Author

Katarina Trebušak Podkrajšek

Observed names: K T Podkrajšek, K Trebušak Podkrajšek, K. Trebusak Podkrajsek, K. Trebušak Podkrajšek, K.T. Podkrajšek, KT Podkrajsek, Katarina Sedej, Katarina T. Podkrajsek, Katarina Trebu??ak-Podkraj??ek, Katarina Trebusak Podkrajsek, Katarina Trebusak-Podkrajsek, Katarina Trebušak-Podkrajšek, Podkrajsek, Katarina Trebusak, Podkrajšek, Katarina Trebušak

Institutions: University of Ljubljana, Ljubljana University Medical Centre

Observed institutions: University of Helsinki, University of Ljubljana, Helsinki University Hospital, Ljubljana University Medical Centre, European Atherosclerosis Society

ORCID: 0000-0002-0154-3547

Observed ORCID: 0000-0002-0154-3547

OpenAlex ID: A5072098806

Chronic mucocutaneous candidiasis in APECED or thymoma patients correlates with autoimmunity to Th17-associated cytokines

2010 · Kai Kisand, Anette S. Bøe Wolff, et al. · The Journal of Experimental Medicine · 677

Global perspective of familial hypercholesterolaemia: a cross-sectional study from the EAS Familial Hypercholesterolaemia Studies Collaboration (FHSC)

2021 · Antonio J. Vallejo-Vaz, Christophe A.T. Stevens, et al. · The Lancet · 314

Preexisting autoantibodies to type I IFNs underlie critical COVID-19 pneumonia in patients with APS-1

2021 · Paul Bastard, Elizaveta Orlova, et al. · The Journal of Experimental Medicine · 299

AIRE-Deficient Patients Harbor Unique High-Affinity Disease-Ameliorating Autoantibodies

2016 · Steffen Meyer, Martin Woodward, et al. · Cell · 292

Universal Screening for Familial Hypercholesterolemia in Children

2015 · Gašper Klančar, Urh Grošelj, et al. · Journal of the American College of Cardiology · 151

Interferon autoantibodies associated with AIRE deficiency decrease the expression of IFN-stimulated genes

2008 · Kai Kisand, Maire Link, et al. · Blood · 129

Universal screening for familial hypercholesterolemia in children: The Slovenian model and literature review

2018 · Urh Groselj, Jernej Kovac, et al. · Atherosclerosis · 117

Pathogenesis of Type 1 Diabetes: Established Facts and New Insights

2022 · Ana Zajec, Katarina Trebušak Podkrajšek, et al. · Genes · 107

Next-Generation Sequencing in Newborn Screening: A Review of Current State

2021 · Ziga I. Remec, Katarina Trebusak Podkrajsek, et al. · Frontiers in Genetics · 86

Familial hypercholesterolaemia in children and adolescents from 48 countries: a cross-sectional study

2023 · Kanika Inamdar Dharmayat, Antonio J. Vallejo-Vaz, et al. · The Lancet · 83

Next generation sequencing as a follow-up test in an expanded newborn screening programme

2017 · Andraz Smon, Barbka Repic Lampret, et al. · Clinical Biochemistry · 63

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

2009 · Tinka Hovnik, Vita Dolžan, et al. · Diabetes Care · 61

Anti-cytokine autoantibodies suggest pathogenetic links with autoimmune regulator deficiency in humans and mice

2012 · J Kärner, A Meager, et al. · Clinical & Experimental Immunology · 58

Autoimmune Regulator-1 Messenger Ribonucleic Acid Analysis in a Novel Intronic Mutation and Two Additional NovelAIREGene Mutations in a Cohort of Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy Patients

2005 · Katarina Trebušak Podkrajšek, Nina Bratanič, et al. · The Journal of Clinical Endocrinology & Metabolism · 56

Telomere Attrition in Neurodegenerative Disorders

2020 · Tina Levstek, Eva Kozjek, et al. · Frontiers in Cellular Neuroscience · 52

Universal screening for familial hypercholesterolemia in 2 populations

2022 · Ursa Sustar, Olga Kordonouri, et al. · Genetics in Medicine · 50

Extracellular Vesicles Derived Human-miRNAs Modulate the Immune System in Type 1 Diabetes

2020 · Tine Tesovnik, Jernej Kovač, et al. · Frontiers in Cell and Developmental Biology · 50

Autoantibody Repertoire in APECED Patients Targets Two Distinct Subgroups of Proteins

2017 · Dmytro Fishman, Kai Kisand, et al. · Frontiers in Immunology · 47

Personalized laboratory medicine: a patient-centered future approach

2018 · Irena Prodan Žitnik, Darko Černe, et al. · Clinical Chemistry and Laboratory Medicine (CCLM) · 42

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

2012 · Urh Groselj, Mojca Zerjav Tansek, et al. · Molecular Genetics and Metabolism · 42

IL‐6‐specific autoantibodies among APECED and thymoma patients

2016 · Jaanika Kärner, Maire Pihlap, et al. · Immunity Inflammation and Disease · 40

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

2008 · Katarina Trebušak Podkrajšek, Tatjana Milenković, et al. · European Journal of Endocrinology · 40

The possible influence of genetic aetiological factors on molar–incisor hypomineralisation

2020 · Luka Hočevar, Jernej Kovač, et al. · Archives of Oral Biology · 39

Biomarkers of Fabry Nephropathy: Review and Future Perspective

2020 · Tina Levstek, Bojan Vujkovac, et al. · Genes · 34

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

2012 · Tinka Hovnik, Nevenka Bratanič, et al. · European Journal of Pediatrics · 34

Works count: 137

Citation count: 3,660

H-index: 29

I10-index: 51