COBISS Co-operative Online Bibliographic system & services COBISS
Momčilo Ristanović
Personal bibliography for the period 2013-2025
2013
1.
HODŽIĆ, Alenka, RISTANOVIĆ, Momčilo, ZORN, Branko, TULIĆ, Cane, MAVER, Aleš, NOVAKOVIĆ,
Ivana, PETERLIN, Borut. Genetic variation in circadian rhythm genes CLOCK and ARNTL
as risk factor for male infertility. PloS one. 2013, vol. 8, iss. 3, str. 1-5, ilustr. ISSN 1932-6203. http://www.plosone.org/article/fetchObject.action?uri=info%3Adoi%2F10.1371%2Fjournal.pone.0059220&representation=PDF, DOI: 10.1371/journal.pone.0059220. [COBISS.SI-ID 830892]
2017
2.
HODŽIĆ, Alenka, RISTANOVIĆ, Momčilo, ZORN, Branko, TULIĆ, Cane, MAVER, Aleš, NOVAKOVIĆ,
Ivana, PLAŠESKA KARANFILSKA, Dijana, PETERLIN, Borut. Genetic variation in leptin
and leptin receptor genes as a risk factor for idiopathic male infertility. Andrology. 2017, vol. 5, no. 1, str. 70-74. ISSN 2047-2919. http://onlinelibrary.wiley.com/doi/10.1111/andr.12295/epdf, DOI: 10.1111/andr.12295. [COBISS.SI-ID 4071340]
2018
3.
HOČEVAR, Keli, PETERLIN, Ana Marija, MITROVIĆ-JOVANOVIĆ, Ana, RISTANOVIĆ, Momčilo,
TUL, Nataša, PETERLIN, Borut. Association between angiotensin-converting enzyme gene
insertion/deletion polymorphism and susceptibility to preterm birth : a case-control
study and meta-analysis. European Journal of Obstetrics, Gynecology and Reproductive Biology. [Print ed.]. Dec. 2018, vol. 231, str. 122-128. ISSN 0301-2115. DOI: 10.1016/j.ejogrb.2018.09.019. [COBISS.SI-ID 5216172]
4.
HODŽIĆ, Alenka, LAVTAR, Polona, RISTANOVIĆ, Momčilo, NOVAKOVIĆ, Ivana, DOTLIĆ, Jelena,
PETERLIN, Borut. Genetic variation in the CLOCK gene is associated with idiopathic
recurrent spontaneous abortion. PloS one. 2018, vol. 13, iss. 5, str. e0196345. ISSN 1932-6203. https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0196345&type=printable, DOI: 10.1371/journal.pone.0196345. [COBISS.SI-ID 5891244]
2021
5.
HODŽIĆ, Alenka, MAVER, Aleš, PLAŠESKA KARANFILSKA, Dijana, RISTANOVIĆ, Momčilo, NOVESKI,
P., ZORN, Branko, TERZIĆ, Mira, KUNEJ, Tanja, PETERLIN, Borut. De novo mutations in
idiopathic male infertility : a pilot study. Andrology. 2021, vol. 9, no. 1, str. 212-220. ISSN 2047-2919. https://onlinelibrary.wiley.com/doi/abs/10.1111/andr.12897, DOI: 10.1111/andr.12897. [COBISS.SI-ID 26668547]
2024
6.
PODGRAJŠEK, Rebeka, HODŽIĆ, Alenka, MAVER, Aleš, ŠTIMPFEL, Martin, ANDJELIĆ, Aleksander,
MILJANOVIĆ, Olivera, RISTANOVIĆ, Momčilo, NOVAKOVIĆ, Ivana, PLAŠESKA KARANFILSKA,
Dijana, NOVESKI, Predrag, OSTOJIĆ, Saša, GRŠKOVIĆ, Antun, BURETIĆ-TOMLJANOVIĆ, Alena,
PETERLIN, Borut. Genetic testing for monogenic forms of male infertility contributes
to the clinical diagnosis of men with idiopathic severe male infertility. European journal of human genetics. 2024, vol. 33, suppl. 1, str. 356-357. ISSN 1018-4813. [COBISS.SI-ID 187654659]
7.
PODGRAJŠEK, Rebeka, HODŽIĆ, Alenka, MAVER, Aleš, ŠTIMPFEL, Martin, ANDJELIĆ, Aleksander,
MILJANOVIĆ, Olivera, RISTANOVIĆ, Momčilo, NOVAKOVIĆ, Ivana, PLAŠESKA KARANFILSKA,
Dijana, NOVESKI, Predrag, PETERLIN, Borut, et al. A multicenter cohort study of whole
exome sequencing-based screening for monogenic causes of male infertility in the Balkan
population. In: KRANJC BREZAR, Simona (ed.), ČEMAŽAR, Maja (ed.), MARKELC, Boštjan
(ed.). 10th Congress of the Genetic Society of Slovenia & 10th meeting of the Slovenian Society
for Human Genetics : book of abstracts : September 25th-28th 2024, Faculty of Tourism
Studies - Turistica, Portorož, Slovenia]. 1st ed. Ljubljana: Genetic Society of Slovenia: Slovenian Society of Human Genetics,
2024. Str. 101-102. ISBN 978-961-93545-9-9. https://genetika24.sgd.si/wp-content/uploads/2024/09/Gen24_Book_of_Abstracts_Web.pdf. [COBISS.SI-ID 211839491]
2025
8.
