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Universal Screening for Familial Hypercholesterolemia in Children

Journal of the American College of Cardiology, 2015-09, Vol.66 (11), p.1250-1257

2015

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Contribution of Retrotransposons to the Pathogenesis of Type 1 Diabetes and Challenges in Analysis Methods

International journal of molecular sciences, 2023-02, Vol.24 (4), p.3104

2023

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Pathogenesis of Type 1 Diabetes: Established Facts and New Insights

Genes, 2022-04, Vol.13 (4), p.706

2022

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PAX5 Alterations in a Consecutive Childhood B-Cell Acute Lymphoblastic Leukemia Cohort Treated Using the ALL IC-BFM 2009 Protocol

Cancers, 2024-03, Vol.16 (6), p.1164

2024

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The Role of Epigenetic Modifications in Late Complications in Type 1 Diabetes

Genes, 2022-04, Vol.13 (4), p.705

2022

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Mnenja o izobraževanju starejših oseb na kulturno-umetniškem področju

AS. Andragoška spoznanja, 2021-04, Vol.27 (1), p.139-151

2021

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Clinical and genetic characteristics of a patient with phosphoribosyl pyrophosphate synthetase 1 deficiency and a systematic literature review

Molecular genetics and metabolism reports, 2023-09, Vol.36, p.100986, Article 100986

2023

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Integrative Transcriptomic Profiling of the Wilms Tumor

Cancers, 2023-07, Vol.15 (15), p.3846

2023

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Challenges in identifying large germline structural variants for clinical use by long read sequencing

Computational and structural biotechnology journal, 2020-01, Vol.18, p.83-92

2020

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

Frontiers in cell and developmental biology, 2020-03, Vol.8, p.202-202

2020

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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, 2022-07, Vol.13 (7), p.1272

2022

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Heterozygous NPR2 Variants in Idiopathic Short Stature

Genes, 2022-06, Vol.13 (6), p.1065

2022

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PRESEJALNO TESTIRANJE NOVOROJENČKOV ZA VROJENE BOLEZNI V SLOVENIJI

Slovenska pediatrija, 2024-05, Vol.31 (2), p.77-84

2024

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Focused peptide library screening as a route to a superior affinity ligand for antibody purification

Scientific reports, 2021-06, Vol.11 (1), p.11650-11650, Article 11650

2021

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Relevant Weight Reduction and Reversed Metabolic Co-morbidities Can Be Achieved by Duodenojejunal Bypass Liner in Adolescents with Morbid Obesity

Obesity surgery, 2020-03, Vol.30 (3), p.1001-1010

2020

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

Archives of oral biology, 2020-10, Vol.118, p.104848-104848, Article 104848

2020

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Long Way to the 2014 Istanbul Convention: Its Role and Significance

The person and the challenges : the journal of theology, education, canon law, and social studies inspired by Pope John Paul II, 2023-01, Vol.13 (2), p.247-263

2023

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Five years of NGS in a diagnostic setup: experience from the Unit of Special Laboratory Diagnostics at the University Children's Hospital in Ljubljana

Arhiv za higijenu rada i toksikologiju, 2018-04, Vol.69 (2), p.A19-A19

Kovač, Jernej

2018

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

Atherosclerosis, 2018-10, Vol.277, p.383-391

2018

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Exploring early DNA methylation alterations in type 1 diabetes: implications of glycemic control

Frontiers in endocrinology (Lausanne), 2024-06, Vol.15, p.1416433

2024

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Does intervention with GLP-1 receptor agonist semaglutide modulate perception of sweet taste in women with obesity: study protocol of a randomized, single-blinded, placebo-controlled clinical trial

Trials, 2021-07, Vol.22 (1), p.464-464, Article 464

2021

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Heterozygous Genetic Variants in Autosomal Recessive Genes of the Leptin-Melanocortin Signalling Pathway Are Associated With the Development of Childhood Obesity

Frontiers in endocrinology (Lausanne), 2022-04, Vol.13, p.832911-832911

2022

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Multifocal gastric adenocarcinoma in a patient with LRBA deficiency

Orphanet journal of rare diseases, 2017-07, Vol.12 (1), p.131-131, Article 131

2017

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

Frontiers in genetics, 2021-05, Vol.12, p.662254-662254

2021

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Association between one’s attachment to parents and subsequent attachment to a partner

The person and the challenges : the journal of theology, education, canon law, and social studies inspired by Pope John Paul II, 2021-01, Vol.11 (1), p.183-199

2021

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Universal Screening for Familial Hypercholesterolemia in Children

Contribution of Retrotransposons to the Pathogenesis of Type 1 Diabetes and Challenges in Analysis Methods

Pathogenesis of Type 1 Diabetes: Established Facts and New Insights

PAX5 Alterations in a Consecutive Childhood B-Cell Acute Lymphoblastic Leukemia Cohort Treated Using the ALL IC-BFM 2009 Protocol

The Role of Epigenetic Modifications in Late Complications in Type 1 Diabetes

Mnenja o izobraževanju starejših oseb na kulturno-umetniškem področju

Clinical and genetic characteristics of a patient with phosphoribosyl pyrophosphate synthetase 1 deficiency and a systematic literature review

Integrative Transcriptomic Profiling of the Wilms Tumor

Challenges in identifying large germline structural variants for clinical use by long read sequencing

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

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

Heterozygous NPR2 Variants in Idiopathic Short Stature

PRESEJALNO TESTIRANJE NOVOROJENČKOV ZA VROJENE BOLEZNI V SLOVENIJI

Focused peptide library screening as a route to a superior affinity ligand for antibody purification

Relevant Weight Reduction and Reversed Metabolic Co-morbidities Can Be Achieved by Duodenojejunal Bypass Liner in Adolescents with Morbid Obesity

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

Long Way to the 2014 Istanbul Convention: Its Role and Significance

Five years of NGS in a diagnostic setup: experience from the Unit of Special Laboratory Diagnostics at the University Children's Hospital in Ljubljana

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

Exploring early DNA methylation alterations in type 1 diabetes: implications of glycemic control

Does intervention with GLP-1 receptor agonist semaglutide modulate perception of sweet taste in women with obesity: study protocol of a randomized, single-blinded, placebo-controlled clinical trial

Heterozygous Genetic Variants in Autosomal Recessive Genes of the Leptin-Melanocortin Signalling Pathway Are Associated With the Development of Childhood Obesity

Multifocal gastric adenocarcinoma in a patient with LRBA deficiency

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

Association between one’s attachment to parents and subsequent attachment to a partner

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