A novel splice-site FHOD3 founder variant is a common cause of hypertrophic cardiomyopathy in the population of the Balkans-A cohort study von Vodnjov, Nina, Toplišek, Janez, Maver, Aleš, Čuturilo, Goran, Jaklič, Helena, Teran, Nataša, Višnjar, Tanja, Škrjanec Pušenjak, Maruša, Hodžić, Alenka, Miljanović, Olivera, Peterlin, Borut, Writzl, Karin

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Identification of rare genetic variation of NLRP1 gene in familial multiple sclerosis von Maver, Ales, Lavtar, Polona, Ristić, Smiljana, Stopinšek, Sanja, Simčič, Saša, Hočevar, Keli, Sepčić, Juraj, Drulović, Jelena, Pekmezović, Tatjana, Novaković, Ivana, Alenka, Hodžić, Rudolf, Gorazd, Šega, Saša, Starčević-Čizmarević, Nada, Palandačić, Anja, Zamolo, Gordana, Kapović, Miljenko, Likar, Tina, Peterlin, Borut

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Association of circadian rhythm genes ARNTL/BMAL1 and CLOCK with multiple sclerosis von Lavtar, Polona, Rudolf, Gorazd, Maver, Aleš, Hodžić, Alenka, Starčević Čizmarević, Nada, Živković, Maja, Šega Jazbec, Saša, Klemenc Ketiš, Zalika, Kapović, Miljenko, Dinčić, Evica, Raičević, Ranko, Sepčić, Juraj, Lovrečić, Luca, Stanković, Aleksandra, Ristić, Smiljana, Peterlin, Borut

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A Single Nucleotide Polymorphism of DNA methyltransferase 3B gene is a risk factor for recurrent spontaneous abortion von Barišić, Anita, Pereza, Nina, Hodžić, Alenka, Ostojić, Saša, Peterlin, Borut

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Transcriptome Profiling Uncovers Potential Common Mechanisms in Fetal Trisomies 18 and 21 von Volk, Marija, Maver, Aleš, Hodžić, Alenka, Lovrečić, Luca, Peterlin, Borut

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Functional single nucleotide polymorphisms of matrix metalloproteinase 7 and 12 genes in idiopathic recurrent spontaneous abortion von Barišić, Anita, Pereza, Nina, Hodžić, Alenka, Kapović, Miljenko, Peterlin, Borut, Ostojić, Saša

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Genetic variation in the CLOCK gene is associated with idiopathic recurrent spontaneous abortion von Hodžić, Alenka, Lavtar, Polona, Ristanović, Momčilo, Novaković, Ivana, Dotlić, Jelena, Peterlin, Borut

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The −2549 insertion/deletion polymorphism in the promoter region of the VEGFA gene in couples with idiopathic recurrent spontaneous abortion von Pereza, Nina, Ostojić, Saša, Smirčić, Anamarija, Hodžić, Alenka, Kapović, Miljenko, 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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Vaginal Microbiome Signature Is Associated With Spontaneous Preterm Delivery von Hočevar, Keli, Maver, Aleš, Vidmar Šimic, Marijana, Hodžić, Alenka, Haslberger, Alexander, Premru Seršen, Tanja, Peterlin, Borut

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Second Case of Gonadal Mosaicism and a Novel Nonsense NR2F1 Gene Variant as the Cause of Bosch–Boonstra–Schaaf Optic Atrophy Syndrome von Hrvatin, Nenad, Pereza, Nina, Čaljkušić‐Mance, Tea, Vučerić, Tamara Mišljenović, Ostojić, Saša, Hodžić, Alenka, Maver, Aleš, Peterlin, Borut

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Transcriptomic signatures for human male infertility von Hodžić, Alenka, Maver, Aleš, Zorn, Branko, Petrovič, Daniel, Kunej, Tanja, Peterlin, Borut

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Loss‐of‐Function Mutations in NR4A2 Cause Dopa‐Responsive Dystonia Parkinsonism von Wirth, Thomas, Mariani, Louise Laure, Bergant, Gaber, Baulac, Michel, Habert, Marie‐Odile, Drouot, Nathalie, Ollivier, Emmanuelle, Hodžić, Alenka, Rudolf, Gorazd, Nitschke, Patrick, Rudolf, Gabrielle, Chelly, Jamel, Tranchant, Christine, Anheim, Mathieu, Roze, Emmanuel

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De novo mutations in idiopathic male infertility—A pilot study von Hodžić, Alenka, Maver, Aleš, Plaseska‐Karanfilska, Dijana, Ristanović, Momčilo, Noveski, Predrag, Zorn, Branko, Terzic, Marija, Kunej, Tanja, Peterlin, Borut

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Genetic variation in circadian rhythm genes CLOCK and ARNTL as risk factor for male infertility von Hodžić, Alenka, Ristanović, Momčilo, Zorn, Branko, Tulić, Cane, Maver, Aleš, Novaković, Ivana, Peterlin, Borut

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Phenotype-driven gene target definition in clinical genome-wide sequencing data interpretation von Ales, Maver, Luca, Lovrecic, Marija, Volk, Gorazd, Rudolf, Karin, Writzl, Ana, Blatnik, Alenka, Hodzic, Peterlin, Borut

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Genetic variation in leptin and leptin receptor genes is a risk factor for idiopathic recurrent spontaneous abortion von Müller, Andrijana, Wagner, Jasenka, Hodžić, Alenka, Maver, Aleš, Škrlec, Ivana, Heffer, Marija, Zibar, Lada, Peterlin, Borut

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How next-generation sequencing improves care of patients with genetic diseases von Maver, Aleš, Hodžić, Alenka, Bergant, Gaber, Višnjar, Tanja, Peterlin, Borut

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A novel splice-site FHOD3 founder variant is a common cause of hypertrophic cardiomyopathy in the population of the Balkans–A cohort study von Nina Vodnjov, Janez Toplišek, Aleš Maver, Goran Čuturilo, Helena Jaklič, Nataša Teran, Tanja Višnjar, Maruša Škrjanec Pušenjak, Alenka Hodžić, Olivera Miljanović, Borut Peterlin, Karin Writzl

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The lack of association between angiotensin‐converting enzyme gene insertion/deletion polymorphism and nicotine dependence in multiple sclerosis von Nadalin, Sergej, Buretić‐Tomljanović, Alena, Lavtar, Polona, Starčević Čizmarević, Nada, Hodžić, Alenka, Sepčić, Juraj, Kapović, Miljenko, Peterlin, Borut, Ristić, Smiljana

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