Glavač D, Jarc-Vidmar M, Vrabec K, Ravnik-Glavač M, Fakin A, Hawlina M.

Clinical and genetic heterogeneity in Slovenian patients with BEST disease Acta Ophthalmol.

2016 Dec;94(8):e786-e794. doi: 10.1111/aos.13202.

Bonnet C, Riahi Z, Chantot-Bastaraud S, Smagghe L, Letexier M, Marcaillou C, Lefèvre GM, Hardelin JP, El-Amraoui A, Singh-Estivalet A, Mohand-Saïd S, Kohl S, Kurtenbach A, Sliesoraityte I, Zobor D, Gherbi S, Testa F, Simonelli F, Banfi S, Fakin A, Glavač D, Jarc-Vidmar M, Zupan A, Battelino S, Martorell Sampol L, Claveria MA, Catala Mora J, Dad S, Møller LB, Rodriguez Jorge J, Hawlina M, Auricchio A, Sahel JA, Marlin S, Zrenner E, Audo I, Petit C.

An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients.

Eur J Hum Genet. 2016 Dec;24(12):1730-1738. doi: 10.1038/ejhg.2016.99.

Zupan A, Hauptman N, Glavač D.

The maternal perspective for five Slovenian regions: The importance of regional sampling.

Ann Hum Biol. 2016;43(1):57-66. doi: 10.3109/03014460.2015.1006678.

Zidar N, Boštjančič E, Jerala M, Kojc N, Drobne D, Štabuc B, Glavač D.

Down-regulation of microRNAs of the miR-200 family and upregulation of Snail and Slug in inflammatory bowel diseases – hallmark of epithelial-mesenchymal transition.

J Cell Mol Med. 2016; 20 (10): 1813–20.