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Browsing by Project [P3-0326]
Showing results 1 to 12 of 12
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2023 | A novel splice-site FHOD3</i> founder variant is a common cause of hypertrophic cardiomyopathy in the population of the Balkans-A cohort study | Vodnjov, 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 |
| 2024 | A novel splice-site FHOD3 founder variant is a common cause of hypertrophic cardiomyopathy in the population of the Balkans - a cohort study | Vodnjov, 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 |
| 2025 | ACE gene and male infertility: a South Slavic case-control study and multi-omics data integration | Kunej, 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;
| Naučni članak | 22M22 - Međunarodni časopis kategorije M22 |
| 2018 | Association between angiotensin-converting enzyme gene insertion/deletion polymorphism and susceptibility to preterm birth: A case-control study and meta-analysis | Hocevar, Keli; Peterlin, Ana; Mitrovic-Jovanovic, Ana; Bozovic, Aleksandra; Ristanovic, Momcilo; Tul, Natasa; Peterlin, Borut | Naučni članak | 22M22 - Međunarodni časopis kategorije M22 |
| 2025 | Biallelic RFC1 Expansions Are a Rare Cause of Early-Onset and Familial Parkinson's Disease | Kovanda, Anja; Šušmelj, Lara; Jaklič, Helena; Lukežič, Tadeja; Maver, Aleš; Petrović, Igor N. ; Dragašević-Mišković, Nataša T. ; Svetel, Marina V. ; Racki, Valentino; Vuletič, Vladimira;
Novakovič, Ivana V.
; Peterlin, Borut; | Информативни прилог | 22M22 - Међународни часопис категорије M22 |
| 2021 | De novo mutations in idiopathic male infertility-A pilot study | Hodzic, Alenka; Maver, Ales; Plaseska-Karanfilska, Dijana; Ristanovic, Momcilo; Noveski, Predrag; Zorn, Branko; Terzic, Marija; Kunej, Tanja; Peterlin, Borut | Научни чланак | 21aM21a - Водећи међународни часопис категорије M21a |
| 2024 | Genetic testing for monogenic forms of male infertility contributes to the clinical diagnosis of men with idiopathic severe male infertility | Podgrajšek, Rebeka; Hodžić, Alenka; Maver, Aleš; Štimpfel, Martin; Anđelić, Aleksander; Miljanović, Olivera; Ristanović, Momčilo ; Novaković, Ivana V. ; Plaseska-Karanfilska, Dijana; Noveski, Predrag;
Ostojić, Saša; Gršković, Antun; Buretić-Tomljanović, Alena; Peterlin, Borut;
| Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
| 2025 | Genetic Testing for Monogenic Forms of Male Infertility Contributes to the Clinical Diagnosis of Men with Severe Idiopathic Male Infertility | Podgrajsek, 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;
| Naučni članak | 21aM21a - Vodeći međunarodni časopis kategorije M21a |
| 2017 | Genetic variation in leptin and leptin receptor genes as a risk factor for idiopathic male infertility | Hodžić, Alenka; Ristanović, Momčilo ; Zorn, Branko; Tulić, Cane ; Maver, Aleš; Novaković, Ivana V. ; Plašeska-Karanfilska, D.; Peterlin, Borut | Naučni članak | 21M21 - Vodeći međunarodni časopis kategorije M21 |
| 2025 | Increased burden of rare variants in GWAS associated genes in familial multiple sclerosis | Turk, Aleksander; Maver, Aleš; Juvan, Peter; Drulović, Jelena S. ; Mesaroš, Šarlota T. ; Novaković, Ivana V. ; Starčević-Čizmarević, Nada; Ristič, Smiljana; Stanković-Matić, Ivana; Peterlin, Borut | Научни чланак | 21M21 - Водећи међународни часопис категорије M21 |
| 2022 | Maternal LINE-1 DNA Methylation in Early Spontaneous Preterm Birth | Barišić, Anita; Stanković, Aleksandra ; Stojković, Ljiljana ; Pereza, Nina; Ostojić, Saša; Peterlin, Ana; Peterlin, Borut; Vraneković, Jadranka | Article | 21aM21a |
| 2025 | The role of DNA mismatch repair mutS/mutL homolog genes in spermatogenesis and male infertility: a systematic review and cohort study | Podgrajšek, Rebeka; Hodžić, Alenka; Maver, Aleš; Stimpfel, Martin; Anđelić, Aleksander; Miljanović, Olivera; Ristanović, Momčilo ; Novaković, Ivana ; Plašeska-Karanfilska, Dijana; Noveski, Predrag;
Ostojić, Saša; Buretić-Tomljanović, Alena; Peterlin, Borut;
| Reviews | 21aM21a |