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Poglavlja u knjizi
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1. Ostojić, Saša; Pereza, Nina.
Genetički i epigenetički čimbenici pobačaja // Genetičko informiranje u praksi / Čulić, Vida ; Pavelić, Jasminka ; Radman, Maja (ur.).
Zagreb : Medicinska naklada, 2015.
Str. 263-267.
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Izvorni znanstveni i pregledni radovi u CC časopisima
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1. Pereza, Nina; Ostojić, Saša; Kapović, Miljenko; Peterlin, Borut.
Systematic review and meta-analysis of genetic association studies in idiopathic recurrent spontaneous abortion. // Fertility and sterility. 107 (2017) , 1; 150-159e2 (članak, znanstveni).  
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2. Pereza, Nina; Ostojić, Saša; Smirčić, Anamarija; Hodžić, Alenka; Kapović, Miljenko; Peterlin, Borut.
The -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 (članak, znanstveni).
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3. Pereza, Nina; Črnjar, Ksenija; Buretić-Tomljanović, Alena; Volk, Marija; Kapović, Miljenko; Peterlin, Borut; Ostojić, Saša.
Y chromosome azoospermia factor region microdeletions are not associated with idiopathic recurrent spontaneous abortion in Slovenian population: association study and literature review. // Fertility and sterility. 99 (2013) , 6; 1663-1667 (članak, znanstveni).
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4. Pereza, Nina; Ostojić, Saša; Kapović, Miljenko; Buretić-Tomljanović, Alena.
Insulin-like growth factor 2 and insulin-like growth factor 2 receptor gene polymorphisms in idiopathic male infertility. // Journal of reproductive medicine. 58 (2013) , 2; 132-136 (članak, znanstveni).
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5. Pereza, Nina; Volk, Marija; Zrakić, Nikolina; Kapović, Miljenko; Peterlin, Borut; Ostojić, Saša.
Genetic variation in tissue inhibitors of metalloproteinases as a risk factor for idiopathic recurrent spontaneous abortion. // Fertility and sterility. 99 (2013) , 7; 1923-1929 (članak, znanstveni).
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6. Pereza, Nina; Ostojić, Saša; Volk, Marija; Kapović, Miljenko; Peterlin, Borut.
Matrix metalloproteinases 1, 2, 3 and 9 functional single-nucleotide polymorphisms in idiopathic recurrent spontaneous abortion. // Reproductive biomedicine online. 24 (2012) , 5; 567-575 (članak, znanstveni).
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7. Pereza, Nina; Ostojić, Saša; Volk, Marija; Maver, Aleš; Kapović, Miljenko; Peterlin, Borut.
The insulin-like growth factor 2 receptor gene Gly1619Arg polymorphism and idiopathic recurrent spontaneous abortion.. // Journal of Maternal-Fetal & Neonatal Medicine. 25 (2012) , 4; 429-431 (kratko priopćenje, znanstveni).
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8. Pereza, Nina; Severinski, Srećko; Ostojić, Saša; Volk, Marija; Maver, Aleš; Dekanić, Kristina, Baraba; Kapović, Miljenko; Peterlin, Borut.
Third case of 8q23.3-q24.13 deletion in a patient with Langer-Giedion syndrome phenotype without TRPS1 gene deletion. // American journal of medical genetics. Part A. 158A (2012) , 3; 659-663 (članak, znanstveni).
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9. Medica, Igor; Ostojić, Saša; Pereza, Nina; Kastrin, Andrej; Peterlin, Borut.
Association between genetic polymorphisms in cytokine genes and recurrent miscarriage – a meta-analysis. // Reproductive biomedicine online. 19 (2009) , 3; 406-414 (pregledni rad, znanstveni). 
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10. Ostojić, Saša; Pereza, Nina; Volk, Marija; Kapović, Miljenko; Peterlin, Borut.
Genetic Predisposition to Idiopathic Recurrent Spontaneous Abortion : Contribution of Genetic Variations in IGF-2 and H19 Imprinted Genes. // American journal of reproductive immunology. 60 (2008) , 2; 111-117 (članak, znanstveni).
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Znanstveni radovi u drugim časopisima
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1. Pereza, Nina; Buretić-Tomljanović, Alena; Ostojić, Saša; Vraneković, Jadranka; Bićanić, Nenad; Kapović, Miljenko.
Izodicentrični X kromosom i složeni mozaicizam 45, X/46, X, idic(X)(q28)/46, XX u bolesnice sa sekundarnom amenorejom, visokim rastom i pretilošću. // Medicina Fluminensis. 47 (2011) , 1; 107-114 (kratko priopćenje, znanstveni).
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2. Pereza, Nina; Zergollern-Čupak, Ljiljana; Ostojić, Saša.
Elektroničke baze podataka humanih genetičkih poremećaja: osnove diferencijalne dijagnostike u kliničkoj genetici. // Medicina. 45 (2009) , 1; 22-37 (pregledni rad, znanstveni).
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3. Pereza, Nina; Ostojić, Saša.
