Jadranka; Stanković, Aleksandra; Peterlin, Ana; Peterlin, Borut; Ostojić, Saša; Pereza, NinaVDR gene polymorphisms and DNA methylation in idiopathic spontaneous preterm birth // The 8th World Congress on Controversies in Preconception, Preimplantation and Prenatal Genetic Diagnosis
online conference, 2021. str. 1-1 (poster, međunarodna recenzija, sažetak, znanstveni) -
9.Mladenić, Tea; Barišić, Anita; Liehr, Thomas; Starčević Čizmarević, Nada; Brajenović-Milić, Bojana; Ostojić, Saša; Vraneković, JadrankaFluorescence in situ hybridization: a Gold Standard in Identification of Small Supernumerary Marker Chromosome in Prenatal Diagnostics // The 8th World Congress on Controversies in Preconception, Preimplantation and Prenatal Genetic Diagnosis
online conference, 2021. str. 1-1 (poster, međunarodna recenzija, sažetak, znanstveni) -
10.Barišić, Anita; Stanković, Aleksandra; Stojković, Ljiljana; Pereza, Nina; Ostojić, Saša; Peterlin, Ana; Peterlin, Borut; Vraneković, JadrankaMaternal LINE-1 DNA methylation in early spontaneous preterm birth // Biological research for nursing, 1 (2021), 1; 1-1 (međunarodna recenzija, članak, znanstveni)
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11.Barišić, Anita; Buretić Tomljanović, Alena; Starčević Čizmarević, Nada; Ostojić, Saša; Romac, Pavle; Vraneković, JadrankaA rare Y-autosome translocation found in a patient with nonobstructive azoospermia: Case report // Systems Biology in Reproductive Medicine, 1 (2021), 1-7 doi:10.1080/19396368.2021.1898701 (međunarodna recenzija, članak, znanstveni)
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12.Vraneković, Jadranka; Babić Božović, Ivana; Bilić Čače, Iva; Brajenović-Milić, BojanaMethylenetetrahydrofolate Reductase Dimer Configuration as a Risk Factor for Maternal Meiosis I-Derived Trisomy 21 // Human heredity, 30 (2021), 1-5 doi:10.1159/000515121 (međunarodna recenzija, kratko priopcenje, znanstveni)
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13.Vraneković, Jadranka; Slivšek, Goran; Majstorović, DijanaMethyltetrahydrofolate-homocysteine methyltransferase reductase gene and congenital heart defects in Down syndrome // Genetics & Applications, 4 (2020), 1; 12-17 doi:10.31383/ga.vol4iss1pp12-17 (međunarodna recenzija, članak, znanstveni)
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14.Barišić, AnitaGenetički i epigenetički čimbenici u idiopatskom spontanom prijevremenom porodu, 2020., doktorska disertacija, Medicinski fakultet, Rijeka
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15.Barišić, Anita; Finderle, Aleks; Petrović, Oleg; Vraneković, JadrankaBifid cardiac apex in Pallister-Killian syndrome: case report // Medicina Fluminensis, 56 (2020), 2; 189-192 (domaća recenzija, prikaz, znanstveni)
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16.Vraneković, Jadranka; Babić Božović, Ivana; Živković, Maja; Stanković, Aleksandra; Brajenović Milić, BojanaLINE-1 DNA METHYLATION AND CONGENITAL HEART DEFECTS IN DOWN SYNDROME // Molecular and Experimental Biology in Medicine, 2 (2019), 1; 34-37 (recenziran, članak, znanstveni)
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17.Vraneković Jadranka, Ivana babić Božović, Goran Slivšek, Iva Bilić Čače, Bojana Brajenović MilićPolymorphisms in folate pathway genes as risk factors for congenital heart defects in Down syndrome // Genetics and Applications / Bajrović Kasim (ur.).
Sarajevo: INGEB, 2019. str. 14-14 (pozvano predavanje, međunarodna recenzija, sažetak, ostalo) -
18.Barišić, Anita; Finderle, Aleks; Petrović, Oleg; Starčević Čizmarević, Nada; Ostojić, Saša; Vraneković, JadrankaBifid cardiac apex in Pallister Killian syndrome: case report // Molecular Cytogenetics
Salzburg, austrija, 2019. str. 1-1 (poster, međunarodna recenzija, sažetak, znanstveni) -
19.Vraneković, Jadranka; Babić Božović, Ivana; Živković, Maja: Stanković, Aleksandra; Brajenović-Milić, BojanaLINE-1 Methylation and Congenital Heart Defects in Down Syndrome // Molecular and experimental biology in medicine, 2 (2019), 1; 34-37 (međunarodna recenzija, članak, znanstveni)
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20.Babić Božović, Ivana; Stanković, Aleksandra; Živković, Maja; Vraneković, Jadranka; Mahulja- Stamenković, Vesna; Brajenović-Milić, BojanaMaternal LINE-1 Methylation and Congenital Heart Defects in Down Syndrome // Frontiers in genetics, 10 (2019), 41; 1-8 doi:10.3389/fgene.2019.00041 (međunarodna recenzija, članak, znanstveni)
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21.Jadranka Vraneković, Ivana Babić-Božović, Maja Živković, Aleksandra Stanković, Iva Bilić-Čače, Bojana Brajenović-MilićDNA METILACIJA I PRIROĐENE SRČANE GREŠKE U DJECE S DOWN SINDROMOM // ZBORNIK SAŽETAKA 13. HRVATSKOG BIOLOŠKOG KONGRESA BOOK OF ABSTRACTS OF THE 13 th CROATIAN BIOLOGICAL CONGRESS / Petar Kružić ; Katarina Caput Mihalić ; Sanja Gottstein ; Dubravko Pavoković ; Mladen Kučinić (ur.).
Zagreb: Hrvatsko biološko društvo SOCIETAS BIOLOGORUM CROATICA Croatian Biological Society, 2018. str. 179-180 (poster, domaća recenzija, sažetak, ostalo) -
22.Barišić, Anita; Vraneković, Jadranka; Babić Božović Ivana; Brajenović-Milić BojanaMarker kromosom - izazov u prenatalnoj dijagnostici: prikaz slučajeva // Paediatria Croatica
Zagreb, Hrvatska, 2018. str. 182-182 (predavanje, domaća recenzija, sažetak, znanstveni) -
23.Barišić, Anita; Vraneković, Jadranka; Babić Božović Ivana; Brajenović-Milić BojanaMarker kromosom - izazov u prenatalnoj dijagnostici: prikaz slučajeva // Dani humane genetike prof.dr.sc. Ljiljana Zergollern Čupak
Zagreb, Hrvatska, 2018. (predavanje, recenziran, ostalo, znanstveni) -
24.Majstorović, Dijana; Vraneković, Jadranka; Štifanić, MauroVažnost edukacije o medicinskoj genetici u sestrinstvu // Suvremeno sestrinstvo / Lovrić Robert, Vrčev Aleksandar (ur.).
Osijek: Fakultet za dentalnu medicinu i zdravstvo Osijek / Sveučilište Josipa Jurja Strosmayera u Osijeku, 2018. str. 110-110 (predavanje, podatak o recenziji nije dostupan, sažetak, znanstveni) -
25.Jadranka Vraneković, Ivana Babić Božović, Bojana Brajenović MilićMethylenetetrahydrofolate reductase dimer configuration and chromosome 21 nondisjunction // "Peti dani humane genetike- prof.dr.sc.Ljiljana Zergollern-Čupak",
Dubrovnik, Hvatska, 2017. (poster, domaća recenzija, neobjavljeni rad, ostalo)
