Search Results - "Alenka, Hodžić" :: K.UTB vyhledávací portál | TBU Library Retrieval Portal

A novel splice-site FHOD3 founder variant is a common cause of hypertrophic cardiomyopathy in the population of the Balkans-A cohort study

A novel splice-site FHOD3 founder variant is a common cause of hypertrophic cardiomyopathy in the population of the Balkans-A cohort study

by 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
Published in PloS one (05.12.2023)

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Identification of rare genetic variation of NLRP1 gene in familial multiple sclerosis

Identification of rare genetic variation of NLRP1 gene in familial multiple sclerosis

by 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
Published in Scientific reports (16.06.2017)

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Association of circadian rhythm genes ARNTL/BMAL1 and CLOCK with multiple sclerosis

Association of circadian rhythm genes ARNTL/BMAL1 and CLOCK with multiple sclerosis

by 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
Published in PloS one (11.01.2018)

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Genetic variation in the maternal vitamin D receptor FokI gene as a risk factor for recurrent pregnancy loss

Genetic variation in the maternal vitamin D receptor FokI gene as a risk factor for recurrent pregnancy loss

by Barišić, Anita, Pereza, Nina, Hodžić, Alenka, Krpina, Milena Gašparović, Ostojić, Saša, Peterlin, Borut
Published in The journal of maternal-fetal & neonatal medicine (18.07.2021)

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Transcriptome Profiling Uncovers Potential Common Mechanisms in Fetal Trisomies 18 and 21

Transcriptome Profiling Uncovers Potential Common Mechanisms in Fetal Trisomies 18 and 21

by Volk, Marija, Maver, Aleš, Hodžić, Alenka, Lovrečić, Luca, Peterlin, Borut
Published in Omics (Larchmont, N.Y.) (01.10.2017)

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A Single Nucleotide Polymorphism of DNA methyltransferase 3B gene is a risk factor for recurrent spontaneous abortion

A Single Nucleotide Polymorphism of DNA methyltransferase 3B gene is a risk factor for recurrent spontaneous abortion

by Barišić, Anita, Pereza, Nina, Hodžić, Alenka, Ostojić, Saša, Peterlin, Borut
Published in American journal of reproductive immunology (1989) (01.12.2017)

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Functional single nucleotide polymorphisms of matrix metalloproteinase 7 and 12 genes in idiopathic recurrent spontaneous abortion

Functional single nucleotide polymorphisms of matrix metalloproteinase 7 and 12 genes in idiopathic recurrent spontaneous abortion

by Barišić, Anita, Pereza, Nina, Hodžić, Alenka, Kapović, Miljenko, Peterlin, Borut, Ostojić, Saša
Published in Journal of assisted reproduction and genetics (01.03.2017)

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The −2549 insertion/deletion polymorphism in the promoter region of the VEGFA gene in couples with idiopathic recurrent spontaneous abortion

The −2549 insertion/deletion polymorphism in the promoter region of the VEGFA gene in couples with idiopathic recurrent spontaneous abortion

by Pereza, Nina, Ostojić, Saša, Smirčić, Anamarija, Hodžić, Alenka, Kapović, Miljenko, Peterlin, Borut
Published in Journal of assisted reproduction and genetics (01.12.2015)

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Genetic variation in the CLOCK gene is associated with idiopathic recurrent spontaneous abortion

Genetic variation in the CLOCK gene is associated with idiopathic recurrent spontaneous abortion

by Hodžić, Alenka, Lavtar, Polona, Ristanović, Momčilo, Novaković, Ivana, Dotlić, Jelena, Peterlin, Borut
Published in PloS one (16.05.2018)

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$Case Report: Non-ossifying fibromas with pathologic fractures in a patient with NONO -associated X-linked syndromic intellectual developmental disorder$

Case Report: Non-ossifying fibromas with pathologic fractures in a patient with NONO -associated X-linked syndromic intellectual developmental disorder

by Writzl, Karin, Mavčič, Blaž, Maver, Aleš, Hodžić, Alenka, Peterlin, Borut
Published in Frontiers in genetics (18.07.2023)

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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

