Borut Peterlin

Study of Three Single Nucleotide Polymorphisms in the SLC6A14 Gene in Association with Male Infertility

B. Peterlin, P. Noveski, T. Plaseski, 2014, Balkan journal of medical genetics : BJMG.

Solving patients with rare diseases through programmatic reanalysis of genome-phenome data

Pieter B. T. Neerincx, Spencer J. Gibson, Farid Yavari Dizjikan, 2021, European Journal of Human Genetics.

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.

Genetic Variation in Osteopontin Gene Is Associated with Susceptibility to Sarcoidosis in Slovenian Population

B. Peterlin, A. Maver, I. Medica, 2010, Disease markers.

Exclusive breastfeeding may be a protective factor in individuals with familial multiple sclerosis. A population registry-based case-control study.

J. Ivanovic, S. Mesaros, N. Veselinović, 2023, Multiple sclerosis and related disorders.

De novo mutations in idiopathic male infertility—A pilot study

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