Pregled po CROSBI profilu: Nina Pereza (CROSBI Profil: 26660, MBZ: 322474)
Pronađeno 69 radova
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1.Mladenić, Tea; Mavrinac, Martina; Dević Pavlić, Sanja; Malnar, Anna; Matić, Matea; Mikić, Sara; Ostojić, Saša; Pereza, NinaNon-genetic physicians’ knowledge, attitudes and behavior towards medical genetics // Wiener klinische Wochenschrift, 1 (2023), 7671, 9 doi:https://pubmed.ncbi.nlm.nih.gov/36763136/ (međunarodna recenzija, članak, znanstveni)
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2.Mladenić, Tea; Mavrinac, Martina; Dević Pavlić, Sanja; Malnar, Anna; Matić, Matea; Mikić, Sara; Ostojić, Saša; Pereza, NinaNon-genetic health professionals' knowledge, attitudes, and behaviors towards medical genetics in Croatia // European Human Genetics Conference (ESHG 2022)
Beč, Austrija, 2022. str. 1-1 (poster, međunarodna recenzija, sažetak, znanstveni) -
3.Mladenić, Tea; Zoričić, Dunja; Batičić, Lara; Ostojić, Saša; Pereza, NinaPravila PRISMA 2020.: ažurirane smjernice za izvještavanje u sustavnim pregledima // Medicina Fluminensis, 57 (2021), 4; 444-465 doi:10.21860/medflum2021_264903 (domaća recenzija, ostalo)
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4.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) -
5.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) -
6.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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7.Dejhalla, Ema; Pereza, Nina; Ostojić, Saša; Peterlin, Borut; Dević Pavlić, SanjaGenetičko testiranje recesivnih monogenskih bolesti: od dijagnostičkog testiranja do suvremenog proširenog genomskog probira nositelja // Medicina Fluminensis, 57 (2021), 1; 25-34 doi:10.21860/medflum2021_365337 (domaća recenzija, pregledni rad, ostalo)
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8.Čargonja, Paola; Mavrinac, Martina; Ostojić, Saša; Pereza, NinaThe impact of needs-based education on the change of knowledge and attitudes towards medical genetics in medical students // European Journal of Human Genetics, / (2021), /; /-/ doi:10.1038/s41431-020-00791-9 (međunarodna recenzija, članak, znanstveni)
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9.Gašparović Krpina, Milena; Barišić, Anita; Peterlin, Ana; Tul, Nataša; Ostojić, Saša; Peterlin, Borut; Pereza, NinaVitamin D receptor polymorphisms in spontaneous preterm birth: a case-control study // Croatian medical journal, 61 (2020), 338-345 (međunarodna recenzija, članak, znanstveni)
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10.Barišić, Anita; Kolak, Maja; Peterlin, Ana; Tul, Nataša; Gašparović Krpina, Milena; Ostojić, Saša; Peterlin Borut; Pereza, NinaDNMT3B rs1569686 and rs2424913 gene polymorphisms are associated with positive family history of preterm birth and smoking status // Croatian medical journal, 61 (2020), 8-17 (međunarodna recenzija, članak, znanstveni)
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11.Barišić, Anita; Kolak, Maja; Peterlin, Ana; Tul, Nataša; Gašparović Krpina, Milena; Ostojić, Saša; Peterlin, Borut; Pereza, NinaGenetic variation in the maternal vitamin D receptor FokI gene as a risk factor for recurrent pregnancy loss // Journal of maternal-fetal & neonatal medicine, 14 (2019), 1-6 (međunarodna recenzija, članak, znanstveni)
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12.Lovrečić, Luca; Pereza, Nina; Jaklič, Helena; Ostojić, Saša; Peterlin, BorutCombination of QF‐PCR and aCGH is an efficient diagnostic strategy for the detection of chromosome aberrations in recurrent miscarriage // Molecular Genetics & Genomic Medicine, 7 (2019) doi:10.1002/mgg3.980 (međunarodna recenzija, članak, znanstveni)
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13.Barišić Anita; Pereza Nina; Hodžić Alenka; Gašparović Krpina Milena; Ostojić Saša; Peterlin BorutGenetic variation in the maternal vitamin D receptor FOKI gene as a risk factor for recurrent pregnancy loss // Journal of maternal-fetal & neonatal medicine, 8 (2019), 1660768, 6 doi:10.1080/14767058.2019.1660768. (međunarodna recenzija, članak, znanstveni)
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14.Belančić, Andrej; Pereza, NinaAssociation between vitamin D receptor sequence variants and obesity/metabolic syndrome: systematic review // Abstract book - 11th ISABS Conference on Forensic and Anthropologic Genetics
