Katarina Trebušak Podkrajšek (Katarina Trebusak Podkrajsek)

Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 27

Top Venues

Genes

Antioxidants (Basel, Switzerland)

International journal of molecular sciences

Medicina (Kaunas, Lithuania)

University of Ljubljana, Faculty of Medicine

This page only lists publications with an associated author ORCID identifier.

Affiliation History

University of Ljubljana, Faculty of Medicine

Slovenia

Associate professor :: Institute od Biochemistry

Publications

Sabina Ugovšek, Andreja Rehberger Likozar, Tina Levstek, Katarina Trebušak Podkrajšek, Janja Zupan, Miran Šebeštjen
Haplotype of the Lipoprotein(a) Gene Variants rs10455872 and rs3798220 Is Associated with Parameters of Coagulation, Fibrinolysis, and Inflammation in Patients after Myocardial Infarction and Highly Elevated Lipoprotein(a) Values. International journal of molecular sciences 25 (2) (2024)
Tina Levstek, Nika Breznik, Bojan Vujkovac, Albina Nowak, Katarina Trebušak Podkrajšek
Dynamics of Leukocyte Telomere Length in Patients with Fabry Disease. Biomedicines 12 (8) (2024)
Sabina Ugovšek, Andreja Rehberger Likozar, Tina Levstek, Katarina Trebušak Podkrajšek, Janja Zupan, Miran Šebeštjen
Haplotype of the Lipoprotein(a) Gene Variants rs10455872 and rs3798220 Is Associated with Parameters of Coagulation, Fibrinolysis, and Inflammation in Patients after Myocardial Infarction and Highly Elevated Lipoprotein(a) Values. International journal of molecular sciences 25 (2) (2024)
Tina Levstek, Nika Breznik, Bojan Vujkovac, Albina Nowak, Katarina Trebušak Podkrajšek
Dynamics of Leukocyte Telomere Length in Patients with Fabry Disease. Biomedicines 12 (8) (2024)
Sabina Ugovšek, Andreja Rehberger Likozar, Tina Levstek, Katarina Trebušak Podkrajšek, Janja Zupan, Miran Šebeštjen
Haplotype of the Lipoprotein(a) Gene Variants rs10455872 and rs3798220 Is Associated with Parameters of Coagulation, Fibrinolysis, and Inflammation in Patients after Myocardial Infarction and Highly Elevated Lipoprotein(a) Values. International journal of molecular sciences 25 (2) (2024)
Tina Levstek, Tina Karun, Andreja Rehberger Likozar, Miran Šebeštjen, Katarina Trebušak Podkrajšek
Interplay between microRNAs, Serum Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9), and Lipid Parameters in Patients with Very High Lipoprotein(a) Treated with PCSK9 Inhibitors. Genes 14 (3) (2023)
Laurence Jonard, Davide Brotto, Miguel Angel Moreno-Pelayo, Ignacio Del Castillo, Hannie Kremer, Ronald J E Pennings, Helena Caria, Graça Fialho, An Boudewyns, Guy Van Camp, Monika Ołdak, Dominika Oziębło, Naïma Deggouj, Romolo Daniele De Siati, Paolo Gasparini, Giorgia Girotto, Margriet Verstreken, Silvia Dossena, Sebastian Roesch, Saba Battelino, Katarina Trebušak Podkrajšek, Athanasia Warnecke, Thomas Lenarz, Anke Lesinski-Schiedat, Michel Mondain, Anne-Françoise Roux, Françoise Denoyelle, Natalie Loundon, Margaux Serey-Gaut, Patrizia Trevisi, Elisa Rubinato, Alessandro Martini, Sandrine Marlin
Genetic Evaluation of Prelingual Hearing Impairment: Recommendations of an European Network for Genetic Hearing Impairment. Audiology research 13 (3) (2023)
Tina Levstek, Katarina Trebušak Podkrajšek
Telomere Attrition in Chronic Kidney Diseases. Antioxidants (Basel, Switzerland) 12 (3) (2023)
Tina Levstek, Katarina Trebušak Podkrajšek
Telomere Attrition in Chronic Kidney Diseases. Antioxidants (Basel, Switzerland) 12 (3) (2023)
Tina Levstek, Tina Karun, Andreja Rehberger Likozar, Miran Šebeštjen, Katarina Trebušak Podkrajšek
Interplay between microRNAs, Serum Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9), and Lipid Parameters in Patients with Very High Lipoprotein(a) Treated with PCSK9 Inhibitors. Genes 14 (3) (2023)
Tina Levstek, Tina Karun, Andreja Rehberger Likozar, Miran Šebeštjen, Katarina Trebušak Podkrajšek
Interplay between microRNAs, Serum Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9), and Lipid Parameters in Patients with Very High Lipoprotein(a) Treated with PCSK9 Inhibitors. Genes 14 (3) (2023)
Katarina Trebušak Podkrajšek, Primož Kotnik
Special Issue "Genetics and Epigenetics in Endocrine Disorders". Genes 14 (9) (2023)
Tina Leban, Katarina Trebušak Podkrajšek, Jernej Kovac, Ales Fidler, Alenka Pavlič
