A. Hodžić

Genetic variation in the maternal vitamin D receptor FokI gene as a risk factor for recurrent pregnancy loss

B. Peterlin, A. Hodzic, N. Pereza, 2019, 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.

Diagnostic exome sequencing of syndromic epilepsy patients in clinical practice

B Peterlin, B. Peterlin, A. Maver, 2018, Clinical genetics.

Case Report: Non-ossifying fibromas with pathologic fractures in a patient with NONO-associated X-linked syndromic intellectual developmental disorder

B. Peterlin, A. Maver, A. Hodzic, 2023, Frontiers in genetics.

Genetic variation in the CLOCK gene is associated with idiopathic recurrent spontaneous abortion

B. Peterlin, J. Dotlic, A. Hodzic, 2018, PloS one.

Association of circadian rhythm genes ARNTL/BMAL1 and CLOCK with multiple sclerosis

B. Peterlin, A. Maver, A. Hodzic, 2018, PloS one.

The lack of association between angiotensin‐converting enzyme gene insertion/deletion polymorphism and nicotine dependence in multiple sclerosis

B. Peterlin, A. Hodzic, S. Ristić, 2016, Brain and behavior.

A novel splice-site FHOD3 founder variant is a common cause of hypertrophic cardiomyopathy in the population of the Balkans–A cohort study

A. Maver, O. Miljanović, Helena Jaklič, 2023, PloS one.

The −2549 insertion/deletion polymorphism in the promoter region of the VEGFA gene in couples with idiopathic recurrent spontaneous abortion

B. Peterlin, A. Hodzic, N. Pereza, 2015, Journal of Assisted Reproduction and Genetics.

De novo mutations in idiopathic male infertility—A pilot study

T. Kunej, B. Peterlin, P. Noveski, 2020, Andrology.