1. Focused peptide library screening as a route to a superior affinity ligand for antibody purificationKrištof Bozovičar, Barbara Jenko Bizjan, Anže Meden, Jernej Kovač, Tomaž Bratkovič, 2021, original scientific article Keywords: biochemistry, biophysics, biotechnology, chemical biology
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2. Clinical and genetic characteristics of two patients with tyrosinemia type 1 in Slovenia – a novel fumarylacetoacetate hydrolase (FAH) intronic disease-causing variantJaka Šikonja, Jernej Brecelj, Mojca Žerjav-Tanšek, Barbka Repič-Lampret, Ana Drole Torkar, Simona Klemenčič, Neža Lipovec, Valentina Stefanova Kralj, Sara Bertok, Jernej Kovač, Barbara Faganel Kotnik, Markéta Tesařová, Žiga Iztok Remec, Maruša Debeljak, Tadej Battelino, Urh Grošelj, 2022, original scientific article Keywords: tyrosinemia, fumarylacetoacetate hydrolase, nitisinone, dried blood spot, succinylacetone, intronic variant
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3. The possible influence of genetic aetiological factors on molar–incisor hypomineralisationLuka Hočevar, Jernej Kovač, Katarina Trebušak Podkrajšek, Saba Battelino, Alenka Pavlič, 2020, original scientific article Keywords: molar–incisor hypomineralisation, aetiology, single nucleotide polymorphism
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4. Association of glycemic control and cell stress with telomere attrition in type 1 diabetesTine Tesovnik, Jernej Kovač, Tinka Hovnik, Klemen Dovč, Nataša Bratina, Tadej Battelino, Katarina Trebušak Podkrajšek, 2018, other scientific articles Keywords: hyperglycemia, abnormal blood glucose level, oxidative stress, type 1 diabetes
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5. Dataset on amelogenesis-related genes variants (ENAM and ENAM interacting genes) and on human leukocyte antigen alleles (DQ2 and DQ8) distribution in children with and without molar–incisor hypomineralisation (MIH)Luka Hočevar, Jernej Kovač, Katarina Trebušak Podkrajšek, Saba Battelino, Alenka Pavlič, 2020, original scientific article Keywords: amelogenesis, molar–incisor hypomineralisation, MIH, genes variants, aetiology, human leukocyte antigen, amelogenesis-related genes, single nucleotide polymorphism
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6. Clinical and genetic characteristics of a patient with phosphoribosyl pyrophosphate synthetase 1 deficiency and a systematic literature reviewKatarina Štajer, Neja Kovač, Jaka Šikonja, Matej Mlinarič, Sara Bertok, Jernej Brecelj, Maruša Debeljak, Jernej Kovač, Gašper Markelj, David Neubauer, Rina Rus, Mojca Žerjav-Tanšek, Ana Drole Torkar, Aleksandra Zver, Tadej Battelino, Rosa Jiménez Torres, Urh Grošelj, 2023, review article Keywords: phosphoribosyl pyrophosphate synthetase 1, PRPS1, PRS-I super-activity, PRS-I deficiency, Arts syndrome, X-linked Charcot-Marie-Tooth neuropathy type 5
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7. Evaluation of body mass index, overweight and obesity status, and cholesterol levels in younger childrenUrša Šuštar, Olga Kordonouri, Stefan Arens, Jernej Kovač, Katarina Sedej, Tadej Battelino, Urh Grošelj, 2023, other scientific articles Keywords: children, overweight, obesity, cholesterol
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