An Intron c.103-3T>C Variant of the AMELX Gene Causes Combined Hypomineralized and Hypoplastic Type of Amelogenesis Imperfecta: Case Series and Review of the Literature . Genes 13 (7) (2022)
Barbara Čugalj Kern, Katarina Trebušak Podkrajšek, Jernej Kovac, Robert Šket, Barbara Jenko Bizjan, Tine Tesovnik, Maruša Debeljak, Tadej Battelino, Nataša Bratina
The Role of Epigenetic Modifications in Late Complications in Type 1 Diabetes. Genes 13 (4) (2022)
Tina Levstek, Nik Podkrajšek, Andreja Rehberger Likozar, Miran Šebeštjen, Katarina Trebušak Podkrajšek
The Influence of Treatment with PCSK9 Inhibitors and Variants in the CRP (rs1800947), TNFA (rs1800629), and IL6 (rs1800795) Genes on the Corresponding Inflammatory Markers in Patients with Very High Lipoprotein(a) Levels. Journal of cardiovascular development and disease 9 (5) (2022)
Tjasa Krasovec, Jaka Šikonja, Mojca Tanšek Žerjav, Marusa Debeljak, Sasa Ilovar, Katarina Trebušak Podkrajšek, Sara Bertok, Tine Tesovnik, Jernej Kovac, Jasna Suput Omladic, Michaela Friederike Hartmann, Stefan A Wudy, Magdalena Avbelj Stefanija, Tadej Battelino, Primoz Kotnik, Urh Groselj
Long-Term Follow-Up of Three Family Members with a Novel NNT Pathogenic Variant Causing Primary Adrenal Insufficiency. Genes 13 (5) (2022)
Ana Zajec, Katarina Trebušak Podkrajšek, Tine Tesovnik, Robert Šket, Barbara Čugalj Kern, Barbara Jenko Bizjan, Darja Šmigoc Schweiger, Tadej Battelino, Jernej Kovac
Pathogenesis of Type 1 Diabetes: Established Facts and New Insights. Genes 13 (4) (2022)
Samar S Hassan, Mohamed Abdullah, Katarina Trebušak Podkrajšek, Salwa Musa, Areej Ibrahim, Omer Babiker, Jernej Kovac, Tadej Battelino, Magdalena Avbelj Stefanija
A Novel Splice-Site Deletion in the POU1F1 Gene Causes Combined Pituitary Hormone Deficiency in Multiple Sudanese Pedigrees. Genes 13 (4) (2022)
Katarina Trebušak Podkrajšek, Tine Tesovnik, Nina Bozanic Urbancic, Saba Battelino
Novel GRHL2 Gene Variant Associated with Hearing Loss: A Case Report and Review of the Literature. Genes 12 (4) (2021)
Tina Levstek, Teo Mlinšek, Marija Holcar, Katja Goričar, Metka Lenassi, Vita Dolzan, Bojan Vujkovac, Katarina Trebušak Podkrajšek
Urinary Extracellular Vesicles and Their miRNA Cargo in Patients with Fabry Nephropathy. Genes 12 (7) (2021)
Tina Levstek, Sara Redenšek, Maja Trošt, Vita Dolzan, Katarina Trebušak Podkrajšek
Assessment of the Telomere Length and Its Effect on the Symptomatology of Parkinson's Disease. Antioxidants (Basel, Switzerland) 10 (1) (2021)
Jera Stritar, Lana Stavber, Maja Ficko, Primož Kotnik, Tadej Battelino, Katarina Trebušak Podkrajšek, Tinka Hovnik
Detection of Del/Dup Inside SHOX/PAR1 Region in Children and Young Adults with Idiopathic Short Stature. Genes 12 (10) (2021)
Jasna Suput Omladic, Maja Pajek, Urh Groselj, Katarina Trebušak Podkrajšek, Magdalena Avbelj Stefanija, Mojca Zerjav Tansek, Primoz Kotnik, Tadej Battelino, Darja Smigoc Schweiger
Central TSH Dysregulation in a Patient with Familial Non-Autoimmune Autosomal Dominant Hyperthyroidism Due to a Novel Thyroid-Stimulating Hormone Receptor Disease-Causing Variant. Medicina (Kaunas, Lithuania) 57 (3) (2021)
Andreja Rehberger Likozar, Ales Blinc, Katarina Trebušak Podkrajšek, Miran Šebeštjen
LPA Genotypes and Haplotypes Are Associated with Lipoprotein(a) Levels but Not Arterial Wall Properties in Stable Post-Coronary Event Patients with Very High Lipoprotein(a) Levels. Journal of cardiovascular development and disease 8 (12) (2021)
Nina Božanić Urbančič, Saba Battelino, Tine Tesovnik, Katarina Trebušak Podkrajšek
The Importance of Early Genetic Diagnostics of Hearing Loss in Children. Medicina (Kaunas, Lithuania) 56 (9) (2020)
Tina Levstek, Bojan Vujkovac, Katarina Trebušak Podkrajšek
Biomarkers of Fabry Nephropathy: Review and Future Perspective. Genes 11 (9) (2020)
Maja Pajek, Magdalena Avbelj Stefanija, Katarina Trebušak Podkrajšek, Jasna Suput Omladic, Mojca Zerjav Tansek, Tadej Battelino, Urh Groselj
Hypercholesterolemia in Two Siblings with Resistance to Thyroid Hormones Due to Disease-Causing Variant in Thyroid Hormone Receptor (THRB) Gene. Medicina (Kaunas, Lithuania) 56 (12) (2020)

Katarina Trebušak Podkrajšek.css-eqlu8i{font-size:small;padding-left:4px;} (Katarina Trebusak Podkrajsek)

Publication Activity (10 Years)

Top Topics

Top Venues

Katarina Trebušak Podkrajšek (Katarina Trebusak Podkrajsek)