Pregled po CROSBI profilu: Saša Ostojić (CROSBI Profil: 17699, MBZ: 238754)
Pronađeno 80 radova
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1.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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2.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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3.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) -
4.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) -
5.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) -
6.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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7.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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8.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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9.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) -
10.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) -
11.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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12.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) -
13.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)
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14.Pereza, Nina; Ostojić, Saša; Kapović, Miljenko; Peterlin, BorutSystematic review and meta-analysis of genetic association studies in idiopathic recurrent spontaneous abortion // Fertility and sterility, 107 (2017), 1; 150-159e2 doi:10.1016/j.fertnstert.2016.10.007 (međunarodna recenzija, članak, znanstveni)
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15.Pereza, Nina; Ostojić, Saša; Kapović, Miljenko; Peterlin, BorutGenetika ponavljajućih spontanih pobačaja: napredci i prijepori // Medicina-fluminensis, 52 (2016), 203-210 (podatak o recenziji nije dostupan, pregledni rad, znanstveni)
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16.Pereza, Nina; Ostojić, Saša; Zdravčević, Matea; Volk, Marija; Kapović, Miljenko; Peterlin, BorutInsertion/deletion polymorphism in intron 16 of ACE gene in idiopathic recurrent spontaneous abortion: case-control study, systematic review and meta-analysis // Reproductive biomedicine online, 32 (2016), 2; 237-246 doi:10.1016/j.rbmo.2015.11.003 (međunarodna recenzija, članak, znanstveni)
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17.Ostojić, Saša; Pereza, NinaGenetički i epigenetički čimbenici pobačaja // Genetičko informiranje u praksi / Čulić, Vida ; Pavelić, Jasminka ; Radman, Maja (ur.).
Zagreb: Medicinska naklada, 2015. str. 263-267 -
18.Pereza, Nina; Ostojić, Saša; Smirčić, Anamarija; Hodžić, Alenka; Kapović, Miljenko; Peterlin, BorutThe -2549 insertion/deletion polymorphism in the promoter region of the VEGFA gene in couples with idiopathic recurrent spontaneous abortion // Journal of assisted reproduction and genetics, 32 (2015), 12; 1789-1794 doi:10.1007/s10815-015-0593-0 (međunarodna recenzija, članak, znanstveni)
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19.Pereza, Nina; Ostojić, Saša; Volk, Marija; Kapović, Miljenko; Peterlin, BorutInsercijsko-delecijski polimorfizmi ACE, NOS3 i VEGFA gena u žena s idiopatskim ponavljajućim spontanim pobačajima // Šesti hrvatski kongres humane genetike
Split, Hrvatska, 2015. (poster, međunarodna recenzija, sažetak, znanstveni) -
20.Pereza, Nina; Ostojić, Saša; Smirčić, Anamarija; Volk, Marija; Kapović, Miljenko; Peterlin, BorutThe -2549 insertion/deletion polymorphism in the promoter region of the VEGFA gene in couples with idiopathic recurrent spontaneous abortion. // 11th Balkan Congress of Human Genetics
Beograd, Srbija, 2015. (poster, međunarodna recenzija, sažetak, znanstveni) -
21.Pereza, Nina; Severinski, Srećko; Ostojić, Saša; Volk, Marija; Maver, Aleš; Dekanić, Kristina Baraba; Kapović, Miljenko; Peterlin, BorutCornelia de Lange syndrome caused by heterozygous deletions of chromosome 8q24: comments on the article by Pereza et al. [2012] // American journal of medical genetics. Part A, 167 (2015), 6; 1426-1427 doi:10.1002/ajmg.a.36974 (podatak o recenziji nije dostupan, pismo uredniku, znanstveni)
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22.Pereza, Nina; Peterlin, Borut; Volk, Marija; Kapović, Miljenko; Ostojić, SašaA critical update on endothelial nitric oxide synthase gene variations in women with idiopathic recurrent spontaneous abortion: genetic association study, systematic review and meta-analyses // Molecular human reproduction, 21 (2015), 5; 466-478 doi:10.1093/molehr/gav008 (međunarodna recenzija, članak, znanstveni)
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23.Ostojić, Saša; Pereza, NinaMedicina Fluminensis na razmeđu polustoljetnog djelovanja – promjene i vizija za novo doba // Medicina Fluminensis, 50 (2014), 4-6 (podatak o recenziji nije dostupan, uvodnik, znanstveni)
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24.Pereza, Nina; Pleša, Ivana; Peterlin, Ana; Jan, Žiga; Tul, Nataša; Kapović, Miljenko; Ostojić, Saša; Peterlin, BorutFunctional Polymorphisms of Matrix Metalloproteinases 1 and 9 Genes in Women with Spontaneous Preterm Birth // Disease markers, 2014 (2014), 171036-1 doi:10.1155/2014/171036 (međunarodna recenzija, članak, znanstveni)
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25.Pereza, NinaVarijabilnost gena matriks metaloproteinaza i tkivnih inhibitora metaloproteinaza u parova s ponavljajućim spontanim pobačajima nepoznate etiologije, 2013., doktorska disertacija, Medicinski fakultet, Rijeka
