Tinka Hovnik

Genetic Polymorphisms in Genes Encoding Antioxidant Enzymes Are Associated With Diabetic Retinopathy in Type 1 Diabetes

Tinka Hovnik, Vita Dolžan, Nataša Bratina et al. · Diabetes Care · 2009 · 63 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Five novel mutations and two large deletions in a population analysis of the phenylalanine hydroxylase gene

Urh Grošelj, Mojca Žerjav Tanšek, Jernej Kovač et al. · Molecular Genetics and Metabolism · 2012 · 42 citations

Life Sciences, Genetics, Molecular Genetics +12

Detection of a complete autoimmune regulator gene deletion and two additional novel mutations in a cohort of patients with atypical phenotypic variants of autoimmune polyglandular syndrome type 1

Katarina Trebušak Podkrajšek, Tatjana Milenković, Roelof J. Odink et al. · European Journal of Endocrinology · 2008 · 39 citations

Life Sciences, Genetics, Molecular Genetics +16

Severe progressive obstructive cardiomyopathy and renal tubular dysfunction in Donohue syndrome with decreased insulin receptor autophosphorylation due to a novel INSR mutation

Tinka Hovnik, Nevenka Bratanič, Katarina Trebušak Podkrajšek et al. · European Journal of Pediatrics · 2012 · 34 citations

Medicine, Endocrinology, Molecular Genetics +17

High frequency of pathogenic ACAN variants including an intragenic deletion in selected individuals with short stature

Lana Stavber, Tinka Hovnik, Primož Kotnik et al. · European Journal of Endocrinology · 2020 · 31 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17