Pregled po CROSBI profilu: Jadranka Vraneković (CROSBI Profil: 29422, MBZ: 270140)
Pronađeno 74 radova
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1.Barišić, Anita; Ravančić Ergović Maja; Majstorović, Dijana; Vraneković, JadrankaMicronutrient status in children and adolescents with Down syndrome: systematic review and meta‐ analysis // JIDR. Journal of intellectual disability research, 1 (2023), 1; 1-1 (međunarodna recenzija, članak, znanstveni)
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2.Tadić, Ana; Barišić, Anita; Jadranka, VranekovićOsvrt na prijmenu neinvazivnog prenatalnog testiranja slobodno cirkulirajuće DNK fetusa iz krvi majke // Liječnički vjesnik : glasilo Hrvatskoga liječničkog zbora, 145 (2023), 1-2; 53-54 (podatak o recenziji nije dostupan, pismo, ostalo)
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3.(Clinical institute of genomic medicine, University Medical Centre Ljubljana, Ljubljana, Slovenia) Majstorović, Dijana; Barišić, Anita; Božović Babić, Ivana; Čače Bilić, Iva; Čače, Neven; Štifanić, Mauro; Vraneković, JadrankaDNMT3B rs2424913 as a Risk Factor for Congenital Heart Defects in Down Syndrome // Genes, 14 (2023), 3; 14030576, 11 doi:10.3390/genes14030576 (recenziran, članak, znanstveni)
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4.D., Gasparini; S., Blazevic Zelic; J, Vranekovic; F., M. Wensveen; T., Turk WensveenEstrogen withdrawal associated psychosis (EWAP) as a result of hormone replacement treatment discontinuation in a patient with 46, XY gonadal dysgenesis // ESE Young Endocrinologists and Scientists (EYES) 2022 / European society of Endocrinology (ur.).
Zagreb: Bioscientifica, 2022. str. 32-32 doi:10.1530/endoabs.83.rdp7 (predavanje, podatak o recenziji nije dostupan, sažetak, stručni) -
5.Barišić, Anita; Tadić, Ana; Vraneković, JadrankaNon-invasive prenatal testing in the screening of the most common aneuploidies: our experience // The 9th World Congress on Controversies in Preconception, Preimplantation and Prenatal Genetic Diagnosis (CoGen)
online konferencija, 2022. str. 1-1 (poster, međunarodna recenzija, sažetak, znanstveni) -
6.Barišić, Anita; Vraneković, JadrankaWill SARS-COV-2 infection accelerate the incidence of Alzheimer's disease in Down syndrome population? // Aging clinical and experimental research, 1 (2022), 1; 1-1 doi:10.1007/s40520-022-02280-z (međunarodna recenzija, pismo uredniku, znanstveni)
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7.Majstorović, Dijana; Barišić, Anita; Štifanić, Mauro; Dobrača, Igor; Vraneković, JadrankaThe Importance of Genomic Literacy and Education in Nursing // The Importance of Genetic Literacy and Education in Medicine / Pereza, Nina ; Peterlin, Borut ; Ostojić, Saša (ur.).
Lausanne: Frontiers Media, 2022. str. 62-68 -
8.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) -
9.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) -
10.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 (ECA 2021)
online, 2021. str. 36-37 (poster, sažetak, znanstveni) -
11.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 BiH with International Participation - Book of Abstracts
Sarajevo: Institute for Genetic Engineering and Biotechnology, University of Sarajevo, 2021. str. 69-69 (poster, međunarodna recenzija, sažetak, znanstveni) -
12.Brajenović - Milić, Bojana; Starčević Čizmarević, Nada; Vraneković, JadrankaPriručnik za vježbe iz predmeta Biologija / Brajenović - Milić, Bojana (ur.).
Rijeka: Medicinski fakultet Sveučilišta u Rijeci, 2021 -
13.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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14.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) -
15.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) -
16.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) -
17.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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18.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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19.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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20.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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21.Barišić, AnitaGenetički i epigenetički čimbenici u idiopatskom spontanom prijevremenom porodu, 2020., doktorska disertacija, Medicinski fakultet, Rijeka
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22.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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23.Vraneković, Jadranka; Babić Božović, Ivana; Slivšek, Goran; Bilić Čače, Iva; Brajenović, BojanaPolimorfizmi gena uključenih u metabolizam folata kao rizični čimbenici za razvoj prirođenih srčanih grešaka kod osoba s Down sindromom // Book of Abstracts — 1st Congress of Geneticists in Bosnia and Herzegovina with International Participation / Bajrović, Kasim (ur.).
Sarajevo: Institute for Genetic Engineering and Biotechnology, 2019. str. 14-14 doi:10.31383/ga.vol3iss2pp1-134 (pozvano predavanje, međunarodna recenzija, sažetak, znanstveni) -
24.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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25.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: Institut za genetičko inženjerstvo i biotehnologiju, 2019. str. 14-14 (pozvano predavanje, međunarodna recenzija, sažetak, ostalo)
