Systematic review and meta-analysis of genetic association studies in idiopathic recurrent spontaneous abortion von Pereza, Nina, M.D., Ph.D, Ostojić, Saša, M.D., Ph.D, Kapović, Miljenko, M.D., Ph.D, Peterlin, Borut, M.D., Ph.D

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Assessment of pathogenic variation in gynecologic cancer genes in a national cohort von Kotnik, Urška, Maver, Aleš, Peterlin, Borut, Lovrecic, Luca

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Responsible implementation of expanded carrier screening von Henneman, Lidewij, Borry, Pascal, Chokoshvili, Davit, Cornel, Martina C, van El, Carla G, Forzano, Francesca, Hall, Alison, Howard, Heidi C, Janssens, Sandra, Kayserili, Hülya, Lakeman, Phillis, Lucassen, Anneke, Metcalfe, Sylvia A, Vidmar, Lovro, de Wert, Guido, Dondorp, Wybo J, Peterlin, Borut

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Increasing Genomic Literacy Through National Genomic Projects von Zimani, Ana Nyasha, Peterlin, Borut, Kovanda, Anja

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Identification of women at risk for hereditary breast and ovarian cancer in a sample of 1000 Slovenian women: a comparison of guidelines von Kotnik, Urska, Peterlin, Borut, Lovrecic, Luca

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Mutations in SCN3A cause early infantile epileptic encephalopathy von Zaman, Tariq, Helbig, Ingo, Božović, Ivana Babić, DeBrosse, Suzanne D., Bergqvist, A. Christina, Wallis, Kimberly, Medne, Livija, Maver, Aleš, Peterlin, Borut, Helbig, Katherine L., Zhang, Xiaohong, Goldberg, Ethan M.

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How to design a national genomic project-a systematic review of active projects von Kovanda, Anja, Zimani, Ana Nyasha, Peterlin, Borut

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Recessive DNAH9 Loss-of-Function Mutations Cause Laterality Defects and Subtle Respiratory Ciliary-Beating Defects von Loges, Niki T., Antony, Dinu, Maver, Ales, Deardorff, Matthew A., Güleç, Elif Yýlmaz, Gezdirici, Alper, Nöthe-Menchen, Tabea, Höben, Inga M., Jelten, Lena, Frank, Diana, Werner, Claudius, Tebbe, Johannes, Wu, Kaman, Goldmuntz, Elizabeth, Čuturilo, Goran, Krock, Bryan, Ritter, Alyssa, Hjeij, Rim, Bakey, Zeineb, Pennekamp, Petra, Dworniczak, Bernd, Brunner, Han, Peterlin, Borut, Tanidir, Cansaran, Olbrich, Heike, Omran, Heymut, Schmidts, Miriam

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Improving diagnostics of rare genetic diseases with NGS approaches von Vinkšel, Mateja, Writzl, Karin, Maver, Aleš, Peterlin, Borut

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Analysis of blood-based gene expression in idiopathic Parkinson disease von Shamir, Ron, Amar, David

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Optical genome mapping in an atypical Pelizaeus-Merzbacher prenatal challenge von Rogac, Mihael, Kovanda, Anja, Lovrečić, Luca, Peterlin, Borut

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Nutraceutical Approaches of Autophagy and Neuroinflammation in Alzheimer's Disease: A Systematic Review von Gruendler, Reinhard, Hippe, Berit, Jengic, Vesna Sendula, Peterlin, Borut, Haslberger, Alexander G.

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The Role of microRNAs in Heart Failure: A Systematic Review von Peterlin, Ana, Pocivavsek, Karolina, Petrovic, Danijel, Peterlin, Borut

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Diagnostic outcomes of exome sequencing in patients with syndromic or non-syndromic hearing loss von Likar, Tina, Hasanhodžić, Mensuda, Teran, Nataša, Maver, Aleš, Peterlin, Borut, Writzl, Karin

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Diagnostic yield of exome sequencing in myopathies: Experience of a Slovenian tertiary centre von Bozovic, Ivana Babic, Maver, Ales, Leonardis, Lea, Meznaric, Marija, Osredkar, Damjan, Peterlin, Borut

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A Systematic Review of Parkinson's Disease Pharmacogenomics: Is There Time for Translation into the Clinics? von Vuletic, Vladimira, Racki, Valentino, Papic, Elisa, Peterlin, Borut

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Pharmacogenomics of Multiple Sclerosis: A Systematic Review von Hočevar, Keli, Ristić, Smiljana, Peterlin, Borut

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Family history tools for primary care: A systematic review von Miroševič, Špela, Klemenc-Ketiš, Zalika, Peterlin, Borut

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Case Report: Non-ossifying fibromas with pathologic fractures in a patient with NONO -associated X-linked syndromic intellectual developmental disorder von Writzl, Karin, Mavčič, Blaž, Maver, Aleš, Hodžić, Alenka, Peterlin, Borut

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Editorial: The Importance of Genetic Literacy and Education in Medicine von Pereza, Nina, Peterlin, Borut, Ostojić, Saša, Poslon, Željka

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