Tinka Hovnik

Ljubljana, Slovenia

Last Updated: 09/26/2026

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Found 22 publications

Persistent Sex Differences in Cardiovascular Disease Risk Factors: A Longitudinal Cohort Study in Youth With Type 1 Diabetes.

Persistent Sex Differences in Cardiovascular Disease Risk Factors: A Longitudinal Cohort Study in Youth With Type 1 Diabetes.

Journal: American journal of preventive medicine

Published: November 25, 2025

A Comprehensive Genetic Analysis of Slovenian Families with Multiple Cases of Orofacial Clefts Reveals Novel Variants in the Genes IRF6, GRHL3, and TBX22.

A Comprehensive Genetic Analysis of Slovenian Families with Multiple Cases of Orofacial Clefts Reveals Novel Variants in the Genes IRF6, GRHL3, and TBX22.

Journal: International journal of molecular sciences

Published: November 25, 2022

Heterozygous NPR2 Variants in Idiopathic Short Stature.

Heterozygous NPR2 Variants in Idiopathic Short Stature.

Journal: Genes

Published: May 14, 2022

Early Discovery of Children With Lysosomal Acid Lipase Deficiency With the Universal Familial Hypercholesterolemia Screening Program.

Early Discovery of Children With Lysosomal Acid Lipase Deficiency With the Universal Familial Hypercholesterolemia Screening Program.

Journal: Frontiers in genetics

Published: May 04, 2022

An Adolescent Boy with Klinefelter Syndrome and 47,XXY/46,XX Mosaicism: Case Report and Review of Literature.

An Adolescent Boy with Klinefelter Syndrome and 47,XXY/46,XX Mosaicism: Case Report and Review of Literature.

Journal: Genes

Published: March 31, 2022

Genetic Variability in Slovenian Cohort of Patients with Oculocutaneous Albinism.

Genetic Variability in Slovenian Cohort of Patients with Oculocutaneous Albinism.

Journal: Acta chimica Slovenica

Published: December 13, 2021

Detection of Del/Dup Inside SHOX/PAR1 Region in Children and Young Adults with Idiopathic Short Stature.

Detection of Del/Dup Inside SHOX/PAR1 Region in Children and Young Adults with Idiopathic Short Stature.

Journal: Genes

Published: August 31, 2021

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

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

Journal: European journal of endocrinology

Published: September 27, 2019

Dual Role of PTPN22 but Not NLRP3 Inflammasome Polymorphisms in Type 1 Diabetes and Celiac Disease in Children.

Dual Role of PTPN22 but Not NLRP3 Inflammasome Polymorphisms in Type 1 Diabetes and Celiac Disease in Children.

Journal: Frontiers in pediatrics

Published: November 07, 2018

Association of Glycemic Control and Cell Stress With Telomere Attrition in Type 1 Diabetes.

Association of Glycemic Control and Cell Stress With Telomere Attrition in Type 1 Diabetes.

Journal: JAMA pediatrics

Published: June 23, 2018

Metabolic control, ApoE genotypes, and dyslipidemia in children, adolescents and young adults with type 1 diabetes.

Metabolic control, ApoE genotypes, and dyslipidemia in children, adolescents and young adults with type 1 diabetes.

Journal: Atherosclerosis

Published: February 12, 2018

Characterization of a de novo sSMC 17 detected in a girl with developmental delay and dysmorphic features.

Characterization of a de novo sSMC 17 detected in a girl with developmental delay and dysmorphic features.

Journal: Molecular cytogenetics

Published: January 13, 2017

Showing 1-12 of 22

Last Updated: 09/26/2026