Split, Hrvatska, 2019. str. 1-1 (poster, recenziran, sažetak, znanstveni) -
15.Barišić, Anita; Mance, Katarina; Peterlin, Ana; Tul, Nataša; Gašparović Krpina, Milena; Ostojić, Saša; Peterlin, Borut; Pereza, NinaGene polymorphisms of tumor necrosis factor alpha in women with spontaneous preterm birth // ISABS Conference on Forensic and anthropologic genetics and Mayo Clinic lectures in individualized medicine
Zagreb, 2019. str. 182-182 (poster, međunarodna recenzija, sažetak, znanstveni) -
16.Barišić, Anita; Pereza, Nina; Kolak, Maja; Peterlin, Ana; Tul, Nataša; Gašparović Krpina, Milena; Ostojić, Saša; Peterlin, BorutGENE POLYMORPHISMS OF DNA METHYLTRANSFERASE 3B IN WOMEN WITH SPONTANEOUS PRETERM BIRTH // Balkan Journal of Medical Genetics
Edirne, Turska, 2019. str. 50-51 (poster, međunarodna recenzija, sažetak, znanstveni) -
17.Pereza, Nina; Ostojić, Saša; Belančić, Andrej; Ploh, MajaMedicina Fluminensis: promotor najmlađih stvaratelja znanosti // Medicina Fluminensis, 54 (2018), 4; 348-352 doi:10.21860/medflum2018_207347 (recenziran, uvodnik, stručni)
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18.Barišić, Anita; Pereza, Nina; Ostojić, Saša; Peterlin, Borut; Hodžić, AlenkaSingle nucleotide polymorphisms of vitamin D receptor and recurrent pregnancy loss // European Human Genetics Conference
Milano, Italija, 2018. E-P01.47, 1 (poster, međunarodna recenzija, sažetak, ostalo) -
19.Belančić, Andrej; Vučinić, Damir; Pereza, Nina; Ostojić, SašaStudentska sekcija časopisa Medicina Fluminensis – jamstvo za svijetlu budućnost // Medicina : glasilo Hrvatskoga liječničkoga zbora, Podružnica Rijeka, 54 (2018), 1; 4-5 doi:10.21860/medflum2018_192874 (recenziran, uvodnik, stručni)
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20.Barišić, Anita; Dević Pavlić, Sanja; Ostojić, Saša; Pereza, NinaMatrix metalloproteinase and tissue inhibitors of metalloproteinases gene polymorphisms in disorders that influence fertility and pregnancy complications: A systematic review and meta- analysis // Gene, 647 (2018), 48-60 doi:10.1016/j.gene.2018.01.010 (međunarodna recenzija, članak, znanstveni)
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21.Gašparović Krpina, Milena; Peterlin, Ana; Tul, Nataša; Peterlin, Borut; Ostojić, Saša; Pereza, NinaThe FokI polymorphism in vitamin D receptor gene in women with spontaneous preterm birth influences new-born birth weight // Program and abstracts – 10th ISABS conference on forensic and anthropologic genetics and Mayo clinic lectures in individualized medicine
Dubrovnik, Hrvatska, 2017. (poster, međunarodna recenzija, sažetak, znanstveni) -
22.Pereza, Nina; Kolak, Maja; Peterlin, Ana; Tul, Nataša; Peterlin, Borut; Ostojić, SašaGene polymorphisms of DNA methyltransferases in women with spontaneous preterm birth // Program and abstracts – 10th ISABS conference on forensic and anthropologic genetics and Mayo clinic lectures in individualized medicine
Dubrovnik, Hrvatska, 2017. (poster, međunarodna recenzija, sažetak, znanstveni) -
23.Barišić, Anita; Pereza, Nina; Hodžić, Alenka; Ostojić, Saša; Peterlin, BorutA single nucleotide polymorphism of DNA methyltransferase 3B gene is a risk factor for recurrent spontaneous abortion // American journal of reproductive immunology, 78 (2017), 6; e12765, 14 doi:10.1111/aji.12765 (podatak o recenziji nije dostupan, članak, znanstveni)
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24.Barišić, Anita; Pereza, Nina; Hodžić, Alenka; Peterlin, Borut; Ostojić, SašaA single nucleotide polymorphism of DNA methyltransferase 3B gene is a potential risk factor for reccurent spontaneous abortion // The Tenth ISABS Conference on Forensic and Anthropologic Genetics and Mayo Clinic Lectures in Individualized Medicine / Ordog, Tamas (ur.).
Zagreb: Grafički zavod Hrvatske, 2017. str. 226-226 (poster, međunarodna recenzija, sažetak, znanstveni) -
25.Barišić, Anita; Pereza, Nina; Hodžić, Alenka; Kapović, Miljenko; Peterlin, Borut; Ostojić, SašaFunctional single nucleotide polymorphisms of matrix metalloproteinase 7 and 12 genes in idiopathic recurrent spontaneous abortion // Journal of assisted reproduction and genetics, 34 (2017), 3; 365-371 (međunarodna recenzija, članak, znanstveni)