Second Case of Gonadal Mosaicism and a Novel Nonsense NR2F1 Gene Variant as the Cause of Bosch-Boonstra-Schaaf Optic Atrophy Syndrome

by Hrvatin, Nenad, Pereza, Nina, Čaljkušić-Mance, Tea, Vučerić, Tamara Mišljenović, Ostojić, Saša, Hodžić, Alenka, Maver, Aleš, Peterlin, Borut
Published in Clinical genetics (30.09.2024)

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Vaginal Microbiome Signature Is Associated With Spontaneous Preterm Delivery

Vaginal Microbiome Signature Is Associated With Spontaneous Preterm Delivery

by Hočevar, Keli, Maver, Aleš, Vidmar Šimic, Marijana, Hodžić, Alenka, Haslberger, Alexander, Premru Seršen, Tanja, Peterlin, Borut
Published in Frontiers in medicine (10.09.2019)

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Loss‐of‐Function Mutations in NR4A2 Cause Dopa‐Responsive Dystonia Parkinsonism

Loss‐of‐Function Mutations in NR4A2 Cause Dopa‐Responsive Dystonia Parkinsonism

by 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
Published in Movement disorders (01.05.2020)

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Phenotype-driven gene target definition in clinical genome-wide sequencing data interpretation

Phenotype-driven gene target definition in clinical genome-wide sequencing data interpretation

by Ales, Maver, Luca, Lovrecic, Marija, Volk, Gorazd, Rudolf, Karin, Writzl, Ana, Blatnik, Alenka, Hodzic, Peterlin, Borut
Published in Genetics in medicine (01.11.2016)

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Transcriptomic signatures for human male infertility

Transcriptomic signatures for human male infertility

by Hodžić, Alenka, Maver, Aleš, Zorn, Branko, Petrovič, Daniel, Kunej, Tanja, Peterlin, Borut
Published in Frontiers in molecular biosciences (21.08.2023)

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De novo mutations in idiopathic male infertility—A pilot study

De novo mutations in idiopathic male infertility—A pilot study

by Hodžić, Alenka, Maver, Aleš, Plaseska‐Karanfilska, Dijana, Ristanović, Momčilo, Noveski, Predrag, Zorn, Branko, Terzic, Marija, Kunej, Tanja, Peterlin, Borut
Published in Andrology (Oxford) (01.01.2021)

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Genetic variation in circadian rhythm genes CLOCK and ARNTL as risk factor for male infertility

Genetic variation in circadian rhythm genes CLOCK and ARNTL as risk factor for male infertility

by Hodžić, Alenka, Ristanović, Momčilo, Zorn, Branko, Tulić, Cane, Maver, Aleš, Novaković, Ivana, Peterlin, Borut
Published in PloS one (18.03.2013)

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Genetic variation in leptin and leptin receptor genes is a risk factor for idiopathic recurrent spontaneous abortion

Genetic variation in leptin and leptin receptor genes is a risk factor for idiopathic recurrent spontaneous abortion

by Müller, Andrijana, Wagner, Jasenka, Hodžić, Alenka, Maver, Aleš, Škrlec, Ivana, Heffer, Marija, Zibar, Lada, Peterlin, Borut
Published in Croatian medical journal (01.12.2016)

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How next-generation sequencing improves care of patients with genetic diseases

How next-generation sequencing improves care of patients with genetic diseases

by Maver, Aleš, Hodžić, Alenka, Bergant, Gaber, Višnjar, Tanja, Peterlin, Borut
Published in Arhiv za higijenu rada i toksikologiju (01.04.2018)

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The lack of association between angiotensin‐converting enzyme gene insertion/deletion polymorphism and nicotine dependence in multiple sclerosis

The lack of association between angiotensin‐converting enzyme gene insertion/deletion polymorphism and nicotine dependence in multiple sclerosis

by Nadalin, Sergej, Buretić‐Tomljanović, Alena, Lavtar, Polona, Starčević Čizmarević, Nada, Hodžić, Alenka, Sepčić, Juraj, Kapović, Miljenko, Peterlin, Borut, Ristić, Smiljana
Published in Brain and behavior (01.01.2017)

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