Funkcionalna nejednakost roditeljskih genoma u etiologiji gestacijskih trofoblastičnih bolesti. // Medicina. 44 (2008) , 1; 22-37 (pregledni rad, znanstveni).
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Plenarna izlaganja
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1. Ostojić, Saša.
Current view on Bioethics and Genetics: Genetic Counselling // 5th International Conference on Clinical Ethics and Consultation: Bioethics & Ethics Consultation in a Diversified World, Conference Proceedings / Chen-tek Tai, Michael (ur.).
Taichung : Taipei : Chungshan Medical University, Academia Sinica, 2009. 64-64 (plenarno predavanje,međunarodna recenzija,sažetak,znanstveni).
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Sažeci u zbornicima skupova
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1. Pereza, Nina; Peterlin, Borut; Kapović, Miljenko; Ostojić, Saša.
Direct and potential (epi)genetic causes of recurrent spontaneous abortion: advances and controversies // Book of abstracts / Lovrečić, Luca ; Maver, Aleš (ur.).
Ljubljana : Slovenian Association of Medical Genetics, 2013. 35-35 (predavanje,međunarodna recenzija,sažetak).
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2. Pereza, Nina; Volk, Marija; Kapović, Miljenko; Peterlin, Borut; Ostojić, Saša.
Single nucleotide polymorphisms of tissue inhibitors of metalloproteinases genes in couples with idiopathic recurrent spontaneous abortion // Book of abstracts / Lovrečić, Luca ; Maver, Aleš (ur.).
Ljubljana : Slovenian Association of Medical Genetics, 2013. 118-118 (poster,međunarodna recenzija,sažetak).
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3. Ostojić, Saša; Pereza, Nina; Kapović, Miljenko; Peterlin, Borut.
Current view on genetics and epigenetics of recurrent spontaneous abortion // Final program and abstracts - The seventh ISABS conference in forensic, anthropologic and medical genetics and Mayo Clinic lectures in translational medicine.
Zagreb, 2011. 262-262 (pozvano predavanje,međunarodna recenzija,sažetak,znanstveni).
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4. Pereza, Nina; Ostojić, Saša; Volk, Marija; Kapović, Miljenko; Peterlin, Borut.
Functional single nucleotide polymorphisms in promoter region of matrix metalloproteinase -1, -2, -3 and -9 as risk factors for recurrent spontaneous abortion // Final program and abstracts - The seventh ISABS conference in forensic, anthropologic and medical genetics and Mayo Clinic lectures in translational medicine.
Zagreb, 2011. 263-263 (predavanje,međunarodna recenzija,sažetak,znanstveni).
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5. Pereza, Nina; Severinski, Srećko; Ostojić, Saša; Volk, Marija; Maver, Aleš; Baraba, Kristina; Kapović, Miljenko; Peterlin, Borut.
A rare case of 8q23.3-q24.13 microdeletion in a patient with Langer-Giedion syndrome without TRPS1 gene deletion // Final program and abstracts - The seventh ISABS conference in forensic, anthropologic and medical genetics and Mayo Clinic lectures in translational medicine.
Zagreb, 2011. 297-297 (poster,međunarodna recenzija,sažetak,znanstveni).
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6. Blatnik, A; Volk, Marija; Ostojić, Saša; Pereza, Nina; Kapović, Miljenko; Peterlin, Borut.
Genetics of recurrent miscarriage // .
(predavanje,međunarodna recenzija,sažetak).
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7. Nina Pereza, Saša Ostojić, Marija Volk, Aleš Maver, Miljenko Kapović, Borut Peterlin.
Insulin-like growth factor 2 receptor gene Gly1619Arg polymorphism in couples with idiopathic recurrent spontaneous abortion. // 1oth Congress of the Croatian Society of Biochemistry and Molecular Biology. „The Secret Life of Biomolecules“, Opatija, 2010..
2010. (poster,međunarodna recenzija,sažetak).
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8. Sorta-Bilajac, Iva; Ostojić, Saša.
Back to Basics: Is there a Place for Virtue-Ethics-Approach in Genetic Counseling? // 5th International Conference on Clinical Ethics and Consultation: Bioethics & Ethics Consultation in a Diversified World, Conference Proceedings / Chen-tek Tai, Michael (ur.).
Taichung : Taipei : Chungshan Medical University, Academia Sinica, 2009. 53-54 (predavanje,međunarodna recenzija,sažetak,znanstveni).
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9. Ostojić, Saša.
Bioethics and Genetics: Current view on Genetic counseling // The Challenge of Croass-Cultural Bioethics in 21st Century / Sorta-Bilajac, Iva ; Blažević, Ivana ; Tancabel, Ana (ur.).
Rijeka : The International Association of Bioethics, University of Rijeka - School of Medicine, Croatian Society for Clinical Bioethics, 2008. 133-133 (pozvano predavanje,međunarodna recenzija,sažetak,znanstveni).
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Disertacije
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Sadržaj objavljen na bib.irb.hr (osim ako je drugačaije navedeno) podložan je pravilima Creative Commons licence
