Rus RR, Ključevšek T, Kojc N.

Vascular Malformation in the Kidney as a Cause of Severe Hypertension in an Infant.

Indian J Pediatr. 2020 Sep; 87(9):762-763.

Stergar J, Dolenec R, Kojc N, Lakota K, Perše M, Tomšič M, Milanic M.

Hyperspectral evaluation of peritoneal fibrosis in mouse models. Biomed Opt Express.

2020 Mar 13; 11 (4): 1991-2006.

Borštnar Š, Večerić-Haler Ž, Boštjančič E, Pipan Tkalec Ž, Kovač D, Lindič J, Kojc N.

Uromodulin and microRNAs in Kidney Transplantation-Association with Kidney Graft Function.

Int J Mol Sci. 2020 Aug 5; 21 (16): 5592.

Kebe Radulović M, Melkić E, Grčar Kuzmanov B, Cimerman D, Strojan Fležar M.

Erythroblastic sarcoma presenting as a unilateral pleural effusion in a patient with myelodysplastic syndrome/myeloproliferative neoplasm-Case report with cytologic and histologic findings.

Diagn Cytopathol. 2020 Dec;48(12):E18-E21.

Kebe Radulović M, Vivoda Tomšič M, Cimerman D, Gutnik H, Strojan Fležar M.

A novel combined animal tissue model for freehand and ultrasound-guided fine needle aspiration biopsy and smear preparation techniques training.

Diagn Cytopathol. 2021 Jan;49(1):39-45.

Jensterle M, Lezaic L, Jeruc J, Janez A.

Periprostatic paraganglioma causing occult Cushing’s syndrome.

Endocrine. 2020 Aug;69(2):461-463.

Zupančič D, Korać-Prlić J, Kreft ME, Franković L, Vilović K, Jeruc J, Romih R, Terzić J.

Vitamin A Rich Diet Diminishes Early Urothelial Carcinogenesis by Altering Retinoic Acid Signaling.

Cancers (Basel). 2020 Jun 28;12(7):1712.

Cokan KB, Urlep Ž, Lorbek G, Matz-Soja M, Skubic C, Perše M, Jeruc J, Juvan P, Režen T, Rozman D.

Chronic Disruption of the Late Cholesterol Synthesis Leads to Female-Prevalent Liver Cancer.

Cancers (Basel). 2020 Nov 9;12(11):3302.

Khan M, Cornelis SS, Pozo-Valero MD, Whelan L, Runhart EH, Mishra K, Bults F, AlSwaiti Y, AlTalbishi A, De Baere E, Banfi S, Banin E, Bauwens M, Ben-Yosef T, Boon CJF, van den Born LI, Defoort S, Devos A, Dockery A, Dudakova L, Fakin A, Glavač D, et al.

Resolving the dark matter of ABCA4 for 1054 Stargardt disease probands through integrated genomics and transcriptomics.

Genetics in Medicine 2020; 22: 1235-1246

Sajovic J, Meglič A, Šuštar M, Jarc-Vidmar M, Cremers F, Khan M, Allikmets R, Glavač D, Maver A, Volk M, Peterlin B, Hawlina M, Fakin A, et al.

Phenotypic characterization of Stargardt disease cases carrying the frequent ABCA4 mutation c.5714 1 5G[ A (p.[= ,Glu1863Leufs*33]) using electrophysiology.

Documenta Ophthalmologica 2020; 1:13.