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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.