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Plos One|January 3, 2018
Diagnostic outcomes of exome sequencing in patients with syndromic or non-syndromic hearing lossTina Likar, Mensuda Hasanhodžić, Nataša Teran, et al.
Fertility and Sterility|March 12, 2013
Genetic variation in tissue inhibitors of metalloproteinases as a risk factor for idiopathic recurrent spontaneous abortionNina Pereza, Marija Volk, Nikolina Zrakić, et al.
Scientific Reports|November 20, 2025
Creating the Slovenian genome database and browser as a source of comprehensive variation of the Slovenian populationAleš Maver, Peter Juvan, Urška Kotnik, et al.
Collegium Antropologicum|January 20, 2009
De novo NEMO gene deletion (delta4-10)--a cause of incontinentia pigmenti in a female infant: a case reportVida Culić, Dragana Gabrić, Neira Puizina-Ivić, et al.
Biomedical Reports|October 20, 2021
Potential protective role of a NOD2 polymorphism in the susceptibility to multiple sclerosis is not associated with interferon therapyAida Zečkanović, Aleš Maver, Smiljana Ristić, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|August 27, 2019
Genetic variation in the maternal vitamin D receptor FokI gene as a risk factor for recurrent pregnancy lossAnita Barišić, Nina Pereza, Alenka Hodžić, et al.
International Journal of Gynaecology and Obstetrics: the Official Organ of the International Federation of Gynaecology and Obstetrics|December 2, 2024
Maternal genetic risk factors for spontaneous preterm birth: A systematic review and meta-analysisTea Mladenić, Anita Barišić, Nina Pereza, et al.
European Journal of Human Genetics : EJHG|February 18, 2025
Towards a patient-centred classification of genetic disease severityMojca Cizek Sajko, Lovro Vidmar, Bernarda Prosenc, et al.
American Journal of Reproductive Immunology (New York, N.Y. : 1989)|October 10, 2007
Polymorphisms in the interleukin-12/18 genes and recurrent spontaneous abortionSasa Ostojić, Marija Volk, Igor Medica, et al.
Clinical Genetics|June 11, 2024
Non-dilated left ventricular cardiomyopathy with arrhythmias is commonly caused by the nonsense variant DSP:c.3793G>T in Slovenian patientsNina Vodnjov, Anja Zupan Mežnar, Aleš Maver, et al.
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