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Fertility and Sterility|February 16, 2013
Y chromosome azoospermia factor region microdeletions are not associated with idiopathic recurrent spontaneous abortion in a Slovenian population: association study and literature reviewNina Pereza, Ksenija Črnjar, Alena Buretić-Tomljanović, et al.
Croatian Medical Journal|September 4, 2020
Vitamin D receptor polymorphisms in spontaneous preterm birth: a case-control studyMilena Gašparović Krpina, Anita Barišić, Ana Peterlin, et al.
International Journal of Molecular Sciences|October 26, 2024
Protective Effect of <i>EBF Transcription Factor 1</i> (<i>EBF1</i>) Polymorphism in Sporadic and Familial Spontaneous Preterm Birth: Insights from a Case-Control StudyTea Mladenić, Jasenka Wagner, Mirta Kadivnik, et al.
Frontiers in Medicine|March 5, 2025
How to create a faculty development program that transforms medical education according to actual institutional needs: evidence-based approach and experience at the University of Rijeka, Faculty of Medicine, CroatiaNina Pereza, Goran Hauser, Sanja Dević Pavlić, et al.
Disease Markers|December 23, 2014
Functional polymorphisms of matrix metalloproteinases 1 and 9 genes in women with spontaneous preterm birthNina Pereza, Ivana Pleša, Ana Peterlin, et al.
Biological Research for Nursing|November 3, 2021
Maternal LINE-1 DNA Methylation in Early Spontaneous Preterm BirthAnita Barišić, Aleksandra Stanković, Ljiljana Stojković, et al.
American Journal of Medical Genetics. Part A|April 23, 2015
Cornelia de Lange syndrome caused by heterozygous deletions of chromosome 8q24: comments on the article by Pereza et al. [2012]Nina Pereza, Srećko Severinski, Saša Ostojić, et al.
Wiener Klinische Wochenschrift|February 10, 2023
Non-genetic physicians' knowledge, attitudes and behavior towards medical geneticsTea Mladenić, Martina Mavrinac, Sanja Dević Pavlić, et al.
Croatian Medical Journal|March 3, 2020
DNMT3B rs1569686 and rs2424913 gene polymorphisms are associated with positive family history of preterm birth and smoking statusAnita Barišić, Maja Kolak, Ana Peterlin, et al.
American Journal of Medical Genetics. Part A|February 9, 2012
Third case of 8q23.3-q24.13 deletion in a patient with Langer-Giedion syndrome phenotype without TRPS1 gene deletionNina Pereza, Srećko Severinski, Saša Ostojić, et al.
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