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Bibliography of the person, including all types of documents, not only theses.

PhD theses (3)

1. Aleš Maver: Sinteza heterogenih genomskih podatkov pri odkrivanju dednih dejavnikov za multifaktorske bolezni
2. Irena Vrečar: Genomika Parkinsonove bolezni na področju javnega zdravja
3. Alenka Hodžić: Genomic biomarkers for male infertility

BSc theses (1)

1. Larisa Goričan: Polimorfizmi v genih clock and bmal-1 kot dejavniki tveganja za ponavljajoče spontane splave

Other documents (18)

1. Mojca Globočnik Petrovič, Tanja Kunej, Borut Peterlin, Peter Dovč, Danijel Petrovič: Gly482Ser polymorphism of the peroxisome proliferator-activated receptor-gammacoactivator-1 gene might be a risk factor for diabetic retinopathy in Slovene population (Caucasians) with type 2 diabetes and the Pro12Ala polymorphism of the PPARgamma gene is not
2. Maja Potrč, Marija Volk, Matteo de Rosa, Jože Pižem, Nataša Teran, Helena Jaklič, Aleš Maver, Brigita Drnovšek-Olup, Michela Bollati, Katarina Vogelnik Žakelj, Alojzija Hočevar, Ana Gornik, Vladimir Pfeifer, Borut Peterlin, Marko Hawlina, Ana Fakin: Clinical and histopathological features of gelsolin amyloidosis associated with a novel GSN variant p.Glu580Lys
3. Nina Vodnjov, Anja Zupan Mežnar, Aleš Maver, Ajda Dolinšek, Borut Peterlin, Karin Writzl: Non-dilated left ventricular cardiomyopathy with arrhythmias is commonly caused by the nonsense variant DSP:c.3793G>T in Slovenian patients
4. Aleksander Turk, Tanja Kunej, Borut Peterlin: MicroRNA-target interaction regulatory network in Alzheimer’s disease
5. Maja Dolanc Merc, Urška Kotnik, Borut Peterlin, Luca Lovrečić: Further exploration of cardiac channelopathy and cardiomyopathy genes in stillbirth
6. Špela Mikec, Živa Zidar, Borut Peterlin, Simon Horvat, Neža Pogorevc, Tanja Kunej: Syndromic male subfertility
7. Alenka Hodžić, Aleš Maver, Branko Zorn, Danijel Petrovič, Tanja Kunej, Borut Peterlin: Transcriptomic signatures for human male infertility
8. Matija Rijavec, Aleš Maver, Paul J. Turner, Keli Hočevar, Mitja Košnik, Amnah Yamani, Simon P. Hogan, Adnan Custovic, Borut Peterlin, Peter Korošec: Integrative transcriptomic analysis in human and mouse model of anaphylaxis identifies gene signatures associated with cell movement, migration and neuroinflammatory signalling
9. Rebeka Podgrajšek, Alenka Hodžić, Martin Štimpfel, Tanja Kunej, Borut Peterlin: Insight into the complexity of male infertility
10. Maja Dolanc Merc, Borut Peterlin, Luca Lovrečić: The genetic approach to stillbirth
11. Helena Jaklič, Ivana Babić Božović, Borut Peterlin, Anja Kovanda: Streamlined two-step fragment analysis PCR and exome sequencing of RFC1 for diagnostic testing of suspected CANVAS patients
12. Nina Vodnjov, Aleš Maver, Nataša Teran, Borut Peterlin, Janez Toplišek, Karin Writzl: Clinical outcome of hypertrophic cardiomyopathy in probands with the founder variant c.913_914del in in MYBPC3
13. Tanja Kunej, Rebeka Podgrajšek, Helena Jaklič, Alenka Hodžić, Martin Štimpfel, Olivera Miljanović, Momčilo Ristanović, Ivana Novaković, Dijana Plašeska Karanfilska, Predrag Noveski, Saša Ostojić, Alena Buretić-Tomljanović, Antun Gršković, Borut Peterlin: ACE gene and male infertility
14. Borut Peterlin, Ana Marija Peterlin: Carrier screening and pregnancy
15. Aleksander Turk: Redke patološke genetske različice kot dejavniki tveganja za multiplo sklerozo
16. Aleksander Turk, Aleš Maver, Peter Juvan, Jelena Drulović, Sarlota Mesaros, Ivana Novaković, Nada Starčević-Čizmarević, Smiljana Ristić, Ivana Stanković Matić, Borut Peterlin: Increased burden of rare variants in GWAS associated genes in familial multiple sclerosis
17. Marija Volk, Aleš Maver, Martina Jarc-Vidmar, Nuša Trošt, Tanja Višnjar, Ana Fakin, Lea Kovač, Maja Šuštar Habjan, Lucija Malinar, Sanja Petrović Pajić, Urška Dragin Jerman, Rok Romih, Marko Hawlina, Borut Peterlin: Discovery of PHB1 as a novel candidate gene in dominant optic atrophy
18. Gaber Bergant, Vesna M. Van Midden, Polina Tsygankova, Dorian Laslo, Valentino Rački, Dejan Georgiev, Eliša Papić, Marija Branković, Milena Janković, Marina Svetel, Nataša Teran, Natasa Dragasević Misković, Igor N. Petrović, Aleš Maver, Ivana Novaković, Zvezdan Pirtošek, Martin Rakuša, Vladimira Vuletić, Borut Peterlin: Enrichment of rare variants in nuclear-encoded mitochondrial metabolism genes in patients with early-onset or familial parkinson’s disease