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Browsing by Author Hodzic, Alenka

Showing results 1 to 8 of 8
Issue DateTitleAuthor(s)TypeМp-cat.
2023A novel splice-site FHOD3</i> founder variant is a common cause of hypertrophic cardiomyopathy in the population of the Balkans-A cohort studyVodnjov, Nina; Toplisek, Janez; Maver, Ales; Cuturilo, Goran; Jaklic, Helena; Teran, Natasa; Visnjar, Tanja; Skrjanec, Pusenjak Marusa; Hodzic, Alenka; Miljanovic, Olivera;
Peterlin, Borut; Writzl, Karin; Mahdieh, Nejat;
Article
21M21
2024A novel splice-site FHOD3 founder variant is a common cause of hypertrophic cardiomyopathy in the population of the Balkans - a cohort studyVodnjov, Nina; Toplisek, Janez; Maver, Ales; Cuturilo, Goran; Jaklic, Helena; Teran, Natasa; Visnjar, Tanja; Pusenjak, Marusa Skrjanec; Hodzic, Alenka; Miljanovic, Olivera;
Peterlin, Borut; Writzl, Karin;
Conference Paper
Mp. category will be shown later
2025ACE gene and male infertility: a South Slavic case-control study and multi-omics data integrationKunej, Tanja; Podgrajsek, Rebeka; Jaklic, Helena; Hodzic, Alenka; Stimpfel, Martin; Miljanovic, Olivera; Ristanović, Momčilo  ; Novaković, Ivana V.  ; Plaseska-Karanfilska, Dijana; Noveski, Predrag;
Ostojic, Sasa; Buretic-Tomljanovic, Alena; Grskovic, Antun; Peterlin, Borut;
Article
22M22
2018Association of circadian rhythm genes ARNTL/BMAL1 and CLOCK with multiple sclerosisLavtar, Polona; Rudolf, Gorazd; Maver, Ales; Hodzic, Alenka; Čizmarević, Nada Starčević; Živković, Maja  ; Jazbec, Sasa Sega; Ketis, Zalika Klemenc; Kapovic, Miljenko; Dinčić, Evica;
Raicevic, Ranko; Sepcic, Juraj; Lovrecic, Luca; Stanković, Aleksandra  ; Ristic, Smiljana; Peterlin, Borut;
Naučni članak
21M21 - Vodeći međunarodni časopis kategorije M21
2025Clinical application of whole exome sequencing in the diagnosis of men with severely impaired spermatogenesisPodgrajsek, Rebeka; Hodzic, Alenka; Maver, Aleš; Stimpfel, Martin; Andjelic, Aleksander; Miljanovic, Olivera; Ristanović, Momčilo  ; Novaković, Ivana V.  ; Plaseska-Karanfilska, Dijana; Noveski, Predrag;
Ostojic, Sasa; Buretic-Tomljanovic, Alena; Peterlin, Borut;
Конференцијски рад
Мп категорија ће бити приказана накнадно.
2018Comprehensive use of extended exome analysis improves diagnostic yield in rare disease: a retrospective survey in 1,059 casesBergant, Gaber; Maver, Ales; Lovrecic, Luca; Čuturilo, Goran  ; Hodzic, Alenka; Peterlin, BorutНаучни чланак
21a+M21a+ - Водећи међународни часопис категорије M21a+
2021De novo mutations in idiopathic male infertility-A pilot studyHodzic, Alenka; Maver, Ales; Plaseska-Karanfilska, Dijana; Ristanovic, Momcilo; Noveski, Predrag; Zorn, Branko; Terzic, Marija; Kunej, Tanja; Peterlin, BorutНаучни чланак
21aM21a - Водећи међународни часопис категорије M21a
2025Genetic Testing for Monogenic Forms of Male Infertility Contributes to the Clinical Diagnosis of Men with Severe Idiopathic Male InfertilityPodgrajsek, Rebeka; Hodzic, Alenka; Maver, Ales; Stimpfel, Martin; Andjelic, Aleksander; Miljanovic, Olivera; Ristanović, Momčilo  ; Novaković, Ivana  ; Plaseska-Karanfilska, Dijana; Noveski, Predrag;
Ostojic, Sasa; Grskovic, Antun; Buretic-Tomljanovic, Alena; Peterlin, Borut;
Научни чланак
21aM21a - Водећи међународни часопис категорије M21a