KUNEJ, Tanja, PODGRAJŠEK, Rebeka, JAKLIČ, Helena, HODŽIĆ, Alenka, ŠTIMPFEL, Martin,
MILJANOVIĆ, Olivera, RISTANOVIĆ, Momčilo, NOVAKOVIĆ, Ivana, PLAŠESKA KARANFILSKA,
Dijana, NOVESKI, Predrag, OSTOJIĆ, Saša, BURETIĆ-TOMLJANOVIĆ, Alena, GRŠKOVIĆ, Antun,
PETERLIN, Borut. ACE gene and male infertility : a South Slavic case-control study
and multi-omics data integration. Systems biology in reproductive medicine. 8. 10. 2025, vol. 71, no. 1, str. 524–537, ilustr. ISSN 1939-6376. https://www.tandfonline.com/doi/full/10.1080/19396368.2025.2566747, Repository of the University of Ljubljana – RUL , DiRROS - Digital repository of Slovenian research organizations, DOI: 10.1080/19396368.2025.2566747. [COBISS.SI-ID 252402691]
9.
PODGRAJŠEK, Rebeka, HODŽIĆ, Alenka, MAVER, Aleš, ŠTIMPFEL, Martin, ANDJELIĆ, Aleksander,
MILJANOVIĆ, Olivera, RISTANOVIĆ, Momčilo, NOVAKOVIĆ, Ivana, PLAŠESKA KARANFILSKA,
Dijana, PETERLIN, Borut, et al. Clinical application of whole exome sequencing in
the diagnosis of men with severely impaired spermatogenesis. In: ESHG 2025 : May 24–27, 2025, Milan, Italy. Vienna: European Society of Human Genetics. 2025, 1 spletni vir. https://cattendee.abstractsonline.com/meeting/21105/presentation/3528. [COBISS.SI-ID 243166467]
10.
PODGRAJŠEK, Rebeka, HODŽIĆ, Alenka, MAVER, Aleš, ŠTIMPFEL, Martin, ANDJELIĆ, Aleksander,
MILJANOVIĆ, Olivera, RISTANOVIĆ, Momčilo, NOVAKOVIĆ, Ivana, PLAŠESKA KARANFILSKA,
Dijana, NOVESKI, Predrag, OSTOJIĆ, Saša, PETERLIN, Borut, et al. Genetic testing for
monogenic forms of male infertility contributes to the clinical diagnosis of men with
severe idiopathic male infertility. The world journal of men's health. 2025, vol. 43, no. 4, str. 908-917. ISSN 2287-4690. https://wjmh.org/DOIx.php?id=10.5534/wjmh.240149, DiRROS - Digital repository of Slovenian research organizations, DOI: 10.5534/wjmh.240149. [COBISS.SI-ID 236589059]
11.
PODGRAJŠEK, Rebeka, HODŽIĆ, Alenka, MAVER, Aleš, ŠTIMPFEL, Martin, ANDJELIĆ, Aleksander,
MILJANOVIĆ, Olivera, RISTANOVIĆ, Momčilo, PETERLIN, Borut, et al. The role of DNA
mismatch repair mutS/mutL homolog genes in spermatogenesis and male infertility :
a systematic review and cohort study. Reproductive biology and endocrinology. 2025, vol. 23, [article no.] 149, str. 1-11, ilustr. ISSN 1477-7827. DiRROS - Digital repository of Slovenian research organizations, DOI: 10.1186/s12958-025-01493-x. [COBISS.SI-ID 257890051]
12.
PODGRAJŠEK, Rebeka, HODŽIĆ, Alenka, MAVER, Aleš, ŠTIMPFEL, Martin, ANDJELIĆ, Aleksander,
MILJANOVIĆ, Olivera, RISTANOVIĆ, Momčilo, NOVAKOVIĆ, Ivana, PLAŠESKA KARANFILSKA,
Dijana, NOVESKI, Predrag, PETERLIN, Borut (author, corresponding author), et al. Toward
clinical application of whole-exome sequencing in the diagnosis of men with severely
impaired spermatogenesis. Fertility and sterility. dec. 2025, vol. [v tisku], no. [v tisku], str. 1-6, ilustr. ISSN 1556-5653. https://www.fertstert.org/article/S0015-0282(25)02296-4/abstract, DOI: 10.1016/j.fertnstert.2025.12.009. [COBISS.SI-ID 271621379]
project: P3–0326; funder: Slovenian Research and Innovation Agency (ARIS)
project: P3–0326; funder: Slovenian Research and Innovation Agency (ARIS)